From 7540546200614d7d5f950cb3219cf53b4d311891 Mon Sep 17 00:00:00 2001 From: Ashwini More Date: Thu, 17 Sep 2026 11:51:46 -0400 Subject: [PATCH 1/2] test: add automated response-time performance checks for listing load, edit, and save --- ...formance-baselines.postman_collection.json | 201 ++++++++++++++++++ .../data/certifiedproductids-test-data.json | 7 + chpl/chpl-api/e2e/script/newman-run.js | 25 +++ 3 files changed, 233 insertions(+) create mode 100644 chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json create mode 100644 chpl/chpl-api/e2e/data/certifiedproductids-test-data.json diff --git a/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json b/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json new file mode 100644 index 0000000000..fed62d2a73 --- /dev/null +++ b/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json @@ -0,0 +1,201 @@ +{ + "info": { + "name": "listing-performance-baselines", + "schema": "https://schema.getpostman.com/json/collection/v2.1.0/collection.json" + }, + "item": [ + { + "name": "Listing performance tests - GET iterates Certified Product IDs", + "item": [ + { + "name": "GET /rest/certified_products/{certifiedProductId}/details - test listing details load time", + "event": [ + { + "listen": "prerequest", + "script": { + "type": "text/javascript", + "exec": [ + "const certifiedProductId= pm.iterationData.get(\"certifiedProductId\");\r\npm.environment.set(\"certifiedProductId\",\"certifiedProductId\");" + ] + } + }, + { + "listen": "test", + "script": { + "type": "text/javascript", + "exec": [ + "const actualSeconds = pm.response.responseTime / 1000;\r\nconst tolerance = parseFloat(pm.environment.get(\"tolerancePercent\"));\r\n\r\nconst baselineSeconds = parseFloat(pm.environment.get(\"baselineSeconds_getDetails\"));\r\nconst maxAllowedSeconds = baselineSeconds * (1 + tolerance);\r\n\r\npm.test(\"Status code is 200\", function () {\r\n pm.response.to.have.status(200);\r\n});\r\n\r\npm.test(`GET details response time (${actualSeconds.toFixed(2)}s) is within ${tolerance * 100}% of the baseline (${baselineSeconds}s) — max allowed ${maxAllowedSeconds.toFixed(2)}s`, function () {\r\n pm.expect(actualSeconds).to.be.below(maxAllowedSeconds);\r\n});\r\n\r\nconsole.log(`[GET details] certifiedProductId=${pm.iterationData.get(\"certifiedProductId\")} actual=${actualSeconds.toFixed(2)}s baseline=${baselineSeconds}s maxAllowed=${maxAllowedSeconds.toFixed(2)}s`);" + ] + } + } + ], + "request": { + "method": "GET", + "header": [ + { + "key": "API-Key", + "value": "{{apiKey}}" + }, + { + "key": "Content-Type", + "value": "application/json" + } + ], + "url": { + "raw": "{{url}}/rest/certified_products/{{certifiedProductId}}/details", + "host": [ + "{{url}}" + ], + "path": [ + "rest", + "certified_products", + "{{certifiedProductId}}", + "details" + ] + } + }, + "response": [] + } + ] + }, + { + "name": "Listing performance tests - PUT uses specific Certified Product IDs", + "item": [ + { + "name": "PUT /rest/certified_products/ {certifiedProductId} - test listing-edit-save performance", + "event": [ + { + "listen": "prerequest", + "script": { + "type": "text/javascript", + "exec": [ + "var ReqBody= {\r\n userName:pm.environment.get(\"emailADMIN\"),password:pm.environment.get(\"passwordADMIN\")\r\n };\r\npm.sendRequest({\r\n url: pm.environment.get(\"authurl\"),\r\n method: \"POST\",\r\n header: {\r\n \"Content-Type\": \"application/json\",\r\n \"API-KEY\": pm.environment.get(\"apiKey\")\r\n },\r\n body: JSON.stringify(ReqBody)\r\n}, function (err, response) {\r\n var jsonData = response.json();\r\n pm.environment.set(\"token\",jsonData[pm.environment.get(\"authTokenField\")])\r\n});" + ] + } + }, + { + "listen": "test", + "script": { + "type": "text/javascript", + "exec": [ + "const actualSeconds = pm.response.responseTime / 1000;\r\nconst tolerance = parseFloat(pm.environment.get(\"tolerancePercent\"));\r\n\r\nconst baselineSeconds = parseFloat(pm.environment.get(\"baselineSeconds_putUpdate\"));\r\nconst maxAllowedSeconds = baselineSeconds * (1 + tolerance);\r\n\r\npm.test(\"Status code is 200\", function () {\r\n pm.response.to.have.status(200);\r\n});\r\n\r\npm.test(`GET details response time (${actualSeconds.toFixed(2)}s) is within ${tolerance * 100}% of the baseline (${baselineSeconds}s) — max allowed ${maxAllowedSeconds.toFixed(2)}s`, function () {\r\n pm.expect(actualSeconds).to.be.below(maxAllowedSeconds);\r\n});\r\n\r\nconsole.log(`[PUT update] certifiedProductId= ${10727} actual=${actualSeconds.toFixed(2)}s baseline=${baselineSeconds}s maxAllowed=${maxAllowedSeconds.toFixed(2)}s`);" + ] + } + } + ], + "request": { + "auth": { + "type": "bearer", + "bearer": [ + { + "key": "token", + "value": "{{token}}", + "type": "string" + } + ] + }, + "method": "PUT", + "header": [ + { + "key": "Content-Type", + "value": "application/json" + }, + { + "key": "API-KEY", + "value": "{{apiKey}}" + } + ], + "body": { + "mode": "raw", + "raw": "{\"listing\":{\"acbCertificationId\":\"15.02.05.1167.BRNT.01.01.1.211119\",\"accessibilityCertified\":true,\"accessibilityStandards\":[{\"accessibilityStandardId\":39,\"accessibilityStandardName\":\"ISO/IEC 40500\",\"id\":1732}],\"businessErrorMessages\":[],\"certificationDate\":1637280000000,\"certificationDay\":\"2021-11-19\",\"certificationEvents\":[{\"eventDay\":\"2021-11-19\",\"id\":25211,\"lastModifiedDate\":null,\"lastModifiedUser\":null,\"reason\":null,\"status\":{\"id\":1,\"name\":\"Active\"}}],\"certificationResults\":[{\"additionalSoftware\":[{\"certificationResultId\":605964,\"certifiedProductId\":null,\"certifiedProductNumber\":null,\"grouping\":null,\"id\":21976,\"justification\":null,\"name\":\"Dr 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Filter\"},\"id\":62208}],\"description\":\"The percentage of children who turned 6 months of age during the measurement year, who had a face-to-face visit between the clinician and the child during child's first 6 months, and who had a maternal depression screening for the mother at least once between 0 and 6 months of life\",\"domain\":\"Community/Population Health\",\"id\":304805,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Maternal Depression Screening\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\",\"v16\"],\"cmsId\":\"CMS90\",\"cqmCriterionId\":657,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":62235},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":62232},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":79278},{\"certificationId\":28,\"certificationNumber\":\"170.315 (c)(4)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-filter\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":28,\"number\":\"170.315 (c)(4)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Filter\"},\"id\":62233}],\"description\":\"Percentage of patients 18 years of age and older with congestive heart failure who completed initial and follow-up patient-reported functional status assessments\",\"domain\":\"Person and Caregiver-Centered Experience and Outcome\",\"id\":304811,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v7\"],\"title\":\"Functional Status Assessments for Congestive Heart Failure\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v2\",\"v1\",\"v3\",\"v4\"],\"cmsId\":\"CMS1028\",\"cqmCriterionId\":1278,\"criteria\":[],\"description\":\"Patients with severe obstetric complications which occur during the inpatient delivery hospitalization.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Severe Obstetric Complications\",\"typeId\":2},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1264\",\"cqmCriterionId\":1295,\"criteria\":[],\"description\":\"This measure assesses the proportion of ED encounters for patients who experience at least one emergency care access or timeliness gap. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (REHQR)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS826\",\"cqmCriterionId\":1285,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients aged 18 and older who suffer the harm of developing a new stage 2, stage 3, stage 4, deep tissue, or unstageable pressure injury\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3498e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Pressure Injury\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v11\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS72\",\"cqmCriterionId\":1267,\"criteria\":[],\"description\":\"Ischemic stroke patients administered antithrombotic therapy by the end of hospital day 2\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Antithrombotic Therapy By End of Hospital Day 2\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS73\",\"cqmCriterionId\":609,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received an overlap of parenteral (intravenous [IV] or subcutaneous [subcu]) anticoagulation and warfarin therapy. For patients who received less than five days of overlap therapy, they should be discharged on both medications or have a reason for discontinuation of overlap therapy. Overlap therapy should be administered for at least five days with an international normalized ratio (INR) greater than or equal to 2 prior to discontinuation of the parenteral anticoagulation therapy, discharged on both medications or have a reason for discontinuation of overlap therapy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0373\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients with Anticoagulation Overlap Therapy\",\"typeId\":2},{\"allVersions\":[\"v16\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS74\",\"cqmCriterionId\":1230,\"criteria\":[],\"description\":\"Percentage of children, age 0-20 years, who received a fluoride varnish application during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Primary Caries Prevention Intervention as Offered by Primary Care Providers, including Dentists\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS75\",\"cqmCriterionId\":1231,\"criteria\":[],\"description\":\"Percentage of children, age 0-20 years, who have had tooth decay or cavities during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Children Who Have Dental Decay or Cavities\",\"typeId\":1},{\"allVersions\":[\"v13\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\"],\"cmsId\":\"CMS147\",\"cqmCriterionId\":1053,\"criteria\":[],\"description\":\"Percentage of patients aged 6 months and older seen for a visit between October 1 and March 31 who received an influenza immunization OR who reported previous receipt of an influenza immunization\",\"domain\":null,\"id\":null,\"nqfNumber\":\"41\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Influenza Immunization\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS148\",\"cqmCriterionId\":560,\"criteria\":[],\"description\":\"Percentage of patients 5-17 years of age with diabetes with a Hemoglobin A1c (HbA1c) test during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"365\",\"success\":false,\"successVersions\":[],\"title\":\"Hemoglobin A1c Test for Pediatric Patients\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS149\",\"cqmCriterionId\":1251,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of dementia for whom an assessment of cognition is performed and the results reviewed at least once within a 12 month period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"2872\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Dementia: Cognitive Assessment\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS71\",\"cqmCriterionId\":1266,\"criteria\":[],\"description\":\"Ischemic stroke patients with atrial fibrillation/flutter who are prescribed or continuing to take anticoagulation therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Anticoagulation Therapy for Atrial Fibrillation/Flutter\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS140\",\"cqmCriterionId\":573,\"criteria\":[],\"description\":\"Percentage of female patients aged 18 years and older with Stage I (T1b) through IIIC, ER or PR positive breast cancer who were prescribed tamoxifen or aromatase inhibitor (AI) during the 12-month reporting period \",\"domain\":null,\"id\":null,\"nqfNumber\":\"0387\",\"number\":\"071\",\"success\":false,\"successVersions\":[],\"title\":\"Breast Cancer: Hormonal Therapy for Stage I (T1b)-IIIC Estrogen Receptor/ Progesterone Receptor (ER/PR) Positive Breast Cancer\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS77\",\"cqmCriterionId\":594,\"criteria\":[],\"description\":\"Percentage of patients aged 13 years and older with a diagnosis of HIV/AIDS, with at least two visits during the measurement year, with at least 90 days between each visit, whose most recent HIV RNA level is <200 copies/mL.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A \",\"number\":\"381\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: RNA control for Patients with HIV\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS141\",\"cqmCriterionId\":623,\"criteria\":[],\"description\":\"Percentage of patients aged 18 through 80 years with AJCC Stage III colon cancer who are referred for adjuvant chemotherapy, prescribed adjuvant chemotherapy, or have previously received adjuvant chemotherapy within the 12-month reporting period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0385\",\"number\":\"072\",\"success\":false,\"successVersions\":[],\"title\":\"Colon Cancer: Chemotherapy for AJCC Stage III Colon Cancer Patients\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS142\",\"cqmCriterionId\":1247,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed with documented communication to the physician who manages the ongoing care of the patient with diabetes mellitus regarding the findings of the macular or fundus exam at least once within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"89\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Communication with the Physician Managing Ongoing Diabetes Care\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS143\",\"cqmCriterionId\":1248,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of primary open-angle glaucoma (POAG) who have an optic nerve head evaluation during one or more office visits within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"86\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Primary Open-Angle Glaucoma (POAG): Optic Nerve Evaluation\",\"typeId\":1},{\"allVersions\":[\"v3\",\"v1\",\"v2\"],\"cmsId\":\"CMS1157\",\"cqmCriterionId\":1284,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of Human Immunodeficiency Virus (HIV) during the first 240 days of the measurement period or before the measurement period who had at least two eligible encounters or at least one eligible encounter and one HIV viral load test that were at least 90 days apart within the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV Annual Retention in Care\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v1\"],\"cmsId\":\"CMS1154\",\"cqmCriterionId\":1291,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS816\",\"cqmCriterionId\":1276,\"criteria\":[],\"description\":\"Inpatient hospitalizations for patients 18 years of age or older at admission, who were administered at least one hypoglycemic medication during the encounter, who suffer the harm of a severe hypoglycemic event during the encounter\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3503e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Severe Hypoglycemia\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS9\",\"cqmCriterionId\":1007,\"criteria\":[],\"description\":\"Exclusive breast milk feeding during the newborn's entire hospitalization\",\"domain\":null,\"id\":null,\"nqfNumber\":\"480\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Exclusive Breast Milk Feeding\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS819\",\"cqmCriterionId\":1281,\"criteria\":[],\"description\":\"This measure assesses the number of inpatient hospitalizations for patients age 18 and older who have been administered an opioid medication and are subsequently administered an opioid antagonist within 12 hours, an indication of an opioid-related adverse event\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3501e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Opioid-Related Adverse Events\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS133\",\"cqmCriterionId\":1241,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of uncomplicated cataract who had cataract surgery and no significant ocular conditions impacting the visual outcome of surgery and had best-corrected visual acuity of 20/40 or better (distance or near) achieved within 90 days following the cataract surgery\",\"domain\":null,\"id\":null,\"nqfNumber\":\"565\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cataracts: 20/40 or Better Visual Acuity within 90 Days Following Cataract Surgery\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS771\",\"cqmCriterionId\":1265,\"criteria\":[],\"description\":\"Percentage of patients with an office visit within the measurement period and with a new diagnosis of clinically significant Benign Prostatic Hyperplasia who have International Prostate Symptoms Score (IPSS) or American Urological Association (AUA) Symptom Index (SI) documented at time of diagnosis and again 6-12 months later with an improvement of 3 points\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"International Prostate Symptom Score (IPSS) or American Urological Association-Symptom Index (AUA-SI) Change 6-12 Months After Diagnosis of Benign Prostatic Hyperplasia\",\"typeId\":1},{\"allVersions\":[\"v11\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS134\",\"cqmCriterionId\":979,\"criteria\":[],\"description\":\"The percentage of patients 18-75 years of age with diabetes who had a nephropathy screening test or evidence of nephropathy during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"62\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetes: Medical Attention for Nephropathy\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS136\",\"cqmCriterionId\":1243,\"criteria\":[],\"description\":\"Percentage of children 6-12 years of age and newly dispensed a medication for attention-deficit/hyperactivity disorder (ADHD) who had appropriate follow-up care. Two rates are reported: a. Percentage of children who had one follow-up visit with a practitioner with prescribing authority during the 30-Day Initiation Phase.; b. Percentage of children who remained on ADHD medication for at least 210 days and who, in addition to the visit in the Initiation Phase, had at least two additional follow-up visits with a practitioner within 270 days (9 months) after the Initiation Phase ended.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"108\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Follow-Up Care for Children Prescribed ADHD Medication (ADD)\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS138\",\"cqmCriterionId\":1245,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older who were screened for tobacco use one or more times within 24 months AND who received tobacco cessation intervention if identified as a tobacco user. Three rates are reported: a. Percentage of patients aged 18 years and older who were screened for tobacco use one or more times within 24 months; b. Percentage of patients aged 18 years and older who were screened for tobacco use and identified as a tobacco user who received tobacco cessation intervention; c. Percentage of patients aged 18 years and older who were screened for tobacco use one or more times within 24 months AND who received tobacco cessation intervention if identified as a tobacco user\",\"domain\":null,\"id\":null,\"nqfNumber\":\"28\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Tobacco Use: Screening and Cessation Intervention\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS132\",\"cqmCriterionId\":867,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of uncomplicated cataract who had cataract surgery and had any of a specified list of surgical procedures in the 30 days following cataract surgery which would indicate the occurrence of any of the following major complications: retained nuclear fragments, endophthalmitis, dislocated or wrong power IOL, retinal detachment, or wound dehiscence\",\"domain\":null,\"id\":null,\"nqfNumber\":\"564\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cataracts: Complications within 30 Days Following Cataract Surgery Requiring Additional Surgical Procedures\",\"typeId\":1},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1244\",\"cqmCriterionId\":1293,\"criteria\":[],\"description\":\"This measure assesses the proportion of ED encounters for patients who experience at least one emergency care access or timeliness gap. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR)\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS50\",\"cqmCriterionId\":1226,\"criteria\":[],\"description\":\"Percentage of patients with referrals, regardless of age, for which the referring provider receives a report from the provider to whom the patient was referred\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Closing the Referral Loop: Receipt of Specialist Report\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS167\",\"cqmCriterionId\":772,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed which included documentation of the level of severity of retinopathy and the presence or absence of macular edema during one or more office visits within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"88\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Documentation of Presence or Absence of Macular Edema and Level of Severity of Retinopathy\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v3\",\"v0\",\"v1\",\"v2\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS52\",\"cqmCriterionId\":843,\"criteria\":[],\"description\":\"Percentage of patients aged 6 weeks and older with a diagnosis of HIV/AIDS who were prescribed Pneumocystis jiroveci pneumonia (PCP) prophylaxis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"405\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Pneumocystis Jiroveci Pneumonia (PCP) Prophylaxis\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS169\",\"cqmCriterionId\":773,\"criteria\":[],\"description\":\"Percentage of patients with depression or bipolar disorder with evidence of an initial assessment that includes an appraisal for alcohol or chemical substance use\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Bipolar Disorder and Major Depression: Appraisal for alcohol or chemical substance use\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS53\",\"cqmCriterionId\":716,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving primary PCI during the hospital stay with a time from hospital arrival to PCI of 90 minutes or less\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Primary PCI Received Within 90 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS844\",\"cqmCriterionId\":1273,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWM outcome measure. It is designed to extract the first resulted set of vital signs and basic laboratory results obtained from encounters for adult Medicare Fee-For-Service patients admitted to acute care short stay hospitals.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3502\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Core Clinical Data Elements for the Hybrid Hospital-Wide (All-Condition, All-Procedure) Risk-Standardized Mortality Measure (HWM)\",\"typeId\":2},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS160\",\"cqmCriterionId\":888,\"criteria\":[],\"description\":\"The percentage of patients age 18 and older with the diagnosis of major depression or dysthymia who have a completed PHQ-9 during each applicable 4 month period in which there was a qualifying visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"712\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Depression Utilization of the PHQ-9 Tool\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v1\",\"v2\",\"v0\",\"v3\",\"v4\"],\"cmsId\":\"CMS163\",\"cqmCriterionId\":584,\"criteria\":[],\"description\":\"Percentage of patients 18-75 years of age with diabetes whose LDL-C was adequately controlled (<100 mg/dL) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"002\",\"success\":false,\"successVersions\":[],\"title\":\"Diabetes: Low Density Lipoprotein (LDL-C) Control (< 100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS55\",\"cqmCriterionId\":717,\"criteria\":[],\"description\":\"Median time from emergency department arrival to time of departure from the emergency room for patients admitted to the facility from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"495\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Admitted ED Patients\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS56\",\"cqmCriterionId\":1227,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who received an elective primary total hip arthroplasty (THA) and completed a functional status assessment within 90 days prior to the surgery and in the 270-365 days after the surgery\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Functional Status Assessment for Total Hip Replacement\",\"typeId\":1},{\"allVersions\":[\"v3\",\"v2\"],\"cmsId\":\"CMS1017\",\"cqmCriterionId\":1289,\"criteria\":[],\"description\":\"This ratio measure assesses the number of inpatient hospitalizations where at least one fall with a major or moderate injury occurs among the total qualifying inpatient hospital days for patients age 18 years and older\",\"domain\":null,\"id\":null,\"nqfNumber\":\"4120e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Falls with Injury\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1154FHIR\",\"cqmCriterionId\":1296,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS61\",\"cqmCriterionId\":626,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years whose risk factors have been assessed and a fasting LDL-C test has been performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Cholesterol - Fasting Low Density Lipoprotein (LDL-C) Test Performed\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS156\",\"cqmCriterionId\":1255,\"criteria\":[],\"description\":\"Percentage of patients 65 years of age and older who were ordered high-risk medications. Two rates are reported: a. Percentage of patients who were ordered at least one high-risk medication.; b. Percentage of patients who were ordered at least two of the same high-risk medications.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"22\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Use of High-Risk Medications in the Elderly\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS62\",\"cqmCriterionId\":586,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of HIV/AIDS with at least two medical visits during the measurement year with a minimum of 90 days between each visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"368\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Medical Visit\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS157\",\"cqmCriterionId\":1256,\"criteria\":[],\"description\":\"Percentage of patient visits, regardless of patient age, with a diagnosis of cancer currently receiving chemotherapy or radiation therapy in which pain intensity is quantified\",\"domain\":null,\"id\":null,\"nqfNumber\":\"384\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Oncology: Medical and Radiation - Pain Intensity Quantified\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS158\",\"cqmCriterionId\":766,\"criteria\":[],\"description\":\"This measure identifies pregnant women who had a HBsAg (hepatitis B) test during their pregnancy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Pregnant women that had HBsAg testing\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS64\",\"cqmCriterionId\":627,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years who had a fasting LDL-C test performed and whose risk stratified fasting LDL-C is at or below the recommended LDL-C goal.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Risk-Stratified Cholesterol -Fasting Low Density Lipoprotein (LDL-C)\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS159\",\"cqmCriterionId\":1257,\"criteria\":[],\"description\":\"The percentage of patients 18 years of age or older with major depression or dysthymia who reached remission 12 months (+/- 30 days) after an index visit.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"710\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Depression Remission at Twelve Months\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS951\",\"cqmCriterionId\":1274,\"criteria\":[],\"description\":\"Percentage of patients aged 18-75 years with a diagnosis of diabetes who received a kidney health evaluation defined by an Estimated Glomerular Filtration Rate (eGFR) AND Urine Albumin-Creatinine Ratio (uACR) within the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Kidney Health Evaluation\",\"typeId\":2},{\"allVersions\":[\"v4\",\"v1\",\"v2\",\"v3\"],\"cmsId\":\"CMS314\",\"cqmCriterionId\":1260,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, diagnosed with HIV prior to or during the first 90 days of the measurement period, with an eligible encounter in the first 240 days of the measurement period, whose last HIV viral load test result was less than 200 copies/mL during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV Viral Suppression\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS832\",\"cqmCriterionId\":1286,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients age 18 and older who have an acute kidney injury (stage 2 or greater) that occurred during the encounter. Acute kidney injury (AKI) stage 2 or greater is defined as a substantial increase in serum creatinine value, or by the initiation of kidney dialysis (continuous renal replacement therapy (CRRT), hemodialysis or peritoneal dialysis).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3713e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Acute Kidney Injury\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS60\",\"cqmCriterionId\":606,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving fibrinolytic therapy during the hospital stay and having a time from hospital arrival to fibrinolysis of 30 minutes or less.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Fibrinolytic Therapy Received Within 30 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS65\",\"cqmCriterionId\":719,\"criteria\":[],\"description\":\"Percentage of patients aged 18-85 years of age with a diagnosis of hypertension whose blood pressure improved during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hypertension: Improvement in Blood Pressure\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS154\",\"cqmCriterionId\":1253,\"criteria\":[],\"description\":\"Percentage of children 3 months-18 years of age who were diagnosed with upper respiratory infection (URI) and were not dispensed an antibiotic prescription on or three days after the episode\",\"domain\":null,\"id\":null,\"nqfNumber\":\"69\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Appropriate Treatment for Children with Upper Respiratory Infection (URI)\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v6\",\"v5\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS68\",\"cqmCriterionId\":1228,\"criteria\":[],\"description\":\"Percentage of visits for patients aged 18 years and older for which the eligible professional or eligible clinician attests to documenting a list of current medications using all immediate resources available on the date of the encounter. This list must include ALL known prescriptions, over-the-counters, herbals, and vitamin/mineral/dietary (nutritional) supplements AND must contain the medications' name, dosage, frequency and route of administration.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"419\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Documentation of Current Medications in the Medical Record\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v1\",\"v2\",\"v3\"],\"cmsId\":\"CMS1188\",\"cqmCriterionId\":1280,\"criteria\":[],\"description\":\"Percentage of patients 13 years of age and older with a diagnosis of HIV who had tests for syphilis, gonorrhea, and chlamydia performed within the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Sexually Transmitted Infection (STI) Testing for People with HIV\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS190\",\"cqmCriterionId\":1270,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after the initial admission (or transfer) to the Intensive Care Unit (ICU) or surgery end date for surgeries that start the day of or the day after ICU admission (or transfer)\",\"domain\":null,\"id\":null,\"nqfNumber\":\"372\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Intensive Care Unit Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS108\",\"cqmCriterionId\":1269,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after hospital admission or surgery end date for surgeries that start the day of or the day after hospital admission\",\"domain\":null,\"id\":null,\"nqfNumber\":\"371\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS109\",\"cqmCriterionId\":620,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received intravenous (IV) UFH therapy dosages AND had their platelet counts monitored using defined parameters such as a nomogram or protocol.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients Receiving Unfractionated Heparin with Dosages/Platelet Count Monitoring by Protocol or Nomogram\",\"typeId\":2},{\"allVersions\":[\"v9\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS506\",\"cqmCriterionId\":1271,\"criteria\":[],\"description\":\"Proportion of inpatient hospitalizations for patients 18 years of age and older prescribed, or continued on, two or more opioids or an opioid and benxodiazepine concurrently at discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3316\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Safe Use of Opioids- Concurrent Prescribing\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS100\",\"cqmCriterionId\":604,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients prescribed aspirin at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0142\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Aspirin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS188\",\"cqmCriterionId\":629,\"criteria\":[],\"description\":\"(PN-6) Immunocompetent patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 1) Immunocompetent ICU patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 2) Immunocompetent non-Intensive Care Unit (ICU) patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0147\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Initial Antibiotic Selection for Community-Acquired Pneumonia (CAP) in Immunocompetent Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v0\",\"v5\",\"v6\"],\"cmsId\":\"CMS102\",\"cqmCriterionId\":729,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients who were assessed for rehabilitation services\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Assessed for Rehabilitation\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS30\",\"cqmCriterionId\":636,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients who are prescribed a statin medication at hospital discharge.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Statin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS31\",\"cqmCriterionId\":712,\"criteria\":[],\"description\":\"This measure assesses the proportion of births that have been screened for hearing loss before hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"1354\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hearing Screening Prior To Hospital Discharge\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v1\",\"v0\",\"v2\",\"v3\",\"v4\",\"v11\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS104\",\"cqmCriterionId\":1268,\"criteria\":[],\"description\":\"Ischemic stroke patients prescribed or continuing to take antithrombotic therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Antithrombotic Therapy\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS105\",\"cqmCriterionId\":1011,\"criteria\":[],\"description\":\"Ischemic stroke patients who are prescribed or continuing to take statin medication at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Statin Medication\",\"typeId\":2},{\"allVersions\":[\"v10\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\"],\"cmsId\":\"CMS347\",\"cqmCriterionId\":1261,\"criteria\":[],\"description\":\"Percentage of the following patients - all considered at high risk of cardiovascular events - who were prescribed or were on statin therapy during the measurement period: Adults aged >= 21 years who were previously diagnosed with or currently have an active diagnosis of clinical atherosclerotic cardiovascular disease (ASCVD); OR Adults aged >= 21 years who have ever had a fasting or direct low-density lipoprotein cholesterol (LDL-C) level >= 190 mg/dL or were previously diagnosed with or currently have an active diagnosis of familial or pure hypercholesterolemia; OR Adults aged 40-75 years with a diagnosis of diabetes with a fasting or direct LDL-C level of 70-189 mg/dL\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Statin Therapy for the Prevention and Treatment of Cardiovascular Disease\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v2\",\"v4\",\"v5\"],\"cmsId\":\"CMS986\",\"cqmCriterionId\":1282,\"criteria\":[],\"description\":\"This measure assesses the percentage of hospitalizations for adults aged 65 years and older at the start of the inpatient encounter during the measurement period with a length of stay equal to or greater than 24 hours who received optimal malnutrition care during the current inpatient hospitalization where care performed was appropriate to the patient's level of malnutrition risk and severity. Malnutrition care best practices recommend that for each hospitalization, adult inpatients are screened for malnutrition risk, assessed to confirm findings of malnutrition risk or for a hospital dietitian referral order, and if identified with a \\\"moderate\\\" or \\\"severe\\\" malnutrition status in the current performed malnutrition assessment, receive a current \\\"moderate\\\" or \\\"severe\\\" malnutrition diagnosis and have a current nutrition care plan performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3592e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Global Malnutrition Composite Score\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS107\",\"cqmCriterionId\":732,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients or their caregivers who were given educational materials during the hospital stay addressing all of the following: activation of emergency medical system, need for follow-up after discharge, medications prescribed at discharge, risk factors for stroke, and warning signs and symptoms of stroke\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Stroke Education\",\"typeId\":2},{\"allVersions\":[\"v9\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS349\",\"cqmCriterionId\":1262,\"criteria\":[],\"description\":\"Percentage of patients 15-65 years of age who have been tested for HIV within that age range\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV Screening\",\"typeId\":1},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1244FHIR\",\"cqmCriterionId\":1292,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support hospital quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR) FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS182\",\"cqmCriterionId\":602,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had a diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had a complete lipid profile performed during the measurement period and whose most recent Low-density Lipoprotein (LDL-C) was adequately controlled (< 100 mg/dL).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"241\",\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Complete Lipid Panel and LDL-C Control (<100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS32\",\"cqmCriterionId\":713,\"criteria\":[],\"description\":\"Median elapsed time from emergency department arrival to emergency room departure for patients discharged from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"496\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Discharged ED Patients\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS185\",\"cqmCriterionId\":618,\"criteria\":[],\"description\":\"Percent of term singleton live births (excluding those with diagnoses originating in the fetal period) who DO NOT have significant complications during birth or the nursery care\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0716\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Healthy Term Newborn\",\"typeId\":2},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS1074\",\"cqmCriterionId\":1287,\"criteria\":[],\"description\":\"This measure provides a standardized method for monitoring the performance of diagnostic CT to discourage unnecessarily high radiation doses, a risk factor for cancer, while preserving image quality. This measure is expressed as a percentage of CT exams that are out-of-range based on having either excessive radiation dose or inadequate image quality relative to evidence-based thresholds based on the clinical indication for the exam. All diagnostic CT exams of specified anatomic sites performed in hospital inpatient care settings are eligible. This eCQM requires the use of additional software to access primary data elements stored within radiology electronic health records and translate them into data elements that can be ingested by this eCQM. Additional details are included in the Guidance field.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3663e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CT) in Adults (Facility IQR)\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS177\",\"cqmCriterionId\":1259,\"criteria\":[],\"description\":\"Percentage of patient visits for those patients aged 6 through 17 years with a diagnosis of major depressive disorder with an assessment for suicide risk\",\"domain\":null,\"id\":null,\"nqfNumber\":\"1365\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Child and Adolescent Major Depressive Disorder (MDD): Suicide Risk Assessment\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS178\",\"cqmCriterionId\":632,\"criteria\":[],\"description\":\"Number of surgical patients whose urinary catheter is removed on Postoperative Day 1 (POD) 1 or Postoperative Day (POD) 2 with day of surgery being day zero.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Urinary catheter removed on Postoperative Day 1 (POD 1) or Postoperative Day 2 (POD 2) with day of surgery being day zero\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS179\",\"cqmCriterionId\":592,\"criteria\":[],\"description\":\"Average percentage of time in which patients aged 18 and older with atrial fibrillation who are on chronic warfarin therapy have International Normalized Ratio (INR) test results within the therapeutic range (i.e., TTR) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"380\",\"success\":false,\"successVersions\":[],\"title\":\"ADE Prevention and Monitoring: Warfarin Time in Therapeutic Range \",\"typeId\":1},{\"allVersions\":[\"v8\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS334\",\"cqmCriterionId\":1275,\"criteria\":[],\"description\":\"Nulliparous women with a term, singleton baby in a vertex position delivered by cesarean birth\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cesarean Birth\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS171\",\"cqmCriterionId\":634,\"criteria\":[],\"description\":\"Surgical patients with prophylactic antibiotics initiated within one hour prior to surgical incision. Patients who received vancomycin or a fluoroquinolone for prophylactic antibiotics should have the antibiotics initiated within two hours prior to surgical incision. Due to the longer infusion time required for vancomycin or a fluoroquinolone, it is acceptable to start these antibiotics within two hours prior to incision time.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0527\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Received Within One Hour Prior to Surgical Incision\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\"],\"cmsId\":\"CMS172\",\"cqmCriterionId\":635,\"criteria\":[],\"description\":\"Surgical patients who received prophylactic antibiotics consistent with current guidelines (specific to each type of surgical procedure).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0528\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Selection for Surgical Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS529\",\"cqmCriterionId\":1272,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWR outcome measure. It is designed to extract the first resulted set of vital signs and basic laboratory results obtained from encounters for adult Medicare Fee-For-Service patients admitted to acute care short stay hospitals.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"2879\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Core Clinical Data Elements for the Hybrid Hospital-Wide Readmission (HWR) Measure with Claims and Electronic Health Record Data\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS126\",\"cqmCriterionId\":554,\"criteria\":[],\"description\":\"Percentage of patients 5- 64 years of age who were identified as having persistent asthma and were appropriately prescribed medication during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"311\",\"success\":false,\"successVersions\":[],\"title\":\"Use of Appropriate Medications for Asthma\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS91\",\"cqmCriterionId\":631,\"criteria\":[],\"description\":\"Acute ischemic stroke patients who arrive at this hospital within 2 hours of time last known well and for whom t-PA was initiated at this hospital within 3 hours of time last known well.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0437\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Thrombolytic Therapy\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS128\",\"cqmCriterionId\":1237,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were treated with antidepressant medication, had a diagnosis of major depression, and who remained on an antidepressant medication treatment. Two rates are reported: a. Percentage of patients who remained on an antidepressant medication for at least 84 days (12 weeks).; b. Percentage of patients who remained on an antidepressant medication for at least 180 days (6 months).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"105\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Anti-depressant Medication Management\",\"typeId\":1},{\"allVersions\":[\"v10\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\"],\"cmsId\":\"CMS645\",\"cqmCriterionId\":1263,\"criteria\":[],\"description\":\"Patients determined as having prostate cancer who are currently starting or undergoing androgen deprivation therapy (ADT), for an anticipated period of 12 months or greater and who receive an initial bone density evaluation. The bone density evaluation must be prior to the start of ADT or within 3 months of the start of ADT.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Bone density evaluation for patients with prostate cancer and receiving androgen deprivation therapy\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS249\",\"cqmCriterionId\":1064,\"criteria\":[],\"description\":\"Percentage of female patients 50 to 64 years of age without select risk factors for osteoporotic fracture who received an order for a dual-energy x-ray absorptiometry (DXA) scan during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Appropriate Use of DXA Scans in Women Under 65 Years Who Do Not Meet the Risk Factor Profile for Osteoporotic Fracture\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS129\",\"cqmCriterionId\":1238,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of prostate cancer at low (or very low) risk of recurrence receiving interstitial prostate brachytherapy, OR external beam radiotherapy to the prostate, OR radical prostatectomy, OR cryotherapy who did not have a bone scan performed at any time since diagnosis of prostate cancer\",\"domain\":null,\"id\":null,\"nqfNumber\":\"389\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prostate Cancer: Avoidance of Overuse of Bone Scan for Staging Low Risk Prostate Cancer Patients\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS646\",\"cqmCriterionId\":1264,\"criteria\":[],\"description\":\"Percentage of patients initially diagnosed with non-muscle invasive bladder cancer and who received intravesical Bacillus-Calmette-Guerin (BCG) within 6 months of bladder cancer staging.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Intravesical Bacillus-Calmette-Guerin for non-muscle invasive bladder cancer\",\"typeId\":2},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS1206\",\"cqmCriterionId\":1288,\"criteria\":[],\"description\":\"This measure is an episode of care measure that provides a standardized method for monitoring the performance of diagnostic CT to discourage unnecessarily high radiation doses, a risk factor for cancer, while preserving image quality. This measure is expressed as a percentage of CT exams that are out-of-range based on having either excessive radiation dose or inadequate image quality relative to evidence-based thresholds based on the clinical indication for the exam. All diagnostic CT exams of specified anatomic sites performed in hospital non-inpatient care settings (including emergency settings) are eligible. This eCQM requires the use of additional software to access primary data elements stored within radiology electronic health records and translate them into data elements that can be ingested by this eCQM. Additional details are included in the Guidance field.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3663e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CT) in Adults (Facility OQR)\",\"typeId\":1},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1264FHIR\",\"cqmCriterionId\":1294,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support rural emergency hospital (REH) quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (REHQR) FHIR\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS1056\",\"cqmCriterionId\":1283,\"criteria\":[],\"description\":\"This measure provides a standardized method for monitoring the performance of diagnostic CT to discourage unnecessarily high radiation doses, a risk factor for cancer, while preserving image quality. It is expressed as a percentage of patients with CT exams that are out-of-range based on having either excessive radiation dose or inadequate image quality relative to evidence-based thresholds based on the clinical indication for the exam. All diagnostic CT exams of specified anatomic sites performed in inpatient, outpatient and ambulatory care settings are eligible. This measure is not telehealth eligible. This eCQM requires the use of additional software to access primary data elements stored within radiology electronic health records and translate them into data elements that can be ingested by this eCQM. Additional details are included in the Guidance field.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3663e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CT) in Adults (Clinician Level)\",\"typeId\":3},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1173\",\"cqmCriterionId\":1222,\"criteria\":[],\"description\":\"Percentage of episodes for patients 18 years of age and older with documented Venous Thromboembolism (VTE) symptoms in the primary care setting and who had a diagnosis of VTE that occurs > 24 hours and within 30 days following the index primary care visit where symptoms for the VTE were first present.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diagnostic Delay of Venous Thromboembolism in Primary Care\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS111\",\"cqmCriterionId\":1013,\"criteria\":[],\"description\":\"Median time (in minutes) from admit decision time to time of departure from the emergency department for emergency department patients admitted to inpatient status.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"497\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Admit Decision Time to ED Departure Time for Admitted Patients\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS871\",\"cqmCriterionId\":1277,\"criteria\":[],\"description\":\"This measure assesses the number of inpatient hospital days with a hyperglycemic event (harm) per the total qualifying inpatient hospital days for that encounter for patients 18 years of age or older at admission\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3533e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Severe Hyperglycemia\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\",\"v6\"],\"cmsId\":\"CMS113\",\"cqmCriterionId\":735,\"criteria\":[],\"description\":\"Patients with elective vaginal deliveries or elective cesarean births at >= 37 and < 39 weeks of gestation completed\",\"domain\":null,\"id\":null,\"nqfNumber\":\"469\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Elective Delivery\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS114\",\"cqmCriterionId\":622,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE during hospitalization (not present at admission) who did not receive VTE prophylaxis between hospital admission and the day before the VTE diagnostic testing order date.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Incidence of Potentially-Preventable Venous Thromboembolism\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS996\",\"cqmCriterionId\":1279,\"criteria\":[],\"description\":\"Percentage of emergency department (ED) encounters for patients 18 years and older with a diagnosis of ST-segment elevation myocardial infarction (STEMI) that received appropriate treatment, defined as fibrinolytic therapy within 30 minutes of ED arrival, percutaneous coronary intervention (PCI) within 90 minutes of ED arrival, or transfer within 45 minutes of ED arrival\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3613e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Appropriate Treatment for ST-Segment Elevation Myocardial Infarction (STEMI) Patients in the Emergency Department (ED)\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS26\",\"cqmCriterionId\":711,\"criteria\":[],\"description\":\"An assessment that there is documentation in the medical record that a Home Management Plan of Care (HMPC) document was given to the pediatric asthma patient/caregiver\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Home Management Plan of Care (HMPC) Document Given to Patient/Caregiver\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS22\",\"cqmCriterionId\":1225,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older seen during the reporting period who were screened for high blood pressure AND a recommended follow-up plan is documented based on the current blood pressure (BP) reading as 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Three rates are reported. 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The bone density evaluation must be prior to the start of ADT or within 3 months of the start of ADT.\",\"domain\":\"Effective Clinical Care\",\"id\":316408,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"Bone density evaluation for patients with prostate cancer and receiving androgen deprivation therapy\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS646\",\"cqmCriterionId\":910,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102190},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - 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This list must include ALL known prescriptions, over-thecounters, herbals, and vitamin/mineral/dietary (nutritional) supplements AND must contain the medications' name, dosage, frequency and route of administration.\",\"domain\":\"Patient Safety\",\"id\":316370,\"nqfNumber\":\"0419\",\"number\":\"130 GPRO CARE-3 \",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Documentation of Current Medications in the Medical Record\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS69\",\"cqmCriterionId\":227,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102076},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102077},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102078}],\"description\":\"Percentage of patients aged 18 years and older with a BMI documented during the current encounter or during the previous six months AND with a BMI outside of normal parameters, a follow-up plan is documented during the encounter or during the previous six months of the current encounter. 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Record and Export\"},\"id\":102079},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102080},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102081}],\"description\":\"Percentage of children, age 0-20 years, who received a fluoride varnish application during the measurement period.\",\"domain\":\"Clinical Process/ Effectiveness.\",\"id\":316372,\"nqfNumber\":\"N/A\",\"number\":\"379\",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Primary Caries Prevention Intervention as Offered by Primary Care Providers, including Dentists\",\"typeId\":1},{\"allVersions\":[\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS771\",\"cqmCriterionId\":838,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102193},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102194},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102195}],\"description\":\"Percentage of patients with an office visit within the measurement period and with a new diagnosis of clinically significant Benign Prostatic Hyperplasia who have International Prostate Symptoms Score (IPSS) or American Urological Association (AUA) Symptom Index (SI) documented at time of diagnosis and again 6-12 months later with an improvement of 3 points\",\"domain\":\"Person and Caregiver- Centered Experience and Outcomes\",\"id\":316410,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"International Prostate Symptom Score (IPSS) or American Urological Association-Symptom Index (AUA-SI) Change 6-12 Months After Diagnosis of Benign Prostatic Hyperplasia\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\",\"v16\"],\"cmsId\":\"CMS90\",\"cqmCriterionId\":341,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102082},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102083},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102084}],\"description\":\"Percentage of patients aged 65 years and older with heart failure who completed initial and follow-up patient reported functional status assessments\",\"domain\":\"Patient and Family Engagement.\",\"id\":316373,\"nqfNumber\":\"N/A\",\"number\":\"377\",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Functional Status Assessment for Complex Chronic Conditions\",\"typeId\":1},{\"allVersions\":[\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS951\",\"cqmCriterionId\":1018,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102196},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102197},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102198}],\"description\":\"Percentage of patients aged 18-75 years with a diagnosis of diabetes who received a kidney health evaluation defined by an Estimated Glomerular Filtration Rate (eGFR) AND Urine Albumin-Creatinine Ratio (uACR) within the measurement period\",\"domain\":\"Promote effective prevention and treatment of chronic disease\",\"id\":316411,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"Kidney Health Evaluation\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v1\",\"v3\",\"v4\"],\"cmsId\":\"CMS1028\",\"cqmCriterionId\":1277,\"criteria\":[],\"description\":\"Patients with severe obstetric complications which occur during the inpatient delivery hospitalization.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Severe Obstetric Complications\",\"typeId\":2},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1264\",\"cqmCriterionId\":1294,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support rural emergency hospital (REH) quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (REHQR)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS826\",\"cqmCriterionId\":1284,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients aged 18 and older who suffer the harm of developing a new stage 2, stage 3, stage 4, deep tissue, or unstageable pressure injury\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3498e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Pressure Injury\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v11\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS72\",\"cqmCriterionId\":1266,\"criteria\":[],\"description\":\"Ischemic stroke patients administered antithrombotic therapy by the end of hospital day 2\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Antithrombotic Therapy By End of Hospital Day 2\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS73\",\"cqmCriterionId\":609,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received an overlap of parenteral (intravenous [IV] or subcutaneous [subcu]) anticoagulation and warfarin therapy. For patients who received less than five days of overlap therapy, they should be discharged on both medications or have a reason for discontinuation of overlap therapy. Overlap therapy should be administered for at least five days with an international normalized ratio (INR) greater than or equal to 2 prior to discontinuation of the parenteral anticoagulation therapy, discharged on both medications or have a reason for discontinuation of overlap therapy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0373\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients with Anticoagulation Overlap Therapy\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS75\",\"cqmCriterionId\":1230,\"criteria\":[],\"description\":\"Percentage of children, age 0-20 years, who have had tooth decay or cavities during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Children Who Have Dental Decay or Cavities\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS148\",\"cqmCriterionId\":560,\"criteria\":[],\"description\":\"Percentage of patients 5-17 years of age with diabetes with a Hemoglobin A1c (HbA1c) test during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"365\",\"success\":false,\"successVersions\":[],\"title\":\"Hemoglobin A1c Test for Pediatric Patients\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS71\",\"cqmCriterionId\":1265,\"criteria\":[],\"description\":\"Ischemic stroke patients with atrial fibrillation/flutter who are prescribed or continuing to take anticoagulation therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Anticoagulation Therapy for Atrial Fibrillation/Flutter\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS140\",\"cqmCriterionId\":573,\"criteria\":[],\"description\":\"Percentage of female patients aged 18 years and older with Stage I (T1b) through IIIC, ER or PR positive breast cancer who were prescribed tamoxifen or aromatase inhibitor (AI) during the 12-month reporting period \",\"domain\":null,\"id\":null,\"nqfNumber\":\"0387\",\"number\":\"071\",\"success\":false,\"successVersions\":[],\"title\":\"Breast Cancer: Hormonal Therapy for Stage I (T1b)-IIIC Estrogen Receptor/ Progesterone Receptor (ER/PR) Positive Breast Cancer\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS77\",\"cqmCriterionId\":594,\"criteria\":[],\"description\":\"Percentage of patients aged 13 years and older with a diagnosis of HIV/AIDS, with at least two visits during the measurement year, with at least 90 days between each visit, whose most recent HIV RNA level is <200 copies/mL.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A \",\"number\":\"381\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: RNA control for Patients with HIV\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS141\",\"cqmCriterionId\":623,\"criteria\":[],\"description\":\"Percentage of patients aged 18 through 80 years with AJCC Stage III colon cancer who are referred for adjuvant chemotherapy, prescribed adjuvant chemotherapy, or have previously received adjuvant chemotherapy within the 12-month reporting period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0385\",\"number\":\"072\",\"success\":false,\"successVersions\":[],\"title\":\"Colon Cancer: Chemotherapy for AJCC Stage III Colon Cancer Patients\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS142\",\"cqmCriterionId\":1246,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed with documented communication to the physician who manages the ongoing care of the patient with diabetes mellitus regarding the findings of the macular or fundus exam at least once within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"89\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Communication with the Physician Managing Ongoing Diabetes Care\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v1\"],\"cmsId\":\"CMS1154\",\"cqmCriterionId\":1290,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS816\",\"cqmCriterionId\":1275,\"criteria\":[],\"description\":\"Inpatient hospitalizations for patients 18 years of age or older at admission, who were administered at least one hypoglycemic medication during the encounter, who suffer the harm of a severe hypoglycemic event during the encounter\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3503e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Severe Hypoglycemia\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS9\",\"cqmCriterionId\":1007,\"criteria\":[],\"description\":\"Exclusive breast milk feeding during the newborn's entire hospitalization\",\"domain\":null,\"id\":null,\"nqfNumber\":\"480\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Exclusive Breast Milk Feeding\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS819\",\"cqmCriterionId\":1280,\"criteria\":[],\"description\":\"This measure assesses the number of inpatient hospitalizations for patients age 18 and older who have been administered an opioid medication and are subsequently administered an opioid antagonist within 12 hours, an indication of an opioid-related adverse event\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3501e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Opioid-Related Adverse Events\",\"typeId\":2},{\"allVersions\":[\"v16\",\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS136\",\"cqmCriterionId\":1242,\"criteria\":[],\"description\":\"Percentage of children 6-12 years of age and newly dispensed a medication for attention-deficit/hyperactivity disorder (ADHD) who had appropriate follow-up care. Two rates are reported: a. Percentage of children who had one follow-up visit with a practitioner with prescribing authority during the 30-Day Initiation Phase.; b. Percentage of children who remained on ADHD medication for at least 210 days and who, in addition to the visit in the Initiation Phase, had at least two additional follow-up visits with a practitioner within 270 days (9 months) after the Initiation Phase ended.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"108\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Follow-Up Care for Children Prescribed ADHD Medication (ADD)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS82\",\"cqmCriterionId\":852,\"criteria\":[],\"description\":\"The percentage of children who turned 6 months of age during the measurement year, who had a face-to-face visit between the clinician and the child during child's first 6 months, and who had a maternal depression screening for the mother at least once between 0 and 6 months of life\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Maternal Depression Screening\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS132\",\"cqmCriterionId\":867,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of uncomplicated cataract who had cataract surgery and had any of a specified list of surgical procedures in the 30 days following cataract surgery which would indicate the occurrence of any of the following major complications: retained nuclear fragments, endophthalmitis, dislocated or wrong power IOL, retinal detachment, or wound dehiscence\",\"domain\":null,\"id\":null,\"nqfNumber\":\"564\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cataracts: Complications within 30 Days Following Cataract Surgery Requiring Additional Surgical Procedures\",\"typeId\":1},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1244\",\"cqmCriterionId\":1292,\"criteria\":[],\"description\":\"This measure assesses the proportion of ED encounters for patients who experience at least one emergency care access or timeliness gap. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS166\",\"cqmCriterionId\":701,\"criteria\":[],\"description\":\"Percentage of patients 18-50 years of age with a diagnosis of low back pain who did not have an imaging study (plain X-ray, MRI, CT scan) within 28 days of the diagnosis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"52\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Use of Imaging Studies for Low Back Pain\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS167\",\"cqmCriterionId\":772,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed which included documentation of the level of severity of retinopathy and the presence or absence of macular edema during one or more office visits within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"88\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Documentation of Presence or Absence of Macular Edema and Level of Severity of Retinopathy\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v3\",\"v0\",\"v1\",\"v2\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS52\",\"cqmCriterionId\":843,\"criteria\":[],\"description\":\"Percentage of patients aged 6 weeks and older with a diagnosis of HIV/AIDS who were prescribed Pneumocystis jiroveci pneumonia (PCP) prophylaxis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"405\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Pneumocystis Jiroveci Pneumonia (PCP) Prophylaxis\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS169\",\"cqmCriterionId\":773,\"criteria\":[],\"description\":\"Percentage of patients with depression or bipolar disorder with evidence of an initial assessment that includes an appraisal for alcohol or chemical substance use\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Bipolar Disorder and Major Depression: Appraisal for alcohol or chemical substance use\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS53\",\"cqmCriterionId\":716,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving primary PCI during the hospital stay with a time from hospital arrival to PCI of 90 minutes or less\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Primary PCI Received Within 90 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS844\",\"cqmCriterionId\":1272,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWM outcome measure. It is designed to extract the first resulted set of vital signs and basic laboratory results obtained from encounters for adult Medicare Fee-For-Service patients admitted to acute care short stay hospitals.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3502\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Core Clinical Data Elements for the Hybrid Hospital-Wide (All-Condition, All-Procedure) Risk-Standardized Mortality Measure (HWM)\",\"typeId\":2},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS160\",\"cqmCriterionId\":888,\"criteria\":[],\"description\":\"The percentage of patients age 18 and older with the diagnosis of major depression or dysthymia who have a completed PHQ-9 during each applicable 4 month period in which there was a qualifying visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"712\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Depression Utilization of the PHQ-9 Tool\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v1\",\"v2\",\"v0\",\"v3\",\"v4\"],\"cmsId\":\"CMS163\",\"cqmCriterionId\":584,\"criteria\":[],\"description\":\"Percentage of patients 18-75 years of age with diabetes whose LDL-C was adequately controlled (<100 mg/dL) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"002\",\"success\":false,\"successVersions\":[],\"title\":\"Diabetes: Low Density Lipoprotein (LDL-C) Control (< 100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS55\",\"cqmCriterionId\":717,\"criteria\":[],\"description\":\"Median time from emergency department arrival to time of departure from the emergency room for patients admitted to the facility from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"495\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Admitted ED Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS164\",\"cqmCriterionId\":770,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had an active diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had documentation of use of aspirin or another antiplatelet during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"68\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Use of Aspirin or Another Antiplatelet\",\"typeId\":1},{\"allVersions\":[\"v3\",\"v2\"],\"cmsId\":\"CMS1017\",\"cqmCriterionId\":1288,\"criteria\":[],\"description\":\"This ratio measure assesses the number of inpatient hospitalizations where at least one fall with a major or moderate injury occurs among the total qualifying inpatient hospital days for patients age 18 years and older\",\"domain\":null,\"id\":null,\"nqfNumber\":\"4120e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Falls with Injury\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1154FHIR\",\"cqmCriterionId\":1295,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS61\",\"cqmCriterionId\":626,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years whose risk factors have been assessed and a fasting LDL-C test has been performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Cholesterol - Fasting Low Density Lipoprotein (LDL-C) Test Performed\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS62\",\"cqmCriterionId\":586,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of HIV/AIDS with at least two medical visits during the measurement year with a minimum of 90 days between each visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"368\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Medical Visit\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS158\",\"cqmCriterionId\":766,\"criteria\":[],\"description\":\"This measure identifies pregnant women who had a HBsAg (hepatitis B) test during their pregnancy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Pregnant women that had HBsAg testing\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS64\",\"cqmCriterionId\":627,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years who had a fasting LDL-C test performed and whose risk stratified fasting LDL-C is at or below the recommended LDL-C goal.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Risk-Stratified Cholesterol -Fasting Low Density Lipoprotein (LDL-C)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS832\",\"cqmCriterionId\":1285,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients age 18 and older who have an acute kidney injury (stage 2 or greater) that occurred during the encounter. Acute kidney injury (AKI) stage 2 or greater is defined as a substantial increase in serum creatinine value, or by the initiation of kidney dialysis (continuous renal replacement therapy (CRRT), hemodialysis or peritoneal dialysis).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3713e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Acute Kidney Injury\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS60\",\"cqmCriterionId\":606,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving fibrinolytic therapy during the hospital stay and having a time from hospital arrival to fibrinolysis of 30 minutes or less.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Fibrinolytic Therapy Received Within 30 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS65\",\"cqmCriterionId\":719,\"criteria\":[],\"description\":\"Percentage of patients aged 18-85 years of age with a diagnosis of hypertension whose blood pressure improved during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hypertension: Improvement in Blood Pressure\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS190\",\"cqmCriterionId\":1269,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after the initial admission (or transfer) to the Intensive Care Unit (ICU) or surgery end date for surgeries that start the day of or the day after ICU admission (or transfer)\",\"domain\":null,\"id\":null,\"nqfNumber\":\"372\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Intensive Care Unit Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS108\",\"cqmCriterionId\":1268,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after hospital admission or surgery end date for surgeries that start the day of or the day after hospital admission\",\"domain\":null,\"id\":null,\"nqfNumber\":\"371\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS109\",\"cqmCriterionId\":620,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received intravenous (IV) UFH therapy dosages AND had their platelet counts monitored using defined parameters such as a nomogram or protocol.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients Receiving Unfractionated Heparin with Dosages/Platelet Count Monitoring by Protocol or Nomogram\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS100\",\"cqmCriterionId\":604,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients prescribed aspirin at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0142\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Aspirin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS188\",\"cqmCriterionId\":629,\"criteria\":[],\"description\":\"(PN-6) Immunocompetent patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 1) Immunocompetent ICU patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 2) Immunocompetent non-Intensive Care Unit (ICU) patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0147\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Initial Antibiotic Selection for Community-Acquired Pneumonia (CAP) in Immunocompetent Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v0\",\"v5\",\"v6\"],\"cmsId\":\"CMS102\",\"cqmCriterionId\":729,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients who were assessed for rehabilitation services\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Assessed for Rehabilitation\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS30\",\"cqmCriterionId\":636,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients who are prescribed a statin medication at hospital discharge.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Statin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS31\",\"cqmCriterionId\":712,\"criteria\":[],\"description\":\"This measure assesses the proportion of births that have been screened for hearing loss before hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"1354\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hearing Screening Prior To Hospital Discharge\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v1\",\"v0\",\"v2\",\"v3\",\"v4\",\"v11\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS104\",\"cqmCriterionId\":1267,\"criteria\":[],\"description\":\"Ischemic stroke patients prescribed or continuing to take antithrombotic therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Antithrombotic Therapy\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS105\",\"cqmCriterionId\":1011,\"criteria\":[],\"description\":\"Ischemic stroke patients who are prescribed or continuing to take statin medication at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Statin Medication\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v4\",\"v5\"],\"cmsId\":\"CMS986\",\"cqmCriterionId\":1281,\"criteria\":[],\"description\":\"This measure assesses the percentage of hospitalizations for adults aged 65 years and older at the start of the inpatient encounter during the measurement period with a length of stay equal to or greater than 24 hours who received optimal malnutrition care during the current inpatient hospitalization where care performed was appropriate to the patient's level of malnutrition risk and severity. Malnutrition care best practices recommend that for each hospitalization, adult inpatients are screened for malnutrition risk, assessed to confirm findings of malnutrition risk or for a hospital dietitian referral order, and if identified with a \\\"moderate\\\" or \\\"severe\\\" malnutrition status in the current performed malnutrition assessment, receive a current \\\"moderate\\\" or \\\"severe\\\" malnutrition diagnosis and have a current nutrition care plan performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3592e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Global Malnutrition Composite Score\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS107\",\"cqmCriterionId\":732,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients or their caregivers who were given educational materials during the hospital stay addressing all of the following: activation of emergency medical system, need for follow-up after discharge, medications prescribed at discharge, risk factors for stroke, and warning signs and symptoms of stroke\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Stroke Education\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1244FHIR\",\"cqmCriterionId\":1291,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support hospital quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR) FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS182\",\"cqmCriterionId\":602,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had a diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had a complete lipid profile performed during the measurement period and whose most recent Low-density Lipoprotein (LDL-C) was adequately controlled (< 100 mg/dL).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"241\",\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Complete Lipid Panel and LDL-C Control (<100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS32\",\"cqmCriterionId\":713,\"criteria\":[],\"description\":\"Median elapsed time from emergency department arrival to emergency room departure for patients discharged from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"496\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Discharged ED Patients\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS185\",\"cqmCriterionId\":618,\"criteria\":[],\"description\":\"Percent of term singleton live births (excluding those with diagnoses originating in the fetal period) who DO NOT have significant complications during birth or the nursery care\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0716\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Healthy Term Newborn\",\"typeId\":2},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS1074\",\"cqmCriterionId\":1286,\"criteria\":[],\"description\":\"This measure provides a standardized method for monitoring the performance of diagnostic CT to discourage unnecessarily high radiation doses, a risk factor for cancer, while preserving image quality. This measure is expressed as a percentage of CT exams that are out-of-range based on having either excessive radiation dose or inadequate image quality relative to evidence-based thresholds based on the clinical indication for the exam. All diagnostic CT exams of specified anatomic sites performed in hospital inpatient care settings are eligible. This eCQM requires the use of additional software to access primary data elements stored within radiology electronic health records and translate them into data elements that can be ingested by this eCQM. Additional details are included in the Guidance field.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3663e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CT) in Adults (Facility IQR)\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS178\",\"cqmCriterionId\":632,\"criteria\":[],\"description\":\"Number of surgical patients whose urinary catheter is removed on Postoperative Day 1 (POD) 1 or Postoperative Day (POD) 2 with day of surgery being day zero.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Urinary catheter removed on Postoperative Day 1 (POD 1) or Postoperative Day 2 (POD 2) with day of surgery being day zero\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS179\",\"cqmCriterionId\":592,\"criteria\":[],\"description\":\"Average percentage of time in which patients aged 18 and older with atrial fibrillation who are on chronic warfarin therapy have International Normalized Ratio (INR) test results within the therapeutic range (i.e., TTR) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"380\",\"success\":false,\"successVersions\":[],\"title\":\"ADE Prevention and Monitoring: Warfarin Time in Therapeutic Range \",\"typeId\":1},{\"allVersions\":[\"v8\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS334\",\"cqmCriterionId\":1274,\"criteria\":[],\"description\":\"Nulliparous women with a term, singleton baby in a vertex position delivered by cesarean birth\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cesarean Birth\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS171\",\"cqmCriterionId\":634,\"criteria\":[],\"description\":\"Surgical patients with prophylactic antibiotics initiated within one hour prior to surgical incision. Patients who received vancomycin or a fluoroquinolone for prophylactic antibiotics should have the antibiotics initiated within two hours prior to surgical incision. Due to the longer infusion time required for vancomycin or a fluoroquinolone, it is acceptable to start these antibiotics within two hours prior to incision time.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0527\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Received Within One Hour Prior to Surgical Incision\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\"],\"cmsId\":\"CMS172\",\"cqmCriterionId\":635,\"criteria\":[],\"description\":\"Surgical patients who received prophylactic antibiotics consistent with current guidelines (specific to each type of surgical procedure).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0528\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Selection for Surgical Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS529\",\"cqmCriterionId\":1271,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWR outcome measure. 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ISO 9001:2015 Sections 7.5.1 and 7.5.2 - Covered by QM-04 ISO 9001:2015 Section 7.5.3 - Covered by QM-04 and IT-01 ISO 9001:2015 Section 8.1 - Covered by SE-01 ISO 9001:2015 Section 8.2 - Covered by SE-01 and SA-01 ISO 9001:2015 Sections 8.3.1, 8.3.2 and 8.3.3 - Covered by SE-01 and DQ-01 ISO 9001:2015 Section 8.3.4, 8.3.5 and 8.3.6 - Covered by DQ-01 ISO 9001:2015 Section 8.4 - Covered by PH-01 ISO 9001:2015 Sections 8.5.1, 8.5.2, 8.5.3 and 8.5.4 - Covered by SU-01 ISO 9001:2015 Section 8.5.5 - Covered by SU-01 and SU-02 ISO 9001:2015 Section 8.5.6 - Covered by SU-01 ISO 9001:2015 Section 8.6 - Covered by SU-01 and SD-05 ISO 9001:2015 Section 8.7 - Covered by DQ-01 ISO 9001:2015 Section 9.1.1 - Covered by QM-03 ISO 9001:2015 Section 9.1.2 - Covered by QM-03, CS-01 and SU-02 ISO 9001:2015 Section 9.1.3 - Covered by QM-03 and CS-01 ISO 9001:2015 Section 9.2 - Covered by QM-06 ISO 9001:2015 Section 9.3 - Covered by QM-02 ISO 9001:2015 Section 10.1 - Covered by QM-02 and QM-07 ISO 9001:2015 Section 10.2 - Covered by QM-07 ISO 9001:2015 Section 10.3 - Covered by QM-02\",\"qmsStandardId\":19,\"qmsStandardName\":\"Modified QMS/Mapped\"}],\"reportFileLocation\":null,\"rwtResultsCheckDate\":\"2026-02-24\",\"rwtResultsUrl\":\"https://www.alterahealth.com/legal/onc-reg-compliance/\",\"sed\":{\"ucdProcesses\":[{\"criteria\":[{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/computerized-provider-order-entry-cpoe-medications\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":1,\"number\":\"170.315 (a)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Computerized Provider Order Entry (CPOE) - 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} + } + }, + "url": { + "raw": "{{url}}/rest/certified_products/11708", + "host": [ + "{{url}}" + ], + "path": [ + "rest", + "certified_products", + "11708" + ] + } + }, + "response": [] + } + ] + } + ] +} diff --git a/chpl/chpl-api/e2e/data/certifiedproductids-test-data.json b/chpl/chpl-api/e2e/data/certifiedproductids-test-data.json new file mode 100644 index 0000000000..4357e4f4db --- /dev/null +++ b/chpl/chpl-api/e2e/data/certifiedproductids-test-data.json @@ -0,0 +1,7 @@ +[ + { "certifiedProductId": "11645" }, + { "certifiedProductId": "10785" }, + { "certifiedProductId": "10794" }, + { "certifiedProductId": "10964" }, + { "certifiedProductId": "11769" } +] \ No newline at end of file diff --git a/chpl/chpl-api/e2e/script/newman-run.js b/chpl/chpl-api/e2e/script/newman-run.js index 71b3a42da8..e80c2a7888 100755 --- a/chpl/chpl-api/e2e/script/newman-run.js +++ b/chpl/chpl-api/e2e/script/newman-run.js @@ -428,6 +428,29 @@ const reportDataCriteriaUpToDateControllerTests = { }, }; +const listingPerformanceBaselinesDataTests = { + ...commonOptions, + collection: collection_path + '/listing-performance-baselines.postman_collection.json', + folder: 'Listing performance tests - GET iterates Certified Product IDs', + iterationData: data_path + '/certifiedproductids-test-data.json', + reporter: { + junit: { + export: reports_path + '/listing-performance-baselines-tests.xml', + }, + }, +}; + +const listingPerformanceBaselinesNoDataTests = { + ...commonOptions, + collection: collection_path + '/listing-performance-baselines.postman_collection.json', + folder: 'Listing performance tests - PUT uses specific Certified Product IDs', + reporter: { + junit: { + export: reports_path + '/listing-performance-baselines-nodata-tests.xml', + }, + }, +}; + const jobs = [ cb => newman.run(acbControllerTests,cb), cb => newman.run(accessibilityStandardsControllerTests,cb), @@ -470,6 +493,8 @@ const jobs = [ cb => newman.run(questionableUrlsControllerTests,cb), cb => newman.run(reportDataCriteriaUpToDateControllerTests,cb), cb => newman.run(reportDataNonConformitiesControllerTests,cb), + cb => newman.run(listingPerformanceBaselinesDataTests,cb), + cb => newman.run(listingPerformanceBaselinesNoDataTests,cb), ]; const responseCallback = (err) => { From c7ce15a7eefdfa72a769df15303005281fe06173 Mon Sep 17 00:00:00 2001 From: Ashwini More Date: Thu, 17 Sep 2026 17:45:04 -0400 Subject: [PATCH 2/2] update PUT request body to match prod data --- .../listing-performance-baselines.postman_collection.json | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json b/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json index fed62d2a73..7ebf9b1f74 100644 --- a/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json +++ b/chpl/chpl-api/e2e/collections/listing-performance-baselines.postman_collection.json @@ -174,7 +174,7 @@ ], "body": { "mode": "raw", - "raw": "{\"listing\":{\"acbCertificationId\":\"15.04.04.3123.Sunr.AH.12.1.250905\",\"accessibilityCertified\":true,\"accessibilityStandards\":[{\"accessibilityStandardId\":23,\"accessibilityStandardName\":\"ISO/IEC 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Three rates are reported. 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The bone density evaluation must be prior to the start of ADT or within 3 months of the start of ADT.\",\"domain\":\"Effective Clinical Care\",\"id\":316408,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"Bone density evaluation for patients with prostate cancer and receiving androgen deprivation therapy\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS646\",\"cqmCriterionId\":910,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102190},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - 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This list must include ALL known prescriptions, over-thecounters, herbals, and vitamin/mineral/dietary (nutritional) supplements AND must contain the medications' name, dosage, frequency and route of administration.\",\"domain\":\"Patient Safety\",\"id\":316370,\"nqfNumber\":\"0419\",\"number\":\"130 GPRO CARE-3 \",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Documentation of Current Medications in the Medical Record\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS69\",\"cqmCriterionId\":227,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102076},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102077},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102078}],\"description\":\"Percentage of patients aged 18 years and older with a BMI documented during the current encounter or during the previous six months AND with a BMI outside of normal parameters, a follow-up plan is documented during the encounter or during the previous six months of the current encounter. 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Record and Export\"},\"id\":102079},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102080},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102081}],\"description\":\"Percentage of children, age 0-20 years, who received a fluoride varnish application during the measurement period.\",\"domain\":\"Clinical Process/ Effectiveness.\",\"id\":316372,\"nqfNumber\":\"N/A\",\"number\":\"379\",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Primary Caries Prevention Intervention as Offered by Primary Care Providers, including Dentists\",\"typeId\":1},{\"allVersions\":[\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS771\",\"cqmCriterionId\":838,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102193},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102194},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102195}],\"description\":\"Percentage of patients with an office visit within the measurement period and with a new diagnosis of clinically significant Benign Prostatic Hyperplasia who have International Prostate Symptoms Score (IPSS) or American Urological Association (AUA) Symptom Index (SI) documented at time of diagnosis and again 6-12 months later with an improvement of 3 points\",\"domain\":\"Person and Caregiver- Centered Experience and Outcomes\",\"id\":316410,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"International Prostate Symptom Score (IPSS) or American Urological Association-Symptom Index (AUA-SI) Change 6-12 Months After Diagnosis of Benign Prostatic Hyperplasia\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\",\"v16\"],\"cmsId\":\"CMS90\",\"cqmCriterionId\":341,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102082},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102083},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102084}],\"description\":\"Percentage of patients aged 65 years and older with heart failure who completed initial and follow-up patient reported functional status assessments\",\"domain\":\"Patient and Family Engagement.\",\"id\":316373,\"nqfNumber\":\"N/A\",\"number\":\"377\",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Functional Status Assessment for Complex Chronic Conditions\",\"typeId\":1},{\"allVersions\":[\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS951\",\"cqmCriterionId\":1018,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102196},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102197},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102198}],\"description\":\"Percentage of patients aged 18-75 years with a diagnosis of diabetes who received a kidney health evaluation defined by an Estimated Glomerular Filtration Rate (eGFR) AND Urine Albumin-Creatinine Ratio (uACR) within the measurement period\",\"domain\":\"Promote effective prevention and treatment of chronic disease\",\"id\":316411,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"Kidney Health Evaluation\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v1\",\"v3\",\"v4\"],\"cmsId\":\"CMS1028\",\"cqmCriterionId\":1277,\"criteria\":[],\"description\":\"Patients with severe obstetric complications which occur during the inpatient delivery hospitalization.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Severe Obstetric Complications\",\"typeId\":2},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1264\",\"cqmCriterionId\":1294,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support rural emergency hospital (REH) quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (REHQR)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS826\",\"cqmCriterionId\":1284,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients aged 18 and older who suffer the harm of developing a new stage 2, stage 3, stage 4, deep tissue, or unstageable pressure injury\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3498e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Pressure Injury\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v11\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS72\",\"cqmCriterionId\":1266,\"criteria\":[],\"description\":\"Ischemic stroke patients administered antithrombotic therapy by the end of hospital day 2\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Antithrombotic Therapy By End of Hospital Day 2\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS73\",\"cqmCriterionId\":609,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received an overlap of parenteral (intravenous [IV] or subcutaneous [subcu]) anticoagulation and warfarin therapy. For patients who received less than five days of overlap therapy, they should be discharged on both medications or have a reason for discontinuation of overlap therapy. Overlap therapy should be administered for at least five days with an international normalized ratio (INR) greater than or equal to 2 prior to discontinuation of the parenteral anticoagulation therapy, discharged on both medications or have a reason for discontinuation of overlap therapy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0373\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients with Anticoagulation Overlap Therapy\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS75\",\"cqmCriterionId\":1230,\"criteria\":[],\"description\":\"Percentage of children, age 0-20 years, who have had tooth decay or cavities during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Children Who Have Dental Decay or Cavities\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS148\",\"cqmCriterionId\":560,\"criteria\":[],\"description\":\"Percentage of patients 5-17 years of age with diabetes with a Hemoglobin A1c (HbA1c) test during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"365\",\"success\":false,\"successVersions\":[],\"title\":\"Hemoglobin A1c Test for Pediatric Patients\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS71\",\"cqmCriterionId\":1265,\"criteria\":[],\"description\":\"Ischemic stroke patients with atrial fibrillation/flutter who are prescribed or continuing to take anticoagulation therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Anticoagulation Therapy for Atrial Fibrillation/Flutter\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS140\",\"cqmCriterionId\":573,\"criteria\":[],\"description\":\"Percentage of female patients aged 18 years and older with Stage I (T1b) through IIIC, ER or PR positive breast cancer who were prescribed tamoxifen or aromatase inhibitor (AI) during the 12-month reporting period \",\"domain\":null,\"id\":null,\"nqfNumber\":\"0387\",\"number\":\"071\",\"success\":false,\"successVersions\":[],\"title\":\"Breast Cancer: Hormonal Therapy for Stage I (T1b)-IIIC Estrogen Receptor/ Progesterone Receptor (ER/PR) Positive Breast Cancer\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS77\",\"cqmCriterionId\":594,\"criteria\":[],\"description\":\"Percentage of patients aged 13 years and older with a diagnosis of HIV/AIDS, with at least two visits during the measurement year, with at least 90 days between each visit, whose most recent HIV RNA level is <200 copies/mL.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A \",\"number\":\"381\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: RNA control for Patients with HIV\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS141\",\"cqmCriterionId\":623,\"criteria\":[],\"description\":\"Percentage of patients aged 18 through 80 years with AJCC Stage III colon cancer who are referred for adjuvant chemotherapy, prescribed adjuvant chemotherapy, or have previously received adjuvant chemotherapy within the 12-month reporting period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0385\",\"number\":\"072\",\"success\":false,\"successVersions\":[],\"title\":\"Colon Cancer: Chemotherapy for AJCC Stage III Colon Cancer Patients\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS142\",\"cqmCriterionId\":1246,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed with documented communication to the physician who manages the ongoing care of the patient with diabetes mellitus regarding the findings of the macular or fundus exam at least once within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"89\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Communication with the Physician Managing Ongoing Diabetes Care\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v1\"],\"cmsId\":\"CMS1154\",\"cqmCriterionId\":1290,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS816\",\"cqmCriterionId\":1275,\"criteria\":[],\"description\":\"Inpatient hospitalizations for patients 18 years of age or older at admission, who were administered at least one hypoglycemic medication during the encounter, who suffer the harm of a severe hypoglycemic event during the encounter\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3503e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Severe Hypoglycemia\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS9\",\"cqmCriterionId\":1007,\"criteria\":[],\"description\":\"Exclusive breast milk feeding during the newborn's entire hospitalization\",\"domain\":null,\"id\":null,\"nqfNumber\":\"480\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Exclusive Breast Milk Feeding\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS819\",\"cqmCriterionId\":1280,\"criteria\":[],\"description\":\"This measure assesses the number of inpatient hospitalizations for patients age 18 and older who have been administered an opioid medication and are subsequently administered an opioid antagonist within 12 hours, an indication of an opioid-related adverse event\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3501e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Opioid-Related Adverse Events\",\"typeId\":2},{\"allVersions\":[\"v16\",\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS136\",\"cqmCriterionId\":1242,\"criteria\":[],\"description\":\"Percentage of children 6-12 years of age and newly dispensed a medication for attention-deficit/hyperactivity disorder (ADHD) who had appropriate follow-up care. Two rates are reported: a. Percentage of children who had one follow-up visit with a practitioner with prescribing authority during the 30-Day Initiation Phase.; b. Percentage of children who remained on ADHD medication for at least 210 days and who, in addition to the visit in the Initiation Phase, had at least two additional follow-up visits with a practitioner within 270 days (9 months) after the Initiation Phase ended.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"108\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Follow-Up Care for Children Prescribed ADHD Medication (ADD)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS82\",\"cqmCriterionId\":852,\"criteria\":[],\"description\":\"The percentage of children who turned 6 months of age during the measurement year, who had a face-to-face visit between the clinician and the child during child's first 6 months, and who had a maternal depression screening for the mother at least once between 0 and 6 months of life\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Maternal Depression Screening\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS132\",\"cqmCriterionId\":867,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of uncomplicated cataract who had cataract surgery and had any of a specified list of surgical procedures in the 30 days following cataract surgery which would indicate the occurrence of any of the following major complications: retained nuclear fragments, endophthalmitis, dislocated or wrong power IOL, retinal detachment, or wound dehiscence\",\"domain\":null,\"id\":null,\"nqfNumber\":\"564\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cataracts: Complications within 30 Days Following Cataract Surgery Requiring Additional Surgical Procedures\",\"typeId\":1},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1244\",\"cqmCriterionId\":1292,\"criteria\":[],\"description\":\"This measure assesses the proportion of ED encounters for patients who experience at least one emergency care access or timeliness gap. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS166\",\"cqmCriterionId\":701,\"criteria\":[],\"description\":\"Percentage of patients 18-50 years of age with a diagnosis of low back pain who did not have an imaging study (plain X-ray, MRI, CT scan) within 28 days of the diagnosis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"52\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Use of Imaging Studies for Low Back Pain\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS167\",\"cqmCriterionId\":772,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed which included documentation of the level of severity of retinopathy and the presence or absence of macular edema during one or more office visits within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"88\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Documentation of Presence or Absence of Macular Edema and Level of Severity of Retinopathy\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v3\",\"v0\",\"v1\",\"v2\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS52\",\"cqmCriterionId\":843,\"criteria\":[],\"description\":\"Percentage of patients aged 6 weeks and older with a diagnosis of HIV/AIDS who were prescribed Pneumocystis jiroveci pneumonia (PCP) prophylaxis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"405\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Pneumocystis Jiroveci Pneumonia (PCP) Prophylaxis\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS169\",\"cqmCriterionId\":773,\"criteria\":[],\"description\":\"Percentage of patients with depression or bipolar disorder with evidence of an initial assessment that includes an appraisal for alcohol or chemical substance use\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Bipolar Disorder and Major Depression: Appraisal for alcohol or chemical substance use\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS53\",\"cqmCriterionId\":716,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving primary PCI during the hospital stay with a time from hospital arrival to PCI of 90 minutes or less\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Primary PCI Received Within 90 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS844\",\"cqmCriterionId\":1272,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWM outcome measure. It is designed to extract the first resulted set of vital signs and basic laboratory results obtained from encounters for adult Medicare Fee-For-Service patients admitted to acute care short stay hospitals.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3502\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Core Clinical Data Elements for the Hybrid Hospital-Wide (All-Condition, All-Procedure) Risk-Standardized Mortality Measure (HWM)\",\"typeId\":2},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS160\",\"cqmCriterionId\":888,\"criteria\":[],\"description\":\"The percentage of patients age 18 and older with the diagnosis of major depression or dysthymia who have a completed PHQ-9 during each applicable 4 month period in which there was a qualifying visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"712\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Depression Utilization of the PHQ-9 Tool\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v1\",\"v2\",\"v0\",\"v3\",\"v4\"],\"cmsId\":\"CMS163\",\"cqmCriterionId\":584,\"criteria\":[],\"description\":\"Percentage of patients 18-75 years of age with diabetes whose LDL-C was adequately controlled (<100 mg/dL) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"002\",\"success\":false,\"successVersions\":[],\"title\":\"Diabetes: Low Density Lipoprotein (LDL-C) Control (< 100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS55\",\"cqmCriterionId\":717,\"criteria\":[],\"description\":\"Median time from emergency department arrival to time of departure from the emergency room for patients admitted to the facility from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"495\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Admitted ED Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS164\",\"cqmCriterionId\":770,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had an active diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had documentation of use of aspirin or another antiplatelet during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"68\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Use of Aspirin or Another Antiplatelet\",\"typeId\":1},{\"allVersions\":[\"v3\",\"v2\"],\"cmsId\":\"CMS1017\",\"cqmCriterionId\":1288,\"criteria\":[],\"description\":\"This ratio measure assesses the number of inpatient hospitalizations where at least one fall with a major or moderate injury occurs among the total qualifying inpatient hospital days for patients age 18 years and older\",\"domain\":null,\"id\":null,\"nqfNumber\":\"4120e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Falls with Injury\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1154FHIR\",\"cqmCriterionId\":1295,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS61\",\"cqmCriterionId\":626,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years whose risk factors have been assessed and a fasting LDL-C test has been performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Cholesterol - Fasting Low Density Lipoprotein (LDL-C) Test Performed\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS62\",\"cqmCriterionId\":586,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of HIV/AIDS with at least two medical visits during the measurement year with a minimum of 90 days between each visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"368\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Medical Visit\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS158\",\"cqmCriterionId\":766,\"criteria\":[],\"description\":\"This measure identifies pregnant women who had a HBsAg (hepatitis B) test during their pregnancy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Pregnant women that had HBsAg testing\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS64\",\"cqmCriterionId\":627,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years who had a fasting LDL-C test performed and whose risk stratified fasting LDL-C is at or below the recommended LDL-C goal.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Risk-Stratified Cholesterol -Fasting Low Density Lipoprotein (LDL-C)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS832\",\"cqmCriterionId\":1285,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients age 18 and older who have an acute kidney injury (stage 2 or greater) that occurred during the encounter. Acute kidney injury (AKI) stage 2 or greater is defined as a substantial increase in serum creatinine value, or by the initiation of kidney dialysis (continuous renal replacement therapy (CRRT), hemodialysis or peritoneal dialysis).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3713e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Acute Kidney Injury\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS60\",\"cqmCriterionId\":606,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving fibrinolytic therapy during the hospital stay and having a time from hospital arrival to fibrinolysis of 30 minutes or less.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Fibrinolytic Therapy Received Within 30 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS65\",\"cqmCriterionId\":719,\"criteria\":[],\"description\":\"Percentage of patients aged 18-85 years of age with a diagnosis of hypertension whose blood pressure improved during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hypertension: Improvement in Blood Pressure\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS190\",\"cqmCriterionId\":1269,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after the initial admission (or transfer) to the Intensive Care Unit (ICU) or surgery end date for surgeries that start the day of or the day after ICU admission (or transfer)\",\"domain\":null,\"id\":null,\"nqfNumber\":\"372\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Intensive Care Unit Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS108\",\"cqmCriterionId\":1268,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after hospital admission or surgery end date for surgeries that start the day of or the day after hospital admission\",\"domain\":null,\"id\":null,\"nqfNumber\":\"371\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS109\",\"cqmCriterionId\":620,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received intravenous (IV) UFH therapy dosages AND had their platelet counts monitored using defined parameters such as a nomogram or protocol.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients Receiving Unfractionated Heparin with Dosages/Platelet Count Monitoring by Protocol or Nomogram\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS100\",\"cqmCriterionId\":604,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients prescribed aspirin at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0142\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Aspirin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS188\",\"cqmCriterionId\":629,\"criteria\":[],\"description\":\"(PN-6) Immunocompetent patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 1) Immunocompetent ICU patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 2) Immunocompetent non-Intensive Care Unit (ICU) patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0147\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Initial Antibiotic Selection for Community-Acquired Pneumonia (CAP) in Immunocompetent Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v0\",\"v5\",\"v6\"],\"cmsId\":\"CMS102\",\"cqmCriterionId\":729,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients who were assessed for rehabilitation services\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Assessed for Rehabilitation\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS30\",\"cqmCriterionId\":636,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients who are prescribed a statin medication at hospital discharge.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Statin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS31\",\"cqmCriterionId\":712,\"criteria\":[],\"description\":\"This measure assesses the proportion of births that have been screened for hearing loss before hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"1354\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hearing Screening Prior To Hospital Discharge\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v1\",\"v0\",\"v2\",\"v3\",\"v4\",\"v11\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS104\",\"cqmCriterionId\":1267,\"criteria\":[],\"description\":\"Ischemic stroke patients prescribed or continuing to take antithrombotic therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Antithrombotic Therapy\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS105\",\"cqmCriterionId\":1011,\"criteria\":[],\"description\":\"Ischemic stroke patients who are prescribed or continuing to take statin medication at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Statin Medication\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v4\",\"v5\"],\"cmsId\":\"CMS986\",\"cqmCriterionId\":1281,\"criteria\":[],\"description\":\"This measure assesses the percentage of hospitalizations for adults aged 65 years and older at the start of the inpatient encounter during the measurement period with a length of stay equal to or greater than 24 hours who received optimal malnutrition care during the current inpatient hospitalization where care performed was appropriate to the patient's level of malnutrition risk and severity. Malnutrition care best practices recommend that for each hospitalization, adult inpatients are screened for malnutrition risk, assessed to confirm findings of malnutrition risk or for a hospital dietitian referral order, and if identified with a \\\"moderate\\\" or \\\"severe\\\" malnutrition status in the current performed malnutrition assessment, receive a current \\\"moderate\\\" or \\\"severe\\\" malnutrition diagnosis and have a current nutrition care plan performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3592e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Global Malnutrition Composite Score\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS107\",\"cqmCriterionId\":732,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients or their caregivers who were given educational materials during the hospital stay addressing all of the following: activation of emergency medical system, need for follow-up after discharge, medications prescribed at discharge, risk factors for stroke, and warning signs and symptoms of stroke\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Stroke Education\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1244FHIR\",\"cqmCriterionId\":1291,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support hospital quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR) FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS182\",\"cqmCriterionId\":602,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had a diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had a complete lipid profile performed during the measurement period and whose most recent Low-density Lipoprotein (LDL-C) was adequately controlled (< 100 mg/dL).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"241\",\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Complete Lipid Panel and LDL-C Control (<100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS32\",\"cqmCriterionId\":713,\"criteria\":[],\"description\":\"Median elapsed time from emergency department arrival to emergency room departure for patients discharged from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"496\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Discharged ED Patients\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS185\",\"cqmCriterionId\":618,\"criteria\":[],\"description\":\"Percent of term singleton live births (excluding those with diagnoses originating in the fetal period) who DO NOT have significant complications during birth or the nursery care\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0716\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Healthy Term Newborn\",\"typeId\":2},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS1074\",\"cqmCriterionId\":1286,\"criteria\":[],\"description\":\"This measure provides a standardized method for monitoring the performance of diagnostic CT to discourage unnecessarily high radiation doses, a risk factor for cancer, while preserving image quality. This measure is expressed as a percentage of CT exams that are out-of-range based on having either excessive radiation dose or inadequate image quality relative to evidence-based thresholds based on the clinical indication for the exam. All diagnostic CT exams of specified anatomic sites performed in hospital inpatient care settings are eligible. This eCQM requires the use of additional software to access primary data elements stored within radiology electronic health records and translate them into data elements that can be ingested by this eCQM. Additional details are included in the Guidance field.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3663e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CT) in Adults (Facility IQR)\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS178\",\"cqmCriterionId\":632,\"criteria\":[],\"description\":\"Number of surgical patients whose urinary catheter is removed on Postoperative Day 1 (POD) 1 or Postoperative Day (POD) 2 with day of surgery being day zero.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Urinary catheter removed on Postoperative Day 1 (POD 1) or Postoperative Day 2 (POD 2) with day of surgery being day zero\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS179\",\"cqmCriterionId\":592,\"criteria\":[],\"description\":\"Average percentage of time in which patients aged 18 and older with atrial fibrillation who are on chronic warfarin therapy have International Normalized Ratio (INR) test results within the therapeutic range (i.e., TTR) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"380\",\"success\":false,\"successVersions\":[],\"title\":\"ADE Prevention and Monitoring: Warfarin Time in Therapeutic Range \",\"typeId\":1},{\"allVersions\":[\"v8\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS334\",\"cqmCriterionId\":1274,\"criteria\":[],\"description\":\"Nulliparous women with a term, singleton baby in a vertex position delivered by cesarean birth\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cesarean Birth\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS171\",\"cqmCriterionId\":634,\"criteria\":[],\"description\":\"Surgical patients with prophylactic antibiotics initiated within one hour prior to surgical incision. Patients who received vancomycin or a fluoroquinolone for prophylactic antibiotics should have the antibiotics initiated within two hours prior to surgical incision. Due to the longer infusion time required for vancomycin or a fluoroquinolone, it is acceptable to start these antibiotics within two hours prior to incision time.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0527\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Received Within One Hour Prior to Surgical Incision\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\"],\"cmsId\":\"CMS172\",\"cqmCriterionId\":635,\"criteria\":[],\"description\":\"Surgical patients who received prophylactic antibiotics consistent with current guidelines (specific to each type of surgical procedure).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0528\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Selection for Surgical Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS529\",\"cqmCriterionId\":1271,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWR outcome measure. 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ISO 9001:2015 Sections 7.5.1 and 7.5.2 - Covered by QM-04 ISO 9001:2015 Section 7.5.3 - Covered by QM-04 and IT-01 ISO 9001:2015 Section 8.1 - Covered by SE-01 ISO 9001:2015 Section 8.2 - Covered by SE-01 and SA-01 ISO 9001:2015 Sections 8.3.1, 8.3.2 and 8.3.3 - Covered by SE-01 and DQ-01 ISO 9001:2015 Section 8.3.4, 8.3.5 and 8.3.6 - Covered by DQ-01 ISO 9001:2015 Section 8.4 - Covered by PH-01 ISO 9001:2015 Sections 8.5.1, 8.5.2, 8.5.3 and 8.5.4 - Covered by SU-01 ISO 9001:2015 Section 8.5.5 - Covered by SU-01 and SU-02 ISO 9001:2015 Section 8.5.6 - Covered by SU-01 ISO 9001:2015 Section 8.6 - Covered by SU-01 and SD-05 ISO 9001:2015 Section 8.7 - Covered by DQ-01 ISO 9001:2015 Section 9.1.1 - Covered by QM-03 ISO 9001:2015 Section 9.1.2 - Covered by QM-03, CS-01 and SU-02 ISO 9001:2015 Section 9.1.3 - Covered by QM-03 and CS-01 ISO 9001:2015 Section 9.2 - Covered by QM-06 ISO 9001:2015 Section 9.3 - Covered by QM-02 ISO 9001:2015 Section 10.1 - Covered by QM-02 and QM-07 ISO 9001:2015 Section 10.2 - Covered by QM-07 ISO 9001:2015 Section 10.3 - Covered by QM-02\",\"qmsStandardId\":19,\"qmsStandardName\":\"Modified QMS/Mapped\"}],\"reportFileLocation\":null,\"rwtResultsCheckDate\":\"2026-02-24\",\"rwtResultsUrl\":\"https://www.alterahealth.com/legal/onc-reg-compliance/\",\"sed\":{\"ucdProcesses\":[{\"criteria\":[{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/computerized-provider-order-entry-cpoe-medications\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":1,\"number\":\"170.315 (a)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Computerized Provider Order Entry (CPOE) - 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Three rates are reported. 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The bone density evaluation must be prior to the start of ADT or within 3 months of the start of ADT.\",\"domain\":\"Effective Clinical Care\",\"id\":316408,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"Bone density evaluation for patients with prostate cancer and receiving androgen deprivation therapy\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS646\",\"cqmCriterionId\":910,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102190},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - 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This list must include ALL known prescriptions, over-thecounters, herbals, and vitamin/mineral/dietary (nutritional) supplements AND must contain the medications' name, dosage, frequency and route of administration.\",\"domain\":\"Patient Safety\",\"id\":316370,\"nqfNumber\":\"0419\",\"number\":\"130 GPRO CARE-3 \",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Documentation of Current Medications in the Medical Record\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS69\",\"cqmCriterionId\":227,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102076},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102077},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102078}],\"description\":\"Percentage of patients aged 18 years and older with a BMI documented during the current encounter or during the previous six months AND with a BMI outside of normal parameters, a follow-up plan is documented during the encounter or during the previous six months of the current encounter. 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Record and Export\"},\"id\":102079},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102080},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102081}],\"description\":\"Percentage of children, age 0-20 years, who received a fluoride varnish application during the measurement period.\",\"domain\":\"Clinical Process/ Effectiveness.\",\"id\":316372,\"nqfNumber\":\"N/A\",\"number\":\"379\",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Primary Caries Prevention Intervention as Offered by Primary Care Providers, including Dentists\",\"typeId\":1},{\"allVersions\":[\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS771\",\"cqmCriterionId\":838,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102193},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102194},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102195}],\"description\":\"Percentage of patients with an office visit within the measurement period and with a new diagnosis of clinically significant Benign Prostatic Hyperplasia who have International Prostate Symptoms Score (IPSS) or American Urological Association (AUA) Symptom Index (SI) documented at time of diagnosis and again 6-12 months later with an improvement of 3 points\",\"domain\":\"Person and Caregiver- Centered Experience and Outcomes\",\"id\":316410,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"International Prostate Symptom Score (IPSS) or American Urological Association-Symptom Index (AUA-SI) Change 6-12 Months After Diagnosis of Benign Prostatic Hyperplasia\",\"typeId\":1},{\"allVersions\":[\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\",\"v16\"],\"cmsId\":\"CMS90\",\"cqmCriterionId\":341,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102082},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102083},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102084}],\"description\":\"Percentage of patients aged 65 years and older with heart failure who completed initial and follow-up patient reported functional status assessments\",\"domain\":\"Patient and Family Engagement.\",\"id\":316373,\"nqfNumber\":\"N/A\",\"number\":\"377\",\"success\":true,\"successVersions\":[\"v5\"],\"title\":\"Functional Status Assessment for Complex Chronic Conditions\",\"typeId\":1},{\"allVersions\":[\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS951\",\"cqmCriterionId\":1018,\"criteria\":[{\"certificationId\":25,\"certificationNumber\":\"170.315 (c)(1)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-record-and-export\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":25,\"number\":\"170.315 (c)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Record and Export\"},\"id\":102196},{\"certificationId\":26,\"certificationNumber\":\"170.315 (c)(2)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-import-and-calculate\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":26,\"number\":\"170.315 (c)(2)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Import and Calculate\"},\"id\":102197},{\"certificationId\":172,\"certificationNumber\":\"170.315 (c)(3)\",\"criterion\":{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/clinical-quality-measures-cqms-report\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":172,\"number\":\"170.315 (c)(3)\",\"removed\":false,\"rule\":{\"id\":4,\"name\":\"Cures\"},\"startDay\":\"2020-06-30\",\"status\":\"ACTIVE\",\"title\":\"Clinical Quality Measures - Report\"},\"id\":102198}],\"description\":\"Percentage of patients aged 18-75 years with a diagnosis of diabetes who received a kidney health evaluation defined by an Estimated Glomerular Filtration Rate (eGFR) AND Urine Albumin-Creatinine Ratio (uACR) within the measurement period\",\"domain\":\"Promote effective prevention and treatment of chronic disease\",\"id\":316411,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":true,\"successVersions\":[\"v1\"],\"title\":\"Kidney Health Evaluation\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v1\",\"v3\",\"v4\"],\"cmsId\":\"CMS1028\",\"cqmCriterionId\":1278,\"criteria\":[],\"description\":\"Patients with severe obstetric complications which occur during the inpatient delivery hospitalization.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Severe Obstetric Complications\",\"typeId\":2},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1264\",\"cqmCriterionId\":1295,\"criteria\":[],\"description\":\"This measure assesses the proportion of ED encounters for patients who experience at least one emergency care access or timeliness gap. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (REHQR)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS826\",\"cqmCriterionId\":1285,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients aged 18 and older who suffer the harm of developing a new stage 2, stage 3, stage 4, deep tissue, or unstageable pressure injury\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3498e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Pressure Injury\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v11\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS72\",\"cqmCriterionId\":1267,\"criteria\":[],\"description\":\"Ischemic stroke patients administered antithrombotic therapy by the end of hospital day 2\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Antithrombotic Therapy By End of Hospital Day 2\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS73\",\"cqmCriterionId\":609,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received an overlap of parenteral (intravenous [IV] or subcutaneous [subcu]) anticoagulation and warfarin therapy. For patients who received less than five days of overlap therapy, they should be discharged on both medications or have a reason for discontinuation of overlap therapy. Overlap therapy should be administered for at least five days with an international normalized ratio (INR) greater than or equal to 2 prior to discontinuation of the parenteral anticoagulation therapy, discharged on both medications or have a reason for discontinuation of overlap therapy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0373\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients with Anticoagulation Overlap Therapy\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS75\",\"cqmCriterionId\":1231,\"criteria\":[],\"description\":\"Percentage of children, age 0-20 years, who have had tooth decay or cavities during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Children Who Have Dental Decay or Cavities\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS148\",\"cqmCriterionId\":560,\"criteria\":[],\"description\":\"Percentage of patients 5-17 years of age with diabetes with a Hemoglobin A1c (HbA1c) test during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"365\",\"success\":false,\"successVersions\":[],\"title\":\"Hemoglobin A1c Test for Pediatric Patients\",\"typeId\":1},{\"allVersions\":[\"v16\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS71\",\"cqmCriterionId\":1266,\"criteria\":[],\"description\":\"Ischemic stroke patients with atrial fibrillation/flutter who are prescribed or continuing to take anticoagulation therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Anticoagulation Therapy for Atrial Fibrillation/Flutter\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS140\",\"cqmCriterionId\":573,\"criteria\":[],\"description\":\"Percentage of female patients aged 18 years and older with Stage I (T1b) through IIIC, ER or PR positive breast cancer who were prescribed tamoxifen or aromatase inhibitor (AI) during the 12-month reporting period \",\"domain\":null,\"id\":null,\"nqfNumber\":\"0387\",\"number\":\"071\",\"success\":false,\"successVersions\":[],\"title\":\"Breast Cancer: Hormonal Therapy for Stage I (T1b)-IIIC Estrogen Receptor/ Progesterone Receptor (ER/PR) Positive Breast Cancer\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS77\",\"cqmCriterionId\":594,\"criteria\":[],\"description\":\"Percentage of patients aged 13 years and older with a diagnosis of HIV/AIDS, with at least two visits during the measurement year, with at least 90 days between each visit, whose most recent HIV RNA level is <200 copies/mL.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A \",\"number\":\"381\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: RNA control for Patients with HIV\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS141\",\"cqmCriterionId\":623,\"criteria\":[],\"description\":\"Percentage of patients aged 18 through 80 years with AJCC Stage III colon cancer who are referred for adjuvant chemotherapy, prescribed adjuvant chemotherapy, or have previously received adjuvant chemotherapy within the 12-month reporting period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0385\",\"number\":\"072\",\"success\":false,\"successVersions\":[],\"title\":\"Colon Cancer: Chemotherapy for AJCC Stage III Colon Cancer Patients\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS142\",\"cqmCriterionId\":1247,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed with documented communication to the physician who manages the ongoing care of the patient with diabetes mellitus regarding the findings of the macular or fundus exam at least once within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"89\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Communication with the Physician Managing Ongoing Diabetes Care\",\"typeId\":1},{\"allVersions\":[\"v2\",\"v1\"],\"cmsId\":\"CMS1154\",\"cqmCriterionId\":1291,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS816\",\"cqmCriterionId\":1276,\"criteria\":[],\"description\":\"Inpatient hospitalizations for patients 18 years of age or older at admission, who were administered at least one hypoglycemic medication during the encounter, who suffer the harm of a severe hypoglycemic event during the encounter\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3503e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Severe Hypoglycemia\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS9\",\"cqmCriterionId\":1007,\"criteria\":[],\"description\":\"Exclusive breast milk feeding during the newborn's entire hospitalization\",\"domain\":null,\"id\":null,\"nqfNumber\":\"480\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Exclusive Breast Milk Feeding\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS819\",\"cqmCriterionId\":1281,\"criteria\":[],\"description\":\"This measure assesses the number of inpatient hospitalizations for patients age 18 and older who have been administered an opioid medication and are subsequently administered an opioid antagonist within 12 hours, an indication of an opioid-related adverse event\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3501e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Opioid-Related Adverse Events\",\"typeId\":2},{\"allVersions\":[\"v16\",\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\",\"v15\"],\"cmsId\":\"CMS136\",\"cqmCriterionId\":1243,\"criteria\":[],\"description\":\"Percentage of children 6-12 years of age and newly dispensed a medication for attention-deficit/hyperactivity disorder (ADHD) who had appropriate follow-up care. Two rates are reported: a. Percentage of children who had one follow-up visit with a practitioner with prescribing authority during the 30-Day Initiation Phase.; b. Percentage of children who remained on ADHD medication for at least 210 days and who, in addition to the visit in the Initiation Phase, had at least two additional follow-up visits with a practitioner within 270 days (9 months) after the Initiation Phase ended.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"108\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Follow-Up Care for Children Prescribed ADHD Medication (ADD)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS82\",\"cqmCriterionId\":852,\"criteria\":[],\"description\":\"The percentage of children who turned 6 months of age during the measurement year, who had a face-to-face visit between the clinician and the child during child's first 6 months, and who had a maternal depression screening for the mother at least once between 0 and 6 months of life\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Maternal Depression Screening\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS132\",\"cqmCriterionId\":867,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of uncomplicated cataract who had cataract surgery and had any of a specified list of surgical procedures in the 30 days following cataract surgery which would indicate the occurrence of any of the following major complications: retained nuclear fragments, endophthalmitis, dislocated or wrong power IOL, retinal detachment, or wound dehiscence\",\"domain\":null,\"id\":null,\"nqfNumber\":\"564\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cataracts: Complications within 30 Days Following Cataract Surgery Requiring Additional Surgical Procedures\",\"typeId\":1},{\"allVersions\":[\"v2\"],\"cmsId\":\"CMS1244\",\"cqmCriterionId\":1293,\"criteria\":[],\"description\":\"This measure assesses the proportion of ED encounters for patients who experience at least one emergency care access or timeliness gap. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS166\",\"cqmCriterionId\":701,\"criteria\":[],\"description\":\"Percentage of patients 18-50 years of age with a diagnosis of low back pain who did not have an imaging study (plain X-ray, MRI, CT scan) within 28 days of the diagnosis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"52\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Use of Imaging Studies for Low Back Pain\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS167\",\"cqmCriterionId\":772,\"criteria\":[],\"description\":\"Percentage of patients aged 18 years and older with a diagnosis of diabetic retinopathy who had a dilated macular or fundus exam performed which included documentation of the level of severity of retinopathy and the presence or absence of macular edema during one or more office visits within 12 months\",\"domain\":null,\"id\":null,\"nqfNumber\":\"88\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Diabetic Retinopathy: Documentation of Presence or Absence of Macular Edema and Level of Severity of Retinopathy\",\"typeId\":1},{\"allVersions\":[\"v9\",\"v3\",\"v0\",\"v1\",\"v2\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS52\",\"cqmCriterionId\":843,\"criteria\":[],\"description\":\"Percentage of patients aged 6 weeks and older with a diagnosis of HIV/AIDS who were prescribed Pneumocystis jiroveci pneumonia (PCP) prophylaxis\",\"domain\":null,\"id\":null,\"nqfNumber\":\"405\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Pneumocystis Jiroveci Pneumonia (PCP) Prophylaxis\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS169\",\"cqmCriterionId\":773,\"criteria\":[],\"description\":\"Percentage of patients with depression or bipolar disorder with evidence of an initial assessment that includes an appraisal for alcohol or chemical substance use\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Bipolar Disorder and Major Depression: Appraisal for alcohol or chemical substance use\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS53\",\"cqmCriterionId\":716,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving primary PCI during the hospital stay with a time from hospital arrival to PCI of 90 minutes or less\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Primary PCI Received Within 90 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS844\",\"cqmCriterionId\":1273,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWM outcome measure. It is designed to extract the first resulted set of vital signs and basic laboratory results obtained from encounters for adult Medicare Fee-For-Service patients admitted to acute care short stay hospitals.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3502\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Core Clinical Data Elements for the Hybrid Hospital-Wide (All-Condition, All-Procedure) Risk-Standardized Mortality Measure (HWM)\",\"typeId\":2},{\"allVersions\":[\"v9\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\"],\"cmsId\":\"CMS160\",\"cqmCriterionId\":888,\"criteria\":[],\"description\":\"The percentage of patients age 18 and older with the diagnosis of major depression or dysthymia who have a completed PHQ-9 during each applicable 4 month period in which there was a qualifying visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"712\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Depression Utilization of the PHQ-9 Tool\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v1\",\"v2\",\"v0\",\"v3\",\"v4\"],\"cmsId\":\"CMS163\",\"cqmCriterionId\":584,\"criteria\":[],\"description\":\"Percentage of patients 18-75 years of age with diabetes whose LDL-C was adequately controlled (<100 mg/dL) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"002\",\"success\":false,\"successVersions\":[],\"title\":\"Diabetes: Low Density Lipoprotein (LDL-C) Control (< 100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS55\",\"cqmCriterionId\":717,\"criteria\":[],\"description\":\"Median time from emergency department arrival to time of departure from the emergency room for patients admitted to the facility from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"495\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Admitted ED Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS164\",\"cqmCriterionId\":770,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had an active diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had documentation of use of aspirin or another antiplatelet during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"68\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Use of Aspirin or Another Antiplatelet\",\"typeId\":1},{\"allVersions\":[\"v3\",\"v2\"],\"cmsId\":\"CMS1017\",\"cqmCriterionId\":1289,\"criteria\":[],\"description\":\"This ratio measure assesses the number of inpatient hospitalizations where at least one fall with a major or moderate injury occurs among the total qualifying inpatient hospital days for patients age 18 years and older\",\"domain\":null,\"id\":null,\"nqfNumber\":\"4120e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Falls with Injury\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1154FHIR\",\"cqmCriterionId\":1296,\"criteria\":[],\"description\":\"Percentage of adult patients with risk factors for type 2 diabetes who are due for glycemic screening for whom the screening process was completed during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Screening for Abnormal Glucose Metabolism in Patients at Risk of Developing Diabetes FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS61\",\"cqmCriterionId\":626,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years whose risk factors have been assessed and a fasting LDL-C test has been performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Cholesterol - Fasting Low Density Lipoprotein (LDL-C) Test Performed\",\"typeId\":1},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS62\",\"cqmCriterionId\":586,\"criteria\":[],\"description\":\"Percentage of patients, regardless of age, with a diagnosis of HIV/AIDS with at least two medical visits during the measurement year with a minimum of 90 days between each visit\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"368\",\"success\":false,\"successVersions\":[],\"title\":\"HIV/AIDS: Medical Visit\",\"typeId\":1},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS158\",\"cqmCriterionId\":766,\"criteria\":[],\"description\":\"This measure identifies pregnant women who had a HBsAg (hepatitis B) test during their pregnancy\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Pregnant women that had HBsAg testing\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS64\",\"cqmCriterionId\":627,\"criteria\":[],\"description\":\"Percentage of patients aged 20 through 79 years who had a fasting LDL-C test performed and whose risk stratified fasting LDL-C is at or below the recommended LDL-C goal.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"316\",\"success\":false,\"successVersions\":[],\"title\":\"Preventive Care and Screening: Risk-Stratified Cholesterol -Fasting Low Density Lipoprotein (LDL-C)\",\"typeId\":1},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS832\",\"cqmCriterionId\":1286,\"criteria\":[],\"description\":\"The measure assesses the number of inpatient hospitalizations for patients age 18 and older who have an acute kidney injury (stage 2 or greater) that occurred during the encounter. Acute kidney injury (AKI) stage 2 or greater is defined as a substantial increase in serum creatinine value, or by the initiation of kidney dialysis (continuous renal replacement therapy (CRRT), hemodialysis or peritoneal dialysis).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3713e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hospital Harm - Acute Kidney Injury\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS60\",\"cqmCriterionId\":606,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients with ST-segment elevation on the ECG closest to arrival time receiving fibrinolytic therapy during the hospital stay and having a time from hospital arrival to fibrinolysis of 30 minutes or less.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Fibrinolytic Therapy Received Within 30 Minutes of Hospital Arrival\",\"typeId\":2},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS65\",\"cqmCriterionId\":719,\"criteria\":[],\"description\":\"Percentage of patients aged 18-85 years of age with a diagnosis of hypertension whose blood pressure improved during the measurement period\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hypertension: Improvement in Blood Pressure\",\"typeId\":1},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS190\",\"cqmCriterionId\":1270,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after the initial admission (or transfer) to the Intensive Care Unit (ICU) or surgery end date for surgeries that start the day of or the day after ICU admission (or transfer)\",\"domain\":null,\"id\":null,\"nqfNumber\":\"372\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Intensive Care Unit Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v11\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS108\",\"cqmCriterionId\":1269,\"criteria\":[],\"description\":\"This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after hospital admission or surgery end date for surgeries that start the day of or the day after hospital admission\",\"domain\":null,\"id\":null,\"nqfNumber\":\"371\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Prophylaxis\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS109\",\"cqmCriterionId\":620,\"criteria\":[],\"description\":\"This measure assesses the number of patients diagnosed with confirmed VTE who received intravenous (IV) UFH therapy dosages AND had their platelet counts monitored using defined parameters such as a nomogram or protocol.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Venous Thromboembolism Patients Receiving Unfractionated Heparin with Dosages/Platelet Count Monitoring by Protocol or Nomogram\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS100\",\"cqmCriterionId\":604,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients prescribed aspirin at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0142\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Aspirin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS188\",\"cqmCriterionId\":629,\"criteria\":[],\"description\":\"(PN-6) Immunocompetent patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 1) Immunocompetent ICU patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines. (Population 2) Immunocompetent non-Intensive Care Unit (ICU) patients with Community-Acquired Pneumonia who receive an initial antibiotic regimen during the first 24 hours that is consistent with current guidelines\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0147\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Initial Antibiotic Selection for Community-Acquired Pneumonia (CAP) in Immunocompetent Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v0\",\"v5\",\"v6\"],\"cmsId\":\"CMS102\",\"cqmCriterionId\":729,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients who were assessed for rehabilitation services\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Assessed for Rehabilitation\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS30\",\"cqmCriterionId\":636,\"criteria\":[],\"description\":\"Acute myocardial infarction (AMI) patients who are prescribed a statin medication at hospital discharge.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Statin Prescribed at Discharge\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS31\",\"cqmCriterionId\":712,\"criteria\":[],\"description\":\"This measure assesses the proportion of births that have been screened for hearing loss before hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"1354\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Hearing Screening Prior To Hospital Discharge\",\"typeId\":2},{\"allVersions\":[\"v15\",\"v1\",\"v0\",\"v2\",\"v3\",\"v4\",\"v11\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\",\"v12\",\"v13\",\"v14\"],\"cmsId\":\"CMS104\",\"cqmCriterionId\":1268,\"criteria\":[],\"description\":\"Ischemic stroke patients prescribed or continuing to take antithrombotic therapy at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Antithrombotic Therapy\",\"typeId\":2},{\"allVersions\":[\"v11\",\"v3\",\"v4\",\"v0\",\"v1\",\"v2\",\"v5\",\"v6\",\"v7\",\"v8\",\"v9\",\"v10\"],\"cmsId\":\"CMS105\",\"cqmCriterionId\":1011,\"criteria\":[],\"description\":\"Ischemic stroke patients who are prescribed or continuing to take statin medication at hospital discharge\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Discharged on Statin Medication\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v2\",\"v4\",\"v5\"],\"cmsId\":\"CMS986\",\"cqmCriterionId\":1282,\"criteria\":[],\"description\":\"This measure assesses the percentage of hospitalizations for adults aged 65 years and older at the start of the inpatient encounter during the measurement period with a length of stay equal to or greater than 24 hours who received optimal malnutrition care during the current inpatient hospitalization where care performed was appropriate to the patient's level of malnutrition risk and severity. Malnutrition care best practices recommend that for each hospitalization, adult inpatients are screened for malnutrition risk, assessed to confirm findings of malnutrition risk or for a hospital dietitian referral order, and if identified with a \\\"moderate\\\" or \\\"severe\\\" malnutrition status in the current performed malnutrition assessment, receive a current \\\"moderate\\\" or \\\"severe\\\" malnutrition diagnosis and have a current nutrition care plan performed.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3592e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Global Malnutrition Composite Score\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS107\",\"cqmCriterionId\":732,\"criteria\":[],\"description\":\"Ischemic or hemorrhagic stroke patients or their caregivers who were given educational materials during the hospital stay addressing all of the following: activation of emergency medical system, need for follow-up after discharge, medications prescribed at discharge, risk factors for stroke, and warning signs and symptoms of stroke\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Stroke Education\",\"typeId\":2},{\"allVersions\":[\"v1\"],\"cmsId\":\"CMS1244FHIR\",\"cqmCriterionId\":1292,\"criteria\":[],\"description\":\"This measure assesses the variation in access and timeliness of emergency care to support hospital quality improvement for patients requiring emergency care in an emergency department (ED). This measure is designed to align with incentives to promote improved care both in EDs and the broader health system to help identify where patients do not receive timely access to emergency care. Emergency care access and timeliness gaps are inclusive of several concepts pertaining to boarding and crowding in an ED, including significantly longer ED wait times, higher left without being seen rates, longer boarding times, and longer total length of stay in the ED.\",\"domain\":null,\"id\":null,\"nqfNumber\":null,\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Emergency Care Access & Timeliness (HOQR) FHIR\",\"typeId\":1},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS182\",\"cqmCriterionId\":602,\"criteria\":[],\"description\":\"Percentage of patients 18 years of age and older who were diagnosed with acute myocardial infarction (AMI), coronary artery bypass graft (CABG) or percutaneous coronary interventions (PCI) in the 12 months prior to the measurement period, or who had a diagnosis of ischemic vascular disease (IVD) during the measurement period, and who had a complete lipid profile performed during the measurement period and whose most recent Low-density Lipoprotein (LDL-C) was adequately controlled (< 100 mg/dL).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"241\",\"success\":false,\"successVersions\":[],\"title\":\"Ischemic Vascular Disease (IVD): Complete Lipid Panel and LDL-C Control (<100 mg/dL)\",\"typeId\":1},{\"allVersions\":[\"v8\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v7\",\"v6\"],\"cmsId\":\"CMS32\",\"cqmCriterionId\":713,\"criteria\":[],\"description\":\"Median elapsed time from emergency department arrival to emergency room departure for patients discharged from the emergency department\",\"domain\":null,\"id\":null,\"nqfNumber\":\"496\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Median Time from ED Arrival to ED Departure for Discharged ED Patients\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS185\",\"cqmCriterionId\":618,\"criteria\":[],\"description\":\"Percent of term singleton live births (excluding those with diagnoses originating in the fetal period) who DO NOT have significant complications during birth or the nursery care\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0716\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Healthy Term Newborn\",\"typeId\":2},{\"allVersions\":[\"v4\",\"v2\",\"v3\"],\"cmsId\":\"CMS1074\",\"cqmCriterionId\":1287,\"criteria\":[],\"description\":\"This measure provides a standardized method for monitoring the performance of diagnostic CT to discourage unnecessarily high radiation doses, a risk factor for cancer, while preserving image quality. This measure is expressed as a percentage of CT exams that are out-of-range based on having either excessive radiation dose or inadequate image quality relative to evidence-based thresholds based on the clinical indication for the exam. All diagnostic CT exams of specified anatomic sites performed in hospital inpatient care settings are eligible. This eCQM requires the use of additional software to access primary data elements stored within radiology electronic health records and translate them into data elements that can be ingested by this eCQM. Additional details are included in the Guidance field.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"3663e\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CT) in Adults (Facility IQR)\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS178\",\"cqmCriterionId\":632,\"criteria\":[],\"description\":\"Number of surgical patients whose urinary catheter is removed on Postoperative Day 1 (POD) 1 or Postoperative Day (POD) 2 with day of surgery being day zero.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Urinary catheter removed on Postoperative Day 1 (POD 1) or Postoperative Day 2 (POD 2) with day of surgery being day zero\",\"typeId\":2},{\"allVersions\":[\"v5\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\"],\"cmsId\":\"CMS179\",\"cqmCriterionId\":592,\"criteria\":[],\"description\":\"Average percentage of time in which patients aged 18 and older with atrial fibrillation who are on chronic warfarin therapy have International Normalized Ratio (INR) test results within the therapeutic range (i.e., TTR) during the measurement period.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":\"380\",\"success\":false,\"successVersions\":[],\"title\":\"ADE Prevention and Monitoring: Warfarin Time in Therapeutic Range \",\"typeId\":1},{\"allVersions\":[\"v8\",\"v4\",\"v5\",\"v6\",\"v7\"],\"cmsId\":\"CMS334\",\"cqmCriterionId\":1275,\"criteria\":[],\"description\":\"Nulliparous women with a term, singleton baby in a vertex position delivered by cesarean birth\",\"domain\":null,\"id\":null,\"nqfNumber\":\"N/A\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Cesarean Birth\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v0\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\"],\"cmsId\":\"CMS171\",\"cqmCriterionId\":634,\"criteria\":[],\"description\":\"Surgical patients with prophylactic antibiotics initiated within one hour prior to surgical incision. Patients who received vancomycin or a fluoroquinolone for prophylactic antibiotics should have the antibiotics initiated within two hours prior to surgical incision. Due to the longer infusion time required for vancomycin or a fluoroquinolone, it is acceptable to start these antibiotics within two hours prior to incision time.\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0527\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Received Within One Hour Prior to Surgical Incision\",\"typeId\":2},{\"allVersions\":[\"v6\",\"v4\",\"v0\",\"v1\",\"v2\",\"v3\",\"v5\"],\"cmsId\":\"CMS172\",\"cqmCriterionId\":635,\"criteria\":[],\"description\":\"Surgical patients who received prophylactic antibiotics consistent with current guidelines (specific to each type of surgical procedure).\",\"domain\":null,\"id\":null,\"nqfNumber\":\"0528\",\"number\":null,\"success\":false,\"successVersions\":[],\"title\":\"Prophylactic Antibiotic Selection for Surgical Patients\",\"typeId\":2},{\"allVersions\":[\"v7\",\"v1\",\"v2\",\"v3\",\"v4\",\"v5\",\"v6\"],\"cmsId\":\"CMS529\",\"cqmCriterionId\":1272,\"criteria\":[],\"description\":\"This logic is intended to extract electronic clinical data. This is not an electronic clinical quality measure and this logic will not produce measure results. Instead, it will produce a file containing the data that CMS will link with administrative claims to risk adjust the Hybrid HWR outcome measure. 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ISO 9001:2015 Sections 7.5.1 and 7.5.2 - Covered by QM-04 ISO 9001:2015 Section 7.5.3 - Covered by QM-04 and IT-01 ISO 9001:2015 Section 8.1 - Covered by SE-01 ISO 9001:2015 Section 8.2 - Covered by SE-01 and SA-01 ISO 9001:2015 Sections 8.3.1, 8.3.2 and 8.3.3 - Covered by SE-01 and DQ-01 ISO 9001:2015 Section 8.3.4, 8.3.5 and 8.3.6 - Covered by DQ-01 ISO 9001:2015 Section 8.4 - Covered by PH-01 ISO 9001:2015 Sections 8.5.1, 8.5.2, 8.5.3 and 8.5.4 - Covered by SU-01 ISO 9001:2015 Section 8.5.5 - Covered by SU-01 and SU-02 ISO 9001:2015 Section 8.5.6 - Covered by SU-01 ISO 9001:2015 Section 8.6 - Covered by SU-01 and SD-05 ISO 9001:2015 Section 8.7 - Covered by DQ-01 ISO 9001:2015 Section 9.1.1 - Covered by QM-03 ISO 9001:2015 Section 9.1.2 - Covered by QM-03, CS-01 and SU-02 ISO 9001:2015 Section 9.1.3 - Covered by QM-03 and CS-01 ISO 9001:2015 Section 9.2 - Covered by QM-06 ISO 9001:2015 Section 9.3 - Covered by QM-02 ISO 9001:2015 Section 10.1 - Covered by QM-02 and QM-07 ISO 9001:2015 Section 10.2 - Covered by QM-07 ISO 9001:2015 Section 10.3 - Covered by QM-02\",\"qmsStandardId\":19,\"qmsStandardName\":\"Modified QMS/Mapped\"}],\"reportFileLocation\":null,\"rwtResultsCheckDate\":\"2026-02-24\",\"rwtResultsUrl\":\"https://www.alterahealth.com/legal/onc-reg-compliance/\",\"sed\":{\"ucdProcesses\":[{\"criteria\":[{\"certificationEdition\":\"2015\",\"certificationEditionId\":3,\"companionGuideLink\":\"https://www.healthit.gov/test-method/computerized-provider-order-entry-cpoe-medications\",\"description\":null,\"editable\":true,\"endDay\":null,\"id\":1,\"number\":\"170.315 (a)(1)\",\"removed\":false,\"rule\":{\"id\":3,\"name\":\"2015\"},\"startDay\":\"2015-10-16\",\"status\":\"ACTIVE\",\"title\":\"Computerized Provider Order Entry (CPOE) - 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