eCQM Title | Venous Thromboembolism Prophylaxis |
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eCQM Identifier (Measure Authoring Tool) | 108 | eCQM Version Number | 10.2.000 |
NQF Number | Not Applicable | GUID | 38b0b5ec-0f63-466f-8fe3-2cd20ddd1622 |
Measurement Period | January 1, 20XX through December 31, 20XX | ||
Measure Steward | The Joint Commission | ||
Measure Developer | The Joint Commission | ||
Endorsed By | None | ||
Description |
This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given between the day of arrival to the day after hospital admission or surgery end date for surgeries that start the day of or the day after hospital admission |
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Copyright |
Measure specifications are in the Public Domain. LOINC(R) copyright 2004-2020 Regenstrief Institute, Inc. This material contains SNOMED Clinical Terms(R) (SNOMED CT[R]) copyright 2004-2020 International Health Terminology Standards Development Organization. ICD-10 copyright 2020 World Health Organization. All Rights Reserved. |
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Disclaimer |
These performance measures are not clinical guidelines and do not establish a standard of medical care, and have not been tested for all potential applications. The measures and specifications are provided without warranty. |
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Measure Scoring | Proportion | ||
Measure Type | Process | ||
Stratification |
None |
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Risk Adjustment |
None |
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Rate Aggregation |
None |
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Rationale |
Hospitalized patients at high-risk for VTE may develop an asymptomatic deep vein thrombosis (DVT), and die from pulmonary embolism (PE) even before the diagnosis is suspected. The majority of fatal events occur as sudden or abrupt death, underscoring the importance of prevention as the most critical action step for reducing death from PE (Geerts et al., 2008). The estimated annual incidence of deep-vein thrombosis (DVT) and pulmonary embolism (PE), known collectively as venous thromboembolism (VTE), is approximately 900,000 (Geerts et al., 2008). Approximately two-thirds of cases of DVT or PE are associated with recent hospitalization. This is consistent with the 2001 report by The Agency for Healthcare Research and Quality (AHRQ). AHRQ indicates that "the appropriate application of effective preventive measures in hospitals has major potential for improving patient safety by reducing the incidence of venous thromboembolism" (Shojania et al., 2001). Despite its proven effectiveness, rates of appropriate thromboprophylaxis remain low in both medical and surgical patients. A recent analysis from the ENDORSE survey, which evaluated prophylaxis rates in 17,084 major surgery patients, found that more than one third of patients at risk for VTE (38%) did not receive prophylaxis and that rates varied by surgery type (Cohen et al., 2008). In a review of evidence-based patient safety practices, the Agency for Healthcare Research and Quality defined thromboprophylaxis against VTE as the "number one patient safety practice" for hospitalized patients (Shojania et al., 2001). Updated "safe practices" published by the National Quality Forum (NQF) recommend routine evaluation of hospitalized patients for risk of VTE and use of appropriate prophylaxis (National Quality Forum, 2006). As noted by the ACCP, a vast number of randomized clinical trials provide irrefutable evidence that thromboprophylaxis reduces VTE events, and there are studies that have also shown that fatal PE is prevented by thromboprophylaxis (Geerts et al., 2008). Some select surgeries have previously been monitored in the Surgical Care Improvement Project; since performance on these surgeries has achieved very high levels, they are not included in this measure. |
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Clinical Recommendation Statement |
Failure to recognize and protect patients at risk for venous thromboembolism (VTE) increases the chances for acutely ill hospitalized patients at high risk for developing a deep vein thrombosis or dying from a pulmonary embolism. Screening all patients is the only evidence based practice in reducing incidence of disease. All hospitalized patients should be evaluated for primary VTE prophylaxis, and given appropriate prophylaxis when indicated. |
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Improvement Notation |
Improvement noted as an increase in rate |
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Reference |
Reference Type: CITATION Reference Text: 'Cohen, A. T., Tapson, V. F., Bergmann, J. F., et al. (2008). Venous thromboembolism risk and prophylaxis in the acute hospital care setting (ENDORSE study): A multinational cross-sectional study. Lancet, 371, 387-394.' |
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Reference |
Reference Type: CITATION Reference Text: 'Geerts, W. H., Bergqvist, D., Pineo, G. F., et al. (2008). Prevention of venous thromboembolism: The Eighth ACCP Conference on Antithrombotic and Thrombolytic Therapy. Chest, 133, 381S-453S.' |
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Reference |
Reference Type: CITATION Reference Text: 'Guyatt, G. H., Akl, E. A., Crowther, M., et al. (2012). Antithrombotic therapy and prevention of thrombosis, 9th edition: American College of Chest Physicians evidence-based clinical practice guidelines. Chest, 141(2 Suppl.), 7S-47S.' |
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Reference |
Reference Type: CITATION Reference Text: 'Kearon, C., Akl, E. A., Comerota, A. J., et al. (2012, February). Antithrombotic therapy for VTE disease: Antithrombotic therapy and prevention of thrombosis, 9th edition: American College of Chest Physicians evidence-based clinical practice guidelines. Chest, 141(2 Suppl.), e419S-e494S.' |
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Reference |
Reference Type: CITATION Reference Text: 'National Quality Forum. (2006). National voluntary consensus standards for prevention and care of venous thromboembolism: Policy, preferred practices, and initial performance measures—A consensus report. Washington, DC: National Quality Forum.' |
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Reference |
Reference Type: CITATION Reference Text: 'Shojania, K. G., Duncan, B. W., McDonald, D. M., et al. (eds.). (2001). Making health care safer: A critical analysis of patient safety practices. Evidence Report/Technology Assessment No. 43. Rockville, MD: Agency for Healthcare Research and Quality.' |
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Reference |
Reference Type: CITATION Reference Text: 'Anderson, D. R., Morgano, G. P., Bennett, C., Dentali, F., Francis, C. W., Garcia, D. A., . . . Dahm, P. (2019). American Society of Hematology 2019 guidelines for management of venous thromboembolism: Prevention of venous thromboembolism in surgical hospitalized patients. Blood Advances, 3(23), 3898–3944. doi: 10.1182/bloodadvances.2019000975.' |
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Definition |
None |
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Guidance |
When low dose unfractionated heparin is administered for VTE Prophylaxis, the intended administration route for low dose unfractionated heparin is subcutaneous. Reasons for no pharmacological and no mechanical VTE prophylaxis must be explicitly documented by the MD/APN/PA or pharmacist and linked with VTE prophylaxis. Ambulation alone is not a sufficient reason for not administering VTE prophylaxis. In order for ambulation/patient ambulating to be considered as an acceptable reason, there needs to be explicit documentation, e.g., "patient out of bed and ambulating in halls - no VTE prophylaxis needed." This eCQM is an episode-based measure. An episode is defined as each inpatient hospitalization or encounter that ends during the measurement period. This version of the eCQM uses QDM version 5.5. Please refer to the eCQI resource center (https://ecqi.healthit.gov/qdm) for more information on the QDM. |
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Transmission Format |
TBD |
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Initial Population |
Inpatient hospitalizations for patients age 18 and older, discharged from hospital inpatient acute care without a diagnosis of venous thromboembolism (VTE) or obstetrics with a length of stay less than or equal to 120 days that ends during the measurement period |
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Denominator |
Initial population |
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Denominator Exclusions |
* Inpatient hospitalizations for patients who have a length of stay less than 2 days * Inpatient hospitalizations for patients with comfort measures documented anytime between the day of arrival and the day after hospital admission * Inpatient hospitalizations for patients with comfort measures documented by the day after surgery end date for surgeries that start the day of or the day after hospital admission * Inpatient hospitalizations for patients who are direct admits to intensive care unit (ICU), or transferred to ICU the day of or the day after hospital admission with ICU length of stay greater than or equal to one day * Inpatient hospitalizations for patients with a principal diagnosis of mental disorders or stroke * Inpatient hospitalizations for patients with a principal procedure of Surgical Care Improvement Project (SCIP) VTE selected surgeries |
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Numerator |
Inpatient hospitalizations for patients who received VTE prophylaxis: - between the day of arrival and the day after hospital admission - the day of or the day after surgery end date for surgeries that end the day of or the day after hospital admission Inpatient hospitalizations for patients who have documentation of a reason why no VTE prophylaxis was given: - between the day of arrival and the day after hospital admission - the day of or the day after surgery end date (for surgeries that end the day of or the day after hospital admission) |
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Numerator Exclusions |
Not Applicable |
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Denominator Exceptions |
None |
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Supplemental Data Elements |
For every patient evaluated by this measure also identify payer, race, ethnicity and sex |
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions"
"Initial Population"
"Encounter Less Than 2 Days" union "Encounter With ICU Location Stay 1 Day or More" union "Encounter With Principal Diagnosis of Mental Disorder or Stroke" union "Encounter With Principal Procedure of SCIP VTE Selected Surgery" union "Encounter With Intervention Comfort Measures From Day of Start of Hospitalization To Day After Admission" union "Encounter With Intervention Comfort Measures on Day of or Day After Procedure"
"Encounter With VTE Prophylaxis Received From Day of Start of Hospitalization To Day After Admission or Procedure" union ( "Encounter With Medication Oral Factor Xa Inhibitor Administered on Day of or Day After Admission or Procedure" intersect ( "Encounter With Prior or Present Diagnosis of Atrial Fibrillation or VTE" union "Encounter With Prior or Present Procedure of Hip or Knee Replacement Surgery" ) ) union "Encounter With Low Risk for VTE or Anticoagulant Administered" union "Encounter With No VTE Prophylaxis Due to Medical Reason" union "Encounter With No VTE Prophylaxis Due to Patient Refusal"
None
None
None
"Initial Population"
"Encounter Less Than 2 Days" union "Encounter With ICU Location Stay 1 Day or More" union "Encounter With Principal Diagnosis of Mental Disorder or Stroke" union "Encounter With Principal Procedure of SCIP VTE Selected Surgery" union "Encounter With Intervention Comfort Measures From Day of Start of Hospitalization To Day After Admission" union "Encounter With Intervention Comfort Measures on Day of or Day After Procedure"
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter where Global."LengthInDays" ( QualifyingEncounter.relevantPeriod ) < 2
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter where exists ( QualifyingEncounter.facilityLocations Location where Location.code in "Intensive Care Unit" and Global."LengthInDays" ( Location.locationPeriod ) >= 1 and Location.locationPeriod starts during Interval[start of QualifyingEncounter.relevantPeriod, Global."ToDate" ( start of QualifyingEncounter.relevantPeriod + 2 days ) ) )
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with "Intervention Comfort Measures" ComfortMeasures such that Coalesce(start of Global."NormalizeInterval"(ComfortMeasures.relevantDatetime, ComfortMeasures.relevantPeriod), ComfortMeasures.authorDatetime)during VTE."FromDayOfStartOfHospitalizationToDayAfterAdmission" ( QualifyingEncounter )
from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, "Intervention Comfort Measures" ComfortMeasures where Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and Coalesce(start of Global."NormalizeInterval"(ComfortMeasures.relevantDatetime, ComfortMeasures.relevantPeriod), ComfortMeasures.authorDatetime)during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter
"Low Risk for VTE or Anticoagulant Administered From Day of Start of Hospitalization To Day After Admission" union "Low Risk for VTE or Anticoagulant Administered on Day of or Day After Procedure"
( VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with ["Medication, Administered": "Oral Factor Xa Inhibitor for VTE Prophylaxis or VTE Treatment"] FactorXaMedication such that Global."NormalizeInterval" ( FactorXaMedication.relevantDatetime, FactorXaMedication.relevantPeriod ) starts during TJC."CalendarDayOfOrDayAfter" ( start of QualifyingEncounter.relevantPeriod ) ) union ( from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, ["Medication, Administered": "Oral Factor Xa Inhibitor for VTE Prophylaxis or VTE Treatment"] FactorXaMedication where Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and Global."NormalizeInterval" ( FactorXaMedication.relevantDatetime, FactorXaMedication.relevantPeriod ) starts during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter )
( "No VTE Prophylaxis Medication Due to Medical Reason From Day of Start of Hospitalization To Day After Admission" intersect "No VTE Prophylaxis Device Due to Medical Reason From Day of Start of Hospitalization To Day After Admission" ) union ( "No VTE Prophylaxis Medication Due to Medical Reason on Day of or Day After Procedure" intersect "No VTE Prophylaxis Device Due to Medical Reason on Day of or Day After Procedure" )
"No VTE Prophylaxis Due to Patient Refusal From Day of Start of Hospitalization To Day After Admission" union "No VTE Prophylaxis Due to Patient Refusal on Day of or Day After Procedure"
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter where exists ( QualifyingEncounter.diagnoses EncounterDiagnoses where EncounterDiagnoses.rank = 1 and ( EncounterDiagnoses.code in "Mental Health Diagnoses" or EncounterDiagnoses.code in "Hemorrhagic Stroke" or EncounterDiagnoses.code in "Ischemic Stroke" ) )
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with ( "SCIP VTE Selected Surgery" Procedure where Procedure.rank = 1 ) SelectedSCIPProcedure such that Global."NormalizeInterval" ( SelectedSCIPProcedure.relevantDatetime, SelectedSCIPProcedure.relevantPeriod ) during QualifyingEncounter.relevantPeriod
( VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with ["Diagnosis": "Atrial Fibrillation/Flutter"] AtrialFibrillation such that AtrialFibrillation.prevalencePeriod starts on or before end of QualifyingEncounter.relevantPeriod ) union ( VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter where exists ( QualifyingEncounter.diagnoses QualifyingEncounterDiagnoses where QualifyingEncounterDiagnoses.code in "Atrial Fibrillation/Flutter" ) ) union ( VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with ["Diagnosis": "Venous Thromboembolism"] VTEDiagnosis such that VTEDiagnosis.prevalencePeriod starts before start of QualifyingEncounter.relevantPeriod )
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with ( ["Procedure, Performed": "Hip Replacement Surgery"] union ["Procedure, Performed": "Knee Replacement Surgery"] ) HipKneeProcedure such that Global."NormalizeInterval" ( HipKneeProcedure.relevantDatetime, HipKneeProcedure.relevantPeriod ) starts on or before end of QualifyingEncounter.relevantPeriod
( VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with "VTE Prophylaxis by Medication Administered or Device Applied" VTEProphylaxis such that Global."NormalizeInterval" ( VTEProphylaxis.relevantDatetime, VTEProphylaxis.relevantPeriod ) starts during VTE."FromDayOfStartOfHospitalizationToDayAfterAdmission" ( QualifyingEncounter ) ) union ( from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, "VTE Prophylaxis by Medication Administered or Device Applied" VTEProphylaxis where Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and Global."NormalizeInterval" ( VTEProphylaxis.relevantDatetime, VTEProphylaxis.relevantPeriod ) starts during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter )
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions"
["Intervention, Order": "Comfort Measures"] union ["Intervention, Performed": "Comfort Measures"]
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with "Low Risk Indicator For VTE" LowRiskForVTE such that LowRiskForVTE.LowRiskDatetime during VTE."FromDayOfStartOfHospitalizationToDayAfterAdmission" ( QualifyingEncounter )
from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, "Low Risk Indicator For VTE" LowRiskForVTE where Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and LowRiskForVTE.LowRiskDatetime during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter
/*The variable "LowRiskDatetime" is to hold VTE Risk Assessment relevant dateTime, INR Laboratory Test result dateTime, and Anticoagulant Medication administration start dateTime.*/ ( ["Assessment, Performed": "Risk for venous thromboembolism"] VTERiskAssessment where VTERiskAssessment.result in "Low Risk" return { id: VTERiskAssessment.id, LowRiskDatetime: Global."EarliestOf" ( VTERiskAssessment.relevantDatetime, VTERiskAssessment.relevantPeriod ) } ) union ( ["Laboratory Test, Performed": "INR"] INRLabTest where INRLabTest.result > 3.0 return { id: INRLabTest.id, LowRiskDatetime: INRLabTest.resultDatetime } ) union ( ( ( ["Medication, Administered": "Unfractionated Heparin"] UnfractionatedHeparin where UnfractionatedHeparin.route in "Intravenous route" ) union ["Medication, Administered": "Direct Thrombin Inhibitor"] union ["Medication, Administered": "Glycoprotein IIb/IIIa Inhibitors"] ) AnticoagulantMedication return { id: AnticoagulantMedication.id, LowRiskDatetime: start of Global."NormalizeInterval" ( AnticoagulantMedication.relevantDatetime, AnticoagulantMedication.relevantPeriod ) } )
["Encounter, Performed": "Encounter Inpatient"] EncounterInpatient where "LengthInDays"(EncounterInpatient.relevantPeriod)<= 120 and EncounterInpatient.relevantPeriod ends during day of "Measurement Period"
["Device, Not Applied": "Intermittent pneumatic compression devices (IPC)"] union ["Device, Not Applied": "Venous foot pumps (VFP)"] union ["Device, Not Applied": "Graduated compression stockings (GCS)"] union ["Device, Not Ordered": "Intermittent pneumatic compression devices (IPC)"] union ["Device, Not Ordered": "Venous foot pumps (VFP)"] union ["Device, Not Ordered": "Graduated compression stockings (GCS)"]
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with "No VTE Prophylaxis Device Applied or Ordered" NoVTEDevice such that NoVTEDevice.negationRationale in "Medical Reason" and NoVTEDevice.authorDatetime during VTE."FromDayOfStartOfHospitalizationToDayAfterAdmission" ( QualifyingEncounter )
from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, "No VTE Prophylaxis Device Applied or Ordered" NoVTEDevice where NoVTEDevice.negationRationale in "Medical Reason" and Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and NoVTEDevice.authorDatetime during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with "No VTE Prophylaxis Medication or Device Due to Patient Refusal" PatientRefusal such that PatientRefusal.authorDatetime during VTE."FromDayOfStartOfHospitalizationToDayAfterAdmission" ( QualifyingEncounter )
from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, "No VTE Prophylaxis Medication or Device Due to Patient Refusal" PatientRefusal where Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and PatientRefusal.authorDatetime during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter
["Medication, Not Administered": "Low Dose Unfractionated Heparin for VTE Prophylaxis"] union ["Medication, Not Administered": "Low Molecular Weight Heparin for VTE Prophylaxis"] union ["Medication, Not Administered": "Injectable Factor Xa Inhibitor for VTE Prophylaxis"] union ["Medication, Not Administered": "Warfarin"] union ["Medication, Not Administered": "Rivaroxaban for VTE Prophylaxis"] union ["Medication, Not Ordered": "Low Dose Unfractionated Heparin for VTE Prophylaxis"] union ["Medication, Not Ordered": "Low Molecular Weight Heparin for VTE Prophylaxis"] union ["Medication, Not Ordered": "Injectable Factor Xa Inhibitor for VTE Prophylaxis"] union ["Medication, Not Ordered": "Warfarin"] union ["Medication, Not Ordered": "Rivaroxaban for VTE Prophylaxis"]
VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter with "No VTE Prophylaxis Medication Administered or Ordered" NoVTEMedication such that NoVTEMedication.negationRationale in "Medical Reason" and NoVTEMedication.authorDatetime during VTE."FromDayOfStartOfHospitalizationToDayAfterAdmission" ( QualifyingEncounter )
from VTE."Encounter With Age Range and Without VTE Diagnosis or Obstetrical Conditions" QualifyingEncounter, ["Procedure, Performed": "General or Neuraxial Anesthesia"] AnesthesiaProcedure, "No VTE Prophylaxis Medication Administered or Ordered" NoVTEMedication where NoVTEMedication.negationRationale in "Medical Reason" and Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ends 1 day after day of start of QualifyingEncounter.relevantPeriod and NoVTEMedication.authorDatetime during TJC."CalendarDayOfOrDayAfter" ( end of Global."NormalizeInterval" ( AnesthesiaProcedure.relevantDatetime, AnesthesiaProcedure.relevantPeriod ) ) return QualifyingEncounter
( "No VTE Prophylaxis Medication Administered or Ordered" union "No VTE Prophylaxis Device Applied or Ordered" ) NoVTEProphylaxis where NoVTEProphylaxis.negationRationale in "Patient Refusal"
"Encounter With VTE Prophylaxis Received From Day of Start of Hospitalization To Day After Admission or Procedure" union ( "Encounter With Medication Oral Factor Xa Inhibitor Administered on Day of or Day After Admission or Procedure" intersect ( "Encounter With Prior or Present Diagnosis of Atrial Fibrillation or VTE" union "Encounter With Prior or Present Procedure of Hip or Knee Replacement Surgery" ) ) union "Encounter With Low Risk for VTE or Anticoagulant Administered" union "Encounter With No VTE Prophylaxis Due to Medical Reason" union "Encounter With No VTE Prophylaxis Due to Patient Refusal"
//'SCIP' stands for Surgical Care Improvement Project ["Procedure, Performed": "General Surgery"] union ["Procedure, Performed": "Gynecological Surgery"] union ["Procedure, Performed": "Hip Fracture Surgery"] union ["Procedure, Performed": "Hip Replacement Surgery"] union ["Procedure, Performed": "Intracranial Neurosurgery"] union ["Procedure, Performed": "Knee Replacement Surgery"] union ["Procedure, Performed": "Urological Surgery"]
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
( ["Medication, Administered": "Low Dose Unfractionated Heparin for VTE Prophylaxis"] VTEMedication where VTEMedication.route in "Subcutaneous route" ) union ["Medication, Administered": "Low Molecular Weight Heparin for VTE Prophylaxis"] union ["Medication, Administered": "Injectable Factor Xa Inhibitor for VTE Prophylaxis"] union ["Medication, Administered": "Warfarin"] union ["Medication, Administered": "Rivaroxaban for VTE Prophylaxis"] union ["Device, Applied": "Intermittent pneumatic compression devices (IPC)"] union ["Device, Applied": "Venous foot pumps (VFP)"] union ["Device, Applied": "Graduated compression stockings (GCS)"]
Global."Inpatient Encounter" InpatientEncounter where not ( exists ( InpatientEncounter.diagnoses EncounterDiagnoses where ( EncounterDiagnoses.code in "Obstetrics" or EncounterDiagnoses.code in "Venous Thromboembolism" or EncounterDiagnoses.code in "Obstetrics VTE" ) ) )
( Global."Inpatient Encounter" InpatientEncounter with ["Patient Characteristic Birthdate": "Birth date"] BirthDate such that Global."CalendarAgeInYearsAt" ( BirthDate.birthDatetime, start of InpatientEncounter.relevantPeriod ) >= 18 ) intersect "Admission Without VTE or Obstetrical Conditions"
years between ToDate(BirthDateTime)and ToDate(AsOf)
if ( HasStart(period)) then start of period else end of period
Earliest(NormalizeInterval(pointInTime, period))
not ( start of period is null or start of period = minimum DateTime )
Encounter Visit let ObsVisit: Last(["Encounter, Performed": "Observation Services"] LastObs where LastObs.relevantPeriod ends 1 hour or less on or before start of Visit.relevantPeriod sort by end of relevantPeriod ), VisitStart: Coalesce(start of ObsVisit.relevantPeriod, start of Visit.relevantPeriod), EDVisit: Last(["Encounter, Performed": "Emergency Department Visit"] LastED where LastED.relevantPeriod ends 1 hour or less on or before VisitStart sort by end of relevantPeriod ) return Interval[Coalesce(start of EDVisit.relevantPeriod, VisitStart), end of Visit.relevantPeriod]
difference in days between start of Value and end of Value
if pointInTime is not null then Interval[pointInTime, pointInTime] else if period is not null then period else null as Interval<DateTime>
DateTime(year from Value, month from Value, day from Value, 0, 0, 0, 0, timezoneoffset from Value)
Interval[Global."ToDate" ( StartValue ), Global."ToDate" ( StartValue + 2 days ) )
Interval[Global."ToDate"(start of Global."HospitalizationWithObservation"(Encounter)), Global."ToDate"(start of Encounter.relevantPeriod + 2 days))
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
Measure Set |
eMeasure Venous Thromboembolism (eVTE) |
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