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CVD Risk Assessment Measure - Proportion of pregnant/postpartum patients who receive CVD Risk Assessment with a standardized tool.

CBE ID
4360
Endorsement Status
E&M Committee Rationale/Justification

Not Endorsed due to No Consensus

1.0 New or Maintenance
Previous Endorsement Cycle
Is Under Review
No
1.6 Measure Description

The University of California, Irvine (UCI) implemented and tested a CVD risk assessment tool that immediately identifies patients who are at increased risk for CVD or developing CVD. This tool can be integrated into the electronic health record (EHR) system. 

 

The population includes all patients who have a prenatal or postpartum visit at a healthcare facility or hospital network office; this includes pregnant and postpartum minors. The denominator in the CVD Risk Assessment Measure is all patients seen for pregnancy or postpartum care at a healthcare facility or hospital network. A hospital network includes Labor and Delivery (L&D), outpatient care in hospitals or at affiliated clinics, and private providers contracted with hospitals for delivery. The measure excludes patients who have another reason for visiting a clinic [not prenatal or postpartum care] and have a positive pregnancy test but plan to terminate the pregnancy or seek prenatal services elsewhere. 

 

This measure determines the percentage of pregnant or postpartum patients at a given clinic who were assessed for CVD risk with a standardized tool, such as the CVD risk assessment algorithm developed by the California Maternal Quality Care Collaborative (CMQCC). The aim is to perform CVD risk assessment using a standardized tool on all (100 %) eligible pregnant/postpartum patients.  All patients should be assessed for CVD risk at least once during their pregnancy and, if needed, additional times when new symptoms present during the pregnancy and/or postpartum period. A threshold has still to be determined (“at least xxx % of patients who received risk assessment”). The measure can be calculated on a quarterly or annual basis.

Measure Specs
General Information
1.7 Measure Type
1.7 Composite Measure
No
1.3 Electronic Clinical Quality Measure (eCQM)
1.10 Measure Rationale

Cardiovascular disease (CVD) is a leading cause of maternal mortality in the United States, responsible for over one-third of pregnancy-related deaths. Misdiagnosis of CVD is expected due to similar symptoms caused by pregnancy. Hence, it is crucial to identify pregnant and postpartum people at risk for CVD disease and/or with previously unknown CVD with a standardized risk assessment. Monitoring of these patients and timely interventions contribute to the prevention and mitigation of CVD-related complications and mortality. The proposed measure will allow clinicians to gauge the extent to which they use a standardized tool in their clinic practice and inform interventions to encourage its use.

1.25 Data Source Details

The California Maternal Quality Care Collaborative (CMQCC) developed a CVD risk assessment tool that guides stratification and initial evaluation of symptomatic or high-risk pregnant or postpartum patients. This is currently (May 2024) the only standardized tool to identify pregnant and postpartum patients who are at risk for CVD.  The acceptability of the tool is further strengthened by the support it has received from ACOG, and its inclusion in the CVD bundle by the Alliance for Innovation for Maternal Health.

The tool is integrated into EPIC and Cerner electronic health records, and all data can be retrieved from the EHR. For facilities that do not have electronic health record systems or patient volumes to warrant the inclusion of the tool in the EHR system, the tool can be administered on a hardcopy and the score calculated manually.  Facilities who administer the tool manually, can monitor follow up of patients with positive risk assessment in an excel file.