Date Updated:
eCQM Title: Post-partum follow up for contraception
eCQM Identifier if already designated: N/A
eCQM Version Number: v0
NQF Number:
MAT GUID:
Measurement Period: 12 months
Lookback Period: 90 days
Measure Steward: CDC
Measure Developer: NACHC
Endorsed By:
Description: This measure is intended to evaluate how many women with a recent pregnancy ending in delivery received post-partum follow up care, contraceptive counseling in the peri- or post-partum period and what contraceptive method, if any, they selected.
Intent: The measure is designed to enable a quality improvement workflow to support closing care gaps around opportunities to identify women at the end of a pregnancy episode that concluded in delivery.
Copyright:
Disclaimer:
Measure Scoring: Composite, proportion
Measure Type: Composite, process and outcome
Stratification: None
Risk Adjustment: None
Rate Aggregation: Describes how to combine information calculated based on logic in each of several populations into one summarized result. It can also serve to describe how to risk adjust the data based on supplemental data elements described in the eCQM.
Rationale: Supports patient-centered decision-making, allowing multiple methods to determine which patients fall out of the measure based on early termination of the pregnancy episode.
Clinical Recommendation Statement: MEC/SPR guidelines
Improvement Notation: Higher score indicates better performance on post-partum visit and contraceptive counseling, higher score indicates higher level of access to contraceptive methods.
Reference(s):
Bernard, Caitlin, et al. “Comparison of an Additional Early Visit to Routine Postpartum Care on Initiation of Long-
Acting Reversible Contraception: a Randomized Trial.” Contraception, 2018,
doi:10.1016/j.contraception.2018.05.010.
Brunner Huber, LR, et al. Factors Associated with Pregnancy Intention among Women Who Have Experienced a
Short Birth Interval: Findings from the 2009 to 2011 Mississippi and 2009 Tennessee Pregnancy Risk Assessment
Monitoring System. Annals of Epidemiology, 29 Mar. 2018.
Lopez, Laureen M, et al. “Education for Contraceptive Use by Women after Childbirth.” Cochrane Database of
Systematic Reviews, 2012, doi:10.1002/14651858.cd001863.pub3.
Lopez, LM, et al. “Strategies for Improving Postpartum Contraceptive Use: Evidence from Non-Randomized Studies.”
The Cochrane Database of Systematic Reviews, 27 Nov. 2014, doi:10.1002/14651858.CD011298.pub2.
Sothornwit, Jen, et al. “Immediate versus Delayed Postpartum Insertion of Contraceptive Implant for
Contraception.” Cochrane Database of Systematic Reviews, 2017, doi:10.1002/14651858.cd011913.pub2.
Trussell, J. Contraceptive Technology. Vol. 20, Ardent Media, Inc., 2011.
Definition: Long-acting contraception (LARC): Intrauterine devices and contraceptive implants.
Estimated Delivery Date (EDD): 40 weeks from LMP or calculated delivery date by gestational age as estimated by ultrasound.
Guidance: Use estimated delivery date (EDD) to determine the approximate delivery date and assume that pregnancy continued to delivery by 42 weeks if no confirmed delivery date is entered into record. Look for 6 week post-partum visit by 8 weeks post-EDD if delivery date is not available. If pregnancy episode started but was either closed by event other than delivery or if record contains termination of pregnancy via method other than delivery then episode should be excluded from criteria. Patients may qualify for contraceptive counseling as early as 34 weeks of pregnancy given that pre-delivery counseling provides option to maximize methods available immediately after delivery including sterilization or IUD.
Transmission Format:
Proportion or Ratio eCQMs: The following sections are found in the header of a Proportion or Ratio measure:
Supplemental Data Elements: CMS defines four required Supplemental Data Elements (payer, ethnicity, race, and sex), which are variables used to aggregate data into various subgroups. Comparison of results across strata can serve to show places disparities exist or areas in which exposing differences in results is necessary. Additional supplemental data elements required for risk adjustment or other purposes of data aggregation can be included in the Supplemental Data Element section. For this measure sex is not relevant because it excludes male patients.
Population Criteria: CQL development not yet defined
• Supplemental Data Elements: This is specific information to be retrieved for each patient reported in the eCQM, such as race, ethnicity, payer, and sex. Supplemental data elements might be used for risk adjustment or population health analytics. For this measure sex is not relevant because it excludes male patients