Evidence map›Paper›PMID 42043918›Full record

ArticleJournal of managed care & specialty pharmacy2026

Compliance with the Veterans Health Administration's Pharmacy Benefit Management guidance for duration of clopidogrel following peripheral vascular interventions: a retrospective cohort study.

Sharon E Kim, Jennifer McCoy, Monique Boudreaux-Kelly, Franya Hutchins, Fran Cunningham, Shari Rogal, Edith Tzeng, Daniel E Hall, Carolyn T Thorpe, Katherine M Reitz

Abstract read
In one paragraph

Article in Journal of managed care & specialty pharmacy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sharon E KimSchool of Medicine, University of Pittsburgh, PA.
Jennifer McCoyOffice of Research and Development StatCore, VA Pittsburgh Healthcare System, PA.
Monique Boudreaux-KellyOffice of Research and Development StatCore, VA Pittsburgh Healthcare System, PA.
Franya HutchinsVA Center for Healthcare Evaluation, Research, and Promotion (CHERP), VA Pittsburgh Health Care System, PA.
Fran CunninghamPharmacy Benefits Management Services Center for Medication Safety, Veterans Health Administration, Hines, IL.
Shari RogalVA Center for Healthcare Evaluation, Research, and Promotion (CHERP), VA Pittsburgh Health Care System, PA.
Edith TzengSchool of Medicine, University of Pittsburgh, PA.
Daniel E HallVA Center for Healthcare Evaluation, Research, and Promotion (CHERP), VA Pittsburgh Health Care System, PA.
Carolyn T ThorpeVA Center for Healthcare Evaluation, Research, and Promotion (CHERP), VA Pittsburgh Health Care System, PA.
Katherine M ReitzSchool of Medicine, University of Pittsburgh, PA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClopidogrel was added to the national formulary of the Veterans Health Administration (VHA) in 2000, with national guidance in the form of Criteria for Use (CFU) generated in 2007 by the Pharmacy Benefits Management office. Although the national CFU restricted the duration of clopidogrel to no more than 30 days following peripheral vascular intervention (PVI) for peripheral artery disease (PAD), each local VHA Veterans Affairs Medical Center (VAMC) determined its own strategies of implementation. Strategies ranged from passive diffusion of information to electronic health record-mandated pharmacist approval for noncompliant CFU prescribing.

objectiveTo characterize patterns of compliance to restricted duration of clopidogrel and determine the factors associated with compliance.

methodsIn a retrospective cohort study, we used the Veterans Affairs Surgical Quality Initiative Program (2007-2022) to identify index PVI performed for PAD and integrated post-PVI medication information from the VA Clinical Data Warehouse. Our primary outcome was to evaluate compliance with the CFU. During the active CFU period (2007-2018), we compared patient, procedural, and VAMC features by CFU compliance and determined their associations with compliance using multivariable logistic regression. We also characterized variation in compliance across the Veterans Integrated Service Network (VISN), VAMC, and surgeons.

resultsAmong 7,206 PVIs with postoperative clopidogrel, 35% and 26% had post-PVI clopidogrel durations of no more than 30 days during and after the CFU period, respectively. During the active CFU period, we found no strong association among patient, PVI, and VAMC characteristics with compliance. Compliance during the active CFU period varied significantly among VISNs (16%-55%), VAMCs (0%-93%), and surgeons (0%-100%).

conclusionsAdherence to no more than 30 days of clopidogrel post-PVI was low during and after the active CFU period and varied substantially among the VISNs, VAMCs, and surgeons. Given that national guidance implementation was directed by local VHA pharmacies, this study highlights the importance and limitations of local implementation strategies on national guidance compliance.

Indexed as

ClopidogrelGuideline AdherencePeripheral Arterial DiseasePlatelet Aggregation InhibitorsAgedFemaleHumansMaleMiddle AgedRetrospective StudiesTime FactorsUnited StatesUnited States Department of Veterans AffairsClopidogrelPlatelet Aggregation Inhibitors

Identifiers

PMID42043918
PMCPMC13119478

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.