ReviewHeart failure reviews2026
Why guideline-directed medical therapy depends on more than guidelines: microeconomics of medication use in heart failure.
Review in Heart failure reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Despite substantial mortality benefits, fewer than 25% of individuals with heart failure with reduced ejection fraction (HFrEF) receive all four pillars of guideline-directed medical therapy (GDMT), with underuse driven in part by economic and policy factors. Three clinician- and policy-relevant considerations may improve GDMT optimization. First, reduce patient cost sharing for GDMT at the public policy level. Evidence from national surveys demonstrates medication cost is a significant driver of nonadherence, particularly among economically vulnerable populations. Economic analyses have repeatedly shown GDMT produces high value welfare gains and cost-efficient savings through hospitalization and morbidity reduction. Second, enhance medication price transparency which is often obscured by insurance benefit design and complex rebate flows. Third, reduce overly burdensome administrative and formulary barriers. Cost containment mechanisms including prior authorizations and formulary limitations may delay or prevent initiation when applied to high-value therapies such as GDMT. Addressing these economic factors at both the policy-level and clinician-level is essential for translating GDMT into population-level survival gains. Therefore, this review integrates publicly available microeconomic data, economic theory, and health policy evidence to identify structural barriers to equitable GDMT optimization as well as provide pragmatic, policy-relevant solutions to aid clinicians in improving national adoption of GDMT.
Indexed as
Identifiers
42663770What OpenQuestion holds
Registered trials
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.