ArticleHealth affairs scholar2026
The changing Part D landscape.
Article in Health affairs scholar, 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
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.
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
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Differences in how Medicare advantage prescription drug plans (MA-PDs) and stand-alone prescription drug plans (PDPs) are financed may contribute to fewer coverage options for traditional Medicare beneficiaries. The Inflation Reduction Act (IRA) capped annual out-of-pocket spending and reduced government reinsurance, thereby placing more cost responsibility on plans and manufacturers and potentially further limiting coverage. Methods: This study draws on 2020-2025 data from the CMS public use files to compare coverage options by cost-sharing categories (defined by mean premium and deductible) across plan types and plan sponsors. Results: A majority of MA-PDs maintained low-premium and low-deductible designs (2020 = 66.0%, 2025 = 62.4%), reflecting cross-subsidies from integrated medical benefits, while enhanced PDPs increasingly pursued low-premium and high-deductible structures (38.2%, 51.5%), and basic/actuarially equivalent (AE) PDPs maintained high-premium and high-deductible structures (66.0%, 65.1%). In 2025, more than half of brand-only drugs in unprotected classes were excluded from Part D formularies (enhanced MA-PDs = 51.8%, enhanced PDPs = 57.3%, basic/AE PDPs = 60.0%), especially in high-spending therapeutic areas. Conclusions: Results reflect increasing consolidation and reduced plan diversity, with potential consequences for access and affordability among traditional Medicare beneficiaries. Policymakers may need to reconsider subsidy and risk-adjustment mechanisms to preserve competition and equitable access across plan types in the evolving Part D marketplace.
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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.