Evidence map›Paper›PMID 41478507›Full record

ArticleJournal of the American Pharmacists Association : JAPhA

Disparity implications of machine-learning-based MTM eligibility criteria.

Chi Chun Steve Tsang, Yan Cui, William C Cushman, Catherine M Crill, Katherine Stracner, Junling Wang

Abstract read
In one paragraph

Article in Journal of the American Pharmacists Association : JAPhA. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Chi Chun Steve Tsang
Yan Cui
William C Cushman
Catherine M Crill
Katherine Stracner
Junling Wang

Funding

Reducing Racial/Ethnic Disparities in Alzheimer's-Type Dementia with MTM ServicesR01AG040146 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Junling None Wang · 2011 to 2026
$3.7M
NIA NIH HHS R01 AG040146
6 · The paper itself

Abstract

backgroundAlthough Medicare Medication Therapy Management (MTM) programs have demonstrated clinical and economic benefits, racial/ethnic minority groups face challenges meeting eligibility criteria for enrollment. In 2017, the Centers for Medicare and Medicaid Services launched the 5-year Enhanced MTM demonstration, granting Part D plans flexibility in identifying eligible beneficiaries. However, because participating plans adopted predictive modeling to determine eligibility, concerns persist that this approach may perpetuate existing racial/ethnic disparities.

objectivesTo assess whether health cost-based MTM eligibility differs across race/ethnicity and whether machine learning models reproduce observed disparities in predicted eligibility.

methodsThis study analyzed 2019 Medicare administrative data linked to the Area Health Resource File for a 10% random sample of fee-for-service beneficiaries. Outcomes were binary indicators of top-quartile medication and health care costs, each measured from the Medicare and health care system perspectives. Multivariable logistic regression was employed to assess racial/ethnic disparities in top-quartile costs, using 6 algorithms - regularized logistic regression, random forest, gradient boosted trees, support vector machine, multilayer perceptron, and a consensus model. Predicted probabilities were computed to assess disparities in model outputs using multivariable fractional logistic regression.

resultsAmong 1,848,654 Medicare beneficiaries, Black and Hispanic individuals had significantly lower adjusted odds of top-quartile costs across all cost outcomes compared to their non-Hispanic White counterparts. For instance, the odds of being in the top quartile for total medication costs were 28% lower for Black beneficiaries (odds ratio [OR] = 0.72, 95% confidence interval [CI] = 0.70-0.75) and 21% lower for Hispanic beneficiaries (OR = 0.79, 95% CI = 0.74-0.84). Machine learning models reproduced these disparities in predicted probabilities, mirroring patterns in the empirical data.

conclusionImplementing cost-based MTM eligibility through predictive algorithms may perpetuate racial/ethnic disparities in MTM program access. Future research should explore strategies to mitigate such a potential when using such modeling to determine MTM eligibility.

Indexed as

Eligibility DeterminationHealthcare DisparitiesMachine LearningMedicare Part DMedication Therapy ManagementAgedAged, 80 and overEthnicityFee-for-Service PlansFemaleHealth Care CostsHumansMaleMedicareUnited States

Identifiers

PMID41478507
PMCPMC12790463

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Registered trials

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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.