Evidence map›Paper›PMID 41144533›Full record

ArticlePloS one2025

Enrollment patterns among medicaid beneficiaries with sickle cell disease: Multistate findings from the sickle cell data collection program.

Ashima Singh, Mahua Dasgupta, Hannah K Peng, Mei Zhou, Catie Clyde, Brandon K Attell, Jhaqueline Valle, Sarah L Reeves, Jeffrey Huebner, Angela B Snyder

Abstract read
In one paragraph

Article in PloS one, 2025. 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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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

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.

Ashima SinghDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.ORCID https://orcid.org/0000-0002-1270-8132
Mahua DasguptaDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Hannah K PengDepartment of Pediatrics, Susan B Meister Child Health Evaluation and Research (CHEAR) Center, University of Michigan, Ann Arbor, Michigan, United States of America.
Mei ZhouGeorgia Health Policy Center, Andrew Young School of Policy Studies, Georgia State University, Atlanta, Georgia, United States of America.
Catie ClydeTracking California Program, Public Health Institute, Oakland, California, United States of America.
Brandon K AttellGeorgia Health Policy Center, Andrew Young School of Policy Studies, Georgia State University, Atlanta, Georgia, United States of America.
Jhaqueline ValleTracking California Program, Public Health Institute, Oakland, California, United States of America.
Sarah L ReevesDepartment of Pediatrics, Susan B Meister Child Health Evaluation and Research (CHEAR) Center, University of Michigan, Ann Arbor, Michigan, United States of America.
Jeffrey HuebnerDepartment of Health Services, Wisconsin Medicaid Program, Madison, Wisconsin, United States of America.
Angela B SnyderGeorgia Health Policy Center, Andrew Young School of Policy Studies, Georgia State University, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-5149-6355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajority of individuals living with sickle cell disease (SCD) in the United States are enrolled in Medicaid. The objective of the study was to determine the patterns of Medicaid enrollment among individuals with SCD.

methodWe determined the enrollment pattern among SCD Medicaid beneficiaries categorizing them in three groups: continuously enrolled, had exit and no return, had gaps in duration of enrollment during 2017-2019, leveraging the data from the Sickle Cell Data Collection Program in four states. We compared characteristics of individuals with gaps and those continuously enrolled using chi square tests.

resultsAmong 5883 children and 9260 adults, 70.5% and 61.8% respectively, were continuously enrolled. Gaps were observed in 12.5% of children and 12.9% of adults. A significantly smaller proportion of adults with gaps as compared to those who had continuous enrollment were disabled (CA:30.6% vs 65.3%; GA:23.7% vs 77.6%; MI:40.1% vs 69.5%; WI:39.8% vs 77.0%). Of all observed gaps, 60% were among adults. Enrollment patterns and gap duration varied by state.

conclusionApproximately 12% of individuals with SCD have gaps in enrollment during our 3-year study period. Individuals with disabilities were more likely to have continuous enrollment. Future work is needed to determine reasons for observed gaps and their impact on SCD health outcomes.

Indexed as

Anemia, Sickle CellMedicaidAdolescentAdultChildChild, PreschoolData CollectionFemaleHumansMaleMiddle AgedUnited StatesYoung Adult

Identifiers

PMID41144533
PMCPMC12558464

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