Time trends in emergency department use among adults with intellectual and developmental disabilities.


Journal

Disability and health journal
ISSN: 1876-7583
Titre abrégé: Disabil Health J
Pays: United States
ID NLM: 101306633

Informations de publication

Date de publication:
04 2022
Historique:
received: 22 06 2021
revised: 21 09 2021
accepted: 14 10 2021
pubmed: 17 11 2021
medline: 7 4 2022
entrez: 16 11 2021
Statut: ppublish

Résumé

Emergency Department (ED) visits are common among adults with intellectual and developmental disabilities (IDD). However, little is known about how ED use has varied over time in this population, or how it has been affected by recent Medicaid policy changes. To examine temporal trends in ED use among adult Medicaid members with IDD in eight states that ranged in the extent to which they had implemented state-level Medicaid policy changes that might affect ED use. We conducted repeated cross-sectional analyses of 2010-2016 Medicaid claims data. Quarterly analyses included adults ages 18-64 years with IDD (identified by diagnosis codes) who were continuously enrolled in Medicaid for the past 12 months. We assessed change in number of ED visits per 1000 member months from 2010 to 2016 overall and interacted with state level policy changes such as Medicaid expansion. States with no Medicaid expansion experienced an increase in ED visits (linear trend coefficient: 1.13, p < 0.01), while states operating expansion via waiver had a much smaller (non-significant) increase, and states with ACA-governed expansion had a decrease in ED visits (linear trend coefficient: 1.17, p < 0.01). Other policy changes had limited or no association with ED visits. Medicaid expansion was associated with modest reduction or limited increase in ED visits compared to no expansion. We found no consistent decrease in ED visits in association with other Medicaid policy changes.

Sections du résumé

BACKGROUND
Emergency Department (ED) visits are common among adults with intellectual and developmental disabilities (IDD). However, little is known about how ED use has varied over time in this population, or how it has been affected by recent Medicaid policy changes.
OBJECTIVE
To examine temporal trends in ED use among adult Medicaid members with IDD in eight states that ranged in the extent to which they had implemented state-level Medicaid policy changes that might affect ED use.
METHODS
We conducted repeated cross-sectional analyses of 2010-2016 Medicaid claims data. Quarterly analyses included adults ages 18-64 years with IDD (identified by diagnosis codes) who were continuously enrolled in Medicaid for the past 12 months. We assessed change in number of ED visits per 1000 member months from 2010 to 2016 overall and interacted with state level policy changes such as Medicaid expansion.
RESULTS
States with no Medicaid expansion experienced an increase in ED visits (linear trend coefficient: 1.13, p < 0.01), while states operating expansion via waiver had a much smaller (non-significant) increase, and states with ACA-governed expansion had a decrease in ED visits (linear trend coefficient: 1.17, p < 0.01). Other policy changes had limited or no association with ED visits.
CONCLUSIONS
Medicaid expansion was associated with modest reduction or limited increase in ED visits compared to no expansion. We found no consistent decrease in ED visits in association with other Medicaid policy changes.

Identifiants

pubmed: 34782255
pii: S1936-6574(21)00198-9
doi: 10.1016/j.dhjo.2021.101225
pmc: PMC10950032
mid: NIHMS1971042
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101225

Subventions

Organisme : Intramural CDC HHS
ID : CC999999
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

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Auteurs

Willi Horner-Johnson (W)

Institute on Development and Disability, Oregon Health & Science University, Portland, OR, USA. Electronic address: hornerjo@ohsu.edu.

Stephan Lindner (S)

Center for Health Systems Effectiveness, Oregon Health & Science University, Portland, OR, USA.

Anna Levy (A)

Center for Health Systems Effectiveness, Oregon Health & Science University, Portland, OR, USA.

Jean Hall (J)

Institute for Health and Disability Policy Studies, University of Kansas, Lawrence, KS, USA.

Noelle Kurth (N)

Institute for Health and Disability Policy Studies, University of Kansas, Lawrence, KS, USA.

Erika Garcia (E)

Michigan Department of Health and Human Services, Lansing, MI, USA.

Alice Frame (A)

Michigan Department of Health and Human Services, Lansing, MI, USA.

Kimberly Phillips (K)

Institute on Disability, University of New Hampshire, Durham, NH, USA.

Elizabeth Momany (E)

Public Policy Center, University of Iowa, Iowa City, IA, USA.

Melissa Lurie (M)

New York State Department of Health, Albany, NY, USA.

Yejee Shin (Y)

New York State Department of Health, Albany, NY, USA.

Emily Lauer (E)

Eunice Kennedy Shriver Center, University of Massachusetts Medical School, Shrewsbury, MA, USA.

Parag Kunte (P)

Commonwealth Medicine, University of Massachusetts Medical School, Shrewsbury, MA, USA.

Robin Silverstein (R)

Montana Department of Public Health & Human Services, Helena, MT, USA.

Catherine Okoro (C)

National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, USA.

Suzanne McDermott (S)

School of Public Health & Health Policy, City University of New York, New York, NY, USA.

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