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Preparing the National Healthcare Disparities Report

Gaps in Data for Assessing Racial, Ethnic, and Socioeconomic Disparities in Health Care

Dados Bibliográficos

ID9101958
AutoresErnest Moy (0000-0002-0681-6866, Agency for Healthcare Research and Quality, autor correspondente), Irma E Arispe (National Center for Health Statistics), Julia S Holmes (National Center for Health Statistics), Roxanne M Andrews (Agency for Healthcare Research and Quality, autor correspondente)
Ano2005
Volume43
FascículoSupplement
PáginasI-9-I-16
Data de publicação2005-03-01
Peer ReviewedSim
Open AccessNão
TipoARTICLE
PeriódicoMedical Care (JOURNAL)
Identificadores do periódicoISSN: 0025-7079 • E-ISSN: 1537-1948
EditoraOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/00005650-200503001-00003
OpenAlexW4297899365
IdiomaEN
Citações recebidas8
Referências citadas10

Background: Efforts to quantify, monitor, understand, and reduce disparities in health care are critically dependent on the collection of high-quality data that support such analyses. In producing the first National Healthcare Disparities Report (NHDR), a number of gaps in data were encountered that limited the ability to assess racial, ethnic, and socioeconomic disparities in health care. Objectives: The objectives of this study were to identify and quantify gaps in data related to disparities in health care and discuss efforts to fill these gaps in future NHDRs. Findings: Data on specific racial, ethnic, and socioeconomic groups were often not collected or collected in formats that differed from federal standards. When collected, data were often insufficient to generate reliable estimates for specific racial, ethnic, and socioeconomic groups. These effects were magnified when attempting to assess disparities within many of the agency's priority populations such as women, children, the elderly, low-income populations, and rural residents. Future NHDRs begin to fill some of these gaps in data, but some gaps will likely persist and new gaps will likely arise as the availability of data for specific populations vary from year to year. Conclusions: Gaps in data limit the ability to address racial, ethnic, and socioeconomic disparities in health care. Although many federal efforts are underway to improve data collection, some groups and populations pose unique challenges for data collection that will be difficult to overcome

Agency (philosophy) · Data collection · Environmental health · Ethnic group · Geography · Health care · Health equity · Political science · Population · Socioeconomic status · Sociology · Global Health Workforce Issues · Healthcare Policy and Management · Medicine · Primary Care and Health Outcomes · Gerontology

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Obras citantes distintas8
Citações por ano0,38
Intervalo de citações2005 - 2014 (10)
Velocidade de citaçãohistorical
Altamente citadoNão
Tipos de citaçãoNeutras: 8
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