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1.
J Palliat Med ; 21(S2): S68-S73, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29313755

RESUMO

BACKGROUND: Care for patients with serious illness is an emerging practice area that has gained attention as value-based purchasing has increased. While the number of programs is growing, their impact on care quality and outcomes is unknown. OBJECTIVE: With support from the Gordon and Betty Moore Foundation, the National Committee for Quality Assurance (NCQA) is assessing the feasibility of creating an accountability program focused on serious illness care. METHODS: This article describes the process of developing an accountability program, findings from our initial work, and our plans to develop measures for a serious illness care accountability program. We focused on three questions: 1. What patient populations should be targeted for measurement? 2. What entities have accountability for ensuring high-quality care for serious illness? 3. What structures, processes, and outcomes should be evaluated in an accountability program for serious illness care? RESULTS: Our environmental scan showed that the evidence base for specific patient populations or care models is not sufficiently mature to justify traditional structure and process measures. In visits to serious illness care programs, we observed different staffing models, care models, care settings, and payment structures. We found a gap between recommended inclusion criteria and services when compared to inclusion criteria and services offered by existing programs. CONCLUSIONS: To address the challenges, NCQA intends to develop outcome measures driven by patient and family priorities. Structure and process measures will focus on building organizations' capacity to measure outcomes, including patient engagement and outcomes, linked to patient goals.


Assuntos
Doença Crônica/terapia , Atenção à Saúde/organização & administração , Qualidade da Assistência à Saúde , Responsabilidade Social , Humanos , Planejamento de Assistência ao Paciente , Desenvolvimento de Programas , Valores Sociais , Aquisição Baseada em Valor
2.
Am J Prev Med ; 24(1): 62-70, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12554025

RESUMO

BACKGROUND: Most health services in the United States are delivered by managed care organizations (MCOs). Publicly available, plan-specific performance information is required to adequately assess healthcare quality provided. Using women's health indicators, we compared performance results for MCOs and evaluated whether those MCOs that publicly report quality-of-care (QOC) results demonstrate better QOC than those plans that restrict public access to data. METHODS: Data from the Health Plan Employer Data and Information Set (HEDIS) for commercial MCOs in 1998 were analyzed for women's QOC indicators. Plan-specific, regional, and national performances were analyzed and results compared to established benchmarks. Public-reporting plans were compared to plans that restrict access to QOC information. Linear regression was used to identify determinants of health plan performance including public release of information. RESULTS: Commercial MCOs had wide variations in QOC indicators and, on average, failed to attain national health goals for most women's health indicators analyzed. Plans that restricted public access to QOC information had poorer performance than those that did not (p<0.05). Results suggest that whether a plan publicly releases its performance information is highly associated with health plan performance even after taking into account other factors. CONCLUSIONS: The voluntary aspect of reporting and the ability of health plans to restrict public access is allowing poorer performing health plans to escape public scrutiny. Variations in QOC have clinical significance and, if publicly available, would enable individuals to select high-quality healthcare products. The ability of health plans to restrict public information is not consistent with the 1973 Health Maintenance Organization Act requiring public information on health plan quality. A national strategy to ensure that QOC information is available on all healthcare systems is past due.


Assuntos
Coleta de Dados/métodos , Programas de Assistência Gerenciada/estatística & dados numéricos , Qualidade da Assistência à Saúde , Serviços de Saúde da Mulher/estatística & dados numéricos , Adulto , Feminino , Humanos , Programas de Assistência Gerenciada/normas , Pessoa de Meia-Idade , Estados Unidos
3.
Womens Health Issues ; 12(1): 46-58, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-11786292

RESUMO

The Health plan Employer Data and Information Set (HEDIS) is limited in its scope of women's health-related performance measures. Realizing this, the National Committee for Quality Assurance developed the Women's Health Measurement Advisory Panel (MAP) to expand and develop HEDIS measures to better represent women's health issues. This paper outlines the development of several new women's health-related performance measures and highlights the complexities of creating new measures to assess the quality of care provided to women through our nation's managed care organizations.


Assuntos
Planos de Assistência de Saúde para Empregados/normas , Programas de Assistência Gerenciada/normas , Indicadores de Qualidade em Assistência à Saúde , Serviços de Saúde da Mulher/normas , Comportamento Contraceptivo , Feminino , Fraturas Ósseas/etiologia , Fraturas Ósseas/prevenção & controle , Humanos , Menopausa , Saúde Mental , Osteoporose/complicações , Osteoporose/diagnóstico , Osteoporose/terapia , Estados Unidos
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