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1.
Artigo em Inglês | MEDLINE | ID: mdl-36497947

RESUMO

Identifying and monitoring of health inequalities requires good-quality data. The aim of this work is to systematically review the evidence base on approaches taken within the healthcare context to improve the quality of data for the identification and monitoring of health inequalities and describe the evidence base on the effectiveness of such approaches or recommendations. Peer-reviewed scientific journal publications, as well as grey literature, were included in this review if they described approaches and/or made recommendations to improve data quality relating to the identification and monitoring of health inequalities. A thematic analysis was undertaken of included papers to identify themes, and a narrative synthesis approach was used to summarise findings. Fifty-seven papers were included describing a variety of approaches. These approaches were grouped under four themes: policy and legislation, wider actions that enable implementation of policies, data collection instruments and systems, and methodological approaches. Our findings indicate that a variety of mechanisms can be used to improve the quality of data on health inequalities at different stages (prior to, during, and after data collection). These findings can inform us of actions that can be taken by those working in local health and care services on approaches to improving the quality of data on health inequalities.


Assuntos
Atenção à Saúde , Políticas
3.
Am J Public Health ; 98(1): 28-38, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-18048802

RESUMO

Healthy People 2010 made it a priority to eliminate health disparities. We used a rapid assessment response and evaluation (RARE) to launch a program of participatory action research focused on health disparities in an urban, disadvantaged Black community serviced by a major south Florida health center. We formed partnerships with community members, identified local health disparities, and guided interventions targeting health disparities. We describe the RARE structure used to triangulate data sources and guide intervention plans as well as findings and conclusions drawn from scientific literature and epidemiological, historic, planning, clinical, and ethnographic data. Disenfranchisement and socioeconomic deprivation emerged as the principal determinants of local health disparities and the most appropriate targets for intervention.


Assuntos
Agentes Comunitários de Saúde/educação , Redes Comunitárias/organização & administração , Participação da Comunidade , Disparidades em Assistência à Saúde/estatística & dados numéricos , Qualidade da Assistência à Saúde , Serviços Urbanos de Saúde/estatística & dados numéricos , Florida , Grupos Focais , Humanos , Projetos Piloto , Pobreza , Serviços Urbanos de Saúde/economia , População Urbana
4.
BMC Public Health ; 3: 8, 2003 Jan 27.
Artigo em Inglês | MEDLINE | ID: mdl-12546708

RESUMO

BACKGROUND: Injuries are a major cause of mortality and morbidity in young people. Despite this, the long-term consequences for young survivors of severe injury are relatively unexplored. METHODS: Population based cohort study involving 5 year post injury structured interview of all cases of major trauma (Injury Severity Score > 15) identified retrospectively for 12 month period (1988 to 1989) within former Yorkshire Health Authority area of the United Kingdom. RESULTS: 125 individuals aged 11-24 years at time of injury were identified. Of these, 109 (87%) were interviewed. Only 20% (95% CI 14-29%) of those interviewed reported no disability. Mean Office of Population Census and Surveys (OPCS) disability score of the remainder was 7.5 (median 5.8, range 0.5 to 19.4). The most commonly encountered areas of disability were behaviour (54%, 95% CI 45-63%), intellectual functioning (39%, 95% CI 31-49%) and locomotion (29%, 95% CI 22-39%). Many respondents reported that their daily lives were adversely affected by their health problems for example, causing problems with work, 54% (95% CI 45-63%), or looking after the home, 28% (95% CI 21-38%). Higher OPCS scores were usually but not always associated with greater impact on daily activities. The burden of caring responsibilities fell largely on informal carers. 51% (95% CI 42-61%) of those interviewed would have liked additional help to cope with their injury and disability. CONCLUSION: The study has revealed significant disability amongst a cohort of young people 5 years post severe injury. Whilst many of these young people were coping well with the consequences of their injuries, others reported continuing problems with the activities of daily life. The factors underpinning the young people's differing experiences and social outcome should be explored.


Assuntos
Efeitos Psicossociais da Doença , Pessoas com Deficiência/reabilitação , Avaliação de Resultados em Cuidados de Saúde , Ferimentos e Lesões/reabilitação , Adaptação Psicológica , Adolescente , Adulto , Cuidadores , Estudos de Coortes , Avaliação da Deficiência , Pessoas com Deficiência/psicologia , Feminino , Seguimentos , Humanos , Escala de Gravidade do Ferimento , Masculino , Prevalência , Autoeficácia , Perfil de Impacto da Doença , Sobreviventes/psicologia , Reino Unido/epidemiologia , Ferimentos e Lesões/classificação , Ferimentos e Lesões/psicologia
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