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The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort.
Walker, Caroline E; Mahede, Trinity; Davis, Geoff; Miller, Laura J; Girschik, Jennifer; Brameld, Kate; Sun, Wenxing; Rath, Ana; Aymé, Ségolène; Zubrick, Stephen R; Baynam, Gareth S; Molster, Caron; Dawkins, Hugh J S; Weeramanthri, Tarun S.
Afiliação
  • Walker CE; Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia.
  • Mahede T; Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia.
  • Davis G; Data Linkage Branch, Purchasing and System Performance, Department of Health, Government of Western Australia, Perth, Australia.
  • Miller LJ; Epidemiology Branch, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia.
  • Girschik J; Epidemiology Branch, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia.
  • Brameld K; Centre for Population Health Research, Curtin University, Perth, Australia.
  • Sun W; Epidemiology Branch, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia.
  • Rath A; INSERM, US14, Paris, France.
  • Aymé S; INSERM, US14, Paris, France.
  • Zubrick SR; Faculty of Education, University of Western Australia, Perth, Australia.
  • Baynam GS; Telethon Kids Institute, Perth, Australia.
  • Molster C; Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia.
  • Dawkins HJS; Telethon Kids Institute, Perth, Australia.
  • Weeramanthri TS; Genetic Services WA, King Edward Memorial Hospital, Perth, Australia.
Genet Med ; 19(5): 546-552, 2017 05.
Article em En | MEDLINE | ID: mdl-27657686
ABSTRACT

PURPOSE:

It has been argued that rare diseases should be recognized as a public health priority. However, there is a shortage of epidemiological data describing the true burden of rare diseases. This study investigated hospital service use to provide a better understanding of the collective health and economic impacts of rare diseases.

METHODS:

Novel methodology was developed using a carefully constructed set of diagnostic codes, a selection of rare disease cohorts from hospital administrative data, and advanced data-linkage technologies. Outcomes included health-service use and hospital admission costs.

RESULTS:

In 2010, cohort members who were alive represented approximately 2.0% of the Western Australian population. The cohort accounted for 4.6% of people discharged from hospital and 9.9% of hospital discharges, and it had a greater average length of stay than the general population. The total cost of hospital discharges for the cohort represented 10.5% of 2010 state inpatient hospital costs.

CONCLUSIONS:

This population-based cohort study provides strong new evidence of a marked disparity between the proportion of the population with rare diseases and their combined health-system costs. The methodology will inform future rare-disease studies, and the evidence will guide government strategies for managing the service needs of people living with rare diseases.Genet Med advance online publication 22 September 2016.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Raras / Serviços de Saúde / Tempo de Internação Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Raras / Serviços de Saúde / Tempo de Internação Idioma: En Ano de publicação: 2017 Tipo de documento: Article