Qualidade de vida relacionada com a saúde em pessoas com artrites reumatoide: Caracterização dos estudos publicados entre 2003-2013] [Calidad de vida relacionada con la salud en personas con artritis reumatoide: Caracterización de los studios publicados entre 2003-2013
Background: Rheumatoid arthritis (RA) decreases physical activity, affects functionality, and increases social and psychological stress, with subsequent deterioration in the quality of life. Objective: To characterize the literature on quality of life in patients with RA. Methods: Systematic review...
- Autores:
-
Franco-Aguirre J.Q.
Cardona Arias, Jaiberth Antonio
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2015
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/42995
- Acceso en línea:
- https://doi.org/10.7705/biomedica.v37i3.3170
https://www.scopus.com/inward/record.uri?eid=2-s2.0-77954725908&doi=10.3233%2fNRE-2010-0583&partnerID=40&md5=1a34971d8cc77927cd526493dfe1f577
https://hdl.handle.net/20.500.12494/42995
- Palabra clave:
- Article
Health Assessment Questionnaire
human
quality of life
rheumatoid arthritis
Short Form 36
systematic review
- Rights
- closedAccess
- License
- http://purl.org/coar/access_right/c_14cb
Summary: | Background: Rheumatoid arthritis (RA) decreases physical activity, affects functionality, and increases social and psychological stress, with subsequent deterioration in the quality of life. Objective: To characterize the literature on quality of life in patients with RA. Methods: Systematic review of the literature in four multidisciplinary databases, using a comprehensive and reproducible protocol; analyses were based on frequencies. Results: 244 studies were characterized, out of them 55.3% were done in Europe and 25.4%, in America, of which 60% were form the United States; 59% corresponded to assessments of quality of life as the primary outcome; 29.1% were intervention studies that measured quality of life as secondary outcome, and 11.9% were scale validation studies. The primary measurement tools were Medical Outcome Study Short - Form 36 (51.6%) and Stanford Health Assessment Questionnaire (39.7%). About half of the studies did not do clinical staging of patients with RA. Conclusion: Our results demonstrate the interest to investigate the quality of life in patients with RA, the availability of multiples generic and specific scales for such purpose, and the concentration of publications in Europe and North America. © 2015 Universidad de Antioquia. All rights reserved. |
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