Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis

Detalhes bibliográficos
Autor(a) principal: Martinez, Tieko Y. [UNIFESP]
Data de Publicação: 2000
Outros Autores: Pereira, Carlos A. C. [UNIFESP], Santos, Manuel L. dos [UNIFESP], Ciconelli, Rozana M. [UNIFESP], Guimarães, Sandra M. [UNIFESP], Martinez, JAB
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/26316
http://dx.doi.org/10.1378/chest.117.6.1627
Resumo: Objective: To validate the use of the 36-item short-form questionnaire (SF-36) for measuring health-related quality of life (HRQL) in patients with idiopathic pulmonary fibrosis (IPF).Design: Observational data at a single point in time,Setting: A specialized outpatient respiratory clinic.Participants: Thirty-four patients (mean +/- SE age, 58.29 +/- 1.87 years) with IPF and no significant comorbidity. A matched control group for HRQL measurements was composed of 34 normal subjects (mean age, 58.00 +/- 1.89 years).Measurements and results: Dyspnea was measured by the baseline dyspnea index (BDI). Respiratory function evaluation included FVC, FEV1, and resting; arterial blood gases. IPF patients showed a mean BDI score of 5.21 +/- 0.46. the mean FVC and FEV1 values were 62.41 +/- 2.96% and 66.41 +/- 3.33%, respectively. the mean Pao(2) was 67 +/- 2.51 mm Hg, and the mean Paco(2) was 37 +/- 1.05 mm Hg. Patients scored significantly worse than control subjects with respect to the SF-36 domains of physical functioning, physical role, general health perceptions, vitality, social functioning, emotional role, and mental health index. BDI scores were significantly correlated with five SF-36 components, and FVC and FEV1 were significantly correlated with two SF-36 components. Significant negative correllations were found between arterial pH and four SF-36 domains.Conclusions: Patients with IPF have a significant impairment of HRQL in both physical and psychological functioning. Dyspnea is the most important factor influencing the quality of life in these subjects. the SF-36 questionnaire is a valid instrument to evaluate HRQL in IPF patients.
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spelling Martinez, Tieko Y. [UNIFESP]Pereira, Carlos A. C. [UNIFESP]Santos, Manuel L. dos [UNIFESP]Ciconelli, Rozana M. [UNIFESP]Guimarães, Sandra M. [UNIFESP]Martinez, JABUniversidade Federal de São Paulo (UNIFESP)2016-01-24T12:31:06Z2016-01-24T12:31:06Z2000-06-01Chest. Northbrook: Amer Coll Chest Physicians, v. 117, n. 6, p. 1627-1632, 2000.0012-3692http://repositorio.unifesp.br/handle/11600/26316http://dx.doi.org/10.1378/chest.117.6.162710.1378/chest.117.6.1627WOS:000087666300021Objective: To validate the use of the 36-item short-form questionnaire (SF-36) for measuring health-related quality of life (HRQL) in patients with idiopathic pulmonary fibrosis (IPF).Design: Observational data at a single point in time,Setting: A specialized outpatient respiratory clinic.Participants: Thirty-four patients (mean +/- SE age, 58.29 +/- 1.87 years) with IPF and no significant comorbidity. A matched control group for HRQL measurements was composed of 34 normal subjects (mean age, 58.00 +/- 1.89 years).Measurements and results: Dyspnea was measured by the baseline dyspnea index (BDI). Respiratory function evaluation included FVC, FEV1, and resting; arterial blood gases. IPF patients showed a mean BDI score of 5.21 +/- 0.46. the mean FVC and FEV1 values were 62.41 +/- 2.96% and 66.41 +/- 3.33%, respectively. the mean Pao(2) was 67 +/- 2.51 mm Hg, and the mean Paco(2) was 37 +/- 1.05 mm Hg. Patients scored significantly worse than control subjects with respect to the SF-36 domains of physical functioning, physical role, general health perceptions, vitality, social functioning, emotional role, and mental health index. BDI scores were significantly correlated with five SF-36 components, and FVC and FEV1 were significantly correlated with two SF-36 components. Significant negative correllations were found between arterial pH and four SF-36 domains.Conclusions: Patients with IPF have a significant impairment of HRQL in both physical and psychological functioning. Dyspnea is the most important factor influencing the quality of life in these subjects. the SF-36 questionnaire is a valid instrument to evaluate HRQL in IPF patients.Universidade Federal de São Paulo, Div Pulm, São Paulo, BrazilUniversidade Federal de São Paulo, Div Rheumatol, São Paulo, BrazilUniversidade Federal de São Paulo, Div Pulm, São Paulo, BrazilUniversidade Federal de São Paulo, Div Rheumatol, São Paulo, BrazilWeb of Science1627-1632engAmer Coll Chest PhysiciansChestdyspneaidiopathic pulmonary fibrosislung functionquality of lifeEvaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/263162023-02-15 11:46:39.962metadata only accessoai:repositorio.unifesp.br:11600/26316Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-02-15T14:46:39Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
title Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
spellingShingle Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
Martinez, Tieko Y. [UNIFESP]
dyspnea
idiopathic pulmonary fibrosis
lung function
quality of life
title_short Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
title_full Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
title_fullStr Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
title_full_unstemmed Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
title_sort Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
author Martinez, Tieko Y. [UNIFESP]
author_facet Martinez, Tieko Y. [UNIFESP]
Pereira, Carlos A. C. [UNIFESP]
Santos, Manuel L. dos [UNIFESP]
Ciconelli, Rozana M. [UNIFESP]
Guimarães, Sandra M. [UNIFESP]
Martinez, JAB
author_role author
author2 Pereira, Carlos A. C. [UNIFESP]
Santos, Manuel L. dos [UNIFESP]
Ciconelli, Rozana M. [UNIFESP]
Guimarães, Sandra M. [UNIFESP]
Martinez, JAB
author2_role author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Martinez, Tieko Y. [UNIFESP]
Pereira, Carlos A. C. [UNIFESP]
Santos, Manuel L. dos [UNIFESP]
Ciconelli, Rozana M. [UNIFESP]
Guimarães, Sandra M. [UNIFESP]
Martinez, JAB
dc.subject.eng.fl_str_mv dyspnea
idiopathic pulmonary fibrosis
lung function
quality of life
topic dyspnea
idiopathic pulmonary fibrosis
lung function
quality of life
description Objective: To validate the use of the 36-item short-form questionnaire (SF-36) for measuring health-related quality of life (HRQL) in patients with idiopathic pulmonary fibrosis (IPF).Design: Observational data at a single point in time,Setting: A specialized outpatient respiratory clinic.Participants: Thirty-four patients (mean +/- SE age, 58.29 +/- 1.87 years) with IPF and no significant comorbidity. A matched control group for HRQL measurements was composed of 34 normal subjects (mean age, 58.00 +/- 1.89 years).Measurements and results: Dyspnea was measured by the baseline dyspnea index (BDI). Respiratory function evaluation included FVC, FEV1, and resting; arterial blood gases. IPF patients showed a mean BDI score of 5.21 +/- 0.46. the mean FVC and FEV1 values were 62.41 +/- 2.96% and 66.41 +/- 3.33%, respectively. the mean Pao(2) was 67 +/- 2.51 mm Hg, and the mean Paco(2) was 37 +/- 1.05 mm Hg. Patients scored significantly worse than control subjects with respect to the SF-36 domains of physical functioning, physical role, general health perceptions, vitality, social functioning, emotional role, and mental health index. BDI scores were significantly correlated with five SF-36 components, and FVC and FEV1 were significantly correlated with two SF-36 components. Significant negative correllations were found between arterial pH and four SF-36 domains.Conclusions: Patients with IPF have a significant impairment of HRQL in both physical and psychological functioning. Dyspnea is the most important factor influencing the quality of life in these subjects. the SF-36 questionnaire is a valid instrument to evaluate HRQL in IPF patients.
publishDate 2000
dc.date.issued.fl_str_mv 2000-06-01
dc.date.accessioned.fl_str_mv 2016-01-24T12:31:06Z
dc.date.available.fl_str_mv 2016-01-24T12:31:06Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Chest. Northbrook: Amer Coll Chest Physicians, v. 117, n. 6, p. 1627-1632, 2000.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/26316
http://dx.doi.org/10.1378/chest.117.6.1627
dc.identifier.issn.none.fl_str_mv 0012-3692
dc.identifier.doi.none.fl_str_mv 10.1378/chest.117.6.1627
dc.identifier.wos.none.fl_str_mv WOS:000087666300021
identifier_str_mv Chest. Northbrook: Amer Coll Chest Physicians, v. 117, n. 6, p. 1627-1632, 2000.
0012-3692
10.1378/chest.117.6.1627
WOS:000087666300021
url http://repositorio.unifesp.br/handle/11600/26316
http://dx.doi.org/10.1378/chest.117.6.1627
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Chest
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1627-1632
dc.publisher.none.fl_str_mv Amer Coll Chest Physicians
publisher.none.fl_str_mv Amer Coll Chest Physicians
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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