Evaluation of the short-form 36-item questionnaire to measure health-related quality of life in patients with idiopathic pulmonary fibrosis
Autor(a) principal: | |
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Data de Publicação: | 2000 |
Outros Autores: | , , , , |
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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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 |
|
_version_ |
1802764199082852352 |