Función pulmonar, capacidad funcional y calidad de vida en pacientes con fibrosis pulmonar idiopática. Revisión de la literatura

Karin Villarroel-Bustamante, Daniel Alejandro Jérez-Mayorga, Christian Campos-Jara, Pedro Delgado-Floody, Iris Paola Guzmán-Guzmán

Resultado de la investigación: Review article

Resumen

Introduction: Idiopathic pulmonary fibrosis (IPF) is an interstitial, chronic and progressive disease that usually appears with dyspnea and progressive deterioration of exercise tolerance and activities of daily living, compromising psychological well-being and social interaction. Objectives: To select and summarize information about functional capacity response, pulmonary function and health-related quality of life in patients with IPF after being subjected to a pulmonary rehabilitation program. Materials and methods: Literature review from 2000 to 2016, using the PubMed and ScienceDirect databases. Results: 10 randomized clinical trials were selected. A tendency to a significant increase in the distance traveled in the 6-minute walk test was found. Regarding pulmonary function, results were variable among the studied populations. Quality of life related to health improvement was observed in all patients undergoing rehabilitation, but dyspnea levels showed discordant results. Conclusion: The trials show benefits in terms of functional capacity and health-related quality of life; however, studies are still scarce, done on small populations, and the effects of rehabilitation programs are not sustained 6 months after post-training evaluation.

Idioma originalSpanish
Páginas (desde-hasta)411-417
Número de páginas7
PublicaciónRevista Facultad de Medicina
Volumen66
N.º3
DOI
EstadoPublished - 1 jul 2018

Huella dactilar

Idiopathic Pulmonary Fibrosis
Rehabilitation
Quality of Life
Dyspnea
Lung
Exercise Tolerance
Interpersonal Relations
Activities of Daily Living
PubMed
Population
Chronic Disease
Randomized Controlled Trials
Databases
Psychology

ASJC Scopus subject areas

  • Medicine(all)

Citar esto

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abstract = "Introduction: Idiopathic pulmonary fibrosis (IPF) is an interstitial, chronic and progressive disease that usually appears with dyspnea and progressive deterioration of exercise tolerance and activities of daily living, compromising psychological well-being and social interaction. Objectives: To select and summarize information about functional capacity response, pulmonary function and health-related quality of life in patients with IPF after being subjected to a pulmonary rehabilitation program. Materials and methods: Literature review from 2000 to 2016, using the PubMed and ScienceDirect databases. Results: 10 randomized clinical trials were selected. A tendency to a significant increase in the distance traveled in the 6-minute walk test was found. Regarding pulmonary function, results were variable among the studied populations. Quality of life related to health improvement was observed in all patients undergoing rehabilitation, but dyspnea levels showed discordant results. Conclusion: The trials show benefits in terms of functional capacity and health-related quality of life; however, studies are still scarce, done on small populations, and the effects of rehabilitation programs are not sustained 6 months after post-training evaluation.",
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Función pulmonar, capacidad funcional y calidad de vida en pacientes con fibrosis pulmonar idiopática. Revisión de la literatura. / Villarroel-Bustamante, Karin; Jérez-Mayorga, Daniel Alejandro; Campos-Jara, Christian; Delgado-Floody, Pedro; Guzmán-Guzmán, Iris Paola.

En: Revista Facultad de Medicina, Vol. 66, N.º 3, 01.07.2018, p. 411-417.

Resultado de la investigación: Review article

TY - JOUR

T1 - Función pulmonar, capacidad funcional y calidad de vida en pacientes con fibrosis pulmonar idiopática. Revisión de la literatura

AU - Villarroel-Bustamante, Karin

AU - Jérez-Mayorga, Daniel Alejandro

AU - Campos-Jara, Christian

AU - Delgado-Floody, Pedro

AU - Guzmán-Guzmán, Iris Paola

PY - 2018/7/1

Y1 - 2018/7/1

N2 - Introduction: Idiopathic pulmonary fibrosis (IPF) is an interstitial, chronic and progressive disease that usually appears with dyspnea and progressive deterioration of exercise tolerance and activities of daily living, compromising psychological well-being and social interaction. Objectives: To select and summarize information about functional capacity response, pulmonary function and health-related quality of life in patients with IPF after being subjected to a pulmonary rehabilitation program. Materials and methods: Literature review from 2000 to 2016, using the PubMed and ScienceDirect databases. Results: 10 randomized clinical trials were selected. A tendency to a significant increase in the distance traveled in the 6-minute walk test was found. Regarding pulmonary function, results were variable among the studied populations. Quality of life related to health improvement was observed in all patients undergoing rehabilitation, but dyspnea levels showed discordant results. Conclusion: The trials show benefits in terms of functional capacity and health-related quality of life; however, studies are still scarce, done on small populations, and the effects of rehabilitation programs are not sustained 6 months after post-training evaluation.

AB - Introduction: Idiopathic pulmonary fibrosis (IPF) is an interstitial, chronic and progressive disease that usually appears with dyspnea and progressive deterioration of exercise tolerance and activities of daily living, compromising psychological well-being and social interaction. Objectives: To select and summarize information about functional capacity response, pulmonary function and health-related quality of life in patients with IPF after being subjected to a pulmonary rehabilitation program. Materials and methods: Literature review from 2000 to 2016, using the PubMed and ScienceDirect databases. Results: 10 randomized clinical trials were selected. A tendency to a significant increase in the distance traveled in the 6-minute walk test was found. Regarding pulmonary function, results were variable among the studied populations. Quality of life related to health improvement was observed in all patients undergoing rehabilitation, but dyspnea levels showed discordant results. Conclusion: The trials show benefits in terms of functional capacity and health-related quality of life; however, studies are still scarce, done on small populations, and the effects of rehabilitation programs are not sustained 6 months after post-training evaluation.

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KW - Fibrosis (mesh)

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