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Quality of life in Parkinson`s Disease

In this review report, current possibilities of evaluation of quality of life in Parkinson’s disease have been critically presented. Health Related Quality of Life (-HRQoL) comprises a wide spectrum of consequences of the disease. Measurement of quality of life has become increasingly relevant as an...

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Detalles Bibliográficos
Autores principales: Opara, JA, Brola, W, Leonardi, M, Błaszczyk, B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539848/
https://www.ncbi.nlm.nih.gov/pubmed/23346238
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author Opara, JA
Brola, W
Leonardi, M
Błaszczyk, B
author_facet Opara, JA
Brola, W
Leonardi, M
Błaszczyk, B
author_sort Opara, JA
collection PubMed
description In this review report, current possibilities of evaluation of quality of life in Parkinson’s disease have been critically presented. Health Related Quality of Life (-HRQoL) comprises a wide spectrum of consequences of the disease. Measurement of quality of life has become increasingly relevant as an outcome parameter, especially in long-term trials. Most of the available QoL instruments depend on patient self-reports. The data can be collected by written questionnaires. There are universal questionnaires of QoL – for many diseases and the specific ones – specially created for one disease. Among universal questionnaires, the Sickness Impact Profile (SIP) and the Short-Form Health Status Survey (SF-36) are the most popular in Parkinson’s disease. As for specific questionnaires: the Parkinson`s Disease Questionnaire (PDQ-39) and the Parkinson`s Disease Quality of Life Questionnaire (PDQL) have been described.
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spelling pubmed-35398482013-02-15 Quality of life in Parkinson`s Disease Opara, JA Brola, W Leonardi, M Błaszczyk, B J Med Life Review In this review report, current possibilities of evaluation of quality of life in Parkinson’s disease have been critically presented. Health Related Quality of Life (-HRQoL) comprises a wide spectrum of consequences of the disease. Measurement of quality of life has become increasingly relevant as an outcome parameter, especially in long-term trials. Most of the available QoL instruments depend on patient self-reports. The data can be collected by written questionnaires. There are universal questionnaires of QoL – for many diseases and the specific ones – specially created for one disease. Among universal questionnaires, the Sickness Impact Profile (SIP) and the Short-Form Health Status Survey (SF-36) are the most popular in Parkinson’s disease. As for specific questionnaires: the Parkinson`s Disease Questionnaire (PDQ-39) and the Parkinson`s Disease Quality of Life Questionnaire (PDQL) have been described. Carol Davila University Press 2012-12-15 2012-12-25 /pmc/articles/PMC3539848/ /pubmed/23346238 Text en ©Carol Davila University Press http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Opara, JA
Brola, W
Leonardi, M
Błaszczyk, B
Quality of life in Parkinson`s Disease
title Quality of life in Parkinson`s Disease
title_full Quality of life in Parkinson`s Disease
title_fullStr Quality of life in Parkinson`s Disease
title_full_unstemmed Quality of life in Parkinson`s Disease
title_short Quality of life in Parkinson`s Disease
title_sort quality of life in parkinson`s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539848/
https://www.ncbi.nlm.nih.gov/pubmed/23346238
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