Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper

Detalhes bibliográficos
Autor(a) principal: Baiardini, I.
Data de Publicação: 2010
Outros Autores: Bousquet, P. J., Brzoza, Z., Canonica, G. W., Compalati, E., Fiocchi, A., Fokkens, W., Gerth van Wijk, R., La Grutta, S., Lombardi, C., Maurer, M., Mota-Pinto, A., Ridolo, E., Senna, G. E., Terreehorst, I., Todo-Bom, A., Bousquet, J., Zuberbier, T., Braido, F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/20340
https://doi.org/10.1111/j.1398-9995.2009.02263.x
Resumo: The aim of this GA2LEN consensus report is to provide recommendations for Patient-Reported Outcomes evaluation in clinical trials for allergic diseases, which constitute a global health problem in terms of physical, psychological, economic and social impact. During the last 40 years PROs have gained large consideration and use in the scientific community, in order to gain a better understanding of patients’ subjective assessment with respect to elements concerning their health condition. They include all health-related reports coming from the patient, without involvement or interpretation by physician or others. PROs assessment should be performed by validated tools (disease-specific tools when available, or generic ones) selected taking into account the aim of the study, the expected intervention effects and the determinant and confounding factors or patient related factors which could influence PROs. Moreover, each tool should be used exclusively in the patient population following the authors’ indications without modification and performing a crosscultural validation if the tool must be used in a language that differs from the original. The result analysis also suggests that the relevance of PROs results in any interventional study should include a pre-post assessment providing information concerning statistical differences within or among groups, rates of response for the PROs outcome and a minimal important difference for the population. The report underlines the importance of further investigation on some topics, such as the quality assessment of existing PROs tools, the definition of inclusion and exclusion criteria and a more extensive evaluation of the correlation between PROs, besides HRQoL, and clinical data.
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spelling Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paperAlergiaGa2LenThe aim of this GA2LEN consensus report is to provide recommendations for Patient-Reported Outcomes evaluation in clinical trials for allergic diseases, which constitute a global health problem in terms of physical, psychological, economic and social impact. During the last 40 years PROs have gained large consideration and use in the scientific community, in order to gain a better understanding of patients’ subjective assessment with respect to elements concerning their health condition. They include all health-related reports coming from the patient, without involvement or interpretation by physician or others. PROs assessment should be performed by validated tools (disease-specific tools when available, or generic ones) selected taking into account the aim of the study, the expected intervention effects and the determinant and confounding factors or patient related factors which could influence PROs. Moreover, each tool should be used exclusively in the patient population following the authors’ indications without modification and performing a crosscultural validation if the tool must be used in a language that differs from the original. The result analysis also suggests that the relevance of PROs results in any interventional study should include a pre-post assessment providing information concerning statistical differences within or among groups, rates of response for the PROs outcome and a minimal important difference for the population. The report underlines the importance of further investigation on some topics, such as the quality assessment of existing PROs tools, the definition of inclusion and exclusion criteria and a more extensive evaluation of the correlation between PROs, besides HRQoL, and clinical data.2010info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/20340http://hdl.handle.net/10316/20340https://doi.org/10.1111/j.1398-9995.2009.02263.xenghttp://onlinelibrary.wiley.com/doi/10.1111/j.1398-9995.2009.02263.x/abstractBaiardini, I.Bousquet, P. J.Brzoza, Z.Canonica, G. W.Compalati, E.Fiocchi, A.Fokkens, W.Gerth van Wijk, R.La Grutta, S.Lombardi, C.Maurer, M.Mota-Pinto, A.Ridolo, E.Senna, G. E.Terreehorst, I.Todo-Bom, A.Bousquet, J.Zuberbier, T.Braido, F.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-05-25T06:05:35Zoai:estudogeral.uc.pt:10316/20340Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:39.660282Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
title Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
spellingShingle Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
Baiardini, I.
Alergia
Ga2Len
title_short Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
title_full Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
title_fullStr Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
title_full_unstemmed Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
title_sort Recommendations for assessing Patient-Reported Outcomes and Health-Related quality of life in clinical trials on allergy: a GA2LEN taskforce position paper
author Baiardini, I.
author_facet Baiardini, I.
Bousquet, P. J.
Brzoza, Z.
Canonica, G. W.
Compalati, E.
Fiocchi, A.
Fokkens, W.
Gerth van Wijk, R.
La Grutta, S.
Lombardi, C.
Maurer, M.
Mota-Pinto, A.
Ridolo, E.
Senna, G. E.
Terreehorst, I.
Todo-Bom, A.
Bousquet, J.
Zuberbier, T.
Braido, F.
author_role author
author2 Bousquet, P. J.
Brzoza, Z.
Canonica, G. W.
Compalati, E.
Fiocchi, A.
Fokkens, W.
Gerth van Wijk, R.
La Grutta, S.
Lombardi, C.
Maurer, M.
Mota-Pinto, A.
Ridolo, E.
Senna, G. E.
Terreehorst, I.
Todo-Bom, A.
Bousquet, J.
Zuberbier, T.
Braido, F.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Baiardini, I.
Bousquet, P. J.
Brzoza, Z.
Canonica, G. W.
Compalati, E.
Fiocchi, A.
Fokkens, W.
Gerth van Wijk, R.
La Grutta, S.
Lombardi, C.
Maurer, M.
Mota-Pinto, A.
Ridolo, E.
Senna, G. E.
Terreehorst, I.
Todo-Bom, A.
Bousquet, J.
Zuberbier, T.
Braido, F.
dc.subject.por.fl_str_mv Alergia
Ga2Len
topic Alergia
Ga2Len
description The aim of this GA2LEN consensus report is to provide recommendations for Patient-Reported Outcomes evaluation in clinical trials for allergic diseases, which constitute a global health problem in terms of physical, psychological, economic and social impact. During the last 40 years PROs have gained large consideration and use in the scientific community, in order to gain a better understanding of patients’ subjective assessment with respect to elements concerning their health condition. They include all health-related reports coming from the patient, without involvement or interpretation by physician or others. PROs assessment should be performed by validated tools (disease-specific tools when available, or generic ones) selected taking into account the aim of the study, the expected intervention effects and the determinant and confounding factors or patient related factors which could influence PROs. Moreover, each tool should be used exclusively in the patient population following the authors’ indications without modification and performing a crosscultural validation if the tool must be used in a language that differs from the original. The result analysis also suggests that the relevance of PROs results in any interventional study should include a pre-post assessment providing information concerning statistical differences within or among groups, rates of response for the PROs outcome and a minimal important difference for the population. The report underlines the importance of further investigation on some topics, such as the quality assessment of existing PROs tools, the definition of inclusion and exclusion criteria and a more extensive evaluation of the correlation between PROs, besides HRQoL, and clinical data.
publishDate 2010
dc.date.none.fl_str_mv 2010
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/20340
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https://doi.org/10.1111/j.1398-9995.2009.02263.x
url http://hdl.handle.net/10316/20340
https://doi.org/10.1111/j.1398-9995.2009.02263.x
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv http://onlinelibrary.wiley.com/doi/10.1111/j.1398-9995.2009.02263.x/abstract
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