Cancer patients quality of life, measured by themselves and proxys.

Detalhes bibliográficos
Autor(a) principal: Oliveira, Alexandra
Data de Publicação: 2008
Outros Autores: Pimentel, Francisco L
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/776
Resumo: Health Related Quality of Life (HRQoL) is an essential factor for cancer patients, particularly in the evaluation of the care's. Most of the information that health care providers have is given by the patient. Family can also provide information about them, appealed or not and the quality of such information isn't studied for Portuguese population. The aim of this study was to examine whether proxies can provide useful information on HRQoL of cancer patients.We studied a sample of 176 ambulatory cancer patients and those 176 respective proxies (family) from Medical Oncology Department. A sociodemographic characterization was made for the simple and a clinical characterization was made only for cancer patients. To measure HRQoL were used the EORTC QLQ-C30. Beyond descriptive techniques, the statistical analysis was done using Interclass Correlation (ICC) and Pearson Correlation (r).We found moderate to good agreement (ICC ranged from 0.55 to 0.82, as well as the Pearson correlation) between responses from patients and those from their proxies for the QLQ-C30 scales. Proxies' group considered patients as having higher degree of fatigue, pain and diarrhea and a more impaired physical and emotional functioning, worse global QoL and total score. Statistically significant differences between patients' and proxies' evaluations were found for these subscales. None of the patients or proxies characteristics showed any relationship with the agreement between patient and proxy QoL evaluations'.The results suggest that proxies only provide valid and useful information about cancer patients QoL for QLQ-C30 domains where the agreement between QoL's responses were high and the means diferrence not significant. For using a HRQoL instrument taking into account as source the proxy, is necessary to recognize the agreement of the HRQoL's domains of the instrument. In this case, for several domains of QLQ-C30 the means difference was statistically significant, so, the instrument should be used with caution for physical and emotional functioning, global QoL fatigue, pain, diarrhoea and total QoL. Proxies are a frequent and a mandatory source of information about patient's status, particularly in palliative care. On a clinical point of view, the knowledge of these differences is very important for that such information be ponderous and contextualized in order to improve better care to the patients.
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spelling Cancer patients quality of life, measured by themselves and proxys.Qualidade de vida dos doentes oncológicos. Avaliada pelo próprio e pelo cuidador.Health Related Quality of Life (HRQoL) is an essential factor for cancer patients, particularly in the evaluation of the care's. Most of the information that health care providers have is given by the patient. Family can also provide information about them, appealed or not and the quality of such information isn't studied for Portuguese population. The aim of this study was to examine whether proxies can provide useful information on HRQoL of cancer patients.We studied a sample of 176 ambulatory cancer patients and those 176 respective proxies (family) from Medical Oncology Department. A sociodemographic characterization was made for the simple and a clinical characterization was made only for cancer patients. To measure HRQoL were used the EORTC QLQ-C30. Beyond descriptive techniques, the statistical analysis was done using Interclass Correlation (ICC) and Pearson Correlation (r).We found moderate to good agreement (ICC ranged from 0.55 to 0.82, as well as the Pearson correlation) between responses from patients and those from their proxies for the QLQ-C30 scales. Proxies' group considered patients as having higher degree of fatigue, pain and diarrhea and a more impaired physical and emotional functioning, worse global QoL and total score. Statistically significant differences between patients' and proxies' evaluations were found for these subscales. None of the patients or proxies characteristics showed any relationship with the agreement between patient and proxy QoL evaluations'.The results suggest that proxies only provide valid and useful information about cancer patients QoL for QLQ-C30 domains where the agreement between QoL's responses were high and the means diferrence not significant. For using a HRQoL instrument taking into account as source the proxy, is necessary to recognize the agreement of the HRQoL's domains of the instrument. In this case, for several domains of QLQ-C30 the means difference was statistically significant, so, the instrument should be used with caution for physical and emotional functioning, global QoL fatigue, pain, diarrhoea and total QoL. Proxies are a frequent and a mandatory source of information about patient's status, particularly in palliative care. On a clinical point of view, the knowledge of these differences is very important for that such information be ponderous and contextualized in order to improve better care to the patients.Health Related Quality of Life (HRQoL) is an essential factor for cancer patients, particularly in the evaluation of the care's. Most of the information that health care providers have is given by the patient. Family can also provide information about them, appealed or not and the quality of such information isn't studied for Portuguese population. The aim of this study was to examine whether proxies can provide useful information on HRQoL of cancer patients.We studied a sample of 176 ambulatory cancer patients and those 176 respective proxies (family) from Medical Oncology Department. A sociodemographic characterization was made for the simple and a clinical characterization was made only for cancer patients. To measure HRQoL were used the EORTC QLQ-C30. Beyond descriptive techniques, the statistical analysis was done using Interclass Correlation (ICC) and Pearson Correlation (r).We found moderate to good agreement (ICC ranged from 0.55 to 0.82, as well as the Pearson correlation) between responses from patients and those from their proxies for the QLQ-C30 scales. Proxies' group considered patients as having higher degree of fatigue, pain and diarrhea and a more impaired physical and emotional functioning, worse global QoL and total score. Statistically significant differences between patients' and proxies' evaluations were found for these subscales. None of the patients or proxies characteristics showed any relationship with the agreement between patient and proxy QoL evaluations'.The results suggest that proxies only provide valid and useful information about cancer patients QoL for QLQ-C30 domains where the agreement between QoL's responses were high and the means diferrence not significant. For using a HRQoL instrument taking into account as source the proxy, is necessary to recognize the agreement of the HRQoL's domains of the instrument. In this case, for several domains of QLQ-C30 the means difference was statistically significant, so, the instrument should be used with caution for physical and emotional functioning, global QoL fatigue, pain, diarrhoea and total QoL. Proxies are a frequent and a mandatory source of information about patient's status, particularly in palliative care. On a clinical point of view, the knowledge of these differences is very important for that such information be ponderous and contextualized in order to improve better care to the patients.Ordem dos Médicos2008-06-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/776oai:ojs.www.actamedicaportuguesa.com:article/776Acta Médica Portuguesa; Vol. 21 No. 2 (2008): March-April; 125-134Acta Médica Portuguesa; Vol. 21 N.º 2 (2008): Março-Abril; 125-1341646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/776https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/776/453Oliveira, AlexandraPimentel, Francisco Linfo:eu-repo/semantics/openAccess2022-12-20T10:56:54Zoai:ojs.www.actamedicaportuguesa.com:article/776Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:45.350369Repositório 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 Cancer patients quality of life, measured by themselves and proxys.
Qualidade de vida dos doentes oncológicos. Avaliada pelo próprio e pelo cuidador.
title Cancer patients quality of life, measured by themselves and proxys.
spellingShingle Cancer patients quality of life, measured by themselves and proxys.
Oliveira, Alexandra
title_short Cancer patients quality of life, measured by themselves and proxys.
title_full Cancer patients quality of life, measured by themselves and proxys.
title_fullStr Cancer patients quality of life, measured by themselves and proxys.
title_full_unstemmed Cancer patients quality of life, measured by themselves and proxys.
title_sort Cancer patients quality of life, measured by themselves and proxys.
author Oliveira, Alexandra
author_facet Oliveira, Alexandra
Pimentel, Francisco L
author_role author
author2 Pimentel, Francisco L
author2_role author
dc.contributor.author.fl_str_mv Oliveira, Alexandra
Pimentel, Francisco L
description Health Related Quality of Life (HRQoL) is an essential factor for cancer patients, particularly in the evaluation of the care's. Most of the information that health care providers have is given by the patient. Family can also provide information about them, appealed or not and the quality of such information isn't studied for Portuguese population. The aim of this study was to examine whether proxies can provide useful information on HRQoL of cancer patients.We studied a sample of 176 ambulatory cancer patients and those 176 respective proxies (family) from Medical Oncology Department. A sociodemographic characterization was made for the simple and a clinical characterization was made only for cancer patients. To measure HRQoL were used the EORTC QLQ-C30. Beyond descriptive techniques, the statistical analysis was done using Interclass Correlation (ICC) and Pearson Correlation (r).We found moderate to good agreement (ICC ranged from 0.55 to 0.82, as well as the Pearson correlation) between responses from patients and those from their proxies for the QLQ-C30 scales. Proxies' group considered patients as having higher degree of fatigue, pain and diarrhea and a more impaired physical and emotional functioning, worse global QoL and total score. Statistically significant differences between patients' and proxies' evaluations were found for these subscales. None of the patients or proxies characteristics showed any relationship with the agreement between patient and proxy QoL evaluations'.The results suggest that proxies only provide valid and useful information about cancer patients QoL for QLQ-C30 domains where the agreement between QoL's responses were high and the means diferrence not significant. For using a HRQoL instrument taking into account as source the proxy, is necessary to recognize the agreement of the HRQoL's domains of the instrument. In this case, for several domains of QLQ-C30 the means difference was statistically significant, so, the instrument should be used with caution for physical and emotional functioning, global QoL fatigue, pain, diarrhoea and total QoL. Proxies are a frequent and a mandatory source of information about patient's status, particularly in palliative care. On a clinical point of view, the knowledge of these differences is very important for that such information be ponderous and contextualized in order to improve better care to the patients.
publishDate 2008
dc.date.none.fl_str_mv 2008-06-27
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dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 21 No. 2 (2008): March-April; 125-134
Acta Médica Portuguesa; Vol. 21 N.º 2 (2008): Março-Abril; 125-134
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