Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey.
BACKGROUND:In most emergency situations or severe illness, patients are unable to consent for clinical trial enrollment. In such circumstances, the decision about whether to participate in a scientific study or not is made by a legally designated representative. OBJECTIVE:To address the willingness...
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doaj-dc58f4ae1fd44eab97bee171555cb1c42021-03-03T21:58:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01158e023667510.1371/journal.pone.0236675Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey.Flavia Julie do Amaral PfeilstickerCarolina Aguiar Sant Anna SiqueriNiklas Soderberg CamposFernanda Guimarães AguiarMaria Laura RomagnoliRenato Carneiro de Freitas ChavesCarolina Scoqui GuimarãesAdriano José PereiraRicardo Luiz CordioliAry Serpa NetoMurillo Santucci Cesar AssuncãoThiago Domingos CorrêaBACKGROUND:In most emergency situations or severe illness, patients are unable to consent for clinical trial enrollment. In such circumstances, the decision about whether to participate in a scientific study or not is made by a legally designated representative. OBJECTIVE:To address the willingness of patients admitted to the intensive care unit (ICU) to be enrolled in a scientific study as volunteers, and to assess the agreement between patients' and their legal representatives' opinion concerning enrollment in a scientific study. METHODS:This survey was conducted in two hospitals in São Paulo, Brazil. Patients (≥18 years) with preserved cognitive functions accompanied by a surrogate admitted to the ICU were eligible for this study. A survey containing 28 questions for patients and 8 questions for surrogates was applied within the first 48h from ICU admission. The survey for patients comprised three sections: demographic characteristics, opinion about participation in clinical research and knowledge about the importance of research. The survey for legal representatives contained two sections: demographic characteristics and assessment of legal representatives' opinion in authorizing patients to be enrolled in research. RESULTS:Between January 2017 and May 2018, 208 pairs of ICU patients and their respective legal representatives answered the survey. Out of 208 ICU patients answering the survey, 73.6% (153/208) were willing to be enrolled in the study as volunteers. Of those patients, 65.1% (97/149) would continue participating in a research even if their legal representative did not support their enrollment. Agreement between patients' and surrogates' opinion concerning participation was poor [Kappa = 0.11 (IC95% -0.02 to 0.25)]. If a consent for study participation had been obtained, 69.1% (103/149) of patients would continue participating in the study until its conclusion, and 23.5% (35/149) would allow researchers to use data collected to date, but would withdraw from the study on that occasion. CONCLUSION:The majority of patients admitted to the ICU were willing to be enrolled in a scientific study as volunteers, also after a deferred informed consent procedure has been used. Nevertheless, contradictory opinions between patients and their and their legal representatives' concerning enrollment in a scientific study were often observed.https://doi.org/10.1371/journal.pone.0236675 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Flavia Julie do Amaral Pfeilsticker Carolina Aguiar Sant Anna Siqueri Niklas Soderberg Campos Fernanda Guimarães Aguiar Maria Laura Romagnoli Renato Carneiro de Freitas Chaves Carolina Scoqui Guimarães Adriano José Pereira Ricardo Luiz Cordioli Ary Serpa Neto Murillo Santucci Cesar Assuncão Thiago Domingos Corrêa |
spellingShingle |
Flavia Julie do Amaral Pfeilsticker Carolina Aguiar Sant Anna Siqueri Niklas Soderberg Campos Fernanda Guimarães Aguiar Maria Laura Romagnoli Renato Carneiro de Freitas Chaves Carolina Scoqui Guimarães Adriano José Pereira Ricardo Luiz Cordioli Ary Serpa Neto Murillo Santucci Cesar Assuncão Thiago Domingos Corrêa Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey. PLoS ONE |
author_facet |
Flavia Julie do Amaral Pfeilsticker Carolina Aguiar Sant Anna Siqueri Niklas Soderberg Campos Fernanda Guimarães Aguiar Maria Laura Romagnoli Renato Carneiro de Freitas Chaves Carolina Scoqui Guimarães Adriano José Pereira Ricardo Luiz Cordioli Ary Serpa Neto Murillo Santucci Cesar Assuncão Thiago Domingos Corrêa |
author_sort |
Flavia Julie do Amaral Pfeilsticker |
title |
Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey. |
title_short |
Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey. |
title_full |
Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey. |
title_fullStr |
Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey. |
title_full_unstemmed |
Intensive care unit patients' opinion on enrollment in clinical research: A multicenter survey. |
title_sort |
intensive care unit patients' opinion on enrollment in clinical research: a multicenter survey. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2020-01-01 |
description |
BACKGROUND:In most emergency situations or severe illness, patients are unable to consent for clinical trial enrollment. In such circumstances, the decision about whether to participate in a scientific study or not is made by a legally designated representative. OBJECTIVE:To address the willingness of patients admitted to the intensive care unit (ICU) to be enrolled in a scientific study as volunteers, and to assess the agreement between patients' and their legal representatives' opinion concerning enrollment in a scientific study. METHODS:This survey was conducted in two hospitals in São Paulo, Brazil. Patients (≥18 years) with preserved cognitive functions accompanied by a surrogate admitted to the ICU were eligible for this study. A survey containing 28 questions for patients and 8 questions for surrogates was applied within the first 48h from ICU admission. The survey for patients comprised three sections: demographic characteristics, opinion about participation in clinical research and knowledge about the importance of research. The survey for legal representatives contained two sections: demographic characteristics and assessment of legal representatives' opinion in authorizing patients to be enrolled in research. RESULTS:Between January 2017 and May 2018, 208 pairs of ICU patients and their respective legal representatives answered the survey. Out of 208 ICU patients answering the survey, 73.6% (153/208) were willing to be enrolled in the study as volunteers. Of those patients, 65.1% (97/149) would continue participating in a research even if their legal representative did not support their enrollment. Agreement between patients' and surrogates' opinion concerning participation was poor [Kappa = 0.11 (IC95% -0.02 to 0.25)]. If a consent for study participation had been obtained, 69.1% (103/149) of patients would continue participating in the study until its conclusion, and 23.5% (35/149) would allow researchers to use data collected to date, but would withdraw from the study on that occasion. CONCLUSION:The majority of patients admitted to the ICU were willing to be enrolled in a scientific study as volunteers, also after a deferred informed consent procedure has been used. Nevertheless, contradictory opinions between patients and their and their legal representatives' concerning enrollment in a scientific study were often observed. |
url |
https://doi.org/10.1371/journal.pone.0236675 |
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