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Attitudes to drug trials among relatives of unconscious intensive care patients

BACKGROUND: In many countries relatives are asked to consent on behalf of ICU patients prior to inclusion in clinical trials. However, the attitudes to drug trials among relatives of unconscious ICU patients are largely unknown. METHODS: We performed a prospective questionnaire survey at two univers...

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Autores principales: Perner, Anders, Ibsen, Michael, Bonde, Jan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890661/
https://www.ncbi.nlm.nih.gov/pubmed/20504325
http://dx.doi.org/10.1186/1471-2253-10-6
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author Perner, Anders
Ibsen, Michael
Bonde, Jan
author_facet Perner, Anders
Ibsen, Michael
Bonde, Jan
author_sort Perner, Anders
collection PubMed
description BACKGROUND: In many countries relatives are asked to consent on behalf of ICU patients prior to inclusion in clinical trials. However, the attitudes to drug trials among relatives of unconscious ICU patients are largely unknown. METHODS: We performed a prospective questionnaire survey at two university hospital ICUs of the next-of-kin to 50 unconscious adult patients. They were asked to complete a questionnaire within 48 hours of the patients' acute ICU admission. RESULTS: Forty-two relatives returned the questionnaire of which 41 were completed by direct family members and in one case by a friend to the patient. The majority of relatives (36/42) were positive/positive with some scepticism towards performing drug trials in unconscious ICU patients and 30/42 would most likely accept trial-participation by their relative. The majority (30/42) agreed that they should decide if their relative was to participate in a drug trial and 24 of these found that the treating clinician/ICU consultant should also consent. The majority (27/42) found that deferred consent would be acceptable if there was a limited time frame for initiation of treatment, however 8 respondents found this unacceptable when the intervention was a new drug. The majority of relatives stipulated that adherence to legislation, treatment benefit for the study patient and for future patients, no patient-risk or -discomfort and development of new drugs were important factors if their relative was to participate in an ICU drug trial. When questioned about doctors' motives for performing drug trials the wish for drug development and better patient care were highly rated among relatives. CONCLUSIONS: In general, relatives to unconscious ICU patients expressed positive attitudes to drug trials in the ICU and the inclusion of their relative in drug trials. Consent by next-of-kin and deferred consent was acceptable to the majority of relatives.
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spelling pubmed-28906612010-06-24 Attitudes to drug trials among relatives of unconscious intensive care patients Perner, Anders Ibsen, Michael Bonde, Jan BMC Anesthesiol Research article BACKGROUND: In many countries relatives are asked to consent on behalf of ICU patients prior to inclusion in clinical trials. However, the attitudes to drug trials among relatives of unconscious ICU patients are largely unknown. METHODS: We performed a prospective questionnaire survey at two university hospital ICUs of the next-of-kin to 50 unconscious adult patients. They were asked to complete a questionnaire within 48 hours of the patients' acute ICU admission. RESULTS: Forty-two relatives returned the questionnaire of which 41 were completed by direct family members and in one case by a friend to the patient. The majority of relatives (36/42) were positive/positive with some scepticism towards performing drug trials in unconscious ICU patients and 30/42 would most likely accept trial-participation by their relative. The majority (30/42) agreed that they should decide if their relative was to participate in a drug trial and 24 of these found that the treating clinician/ICU consultant should also consent. The majority (27/42) found that deferred consent would be acceptable if there was a limited time frame for initiation of treatment, however 8 respondents found this unacceptable when the intervention was a new drug. The majority of relatives stipulated that adherence to legislation, treatment benefit for the study patient and for future patients, no patient-risk or -discomfort and development of new drugs were important factors if their relative was to participate in an ICU drug trial. When questioned about doctors' motives for performing drug trials the wish for drug development and better patient care were highly rated among relatives. CONCLUSIONS: In general, relatives to unconscious ICU patients expressed positive attitudes to drug trials in the ICU and the inclusion of their relative in drug trials. Consent by next-of-kin and deferred consent was acceptable to the majority of relatives. BioMed Central 2010-05-26 /pmc/articles/PMC2890661/ /pubmed/20504325 http://dx.doi.org/10.1186/1471-2253-10-6 Text en Copyright ©2010 Perner et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Perner, Anders
Ibsen, Michael
Bonde, Jan
Attitudes to drug trials among relatives of unconscious intensive care patients
title Attitudes to drug trials among relatives of unconscious intensive care patients
title_full Attitudes to drug trials among relatives of unconscious intensive care patients
title_fullStr Attitudes to drug trials among relatives of unconscious intensive care patients
title_full_unstemmed Attitudes to drug trials among relatives of unconscious intensive care patients
title_short Attitudes to drug trials among relatives of unconscious intensive care patients
title_sort attitudes to drug trials among relatives of unconscious intensive care patients
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890661/
https://www.ncbi.nlm.nih.gov/pubmed/20504325
http://dx.doi.org/10.1186/1471-2253-10-6
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