Literature DB >> 23612757

ICU research: the impact of invasiveness on informed consent.

Fabienne Gigon1, Paolo Merlani, Catherine Chenaud, Bara Ricou.   

Abstract

PURPOSE: Studies into the preferences of patients and relatives regarding informed consent for intensive care unit (ICU) research are ongoing. We investigated the impact of a study's invasiveness on the choice of who should give consent and on the modalities of informed consent.
METHODS: At ICU discharge, randomized pairs of patients and relatives were asked to answer a questionnaire about informed consent for research. One group received a vignette of a noninvasive study; the other, of an invasive study. Each study comprised two scenarios, featuring either a conscious or unconscious patient. Multivariate models assessed independent factors related to their preferences.
RESULTS: A total of 185 patients (40 %) and 125 relatives (68 %) responded. The invasiveness of a study had no impact on which people were chosen to give consent. This increased the desire to get more than one person to give consent and decreased the acceptance of deferred or two-step consent. Up to 31 % of both patients and relatives chose people other than the patient himself to give consent, even when the patient was conscious. A range of 3 to 17 % of the respondents reported that they would accept a waiving of consent. Younger respondents and individuals feeling coerced into study participation wanted to be the decision makers.
CONCLUSIONS: Study invasiveness had no impact on patients' and relatives' preferences about who should give consent. Many patients and relatives were reluctant to give consent alone. Deferred and two-step consent were less acceptable for the invasive study. Further work should investigate whether sharing the burden of informed consent with a second person facilitates participation in ICU research.

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Mesh:

Year:  2013        PMID: 23612757     DOI: 10.1007/s00134-013-2908-x

Source DB:  PubMed          Journal:  Intensive Care Med        ISSN: 0342-4642            Impact factor:   17.440


  35 in total

1.  Considering the vulnerabilities of surrogate decision-makers when obtaining consent for critical care research.

Authors:  Kali A Barrett; Damon C Scales
Journal:  Intensive Care Med       Date:  2011-11-26       Impact factor: 17.440

2.  Why substitute decision makers provide or decline consent for ICU research studies: a questionnaire study.

Authors:  Sangeeta Mehta; Friederike Quittnat Pelletier; Maedean Brown; Cheryl Ethier; David Wells; Lisa Burry; Rod MacDonald
Journal:  Intensive Care Med       Date:  2011-11-26       Impact factor: 17.440

Review 3.  The kappa statistic in reliability studies: use, interpretation, and sample size requirements.

Authors:  Julius Sim; Chris C Wright
Journal:  Phys Ther       Date:  2005-03

4.  Effect of consent rituals on mortality in emergency care research.

Authors:  Ian Roberts; David Prieto-Merino; Haleema Shakur; Iain Chalmers; Jon Nicholl
Journal:  Lancet       Date:  2011-03-26       Impact factor: 79.321

5.  Surrogate decision makers' attitudes towards research decision making for critically ill patients.

Authors:  Kali A Barrett; Niall D Ferguson; Valerie Athaide; Deborah J Cook; Jan O Friedrich; Ellen McDonald; Ruxandra Pinto; Orla M Smith; James Stevenson; Damon C Scales
Journal:  Intensive Care Med       Date:  2012-07-24       Impact factor: 17.440

6.  Real-time perspectives of surrogate decision-makers regarding critical illness research: findings of focus group participants.

Authors:  Ellen Iverson; Aaron Celious; Carie R Kennedy; Erica Shehane; Alexander Eastman; Victoria Warren; Dragana Bolcic-Jankovic; Brian Clarridge; Bradley D Freeman
Journal:  Chest       Date:  2012-12       Impact factor: 9.410

7.  Research participants' opinions of delayed consent for a randomised controlled trial of glucose control in intensive care.

Authors:  J E Potter; S McKinley; A Delaney
Journal:  Intensive Care Med       Date:  2012-10-25       Impact factor: 17.440

Review 8.  Confronting the ethical challenges to informed consent in emergency medicine research.

Authors:  Terri A Schmidt; David Salo; Jason A Hughes; Jean T Abbott; Joel M Geiderman; Catherine X Johnson; Katie B McClure; Mary Pat McKay; Junaid A Razzak; Raquel M Schears; Robert C Solomon
Journal:  Acad Emerg Med       Date:  2004-10       Impact factor: 3.451

9.  Protecting subjects without hampering research progress: guidance from the office for human research protections.

Authors:  Bernard A Schwetz
Journal:  Cleve Clin J Med       Date:  2007-03       Impact factor: 2.321

10.  Protecting vulnerable research subjects in critical care trials: enhancing the informed consent process and recommendations for safeguards.

Authors:  Henry Silverman
Journal:  Ann Intensive Care       Date:  2011-04-13       Impact factor: 6.925

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  5 in total

1.  Research to inform the consent-to-research process.

Authors:  Damon C Scales
Journal:  Intensive Care Med       Date:  2013-06-28       Impact factor: 17.440

2.  Increasing participation in critical care studies: the need to understand surrogate decision-makers for critically ill patients.

Authors:  Christiane S Hartog; Anders Aneman; Bara Ricou
Journal:  Intensive Care Med       Date:  2015-01-09       Impact factor: 17.440

3.  Year in review in Intensive Care Medicine 2013: II. Sedation, invasive and noninvasive ventilation, airways, ARDS, ECMO, family satisfaction, end-of-life care, organ donation, informed consent, safety, hematological issues in critically ill patients.

Authors:  Elie Azoulay; Giuseppe Citerio; Jan Bakker; Matteo Bassetti; Dominique Benoit; Maurizio Cecconi; J Randall Curtis; Glenn Hernandez; Margaret Herridge; Samir Jaber; Michael Joannidis; Laurent Papazian; Mark Peters; Pierre Singer; Martin Smith; Marcio Soares; Antoni Torres; Antoine Vieillard-Baron; Jean-François Timsit
Journal:  Intensive Care Med       Date:  2014-01-24       Impact factor: 17.440

Review 4.  Trials using deferred consent in the emergency setting: a systematic review and narrative synthesis of stakeholders' attitudes.

Authors:  Aran Fitzpatrick; Fiona Wood; Victoria Shepherd
Journal:  Trials       Date:  2022-05-16       Impact factor: 2.728

Review 5.  Key stakeholder perceptions about consent to participate in acute illness research: a rapid, systematic review to inform epi/pandemic research preparedness.

Authors:  Nina H Gobat; Micaela Gal; Nick A Francis; Kerenza Hood; Angela Watkins; Jill Turner; Ronald Moore; Steve A R Webb; Christopher C Butler; Alistair Nichol
Journal:  Trials       Date:  2015-12-29       Impact factor: 2.279

  5 in total

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