Literature DB >> 16264077

Resuscitation research involving vulnerable populations: are additional protections needed for emergency exception from informed consent?

Jill M Baren1, Susan S Fish.   

Abstract

The application of basic ethical principles to resuscitation research and other research in the emergency and critical care settings presents a particular challenge. The emergency exception from informed consent (EFIC) rule (21 CFR 50.24 and 45 CFR 46.101[i]) addresses a particular vulnerability: that which occurs when persons cannot consent due to acute loss of decisional capacity. The question arises as to whether populations defined as "vulnerable" are unique within studies to which EFIC applies. This report details the proceedings of a breakout session of the 2005 Academic Emergency Medicine Consensus Conference, "Ethical Conduct of Resuscitation Research," that dealt with this issue. Topics addressed were 1) the applicability of the term "vulnerable" in research using EFIC; 2) the relationship between vulnerability, exploitability, and capacity; 3) the significance of vulnerability in research design; 4) the adaptation of the informed consent process to the emergency setting; and 5) the role of the institutional review board. Ten consensus recommendations emerged from the discussion. Of particular importance was the endorsement of the idea that research using EFIC is as important in vulnerable populations as in the general population and that the systematic exclusion of vulnerable populations from resuscitation research is inappropriate.

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Year:  2005        PMID: 16264077     DOI: 10.1197/j.aem.2005.06.020

Source DB:  PubMed          Journal:  Acad Emerg Med        ISSN: 1069-6563            Impact factor:   3.451


  8 in total

1.  Variation of community consultation and public disclosure for a pediatric multi-centered "Exception from Informed Consent" trial.

Authors:  Maija Holsti; Roger Zemek; Jill Baren; Rachel M Stanley; Prashant Mahajan; Cheryl Vance; Kathleen M Brown; Victor Gonzalez; Denise King; Kammy Jacobsen; Kate Shreve; Katrina van de Bruinhorst; Anne Marie Jones; James M Chamberlain
Journal:  Clin Trials       Date:  2014-11-04       Impact factor: 2.486

2.  ICU research: the impact of invasiveness on informed consent.

Authors:  Fabienne Gigon; Paolo Merlani; Catherine Chenaud; Bara Ricou
Journal:  Intensive Care Med       Date:  2013-04-24       Impact factor: 17.440

3.  Perceived challenges to obtaining informed consent for a time-sensitive emergency department study of pediatric status epilepticus: results of two focus groups.

Authors:  James M Chamberlain; Kathleen Lillis; Cheryl Vance; Kathleen M Brown; Olubunmi Fawumi; Shari Nichols; Colleen O Davis; Tasmeen Singh; Jill M Baren
Journal:  Acad Emerg Med       Date:  2009-08       Impact factor: 3.451

Review 4.  Use of deferred consent for severely ill children in a multi-centre phase III trial.

Authors:  Kathryn Maitland; Sassy Molyneux; Mwamvua Boga; Sarah Kiguli; Trudie Lang
Journal:  Trials       Date:  2011-03-31       Impact factor: 2.279

5.  Informed consent in paediatric critical care research--a South African perspective.

Authors:  Brenda M Morrow; Andrew C Argent; Sharon Kling
Journal:  BMC Med Ethics       Date:  2015-09-09       Impact factor: 2.652

6.  Ethical tensions in the informed consent process for randomized clinical trials in emergency obstetric and newborn care in low and middle-income countries.

Authors:  Dan K Kaye; Gershom Chongwe; Nelson K Sewankambo
Journal:  BMC Med Ethics       Date:  2019-04-27       Impact factor: 2.652

7.  PRagMatic Pediatric Trial of Balanced vs nOrmaL Saline FlUid in Sepsis: study protocol for the PRoMPT BOLUS randomized interventional trial.

Authors:  Scott L Weiss; Fran Balamuth; Elliot Long; Graham C Thompson; Katie L Hayes; Hannah Katcoff; Marlena Cook; Elena Tsemberis; Christopher P Hickey; Amanda Williams; Sarah Williamson-Urquhart; Meredith L Borland; Stuart R Dalziel; Ben Gelbart; Stephen B Freedman; Franz E Babl; Jing Huang; Nathan Kuppermann
Journal:  Trials       Date:  2021-11-06       Impact factor: 2.728

Review 8.  Clinical research without consent in adults in the emergency setting: a review of patient and public views.

Authors:  Jan Lecouturier; Helen Rodgers; Gary A Ford; Tim Rapley; Lynne Stobbart; Stephen J Louw; Madeleine J Murtagh
Journal:  BMC Med Ethics       Date:  2008-04-29       Impact factor: 2.652

  8 in total

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