Literature DB >> 18404082

Impediments to obtaining informed consent for clinical research in trauma patients.

Richard P Dutton1, Lynn G Stansbury, Bethany Hemlock, John R Hess, Thomas M Scalea.   

Abstract

BACKGROUND: Informed consent is required for, but a substantial barrier to, clinic research in trauma care. Exceptions have been established but remain controversial, and little objective data are available to illuminate this debate.
METHODS: We prospectively assessed 2,011 consecutive patients admitted to the R Adams Cowley Shock Trauma Center of the University of Maryland Medical System for the potential to give consent for a hypothetical research trial within 1 hour of admission or whether consent could be obtained from a legally authorized representative (LAR) within 3 hours. These data were then linked with demographic, transport, physiologic, and injury data.
RESULTS: Complete data were available for 1,734 patients: 982 (57%) appeared able to consent and 752 (43%) appeared unable to consent. Of the latter, LAR consent was potentially available for 404, leaving 348 (46%, 20% of all admissions) unconsentable. Those apparently able to consent were significantly less injured than those unable, but a third were subsequently found to have objective barriers to giving consent, and a further third had findings strongly suggestive of impairment. For those unable to consent, subsequent LAR consent was strongly associated with being a minor or being a woman. Lack of LAR consent was strongly associated with being the victim of intentional injury, with being an African-American male and-for European-American men only-with being transported greater distances.
CONCLUSIONS: Severely injured trauma patients can seldom provide consent for research studies, and LARs are often unavailable. Further efforts to develop workable mechanisms for exception from informed consent are justified.

Entities:  

Mesh:

Year:  2008        PMID: 18404082     DOI: 10.1097/TA.0b013e318165c15c

Source DB:  PubMed          Journal:  J Trauma        ISSN: 0022-5282


  15 in total

1.  Coordination and management of multicenter clinical studies in trauma: Experience from the PRospective Observational Multicenter Major Trauma Transfusion (PROMMTT) Study.

Authors:  Mohammad H Rahbar; Erin E Fox; Deborah J del Junco; Bryan A Cotton; Jeanette M Podbielski; Nena Matijevic; Mitchell J Cohen; Martin A Schreiber; Jiajie Zhang; Parsa Mirhaji; Sarah J Duran; Robert J Reynolds; Ruby Benjamin-Garner; John B Holcomb
Journal:  Resuscitation       Date:  2011-10-12       Impact factor: 5.262

2.  Exception from informed consent for emergency research: consulting the trauma community.

Authors:  Carrie A Sims; Joshua A Isserman; Daniel Holena; Latha Mary Sundaram; Nikolai Tolstoy; Sarah Greer; Seema Sonnad; Jose Pascual; Patrick Reilly
Journal:  J Trauma Acute Care Surg       Date:  2013-01       Impact factor: 3.313

3.  Exploring ethical conflicts in emergency trauma research: the COMBAT (Control of Major Bleeding after Trauma) study experience.

Authors:  Theresa L Chin; Ernest E Moore; Marilyn E Coors; James G Chandler; Arsen Ghasabyan; Jeffrey N Harr; John R Stringham; Christopher R Ramos; Sarah Ammons; Anirban Banerjee; Angela Sauaia
Journal:  Surgery       Date:  2014-10-14       Impact factor: 3.982

4.  Emergency medical service providers' attitudes and experiences regarding enrolling patients in clinical research trials.

Authors:  Terri A Schmidt; Maria Nelson; Mohamud Daya; Nicole M DeIorio; Denise Griffiths; Pontine Rosteck
Journal:  Prehosp Emerg Care       Date:  2009 Apr-Jun       Impact factor: 3.077

5.  The use of delayed telephone informed consent for observational emergency medicine research is ethical and effective.

Authors:  Steven R Offerman; Daniel K Nishijima; Dustin W Ballard; Uli K Chetipally; David R Vinson; James F Holmes
Journal:  Acad Emerg Med       Date:  2013-04       Impact factor: 3.451

6.  Waiver of consent in noninterventional, observational emergency research: the PROMMTT experience.

Authors:  Erin E Fox; Eileen M Bulger; Aisha S Dickerson; Deborah J del Junco; Patricia Klotz; Jeanette Podbielski; Nena Matijevic; Karen J Brasel; John B Holcomb; Martin A Schreiber; Bryan A Cotton; Herb A Phelan; Mitchell J Cohen; John G Myers; Louis H Alarcon; Peter Muskat; Charles E Wade; Mohammad H Rahbar
Journal:  J Trauma Acute Care Surg       Date:  2013-07       Impact factor: 3.313

Review 7.  Exceptions to the rule of informed consent for research with an intervention.

Authors:  Susanne Rebers; Neil K Aaronson; Flora E van Leeuwen; Marjanka K Schmidt
Journal:  BMC Med Ethics       Date:  2016-02-06       Impact factor: 2.652

8.  Enrollment with and without exception from informed consent in a pilot trial of tranexamic acid in children with hemorrhagic injuries.

Authors:  Seth W Linakis; Nathan Kuppermann; Rachel M Stanley; Hilary Hewes; Sage Myers; John M VanBuren; T Charles Casper; Matthew Bobinski; Simona Ghetti; Walton O Schalick; Daniel K Nishijima
Journal:  Acad Emerg Med       Date:  2021-08-06       Impact factor: 3.451

9.  Symptom cluster profiles following traumatic orthopedic injuries: A protocol.

Authors:  Stephen Breazeale; Susan G Dorsey; Joan Kearney; Samantha Conley; Sangchoon Jeon; Brad Yoo; Nancy S Redeker
Journal:  Res Nurs Health       Date:  2020-12-25       Impact factor: 2.228

10.  Exploring the experiences of substitute decision-makers with an exception to consent in a paediatric resuscitation randomised controlled trial: study protocol for a qualitative research study.

Authors:  Melissa J Parker; Sonya de Laat; Lisa Schwartz
Journal:  BMJ Open       Date:  2016-09-13       Impact factor: 2.692

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.