Initial Experience Using the Food and Drug Administration Guidelines for Emergency Research Without Consent
Autor: | Linda Gregg, Mark Stuart Kremers, Laurie Silvus Lowder, Diane Roe Whisnant |
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Rok vydání: | 1999 |
Předmět: |
medicine.medical_specialty
medicine.medical_treatment Consultation process Guidelines as Topic Truth Disclosure Food and drug administration Emergency research Informed consent medicine Humans Cardiopulmonary resuscitation Protocol (science) Informed Consent United States Food and Drug Administration business.industry Research Investigational Device medicine.disease Cardiopulmonary Resuscitation Community-Institutional Relations United States Additional research Surgery Baltimore Costs and Cost Analysis Emergency Medicine Medical emergency business |
Zdroj: | Annals of Emergency Medicine. 33:224-229 |
ISSN: | 0196-0644 |
DOI: | 10.1016/s0196-0644(99)70399-9 |
Popis: | Beginning November 6, 1996, Food and Drug Administration regulation 21 CFR 50.24 has allowed research without consent in limited circumstances while requiring additional patient protection in the form of community consultation and disclosure. We report our experience in complying with these regulations in Multicenter Vest CPR protocol, the first investigational device study done under this new ruling. We found uncertainty in inter-pretation of the requirements for community consultation. The acceptance of research without consent varied among the parties exposed to this protocol, but neither physicians nor the lay public expressed major reservations. The consultation process was time-consuming, demanding, and relatively costly. Further clarification of the community consultation standard and additional dialogue on this important topic will help to foster additional research in cardiopulmonary resuscitation. [Kremers MS, Whisnant DR, Lowder LS, Gregg L: Initial experience using the Food and Drug Administration guidelines for emergency research without consent. Ann Emerg Med February 1999;33:224-229.] |
Databáze: | OpenAIRE |
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