Literature DB >> 12042405

Medical research in clinical emergency settings in Europe.

S Lötjönen1.   

Abstract

Clinical emergencies necessitate immediate action to avert the danger to the patient's life or health. Emergency patients might be in greatest need of novel therapies, and even presumed willing to assume some risk, but research into emergency conditions should be conducted under commonly accepted principles that fulfil the scientific, ethical, and legal criteria. Such criteria already exist in the US, but are still under development in Europe. This article introduces criteria upon which trials in emergency settings may be ethically and legally justified in Europe. Based on both legal texts and professional guidelines, the author has established seven conditions for emergency research, of which informed consent and its substitutes, as well as the conditions of direct benefit requirement and necessity, are considered most problematic and therefore analysed more closely. Other conditions include absence of alternative methods, scientific validity, and approval by an ethics committee.

Entities:  

Keywords:  Biomedical and Behavioral Research; European Convention on Human Rights and Biomedicine

Mesh:

Year:  2002        PMID: 12042405      PMCID: PMC1733601          DOI: 10.1136/jme.28.3.183

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  12 in total

Review 1.  31st Bethesda Conference. Emergency Cardiac Care. Task force 3: Special aspects of research conduct in the emergency setting: Waiver of informed consent.

Authors:  E R Passamani; M L Weisfeldt
Journal:  J Am Coll Cardiol       Date:  2000-03-15       Impact factor: 24.094

2.  Deferred consent.

Authors:  R J Levine
Journal:  Control Clin Trials       Date:  1991-08

3.  Initial experience using the Food and Drug administration guidelines for emergency research without consent.

Authors:  M S Kremers; D R Whisnant; L S Lowder; L Gregg
Journal:  Ann Emerg Med       Date:  1999-02       Impact factor: 5.721

Review 4.  Advance directives for non-therapeutic dementia research: some ethical and policy considerations.

Authors:  R L Berghmans
Journal:  J Med Ethics       Date:  1998-02       Impact factor: 2.903

5.  When is surgery research? Towards an operational definition of human research.

Authors:  C E Margo
Journal:  J Med Ethics       Date:  2001-02       Impact factor: 2.903

6.  Informed consent in emergency research. Prehospital thrombolytic therapy for acute myocardial infarction.

Authors:  P S Grim; P A Singer; G P Gramelspacher; T Feldman; R W Childers; M Siegler
Journal:  JAMA       Date:  1989-07-14       Impact factor: 56.272

7.  A retrospective analysis of institutional review board and informed consent practices in EMS research.

Authors:  D T Kim; W H Spivey
Journal:  Ann Emerg Med       Date:  1994-01       Impact factor: 5.721

8.  UK collaborative randomised trial of neonatal extracorporeal membrane oxygenation. UK Collaborative ECMO Trail Group.

Authors: 
Journal:  Lancet       Date:  1996-07-13       Impact factor: 79.321

9.  Evaluation of active compression-decompression CPR in victims of out-of-hospital cardiac arrest.

Authors:  K G Lurie; J J Shultz; M L Callaham; T M Schwab; T Gisch; T Rector; R J Frascone; L Long
Journal:  JAMA       Date:  1994-05-11       Impact factor: 56.272

10.  A randomized clinical trial of calcium entry blocker administration to comatose survivors of cardiac arrest. Design, methods, and patient characteristics. The Brain Resuscitation Clinical Trial II Study Group.

Authors: 
Journal:  Control Clin Trials       Date:  1991-08
View more
  7 in total

1.  The European Union Directive on Clinical Research: present status of implementation in EU member states' legislations with regard to the incompetent patient.

Authors:  F Lemaire; J Bion; J Blanco; P Damas; C Druml; K Falke; J Kesecioglu; A Larsson; J Mancebo; D Matamis; A Pesenti; J Pimentel; M Ranieri
Journal:  Intensive Care Med       Date:  2005-02-15       Impact factor: 17.440

Review 2.  H1-antihistamines for the treatment of anaphylaxis with and without shock.

Authors:  A Sheikh; V m ten Broek; S G A Brown; F E R Simons
Journal:  Cochrane Database Syst Rev       Date:  2007-01-24

3.  The inability to consent in critical care research: emergency or impairment of cognitive function?

Authors:  François Lemaire
Journal:  Intensive Care Med       Date:  2006-09-21       Impact factor: 17.440

4.  Emergency research without consent under Polish law.

Authors:  Joanna Rózyńska; Marek Czarkowski
Journal:  Sci Eng Ethics       Date:  2007-09-14       Impact factor: 3.525

5.  Informed consent procedure for clinical trials in emergency settings: the Polish perspective.

Authors:  Piotr S Iwanowski
Journal:  Sci Eng Ethics       Date:  2007-07-28       Impact factor: 3.525

6.  Patients' preferences for enrolment into critical-care trials.

Authors:  Damon C Scales; Orla M Smith; Ruxandra Pinto; Kali A Barrett; Jan O Friedrich; Neil M Lazar; Deborah J Cook; Niall D Ferguson
Journal:  Intensive Care Med       Date:  2009-06-24       Impact factor: 17.440

7.  Informed consent for clinical trials in acute coronary syndromes and stroke following the European Clinical Trials Directive: investigators' experiences and attitudes.

Authors:  Piotr Iwanowski; Andrzej Budaj; Anna Członkowska; Wojciech Wasek; Beata Kozłowska-Boszko; Urszula Oledzka; Wojciech Masełbas
Journal:  Trials       Date:  2008-07-21       Impact factor: 2.279

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.