tailieunhanh - Báo cáo khoa học: "nformed consent for research obtained during the intensive care unit stay"

Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Critical Care giúp cho các bạn có thêm kiến thức về ngành y học đề tài: nformed consent for research obtained during the intensive care unit stay. | Available online http content 10 6 R170 Research Informed consent for research obtained during the intensive care unit stay Catherine Chenaud Paolo Merlani Samuel Luyasu and Bara Ricou Service of Intensive Care Department of Anesthesiology Pharmacology and Intensive Care University Hospital of Geneva Rue Micheli-du-Crest 24 1211 Geneva 14 Switzerland Corresponding author Catherine Chenaud Received 12 Jul 2006 Revisions requested 10 Aug 2006 Revisions received 8 Sep 2006 Accepted 8 Dec 2006 Published 8 Dec 2006 Critical Care 2006 10 R170 doi cc5120 This article is online at http content 10 6 R1 70 2006 Chenaud et al. licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Open Access Abstract Introduction Patients in the intensive care unit ICU may be in an inadequate condition to give their informed consent for research. The aim of this study was to analyse the ability to recall participation in a clinical trial for which ICU patients had given their consent. Methods The data presented are a two-step observational study first a protocolled informed consent procedure was conducted then the informed consent was given by the patient and second a patient interview was held 10 2 days later by the same investigator. The primary endpoints were the ability to recall their participation in the clinical trial as well as its purpose and related risks. As secondary endpoints we investigated whether asking questions about the clinical trial or reading the informative leaflet was related to the recall. To be included in the study the patient had to have a Glasgow Coma Scale score of 15 be fully oriented and free of mechanical ventilation and be judged competent by both the investigator .

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