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JAMA Netw Open. 2022 May 2;5(5):e2214052. doi: 10.1001/jamanetworkopen.2022.14052.
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本文引用的文献

1
Effect of C-Reactive Protein-Guided Antibiotic Treatment Duration, 7-Day Treatment, or 14-Day Treatment on 30-Day Clinical Failure Rate in Patients With Uncomplicated Gram-Negative Bacteremia: A Randomized Clinical Trial.C-反应蛋白指导的抗生素治疗持续时间、7 天疗程或 14 天疗程对无并发症革兰氏阴性菌血症患者 30 天临床失败率的影响：一项随机临床试验。
JAMA. 2020 Jun 2;323(21):2160-2169. doi: 10.1001/jama.2020.6348.
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Comprehension and recall from the informed consent process by phase I healthy volunteers before dose administration.知情同意过程中 I 期健康志愿者在给药前的理解和回忆。
Clin Trials. 2019 Jun;16(3):283-289. doi: 10.1177/1740774519834257. Epub 2019 Feb 28.
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Closing the evidence gap in infectious disease: point-of-care randomization and informed consent.缩小传染病领域的证据缺口：即时随机化和知情同意。
Clin Microbiol Infect. 2017 Feb;23(2):73-77. doi: 10.1016/j.cmi.2016.07.029. Epub 2016 Aug 3.
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Informed consent for research obtained during the intensive care unit stay.在重症监护病房住院期间获得的研究知情同意书。
Crit Care. 2006;10(6):R170. doi: 10.1186/cc5120.
5
Informed consent in clinical trials.临床试验中的知情同意。
Health Policy. 1996 May;36(2):131-53. doi: 10.1016/0168-8510(95)00805-5.

患者和代理人在书面或口头知情同意参与干预性试验后的回忆。

Patient and Proxy Recall After Providing Written or Oral Informed Consent to Participate in an Interventional Trial.

机构信息

Division of Infectious Diseases, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.

Center for Clinical Research, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.

出版信息

JAMA Netw Open. 2022 May 2;5(5):e2214052. doi: 10.1001/jamanetworkopen.2022.14052.

DOI:10.1001/jamanetworkopen.2022.14052
PMID:35560052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9107023/
Abstract

This cohort study assesses recall rates among patients and their proxies who consented to participate in a randomized clinical trial.

摘要

本队列研究评估了同意参与随机临床试验的患者及其代理人的回忆率。