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本文引用的文献

1
Physician rewards for postmarketing surveillance (seeding studies) in the US.
Pharmacoeconomics. 1995 Mar;7(3):187-90. doi: 10.2165/00019053-199507030-00001.
2
"How much do you get paid if I volunteer?" Suggested institutional policy on reward, consent, and research.“如果我做志愿者，能得到多少报酬？”关于奖励、同意和研究的机构政策建议。
Hosp Health Serv Adm. 1994 Summer;39(2):193-203.
3
Marketing aspects of company-sponsored postmarketing surveillance studies.公司赞助的上市后监测研究的营销方面
Drug Saf. 1993 Jan;8(1):1-8. doi: 10.2165/00002018-199308010-00001.
4
Evaluating drugs after their approval for clinical use.在药物获批临床使用后对其进行评估。
N Engl J Med. 1993 Dec 30;329(27):2029-32. doi: 10.1056/NEJM199312303292710.

作为上市后研究知情同意一部分的经济关联。美国医生和患者的态度。

Financial ties as part of informed consent to postmarketing research. Attitudes of American doctors and patients.

作者信息

La Puma J, Stocking C B, Rhoades W D, Darling C M, Ferner R E, Neuberger J, VandenBurg M, Dews I, Tobias J S

机构信息

Center for Clinical Medical Ethics, University of Chicago, IL 60637, USA.

出版信息

BMJ. 1995 Jun 24;310(6995):1660-3. doi: 10.1136/bmj.310.6995.1660.

DOI:10.1136/bmj.310.6995.1660
PMID:7795459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2550020/
Abstract

Postmarketing research, often called phase IV trials, is intended to familiarise doctors and patients with newly approved drugs. La Puma and colleagues, in Chicago, studied doctors' and patients' attitudes to whether doctors should receive payment for taking part in such research. We asked for commentaries on their findings from four ethical experts, who put the study in a British context, present the views of patients, and examine some methodological assumptions.

摘要

上市后研究，通常称为IV期试验，旨在让医生和患者熟悉新批准的药物。芝加哥的拉普马及其同事研究了医生和患者对于医生参与此类研究是否应获得报酬的态度。我们邀请了四位伦理专家对他们的研究结果发表评论，这些专家将该研究置于英国背景下，阐述了患者的观点，并审视了一些方法学假设。