编者评论:评估监管科学中的最坏情况

J. R. Turner
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引用次数: 2

摘要

去年,我们引入了几个新的投稿类别,包括给编辑的信。前两封信发表在2011年9月的《华尔街日报》上,一封来自Norman Stockbridge博士(FDA),另一封来自Larry Satin博士(Cardiocore)。这两封信都回应了Eoin O 'Brien教授关于动态血压测量(ABPM)的专家评论,题为“为什么在所有降压药试验中都应该强制进行动态血压测量”。值得注意的是,斯托克布里奇博士信中的一个评论已经在几个国际会议上被发言人强调,因此引发了持续的讨论。本期杂志包含两篇评论,一篇来自副主编彼得·皮茨(纽约公共利益医学中心主席),另一篇来自迈克尔·韦伯博士(纽约州立大学下州医学院医学教授,公共利益医学中心主席)。他们讨论对美国医学实践至关重要的问题,并鼓励读者就这些问题给编辑写信。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Editor’s Commentary: Assessing Worst-Case Scenarios in Regulatory Science
Last year we introduced several new categories of submissions, including Letters to the Editor. The first two letters were published in the September 2011 issue of the Journal, one from Dr Norman Stockbridge (FDA) and the other from Dr Larry Satin (Cardiocore). Both letters addressed an Expert Commentary on ambulatory blood pressure measurement (ABPM) by Professor Eoin O’Brien entitled ‘‘Why ABPM Should Be Mandatory in All Trials of Blood Pressure–Lowering Drugs.’’ Of note is that one comment contained in Dr Stockbridge’s letter has already been highlighted by speakers at several international conferences, and has therefore generated ongoing discussion. This issue of the Journal contains two Commentary pieces, one from Associate Editor Peter Pitts (president, Center for Medicine in the Public Interest, New York) and the other from Dr Michael Weber (professor of medicine at SUNY Downstate College of Medicine and chairman of the Center for Medicine in the Public Interest). They discuss issues of central importance to the practice of medicine in the United States, and Letters to the Editor from readers in response to these issues are encouraged.
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