对“突然停止治疗用氧酸钠(GHB)可能引起戒断症状”的评论的回复

D. Zvosec, Stephen W. Smith
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引用次数: 2

摘要

我们感谢Zvosec博士对Xyrem多中心研究小组最近发表的文章的关注(1)。对许多人来说,GHB是一个充满情感的主题,孤儿医学很感激有机会代表作者进一步澄清她的担忧。超过25年的临床研究经验表明,在治疗发作性睡病时,没有任何药物渴求、耐受性或戒断提示身体依赖的报告(2-9)。本报告的作者以前也得到过类似的结果(10,11)。综上所述,上述文献几乎没有提供任何理由来预测参与目前正在讨论的试验的患者的成瘾和随后的戒断症状;然而,我们要对兹沃塞克博士的评论作出回应。如引言(1)所述,本研究报告的结果是在一项随机、安慰剂对照、长期疗效试验中获得的,在该试验中,患者以盲法突然从慢性开放标签治疗中移除7至44个月的碳酸钠。这项研究的目的是为了证明氢氧化钠(当时是一种正在研究的新药)治疗中风的长期疗效,而不会给患者带来数月接受安慰剂治疗的困难。该方案得到了地方和区域伦理委员会以及美国食品和药物管理局的批准。报告不良事件的系统是不良反应术语词典编码符号,通常称为COSTART(12)。在进行这项试验时,COSTART是fda首选的标准化不良事件报告方法。患者报告的对不良事件的逐字描述被转发给临床研究机构,在那里逐字术语被翻译成COSTART术语。值得注意的是,COSTART将转化为成瘾、药物依赖和戒断综合征的术语逐字记录为不良事件。随附的表格列出了在双盲研究阶段安慰剂患者报告的不良事件的逐字和COSTART描述。
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A Reply to “Comment on ‘The Abrupt Cessation of Therapeutically Administered Sodium Oxybate (GHB) May Cause Withdrawal Symptoms’”
We appreciate the care with which Dr. Zvosec reviewed the recently published article by the Xyrem Multicenter Study Group (1). For many, GHB is an emotionally charged subject, and Orphan Medical is grateful for the opportunity to provide additional clarity to her concerns on behalf of the authors. More than 25 yrs of clinical research experience with sodium oxybate has not provided any reports of drug craving, tolerance, or withdrawal suggestive of physical dependence when used in the treatment of narcolepsy (2–9). Similar results have been previously obtained by the authors of the current report (10,11). Taken together, the above body of literature provides little reason to anticipate addiction and subsequent withdrawal symptoms in patients participating in the trial presently under discussion; nevertheless, we would like to respond to the comments of Dr. Zvosec. As stated in the introduction (1), the results reported in the present study were obtained during a randomized, placebo-controlled, long-term efficacy trial, in which patients were abruptly removed in blinded fashion from chronic open-label treatment with sodium oxybate for 7 to 44 months. This study was designed to demonstrate long-term efficacy of sodium oxybate, at the time an investigational new drug, for the treatment of cataplexy without imposing the hardship of receiving placebo treatment for many months. This protocol was approved by local and regional ethics committees as well as the U.S. Food and Drug Administration. The system used for reporting adverse events was the Coding Symbols for a Thesaurus of Adverse Reaction Terms dictionary, commonly referred to as COSTART (12). At the time this trial was being conducted, COSTART was the FDA-preferred means of standardized adverse event reporting. The verbatim description of an adverse event, as reported by the patient, was forwarded to a clinical research organization where verbatim terms were translated into COSTART terms. Of note, COSTART captures verbatim terms that translate to Addiction, Drug Dependence, and Withdrawal Syndrome as adverse events. The accompanying table lists verbatim and COSTART descriptions of the adverse events reported in placebo patients during the double-blind phase of the study.
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