Rocky Mountain Poison and Drug Center, Denver University of Colorado Denver School of Medicine, Aurora, USA.
Br J Clin Pharmacol. 2010 Dec;70(6):794-8. doi: 10.1111/j.1365-2125.2010.03747.x.
The aim of this review was to describe a patient with serotonin toxicity after an overdose of dextromethorphan and chlorphenamine and to perform a systematic literature review exploring whether dextromethorphan and chlorphenamine may be equally contributory in the development of serotonin toxicity in overdose. A Medline literature review was undertaken to identify cases of serotonin toxicity due to dextromethorphan and/or chlorphenamine. Case reports were included if they included information on the ingested dose or plasma concentrations of dextromethorphan and/or chlorphenamine, information about co-ingestions and detailed clinical information to evaluate for serotonin toxicity. Cases were reviewed by two toxicologists and serotonin toxicity, defined by the Hunter criteria, was diagnosed when appropriate. The literature was then reviewed to evaluate whether chlorphenamine may be a serotonergic agent. One hundred and fifty-five articles of dextromethorphan or chlorphenamine poisoning were identified. There were 23 case reports of dextromethorphan, of which 18 were excluded for lack of serotonin toxicity. No cases were identified in which serotonin toxicity could be solely attributed to chlorphenamine. This left six cases of dextrometorphane and/or chlorphenamine overdose, including our own, in which serotonin toxicity could be diagnosed based on the presented clinical information. In three of the six eligible cases dextromethorphan and chlorphenamine were the only overdosed drugs. There is substantial evidence from the literature that chlorphenamine is a similarly potent serotonin re-uptake inhibitor when compared with dextrometorphan. Chlorphenamine is a serotonergic medication and combinations of chlorphenamine and dextromethorphan may be dangerous in overdose due to an increased risk of serotonin toxicity.
本综述的目的是描述 1 例过量使用右美沙芬和氯苯那敏后出现 5-羟色胺毒性的患者,并对探索右美沙芬和氯苯那敏是否同样可能导致过量使用时出现 5-羟色胺毒性的系统文献进行综述。对 Medline 文献进行综述,以确定因右美沙芬和/或氯苯那敏引起的 5-羟色胺毒性病例。如果病例报告中包含右美沙芬和/或氯苯那敏的摄入剂量或血浆浓度信息、共摄入信息以及详细的临床信息以评估 5-羟色胺毒性,则将其纳入。由两名毒理学家对病例进行审查,并在适当情况下根据 Hunter 标准诊断 5-羟色胺毒性。然后对文献进行综述,以评估氯苯那敏是否可能是一种 5-羟色胺能药物。确定了 155 篇关于右美沙芬或氯苯那敏中毒的文章。有 23 例右美沙芬中毒的病例报告,其中 18 例因缺乏 5-羟色胺毒性而被排除。没有发现可以仅归因于氯苯那敏的 5-羟色胺毒性病例。这留下了 6 例右美沙芬和/或氯苯那敏过量的病例,包括我们自己的病例,根据提供的临床信息可以诊断为 5-羟色胺毒性。在这 6 例合格病例中,有 3 例右美沙芬和氯苯那敏是唯一过量的药物。文献中有大量证据表明,氯苯那敏与右美沙芬相比,同样是一种有效的 5-羟色胺再摄取抑制剂。氯苯那敏是一种 5-羟色胺能药物,氯苯那敏和右美沙芬的组合在过量使用时可能会很危险,因为会增加出现 5-羟色胺毒性的风险。