六丙酸自身中毒引起严重和持久的临床症状。

L L Gustafsson, A Berg, A Magnusson, H O Malmlund, B M Sandell, R Stig
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引用次数: 2

摘要

在两年半的时间(1985年至1987年)内收集了瑞典城市地区(42万居民)需要重症监护的六丙酸酯中毒病例。仅纳入血清六丙酸盐浓度高于5.5 mg/L (30 μ mol/L)且有三环类抗抑郁药、吩噻嗪类、巴比妥类、抗组胺药和阿片类药物阴性史的患者。回顾性分析6例患者8例中毒事件的临床资料。最初的症状包括昏迷、低血压、体温过低和呼吸不足。最大昏迷深度(格拉斯哥昏迷评分)在8个事件中的5个中为3至5。7例需要辅助通气(5例持续12小时或更长时间)。血清六丙酸浓度与临床症状的严重程度没有关系。所有患者都存活了下来。对1例患者药物消除的详细分析显示,最终消除半衰期为21小时,比先前报道的5小时更长。使用这种催眠药物的适应症可能因医生而异,因为1987年瑞典各县之间的药物处方有8倍的差异。六丙酸中毒是一种严重的情况,可能需要在重症监护病房对症治疗。临床表现与巴比妥中毒相似。没有主动强制消除药物的作用。这种药物的毒性是否超过了它的临床价值,这是值得怀疑的。
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Hexapropymate self-poisoning causes severe and long-lasting clinical symptoms.

Cases of hexapropymate poisoning requiring intensive care in an urban region of Sweden (420,000 inhabitants) were collected over 2.5 years (1985 to 1987). Only patients with serum hexapropymate concentrations above 5.5 mg/L (30 mumol/L) and with a negative history for intake of tricyclic antidepressants, phenothiazines, barbiturates, antihistaminic drugs and opiates were included. Clinical data about 8 intoxication events in 6 patients were evaluated retrospectively. Initial symptoms included coma, hypotension, hypothermia, and hypoventilation. Maximum coma depth (Glasgow coma score) was 3 to 5 in 5 out of 8 events. On 7 occasions assisted ventilation was required (for 12 hours or more in 5 events). There was no relationship between serum concentrations of hexapropymate and severity of clinical symptoms. All patients survived. Detailed analysis of the drug elimination in one patient showed a terminal elimination half-life of 21 hours, which is longer than previously reported (5 hours). The indications for use of this hypnotic drug may vary between doctors since an 8-fold variation was seen in drug prescription between Swedish counties in 1987. Poisoning with hexapropymate is a serious condition which may require symptomatic treatment in the intensive care unit. The clinical picture is similar to that seen in patients with burbiturate intoxication. There is no role for active forced elimination of the drug. It is questionable whether the clinical value of the drug is outweighted by its toxicity.

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