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抗抑郁药过量:临床与药代动力学方面

Overdosage of antidepressants: clinical and pharmacokinetic aspects.

作者信息

Pedersen O L, Gram L F, Kristensen C B, Møller M, Thayssen P, Bjerre M, Kragh-SøRensen P, Klitgaard N A, Sindrup E, Hole P, Brinklø M

出版信息

Eur J Clin Pharmacol. 1982;23(6):513-21. doi: 10.1007/BF00637499.

Abstract

Twenty-nine cases of self-poisoning with antidepressants (amitriptyline, imipramine, clomipramine, maprotiline, doxepine, nortriptyline, opipramol) were examined by frequent observation of CNS effects, heart rate, blood pressure and standard ECG, 24h-ECG-monitoring, measurement of systolic time intervals, EEG recordings and frequent measurement of serum levels of antidepressants and primary metabolites. None of the patients died. Maximum total serum antidepressant level (parent compound + desmethyl metabolite) ranged from 20 to 2200 micrograms/l, with concentrations above 500 micrograms/l in 11 cases. The serum amitriptyline concentration remained high for 3-4 days in some of the severely intoxicated patients and the decay curves were compatible with partly saturated elimination. A degree of unconsciousness and the occurrence of excitation and hallucinations were generally seen in cases with total serum antidepressant levels above 500 micrograms/l. Grand mal seizures occurred more frequently at high antidepressant levels, but could not be predicted from the EEG recordings. Increased heart rate and prolonged QRS- and QTc-intervals were significantly correlated with the total serum antidepressant level. 24 h-ECG-monitoring revealed no serious arrhythmias or instances of heart block. Hypotension was only seen initially in few patients. Systolic time interval measurements showed changes suggesting impaired myocardial performance (elevated PEP/LVET ratio) at intermediate (60-500 micrograms/l) but not high (greater than 500 micrograms/l) total serum antidepressant levels. Measurement of serum concentration in antidepressant intoxication is important for identification of patients with high serum levels and the corresponding risk of developing toxic reactions, and to exclude patients with a low concentration who do not require intensive observation.

摘要

对29例服用抗抑郁药(阿米替林、丙咪嗪、氯米帕明、马普替林、多塞平、去甲替林、奥匹哌醇)进行自我中毒的患者,通过频繁观察中枢神经系统效应、心率、血压和标准心电图、24小时心电图监测、收缩期时间间期测量、脑电图记录以及频繁测量抗抑郁药及其主要代谢产物的血清水平进行了检查。所有患者均未死亡。血清抗抑郁药总水平最大值(母体化合物+去甲基代谢产物)为20至2200微克/升,11例患者浓度高于500微克/升。在一些重度中毒患者中,血清阿米替林浓度在3 - 4天内持续较高,衰减曲线符合部分饱和消除。血清抗抑郁药总水平高于500微克/升的病例通常会出现一定程度的意识丧失、兴奋和幻觉。癫痫大发作在抗抑郁药水平较高时更频繁发生,但无法从脑电图记录中预测。心率加快以及QRS和QTc间期延长与血清抗抑郁药总水平显著相关。24小时心电图监测未发现严重心律失常或心脏传导阻滞情况。仅少数患者最初出现低血压。收缩期时间间期测量显示,在血清抗抑郁药总水平处于中等(60 - 500微克/升)而非高(大于500微克/升)水平时,有提示心肌功能受损的变化(PEP/LVET比值升高)。测量抗抑郁药中毒时的血清浓度对于识别血清水平高且有发生毒性反应相应风险的患者很重要,同时也可排除血清浓度低且不需要密切观察的患者。

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