[Acute diltiazem (DTZ) poisoning. Survey of french poison control centers].

H Lambert, M Weber, D Renaud
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Abstract

Unlabelled: The end-points of this study upon 134 cases reports by the french Poison Centers from 1979 to 1988 (10 years) were to specify the acute toxicity of diltiazem (DTZ). There were 83 self-poisonings in adults, with diltiazem alone (36 cases) or associated with other non cardiotoxic drugs (47), the doses of DTZ ranging from 300 to 5400 mg, and 51 acute accidental overdose in children, the doses of DTZ ranging from 60 to 420 mg. One case of hypotension was observed in a child, without rhythmic disorder, occurring twelve hours post-ingestion of 180 mg of DTZ. In adults, the clinical effects were observed following 360 mg of dose DTZ, occurring 1 1/2 hour post-ingestion. There were discomfort, brady-cardia in 16% of the cases, hypotension in 23% of the cases, cardiogenic shock in 4% of the cases and cardiac arrest in 2.4% of the cases. The rhythmic disorders occurred 2 to 15 hours post-ingestion. There were conduction defects like atrio-ventricular heart bloc I degree in 9% of the cases, II degree in 2.4% of the cases and III degree in 9% of the cases. Less frequently, sinusal bradycardia in 11% of the cases or sino-auricular heart block in 4% of the cases with sometimes auriculo ventricular heart block. These cardiac disorders occurred with 600 mg of DTZ. A cardiac arrest happened in a young healthy man who had absorbed 5400 mg of DTZ. The cardiogenic shocks occurred in patients with an history of coronary on heart disease. The poison removal is likely to prevent the occurrence of clinical or EKG effects when performed within 2 hours post-ingestion, whatever toxic the dose is. The inotropic drugs have been used in 18% of the cases; a percutaneous ventricular pacing was always effective in patients with II or III degree atrio-ventricular block or/and cardiogenir shock. These data confirm the data in thirteen patients of the literature.

In conclusion: The acute diltiazem poisoning can occur after 600 mg of DTZ and can induce severe cardiac disorders which can be prevented with poison removal or treated with supportive care.

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急性地尔硫卓(DTZ)中毒。法国中毒控制中心调查[j]。
未标记:本研究的终点是法国毒物中心从1979年到1988年(10年)报告的134例病例,目的是明确地尔硫卓(DTZ)的急性毒性。成人自行中毒83例,单独使用地尔硫卓(36例)或与其他非心脏毒性药物联合使用(47例),DTZ剂量300 ~ 5400 mg,儿童急性意外过量51例,DTZ剂量60 ~ 420 mg。在儿童中观察到一例低血压,无节律障碍,在摄入180mg DTZ后12小时发生。在成人中,在服用360毫克剂量的DTZ后1个半小时观察到临床效果。有不适,16%的病例心动过缓,23%的病例低血压,4%的病例心源性休克,2.4%的病例心脏骤停。进食后2 ~ 15小时出现节律性障碍。房室心脏块I度占9%,II度占2.4%,III度占9%。较少见的是,11%的病例有窦性心动过缓,4%的病例有窦性心传导阻滞,有时伴有耳室性心传导阻滞。这些心脏疾病发生在600毫克的DTZ。一名年轻健康男子在服用了5400毫克的DTZ后发生了心脏骤停。心源性休克发生在有冠心病史的患者中。无论中毒剂量如何,如果在摄入后2小时内进行脱毒,都有可能防止临床或心电图的发生。18%的病例使用了肌力药物;经皮心室起搏对于II或III度房室传导阻滞或/和心源性休克患者总是有效的。这些数据证实了文献中13例患者的数据。结论:600 mg DTZ可引起急性地尔硫卓中毒,可引起严重的心脏疾病,可通过排毒预防或支持性护理治疗。
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