Janssen F, Rambeck B, Schnabel R
Neuropediatrics. 1985 Nov;16(4):235-8. doi: 10.1055/s-2008-1059544.
A healthy twenty-month-old boy ingested a maximal dose of valproate from which about 750 mg/kg were absorbed. Cerebral coma, which lasted for twenty hrs, was followed by an undisturbed period of approximately sixteen hrs. Death from cardiorespiratory failure due to severe bronchopneumonia occurred 46.5 hrs after the ingestion of the drug. The serum valproic acid concentration reached a peak of 1061 micrograms/ml within three hours, and fifteen minutes before death it had fallen to 187 micrograms/ml. The half-life of 16.6 hrs was within the range usually found. Metabolic acidosis, hypernatraemia and hyperosmolarity could be corrected, unlike the hypocalcaemia, which developed later. Bilirubin, GOT, GPT, gamma-GT, alkaline phosphatase, blood glucose, diastase, urea, creatinine, haemoglobin as well as PT and PTT and the platelet count were all normal. Leucopenia with 1,600 per microliter developed only during the bronchopneumonial stage. The histo-pathological findings were acute hypoxic damage of the myocardium, kidneys and certain neurones of vulnerable areas of the brain (neuronal microvesiculation and tigrolysis) in addition to a severe cerebral oedema in the final stage. A morphological substrate of an acute valproate encephalopathy was not demonstrable. The liver showed no necrosis or cholostasis. The vertebral marrow was inconspicuous. All the results indicate that liver function was not impaired in spite of the initial maximal concentration of valproic acid. In all probability the patient might have survived the acute valproate intoxication had it not been for the bronchopneumonia.
一名健康的20个月大男孩摄入了最大剂量的丙戊酸盐,吸收量约为750毫克/千克。脑昏迷持续了20小时,随后是约16小时的平稳期。服药后46.5小时,因严重支气管肺炎导致心肺功能衰竭死亡。血清丙戊酸浓度在三小时内达到峰值1061微克/毫升,死亡前15分钟降至187微克/毫升。16.6小时的半衰期在通常范围内。代谢性酸中毒、高钠血症和高渗性可以纠正,与后来出现的低钙血症不同。胆红素、谷草转氨酶、谷丙转氨酶、γ-谷氨酰转肽酶、碱性磷酸酶、血糖、淀粉酶、尿素、肌酐、血红蛋白以及凝血酶原时间和部分凝血活酶时间以及血小板计数均正常。仅在支气管肺炎阶段出现白细胞减少,每微升1600个。组织病理学发现除了在最后阶段出现严重脑水肿外,还有心肌、肾脏和大脑易损区域某些神经元的急性缺氧损伤(神经元微泡形成和虎斑溶解)。未发现急性丙戊酸脑病的形态学基础。肝脏未显示坏死或胆汁淤积。脊椎骨髓不明显。所有结果表明,尽管丙戊酸最初浓度达到最大值,但肝功能并未受损。如果不是支气管肺炎,该患者很可能会从急性丙戊酸盐中毒中幸存下来。