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Sodium stibogluconate (pentostan) overdose in a patient with acquired immunodeficiency syndrome.

机译:患有后天免疫机能丧失综合症的患者中,stibogluconate钠(戊烷)过量。

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A 32-year-old man with acquired immunodeficiency syndrome (AIDS) admitted to the hospital for treatment of visceral leishmaniasis was inadvertently given 10 times the prescribed first dose of sodium stibogluconate ([Sb] 6.5 g instead of 0.65 g). He experienced no immediate major toxicity during the first 48 hours, but a significant rise of pancreatic enzyme activities was observed (amylase at 10 times the upper limit of normal, lipase at 50 times the upper limit of normal) without clinical signs or indications on computed tomography (CT) of pancreatitis. The third day after the overdose, he developed appendicitis, which appeared coincidental; he recovered uneventfully from surgery. Most of the overdose of Sb was eliminated within the first few hours. Pharmacokinetics remained linear; the rapid, long elimination half-lives (2.7 hours and 54 hours, respectively) were similar to those in previously published results. The administration of a chelating agent, dimercaptosuccinic acid (DMSA), 72 hours after the Sb overdose did not modify the pharmacokinetics of the medication.
机译:入院治疗内脏利什曼病的一名32岁患有获得性免疫缺陷综合症(AIDS)的男子不经意地服用了规定的第一剂量的葡糖苷钠([Sb] 6.5 g而不是0.65 g)的10倍。在最初的48小时内,他没有立即发生重大毒性反应,但是观察到胰腺酶活性显着升高(淀粉酶的水平是正常上限的10倍,脂肪酶的水平是正常上限的50倍),但没有计算出的临床体征或适应症胰腺炎的断层扫描(CT)。用药过量的第三天,他出现了阑尾炎,这似乎是巧合。他从手术中康复得很顺利。在最初的几个小时内,大部分过量的Sb被消除。药代动力学保持线性;快速,长消除半衰期(分别为2.7小时和54小时)与先前发表的结果相似。 Sb过量服用72小时后,螯合剂二巯基琥珀酸(DMSA)的给药不会改变药物的药代动力学。

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