Al Aly Ziyad, Yalamanchili Praveen, Gonzalez Esther
Division of Nephrology, Saint Louis University, St. Louis, Missouri 63110, USA.
Semin Dial. 2005 Jan-Feb;18(1):62-6. doi: 10.1111/j.1525-139X.2005.18106.x.
The incidence of intentional or accidental valproic acid (VPA) overdose is increasing. Severe VPA toxicity may lead to coma and death. Traditionally the treatment of patients with VPA toxicity has been limited to supportive measures. VPA is highly protein bound and therefore it is considered not to be removable by extracorporeal means. However, studies of VPA toxicokinetics indicate that at blood levels that exceed therapeutic concentrations, VPA protein binding sites become saturated, leading to increased concentration of the free unbound drug. The free unbound drug has a small molecular weight and therefore it is theoretically amenable to removal by extracorporeal means. We present a patient with VPA toxicity who was successfully treated with "in-series" hemodialysis and hemoperfusion followed by continuous venovenous hemodiafiltration (CVVHDF) and review the literature on the management of VPA toxicity using extracorporeal therapies.
丙戊酸(VPA)故意或意外过量服用的发生率正在上升。严重的VPA毒性可能导致昏迷和死亡。传统上,VPA中毒患者的治疗仅限于支持性措施。VPA与蛋白质高度结合,因此被认为不能通过体外手段清除。然而,VPA毒代动力学研究表明,当血液水平超过治疗浓度时,VPA蛋白质结合位点会饱和,导致游离未结合药物浓度增加。游离未结合药物分子量小,因此理论上可通过体外手段清除。我们报告了一名VPA中毒患者,该患者通过“串联”血液透析和血液灌流,随后进行连续性静脉-静脉血液透析滤过(CVVHDF)成功治疗,并回顾了使用体外疗法治疗VPA毒性的文献。