Richmond Caroline, Coveart Stephanie
Memphis Veterans Affairs Medical Center, Tennessee.
University of Tennessee College of Pharmacy, Memphis.
Fed Pract. 2022 Apr;39(4):182-185. doi: 10.12788/fp.0247. Epub 2022 Apr 11.
Valproic acid (VPA) and its derivative, divalproex (DVP) can cause various hematologic dyscrasias, the most common being thrombocytopenia. Neutropenia and leukopenia have been reported in isolated cases, most occurring in pediatric patients or patients with epilepsy. We report a case of leukopenia and neutropenia that presented after cross taper from quetiapine to DVP for the treatment of borderline personality disorder.
A 34-year-old male patient with history of posttraumatic stress disorder, opioid use disorder, alcohol use disorder, stimulant use disorder, cannabis use, and borderline personality disorder underwent a cross taper from quetiapine to divalproex (DVP). DVP was titrated to 1000 mg per day, complete blood count (CBC) was obtained after completion of cross taper and revealed neutropenia and leukopenia with no documented history of blood dyscrasias. Nine days after discontinuation of DVP, neutrophil and white blood cell count returned to normal limits. With a score of 7 on the Naranjo Adverse Drug Reaction Probability Scale, an adverse reaction of probable DVP-induced neutropenia was documented and medication was not resumed.
This case suggests that there may be a correlation between DVP and isolated neutropenia and leukopenia. Although a CBC is collected routinely to monitor for thrombocytopenia, health care practitioners also should consider other blood dyscrasias. Further studies are warranted to determine incidence of neutropenia and leukopenia with DVP therapy and evaluate whether the medication can be safely continued in cases of mild-to-moderate neutropenia with close monitoring.
丙戊酸(VPA)及其衍生物丙戊酸盐(DVP)可导致各种血液系统异常,最常见的是血小板减少症。孤立病例报告过中性粒细胞减少症和白细胞减少症,大多发生在儿科患者或癫痫患者中。我们报告一例在从喹硫平交叉减量至DVP以治疗边缘性人格障碍后出现白细胞减少症和中性粒细胞减少症的病例。
一名34岁男性患者,有创伤后应激障碍、阿片类物质使用障碍、酒精使用障碍、兴奋剂使用障碍、大麻使用及边缘性人格障碍病史,接受了从喹硫平到丙戊酸盐(DVP)的交叉减量。DVP滴定至每日1000毫克,交叉减量完成后进行全血细胞计数(CBC),结果显示中性粒细胞减少症和白细胞减少症,且无血液系统异常的既往记录。停用DVP九天后,中性粒细胞和白细胞计数恢复至正常范围。根据Naranjo药物不良反应概率量表评分为7分,记录为可能由DVP引起的中性粒细胞减少症不良反应,未恢复用药。
该病例提示DVP与孤立性中性粒细胞减少症和白细胞减少症之间可能存在关联。尽管常规采集CBC以监测血小板减少症,但医护人员也应考虑其他血液系统异常。有必要进一步研究以确定DVP治疗引起中性粒细胞减少症和白细胞减少症的发生率,并评估在密切监测下轻度至中度中性粒细胞减少症患者能否安全继续使用该药物。