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Carbamazepine and the active epoxide metabolite are effectively cleared by hemodialysis followed by continuous venovenous hemodialysis in an acute overdose

机译:血液透析和活性环氧化物代谢物有效地清除了血液透析,然后在急性过量氧化剂中有效地清除了连续的静脉血液透析

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摘要

Hemodialysis (HD) and continuous venovenous hemodialysis (CVVHD) have an unproven role in the management of carbamazepine overdose. Albumin‐enhanced CVVHD may accelerate carbamazepine (CBZ) clearance, but no pharmacokinetic data has been reported for traditional CVVHD without albumin enhancement. In addition, it is unclear whether the active CBZ‐epoxide metabolite is removed with either mode of dialysis. We present a case of CBZ intoxication successfully managed with sequential HD and CVVHD. The CBZ half‐life during CVVHD was 14.7 hours, compared with the patient's endogenous half‐life of 30.8 hours. The CBZ‐epoxide half‐life was 3.2 hours during HD. We conclude that HD and CVVHD provide effective clearance of CBZ and the epoxide metabolite and should be considered in the management of an acute toxic ingestion.
机译:血液透析(HD)和连续的静脉血液透析(CVVHD)在胭脂动物过量的管理中具有未经证实的作用。白蛋白增强的CVVHD可以加速胭脂动物(CBZ)间隙,但没有针对没有白蛋白增强的传统CVVHD报告药代动力学数据。另外,目前还不清楚是否用任一透析模式除去活性CBZ-环氧化物代谢物。我们提出了CBZ中毒的情况,用顺序高清和CVVHD成功管理。 CVVHD期间CBZ半衰期为14.7小时,与患者的内源性半衰期为30.8小时。高清中CBZ-环氧半衰期为3.2小时。我们得出结论,HD和CVVHD提供了CBZ和环氧化物代谢物的有效许可,应考虑在急性毒性摄取的管理中。

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