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血栓性血小板减少性紫癜患者血浆置换后血浆游离苯妥英浓度的反弹

Rebound of plasma free phenytoin concentration following plasmapheresisin a patient with thrombotic thrombocytopenic purpura.

作者信息

Mansur L I, Murrow R W, Garrelts J C, Minns G O

机构信息

Department of Internal Medicine, University of Kansas School of Medicine, Wichita.

出版信息

Ann Pharmacother. 1995 Jun;29(6):592-5. doi: 10.1177/106002809502900608.

Abstract

OBJECTIVE

To measure the total and free serum phenytoin concentrations and phenytoin clearance in a patient with thrombotic thrombocytopenic purpura undergoing plasmapheresis.

CASE SUMMARY

A dose of phenytoin 400 mg i.v. was administered daily 2.5 hours after the completion of plasmapheresis. Intravenous samples were obtained to measure the free and total phenytoin concentrations on 4 consecutive days. These samples were obtained before, at the midpoint, upon completion, and 30, 60, and 120 minutes after completion of plasmapheresis. The samples were centrifuged and stored at 4 degrees C until analysis using the same fluorescence polarization immunoassay kit. The free phenytoin was separated by ultracentrifugation.

DISCUSSION

Despite a decrease in total and free serum phenytoin concentrations measured during the procedure, a marked rebound in the free phenytoin concentration was noted 30 minutes after completion of the procedure. However, by 120 minutes after the procedure, the free phenytoin concentration had decreased to the preprocedure value. The total amount of phenytoin removed by the procedure was less than 5%.

CONCLUSIONS

Despite the decrease in total and free serum phenytoin concentrations observed during plasmapheresis, patients undergoing plasmapheresis may not need supplemental phenytoin, as a rapid reequilibration of the therapeutically active free serum phenytoin occurs following the completion of the procedure. In addition, less than 5% of the total body phenytoin is removed. Second, if the patient experiences symptoms of phenytoin toxicity immediately after the procedure, a free serum phenytoin concentration may be obtained, as this concentration may reflect the reason for toxicity despite a decreased total phenytoin concentration.

摘要

目的

测定一名正在接受血浆置换的血栓性血小板减少性紫癜患者的血清苯妥英总浓度、游离浓度及苯妥英清除率。

病例摘要

在血浆置换结束后2.5小时,每日静脉注射一剂400mg苯妥英。连续4天采集静脉血样以测定游离和总苯妥英浓度。这些血样在血浆置换前、置换中点、置换结束时以及置换结束后30、60和120分钟采集。血样经离心后保存在4℃,直至使用同一荧光偏振免疫分析试剂盒进行分析。游离苯妥英通过超速离心分离。

讨论

尽管在操作过程中测得血清苯妥英总浓度和游离浓度有所下降,但在操作结束后30分钟时,游离苯妥英浓度出现明显反弹。然而,在操作结束后120分钟时,游离苯妥英浓度已降至操作前的值。该操作去除的苯妥英总量不到5%。

结论

尽管在血浆置换过程中观察到血清苯妥英总浓度和游离浓度下降,但接受血浆置换的患者可能不需要补充苯妥英,因为在操作结束后,具有治疗活性的游离血清苯妥英会迅速重新达到平衡。此外,全身苯妥英的去除量不到5%。其次,如果患者在操作后立即出现苯妥英中毒症状,可检测游离血清苯妥英浓度,因为尽管总苯妥英浓度降低,但该浓度可能反映中毒原因。

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