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治疗性血浆置换期间系统性普通肝素抗凝的管理

Management of systemic unfractionated heparin anticoagulation during therapeutic plasma exchange.

作者信息

Kaplan Alesia, Raut Prachi, Totoe Grace, Morgan Shanna, Zantek Nicole D

机构信息

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.

Acute Care Medicine, Department of Hospital Medicine, North Memorial Medical Center, Robbinsdale, Minnesota.

出版信息

J Clin Apher. 2016 Dec;31(6):507-515. doi: 10.1002/jca.21441. Epub 2016 Jan 11.

Abstract

BACKGROUND

Therapeutic plasma exchange (TPE) may remove medications from the patient's plasma. Data is limited on the effect of TPE on unfractionated heparin (UFH).

STUDY DESIGN AND METHODS

A retrospective review was performed of patients receiving TPE and continuous IV infusion UFH from 1/1/2008 to 6/30/2010. TPE with plasma or 5% albumin for replacement fluid and pre and post anti-Xa levels within approximately six hours were analyzed.

RESULTS

Three patients had 15 TPE with plasma replacement. Anti-Xa levels decreased 47% (mean, -0.25 IU/mL) for two TPE when UFH was not changed, 78% (-0.35 IU/mL) for one TPE when the UFH rate was decreased 25%; and 61% (mean -0.72 IU/mL) for two single volume TPE and 87% (-0.65 IU/mL) for one 1.5 plasma volume TPE when UFH was stopped. During nine TPE, the UFH rate was increased by 65% resulting in a mean increase in the anti-Xa level (mean 0.06 IU/mL, 30%). One patient had five single plasma volume TPE with 5% albumin. Anti-Xa levels decreased when the UFH was not changed (-0.06 IU/mL, 38%) and increased when UFH was increased by 30% (0.19 IU/mL, 61%) and 69% (mean 0.04 IU/mL, 15% in three TPE). The PTT increased with all albumin procedures, with more marked increases observed when the UFH rate was increased, while the antithrombin level decreased (mean 65%).

CONCLUSION

Heparin was removed from the patient's plasma during TPE. Adjustment of the dose during TPE may be necessary to maintain therapeutic drug levels. Methods for monitoring UFH therapy may not agree. J. Clin. Apheresis 31:507-515, 2016. © 2016 Wiley Periodicals, Inc.

摘要

背景

治疗性血浆置换(TPE)可能会从患者血浆中清除药物。关于TPE对普通肝素(UFH)影响的数据有限。

研究设计与方法

对2008年1月1日至2010年6月30日期间接受TPE和持续静脉输注UFH的患者进行回顾性研究。分析使用血浆或5%白蛋白作为置换液的TPE以及大约6小时内的抗Xa水平前后变化。

结果

3例患者进行了15次血浆置换的TPE。当UFH未改变时,两次TPE的抗Xa水平下降47%(平均,-0.25 IU/mL);当UFH速率降低25%时,一次TPE的抗Xa水平下降78%(-0.35 IU/mL);当停用UFH时,两次单倍体积TPE的抗Xa水平下降61%(平均-0.72 IU/mL),一次1.5倍血浆体积TPE的抗Xa水平下降87%(-0.65 IU/mL)。在9次TPE期间,UFH速率增加65%,导致抗Xa水平平均增加(平均0.06 IU/mL,30%)。1例患者进行了5次使用5%白蛋白的单倍血浆体积TPE。当UFH未改变时,抗Xa水平下降(-0.06 IU/mL,38%),当UFH增加30%时,抗Xa水平升高(0.19 IU/mL,61%),在三次TPE中升高69%(平均0.04 IU/mL,15%)。所有白蛋白置换程序的部分凝血活酶时间(PTT)均升高,当UFH速率增加时升高更明显,而抗凝血酶水平下降(平均65%)。

结论

TPE期间肝素从患者血浆中被清除。TPE期间可能需要调整剂量以维持治疗药物水平。监测UFH治疗的方法可能不一致。《临床血液分离杂志》31:507 - 515,2016年。©2016威利期刊公司

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