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由于环孢素和他克莫司可逆转地吸附于中心静脉导管,导致其浓度在较长时间内假性升高。

Falsely elevated cyclosporin and tacrolimus concentrations over prolonged periods of time due to reversible adsorption to central venous catheters.

作者信息

Hacker Charlotte, Verbeek Mareike, Schneider Heike, Steimer Werner

机构信息

Institut für Klinische Chemie und Pathobiochemie, Klinikum rechts der Isar, Technische Universität München, Germany.

III. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, Germany.

出版信息

Clin Chim Acta. 2014 Jun 10;433:62-8. doi: 10.1016/j.cca.2014.02.031. Epub 2014 Mar 11.

DOI:10.1016/j.cca.2014.02.031
PMID:24631133
Abstract

Falsely elevated concentrations of immunosuppressants can be caused by reversible adsorption to central venous catheter (CVC) systems. If undetected, this may lead to dose reduction resulting in underdosage which may even entail graft-versus-host disease or organ rejection. We analyzed the adsorption and release for cyclosporine A (CsA) and tacrolimus (Tac) in vitro and in vivo. Four types of CVCs were examined in vitro: two made from polyurethane (PU), one from silicone and one from PU with an incorporated silver ion-based antimicrobial agent. All 26 CVCs analyzed in vitro showed significant reversible adsorption of CsA (n=13; p=0.001) and Tac (n=13; p=0.001, Wilcoxon signed rank test). Immediately after infusing the drugs, the mean concentrations of 6420ng/mL of CsA and 250ng/mL of Tac were measured. Flushing with NaCl lowered the drug release. Besides, blood samples of fifteen patients were taken simultaneously from all lumina of the CVC and via venipuncture. The samples from contaminated lumina showed the mean elevations by a factor of 11 for CsA (n=12) and 89 for Tac (n=3). Blood sampling for immunosuppressant monitoring should thus never be performed from lumina previously used for infusing the drug even after prolonged periods of time and extensive rinsing.

摘要

免疫抑制剂浓度的假性升高可能是由于其可逆吸附于中心静脉导管(CVC)系统所致。若未被检测到,这可能导致剂量减少,进而造成用药不足,甚至可能引发移植物抗宿主病或器官排斥反应。我们对环孢素A(CsA)和他克莫司(Tac)在体外和体内的吸附及释放情况进行了分析。在体外检测了四种类型的CVC:两种由聚氨酯(PU)制成,一种由硅胶制成,一种由含银离子抗菌剂的PU制成。体外分析的所有26根CVC均显示出CsA(n = 13;p = 0.001)和Tac(n = 13;p = 0.001,Wilcoxon符号秩检验)有显著的可逆吸附。输注药物后立即测得CsA的平均浓度为6420ng/mL,Tac的平均浓度为250ng/mL。用氯化钠冲洗可降低药物释放。此外,同时从15名患者的CVC所有管腔及通过静脉穿刺采集血样。来自受污染管腔的样本显示,CsA(n = 12)平均升高11倍,Tac(n = 3)平均升高89倍。因此,即使在长时间和大量冲洗后,也绝不应从先前用于输注药物的管腔采集用于免疫抑制剂监测的血样。

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