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首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Anticoagulation with low-molecular-weight heparin (dalteparin) in plasmapheresis therapy: initial experience.
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Anticoagulation with low-molecular-weight heparin (dalteparin) in plasmapheresis therapy: initial experience.

机译:在血浆置换术中使用低分子量肝素(达肝素)进行抗凝治疗:初步经验。

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BACKGROUND: In contrast to other extracorporeal treatments no established regime exists for anticoagulation with low-molecular-weight heparin (LMWH) in plasmapheresis therapy. A study was conducted to investigate whether LMWH (dalteparin-Na) is suitable as an effective anticoagulant in plasmapheresis therapy. STUDY DESIGN AND METHODS: Eleven patients with autoimmune neurological diseases and the necessity for a plasmapheresis therapy were enrolled. A capillary membrane filter was used. A total of 2000 mL of human plasma was isovolumetrically exchanged per plasmapheresis cycle. The anticoagulation was accomplished with a single bolus of LMWH (dalteparin) of 80 to 90 IU per kg of body weight. The system was visually monitored. Anti-factor (F)Xa activity, thrombin-antithrombin III complex (TAT), and prothrombin fragment 1+2 (F 1+2) were determined at regular intervals. Samples were taken from the collected plasma pool to determine the loss of LMWH during the plasmapheresis procedure. RESULTS: All plasmapheresis cycles with LMWH were successful without complications. Approximately 40 percent of the initially administered LMWH bolus was lost by the large porous filter during the plasmapheresis. The anti-FXa values were determined to be 0.5 IU per mL during the entire plasmapheresis. TAT values were elevated (TAT median, 14.3 microg/L). F 1+2 values measured before the filter cartridge remained within the normal range for the entire plasmapheresis cycle (<1.2 nmol/L) and were increasingly elevated after the filter. CONCLUSION: Our initial experiences with LMWH for anticoagulation in plasmapheresis indicate that a body weight adjusted dose of LMWH (dalteparin) is suitable for anticoagulation in plasmapheresis therapy. No complications were observed. The data are encouraging. Further investigations will show if and how the present anticoagulation regime could be further optimized.
机译:背景:与其他体外治疗相比,血浆置换术中不存在使用低分子量肝素(LMWH)进行抗凝的既定方案。进行了一项研究,以调查LMWH(达肝素钠)是否适合用作血浆置换术中的有效抗凝剂。研究设计和方法:招募了11例自身免疫性神经系统疾病患者,并进行了血浆置换治疗。使用毛细管膜过滤器。每个血浆置换周期共等体积交换2000 mL人血浆。抗凝是通过每公斤体重80到90 IU的LMWH(达肝素)单次推注完成的。对该系统进行视觉监控。定期测定抗因子(F)Xa活性,凝血酶-抗凝血酶III复合物(TAT)和凝血酶原片段1 + 2(F 1 + 2)。从收集的血浆池中取样以测定血浆置换过程中LMWH的损失。结果:LMWH的所有血浆置换周期均成功,无并发症。在血浆置换过程中,大型多孔过滤器损失了最初给予的LMWH推注约40%的剂量。在整个血浆置换过程中,抗FXa值确定为0.5 IU / mL。 TAT值升高(TAT中位数,14.3 microg / L)。 F 1 + 2值在滤筒在整个血浆置换周期内均保持在正常范围内(<1.2 nmol / L),并在过滤后逐渐升高。结论:我们在血浆置换术中使用LMWH进行抗凝的初步经验表明,体重调整剂量的LMWH(达肝素)适用于血浆置换术中的抗凝。没有观察到并发症。数据令人鼓舞。进一步的研究将显示是否以及如何进一步优化当前的抗凝方案。

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