用CRIT-LINE评价不同替代液方案对治疗性采血的血流动力学影响

IF 2.7 4区 医学 Q4 HEMATOLOGY
Hajar Elassas, Olivier Moranne
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引用次数: 0

摘要

在治疗性采血(TA)过程中,必须给予人白蛋白溶液(HAS)以预防低血压发作。CRIT-LINE监测仪用于血液透析评估相对血容量(RBV)的变化,以预防此类低血压发作。本研究的目的是根据不同的液体置换方案评估治疗性血浆置换(TPE)和双滤过血浆置换(DFPP)期间RBV的变化,以确定最佳方案。回顾性的病例系列研究进行了三名患者在三级中心的CIDP。使用CRIT-LINE监视器评估每位患者的TA疗程,以比较液体替代方案。对TPE的以下方案进行了评估:(TPE1) 100%体积替换,补充4%白蛋白;(TPE2)在初始阶段使用70%体积加4%白蛋白和30%生理盐水的组合;(TPE3)在疗程的最后阶段与生理盐水相同的组合。关于DFPP,评估了以下方案:DFPP1:在整个疗程中持续输注4%白蛋白,DFPP2:在疗程的最后20分钟输注4%白蛋白。对于这三名患者,在TPE期间,TPE1、TPE2和TPE3方案的RBV最低点分别为- 10%至- 13%、- 11%至- 17%和- 17%至- 20%。在3例患者中观察到低血压发作,这些患者在治疗结束时联合输液和注入生理盐水(TPE3)。在DFPP会话中,DFPP1和DFPP2协议的RBV变化的最低点分别为- 7%至- 15%和- 10%至- 20%。在疗程结束时输注白蛋白,RBV的最低点更高。我们的研究结果表明,在TA期间持续监测RBV,以确定更好的替代液体方案,并预防治疗期间的低血压,可能具有至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hemodynamic Effect of Different Replacement Fluid Protocols During Therapeutic Apheresis Evaluated With CRIT-LINE

Hemodynamic Effect of Different Replacement Fluid Protocols During Therapeutic Apheresis Evaluated With CRIT-LINE

In therapeutic apheresis (TA) procedures, it is essential to administrate human albumin solution (HAS) to prevent hypotensive episodes. The CRIT-LINE monitor is used in hemodialysis to estimate changes in relative blood volume (RBV) to prevent such hypotensive episodes. The aim of this study was to evaluate the change in RBV during therapeutic plasma exchange (TPE) and double filtration plasmapheresis (DFPP) according to different fluid replacement protocols in order to identify the best protocol. A retrospective case series study was conducted on three patients with CIDP at a tertiary center. Each patient's TA sessions were evaluated with the CRIT-LINE monitor to compare fluid replacement protocols. The following protocols were evaluated for TPE: (TPE1) 100% volume replacement with 4% albumin supplementation; (TPE2) a combination of a 70% volume with 4% albumin and 30% normal saline in the initial phase of the session; and (TPE3) the same combination with normal saline in the final phase of the session. With regard to DFPP, the following protocols were evaluated: DFPP1: continuous infusion of 4% albumin throughout the entire session, and DFPP2: 4% albumin the last 20 min of the session. For the three patients, during the TPE sessions, the nadir for RBV was −10% to −13%, −11% to −17%, and −17% to −20% for TPE1, TPE2, and TPE3 protocols, respectively. Hypotensive episodes were observed in three patients with a combination of fluid replacement with normal saline infused at the end of the session (TPE3). In the DFPP sessions, the nadir for the change in RBV was −7% to −15% and −10% to −20% for DFPP1 and DFPP2 protocols, respectively. The nadir for RBV was higher with albumin infusion at the end of the session. Our results suggest a potentially crucial role of continuous RBV monitoring during TA to identify the better substitution fluid protocol and prevent hypotension during sessions.

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来源期刊
CiteScore
2.80
自引率
13.30%
发文量
70
审稿时长
>12 weeks
期刊介绍: The Journal of Clinical Apheresis publishes articles dealing with all aspects of hemapheresis. Articles welcomed for review include those reporting basic research and clinical applications of therapeutic plasma exchange, therapeutic cytapheresis, therapeutic absorption, blood component collection and transfusion, donor recruitment and safety, administration of hemapheresis centers, and innovative applications of hemapheresis technology. Experimental studies, clinical trials, case reports, and concise reviews will be welcomed.
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