A single center retrospective study: Comparison between centrifugal separation plasma exchange with ACD-A and membrane separation plasma exchange with heparin on acute liver failure and acute on chronic liver failure

IF 1.4 4区 医学 Q4 HEMATOLOGY
Xin-Fang Zhu, Jia-Qiang Li, Tian-Tian Liu, Yuan Wang, Yao Zhong, Qing-Mei Gao, Qi Zhang, Kang-Kang Yu, Chong Huang, Ning Li, Qing Lu, Wen-Hong Zhang, Ji-Ming Zhang, Rong Xia, Jian-Ming Zheng
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Abstract

The purpose of this retrospective study is to compare the efficacy and safety of the centrifugal separation therapeutic plasma exchange (TPE) using citrate anticoagulant (cTPEc) with membrane separation TPE using heparin anticoagulant (mTPEh) in liver failure patients. The patients treated by cTPEc were defined as cTPEc group and those treated by mTPEh were defined as mTPEh group, respectively. Clinical characteristics were compared between the two groups. Survival analyses of two groups and subgroups classified by the model for end-stage liver disease (MELD) score were performed by Kaplan–Meier method and were compared by the log-rank test. In this study, there were 51 patients in cTPEc group and 18 patients in mTPEh group, respectively. The overall 28-day survival rate was 76% (39/51) in cTPEc group and 61% (11/18) in mTPEh group (P > .05). The 90-day survival rate was 69% (35/51) in cTPEc group and 50% (9/18) in mTPEh group (P > .05). MELD score = 30 was the best cut-off value to predict the prognosis of patients with liver failure treated with TPE, in mTPEh group as well as cTPEc group. The median of total calcium/ionized calcium ratio (2.84, range from 2.20 to 3.71) after cTPEc was significantly higher than the ratio (1.97, range from 1.73 to 3.19) before cTPEc (P < .001). However, there was no significant difference between the mean concentrations of total calcium before cTPEc and at 48 h after cTPEc. Our study concludes that there was no statistically significant difference in survival rate and complications between cTPEc and mTPEh groups. The liver failure patients tolerated cTPEc treatment via peripheral vascular access with the prognosis similar to mTPEh. The prognosis in patients with MELD score < 30 was better than in patients with MELD score ≥ 30 in both groups. In this study, the patients with acute liver failure (ALF) and acute on chronic liver failure (ACLF) treated with cTPEc tolerated the TPE frequency of every other day without significant clinical adverse event of hypocalcemia with similar outcomes to the mTPEh treatment. For liver failure patients treated with cTPEc, close clinical observation and monitoring ionized calcium are necessary to ensure the patients' safety.

Abstract Image

单中心回顾性研究:用ACD-A进行离心分离血浆置换与用肝素进行膜分离血浆置换治疗急性肝衰竭和急性慢性肝衰竭的比较
这项回顾性研究旨在比较使用枸橼酸抗凝剂的离心分离治疗性血浆置换术(TPE)(cTPEc)和使用肝素抗凝剂的膜分离治疗性血浆置换术(mTPEh)对肝衰竭患者的疗效和安全性。采用 cTPEc 治疗的患者被定义为 cTPEc 组,采用 mTPEh 治疗的患者被定义为 mTPEh 组。比较两组患者的临床特征。采用 Kaplan-Meier 法对两组患者及按终末期肝病模型(MELD)评分划分的亚组进行生存期分析,并采用对数秩检验进行比较。在这项研究中,cTPEc 组和 mTPEh 组分别有 51 名和 18 名患者。cTPEc 组的 28 天总生存率为 76%(39/51),mTPEh 组为 61%(11/18)(P > .05)。cTPEc 组的 90 天存活率为 69%(35/51),mTPEh 组为 50%(9/18)(P > .05)。在 mTPEh 组和 cTPEc 组中,MELD 评分 = 30 是预测接受 TPE 治疗的肝衰竭患者预后的最佳临界值。cTPEc 治疗后总钙/电离钙比值的中位数(2.84,范围在 2.20 到 3.71 之间)明显高于 cTPEc 治疗前的比值(1.97,范围在 1.73 到 3.19 之间)(P <.001)。但 cTPEc 前和 cTPEc 后 48 小时的总钙平均浓度没有明显差异。我们的研究得出结论,cTPEc 组和 mTPEh 组在存活率和并发症方面没有明显的统计学差异。肝衰竭患者可以耐受经外周血管入路的 cTPEc 治疗,其预后与 mTPEh 相似。两组患者中,MELD评分< 30分的患者预后均优于MELD评分≥30分的患者。在这项研究中,接受 cTPEc 治疗的急性肝衰竭(ALF)和急性慢性肝衰竭(ACLF)患者能够耐受每隔一天一次的 TPE 频率,不会出现低钙血症等明显的临床不良事件,治疗效果与 mTPEh 相似。对于接受 cTPEc 治疗的肝衰竭患者,有必要进行密切的临床观察和离子钙监测,以确保患者的安全。
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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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