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用于肝衰竭的白蛋白透析:一项系统评价

Albumin Dialysis for Liver Failure: A Systematic Review.

作者信息

Tsipotis Evangelos, Shuja Asim, Jaber Bertrand L

机构信息

Division of Nephrology, Department of Medicine, St. Elizabeth's Medical Center, Boston, MA; Department of Medicine, Tufts University School of Medicine, Boston, MA.

Division of Nephrology, Department of Medicine, St. Elizabeth's Medical Center, Boston, MA; Department of Medicine, Tufts University School of Medicine, Boston, MA.

出版信息

Adv Chronic Kidney Dis. 2015 Sep;22(5):382-90. doi: 10.1053/j.ackd.2015.05.004.

DOI:10.1053/j.ackd.2015.05.004
PMID:26311600
Abstract

Albumin dialysis is the best-studied extracorporeal nonbiologic liver support system as a bridge or destination therapy for patients with liver failure awaiting liver transplantation or recovery of liver function. We performed a systematic review to examine the efficacy and safety of 3 albumin dialysis systems (molecular adsorbent recirculating system [MARS], fractionated plasma separation, adsorption and hemodialysis [Prometheus system], and single-pass albumin dialysis) in randomized trials for supportive treatment of liver failure. PubMed, Ovid, EMBASE, Cochrane's Library, and ClinicalTrials.gov were searched. Two authors independently screened citations and extracted data on patient characteristics, quality of reports, efficacy, and safety end points. Ten trials (7 of MARS and 3 of Prometheus) were identified (620 patients). By meta-analysis, albumin dialysis achieved a net decrease in serum total bilirubin level relative to standard medical therapy of 8.0 mg/dL (95% confidence interval [CI], -10.6 to -5.4) but not in serum ammonia or bile acids. Albumin dialysis achieved an improvement in hepatic encephalopathy relative to standard medical therapy with a risk ratio of 1.55 (95% CI, 1.16-2.08) but had no effect survival with a risk ratio of 0.95 (95% CI, 0.84-1.07). Because of inconsistency in the reporting of adverse events, the safety analysis was limited but did not demonstrate major safety concerns. Use of albumin dialysis as supportive treatment for liver failure is successful at removing albumin-bound molecules, such as bilirubin and at improving hepatic encephalopathy. Additional experience is required to guide its optimal use and address safety concerns.

摘要

白蛋白透析是研究最为充分的体外非生物性肝脏支持系统,可作为肝衰竭患者等待肝移植或肝功能恢复期间的过渡或终极治疗手段。我们进行了一项系统评价,以考察3种白蛋白透析系统(分子吸附再循环系统[MARS]、血浆成分分离吸附与血液透析[普罗米修斯系统]以及单程白蛋白透析)在肝衰竭支持治疗随机试验中的疗效和安全性。检索了PubMed、Ovid、EMBASE、Cochrane图书馆和ClinicalTrials.gov。两名作者独立筛选文献并提取有关患者特征、报告质量、疗效和安全性终点的数据。共纳入10项试验(7项MARS试验和3项普罗米修斯试验)(620例患者)。通过荟萃分析,相对于标准药物治疗,白蛋白透析使血清总胆红素水平净下降8.0mg/dL(95%置信区间[CI],-10.6至-5.4),但对血清氨或胆汁酸水平无影响。相对于标准药物治疗,白蛋白透析改善了肝性脑病,风险比为1.55(95%CI,1.16 - 2.08),但对生存率无影响,风险比为0.95(95%CI,0.84 - 1.07)。由于不良事件报告存在不一致性,安全性分析受到限制,但未显示出重大安全问题。使用白蛋白透析作为肝衰竭的支持治疗可成功清除与白蛋白结合的分子,如胆红素,并改善肝性脑病。需要更多经验来指导其最佳应用并解决安全问题。

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