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首页> 外文期刊>Liver >First clinical experience with Molecular Adsorbent Recirculating System (MARS) in six patients with severe acute on chronic liver failure.
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First clinical experience with Molecular Adsorbent Recirculating System (MARS) in six patients with severe acute on chronic liver failure.

机译:分子吸附剂再循环系统(MARS)在6名患有慢性肝功能衰竭的严重急性患者中的首次临床经验。

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Despite recent advances in general supportive care, the mortality rate of patients with severe liver insufficiency remains high. Recently a new artificial liver support system MARS has been used for selective removal of albumin-bound toxins. Aim: To assess the safety and efficacy of MARS treatment in patients with acute on chronic liver disease (n = 5) or liver failure after extended hepatic resection (n = 1). Design/Patients: Six patients, aged 34-58 years, with severe liver insufficiency (mean MELD-score 31 (range 24-35)) were treated one to 16 times with the MARS system. At baseline three patients were intubated, three were encephalopathic (HE) and three had multifactorial kidney failure requiring kidney replacement therapy. Results and Conclusion: In all the patients MARS treatment significantly reduced the serum bilirubin levels. In three patients encephalopathy improved. In two patients the extracorporeal treatment precipitated a disseminated intravascular coagulation with clinically significant bleeding. Bridging to liver transplantation was possible in one patient, the other five patients died 30 days (2-74 days) after starting MARS therapy. Our case series shows that MARS treatment in general can be safely performed in patients with severe liver disease. However, in patients with an activated clotting system severe bleeding complication can be triggered and MARS treatment should be used very cautiously in these situations. MARS seems to be a promising new treatment option for patients with acute on chronic liver failure. However, carefully conducted randomized controlled trials are necessary to define its potential place in the treatment of patients with severe liver disease.
机译:尽管最近在一般支持治疗方面取得了进展,但是严重肝功能不全患者的死亡率仍然很高。最近,一种新的人工肝支持系统MARS已用于选择性去除白蛋白结合的毒素。目的:评估MARS治疗对慢性肝病急性发作(n = 5)或扩大肝切除术后肝衰竭(n = 1)患者的安全性和有效性。设计/患者:6例年龄在34-58岁之间,严重肝功能不全(平均MELD评分31(范围24-35))的患者接受了MARS系统的治疗1到16次。在基线时,对三名患者进行了插管,三名患有脑病(HE),三名患有多因素肾衰竭,需要进行肾脏替代治疗。结果与结论:在所有患者中,MARS治疗均显着降低了血清胆红素水平。三例患者脑病得到改善。在两名患者中,体外治疗引起弥散性血管内凝血,并伴有临床上明显的出血。一名患者可能桥接到肝移植,其他五名患者在开始MARS治疗后30天(2-74天)死亡。我们的病例系列表明,重症肝病患者一般可以安全地进行MARS治疗。但是,在具有激活的凝血系统的患者中,可能会引发严重的出血并发症,在这些情况下应非常谨慎地使用MARS治疗。对于患有慢性肝功能衰竭的急性患者,MARS似乎是一种有希望的新治疗选择。但是,有必要进行仔细的随机对照试验来确定其在重症肝病患者治疗中的潜在地位。

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