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Outcomes after successful direct-acting antiviral therapy for patients with chronic hepatitis C and decompensated cirrhosis

机译:成功直接作用抗病毒治疗慢性丙型肝炎和失代偿期肝硬化患者的结果

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摘要

Background & AimsududDirect-acting antivirals have become widely used for patients with chronic hepatitis C virus infection with decompensated cirrhosis. Virological responses are excellent and early improvements in liver function, at least in a proportion of patients, have been observed but the longer term impact of viral clearance on end-stage liver disease complications is unclear.ududMethods:ududProspective study of patients with decompensated cirrhosis who received 12 weeks of all-oral direct-acting antivirals through the English Expanded Access Programme. Endpoints were deaths, liver transplantation, hepatocellular carcinoma, serious decompensation events, sepsis or hospitalisations, and MELD scores between start of therapy to 15 months post-treatment start. An untreated cohort of patients was retrospectively studied over 6 months for comparison.ududResults:ududAmongst 317/406 patients who achieved sustained virological response at 24 weeks post-treatment, there were 9 deaths (3%), 17 new liver cancers (5%), 39 transplantations (12%) and 52 with serious decompensations (16%), over 15 months.ududWhen compared to the first six months from treatment start and to untreated patients, there was a reduction in incidence of decompensations [30/406 (7%) in months 6–15 and 72/406 (18%) in months 0–6 for treated patients vs. 73/261 (28%) in untreated patients]. There was no significant difference in liver cancer incidence (10/406 (2.5%) in months 6–15 and 17/406 (4%) in months 0–6 for treated patients vs. 11/261 (4%) in untreated patients).ududConclusions:ududThis study suggests that antiviral therapy in patients with decompensated cirrhosis led to prolonged improvement in liver function, with no evidence of paradoxical adverse impact nor increase in liver malignancy.
机译:背景与目的直接作用抗病毒药已广泛用于患有慢性代偿性肝硬化的慢性丙型肝炎病毒感染患者。病毒学应答非常好,并且至少在一定比例的患者中,肝功能得到了早期改善,但是病毒清除对终末期肝病并发症的长期影响尚不清楚。 ud ud方法: ud ud前瞻性研究失代偿期肝硬化的患者中,通过英语扩展访问计划接受了12周全口服直接作用抗病毒药物的治疗。终点是死亡,肝移植,肝细胞癌,严重的代偿失调事件,败血症或住院以及治疗开始至治疗后15个月之间的MELD评分。对未经治疗的一组患者进行了为期6个月的回顾性研究,以进行比较。 ud ud结果: ud ud在317/406名在治疗后24周获得持续病毒学应答的患者中,有9例死亡(3%),17例新肝癌(5%),39例移植手术(12%)和52例严重代偿失调(16%)的病程超过15个月。 ud ud与治疗开始和未治疗的患者头六个月相比,代偿失调的发生率[接受治疗的患者在6-15个月时为30/406(7%),在0-6个月为72/406(18%),而未经治疗的患者为73/261(28%)。治疗患者的肝癌发生率在6-15个月时为10/406(2.5%),0-6个月为17/406(4%),而未治疗患者为11/261(4%) ud ud结论: ud ud这项研究表明,代偿性肝硬化患者进行抗病毒治疗可延长肝功能,没有悖论性不良影响或肝恶性程度增加的证据。

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