Recompensation of Chronic Hepatitis C-Related Decompensated Cirrhosis Following Direct-Acting Antiviral Therapy: Prospective Cohort Study From a Hepatitis C Virus Elimination Program.

IF 25.7 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Gastroenterology Pub Date : 2024-12-01 Epub Date: 2024-08-23 DOI:10.1053/j.gastro.2024.08.018
Madhumita Premkumar, Radha K Dhiman, Ajay Duseja, Rohit Mehtani, Sunil Taneja, Ekta Gupta, Pankaj Gupta, Anchal Sandhu, Prerna Sharma, Sahaj Rathi, Nipun Verma, Anand V Kulkarni, Harish Bhujade, Sreedhara B Chaluvashetty, Naveen Kalra, Gagandeep S Grover, Jasvinder Nain, K Rajender Reddy
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引用次数: 0

Abstract

Background & aims: Chronic hepatitis C-related decompensated cirrhosis is associated with lower sustained virologic response (SVR)-12 rates and variable regression of disease severity after direct-acting antiviral agents. We assessed rates of SVR-12, recompensation (Baveno VII criteria), and survival in such patients.

Methods: Between July 2018 and July 2023, patients with decompensated chronic hepatitis C-related cirrhosis after direct-acting antiviral agents treatment were evaluated for SVR-12 and then had 6-monthly follow-up.

Results: Of 6516 patients with cirrhosis, 1152 with decompensated cirrhosis (age 53.2 ± 11.5 years; 63% men; Model for End-stage Liver Disease-Sodium [MELD-Na]: 16.5 ± 4.6; 87% genotype 3) were enrolled. SVR-12 was 81.8% after 1 course; ultimately SVR was 90.8% after additional treatment. Decompensation events included ascites (1098; 95.3%), hepatic encephalopathy (191; 16.6%), and variceal bleeding (284; 24.7%). Ascites resolved in 86% (diuretic withdrawal achieved in 24% patients). Recompensation occurred in 284 (24.7%) at a median time of 16.5 (interquartile range, 14.5-20.5) months. On multivariable Cox proportional hazards analysis, low bilirubin (adjusted hazard ratio [aHR], 0.6; 95% confidence interval [CI], 0.5-0.8; P < 0.001), international normalized ratio (aHR, 0.2; 95% CI, 0.1-0.3; P < 0.001), absence of large esophageal varices (aHR, 0.4; 95% CI, 0.2-0.9; P = 0.048), or gastric varices (aHR, 0.5; 95% CI, 0.3-0.7; P = 0.022) predicted recompensation. Portal hypertension progressed in 158 (13.7%) patients, with rebleed in 4%. Prior decompensation with variceal bleeding (aHR, 1.6; 95% CI, 1.2-2.8; P = 0.042), and presence of large varices (aHR, 2.9; 95% CI, 1.3-6.5; P < 0.001) were associated with portal hypertension progression. Further decompensation was seen in 221 (19%); 145 patients died and 6 underwent liver transplantation. A decrease in MELDNa of ≥3 was seen in 409 (35.5%) and a final MELDNa score of <10 was seen in 335 (29%), but 2.9% developed hepatocellular carcinoma despite SVR-12.

Conclusions: SVR-12 in hepatitis C virus-related decompensated cirrhosis in a predominant genotype 3 population led to recompensation in 24.7% of patients over a follow-up of 4 years in a public health setting. Despite SVR-12, new hepatic decompensation evolved in 19% and hepatocellular carcinoma developed in 2.9% of patients. (ClinicalTrials.gov, Number: NCT03488485).

直接作用抗病毒疗法后慢性丙型肝炎相关失代偿性肝硬化的恢复:一项消除丙型肝炎病毒计划的前瞻性队列研究。
背景和目的:与慢性丙型肝炎(CHC)相关的失代偿性肝硬化与较低的 SVR-12 率以及直接作用抗病毒药物(DAAs)治疗后疾病严重程度的不同恢复有关。我们评估了这类患者的 SVR-12 率、失代偿率(巴韦诺 VII 标准)和存活率:2018年7月至2023年7月期间,对DAAs治疗后的CHC相关肝硬化失代偿期患者进行SVR-12评估,然后进行6个月随访:在6516名肝硬化患者中,有1152名失代偿期肝硬化患者(年龄53.2±11.5岁,63%为男性,MELD-Na:16.5±4.6,87%为基因3型)入组。一个疗程后,SVR-12 为 81.8%;继续治疗后,SVR 最终为 90.8%。失代偿事件包括腹水(1098 例,95.3%)、肝性脑病(191 例,16.6%)和静脉曲张出血(284 例,24.7%)。86%的患者腹水得到缓解(24%的患者停用了利尿剂)。284例(24.7%)患者在16.5(IQR-14.5-20.5)个月的中位时间内恢复。在多变量考克斯比例危险度分析中,低胆红素(aHR-0.6,95%CI-0.5-0.8,PConclusions:在以基因 3 型为主的人群中,HCV 相关失代偿性肝硬化患者 SVR-12 后,24.7% 的患者在 4 年的公共卫生随访中得到了恢复。尽管获得了 SVR-12,但仍有 19% 的患者出现了新的肝功能失代偿,2.9% 的患者发展为 HCC。
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来源期刊
Gastroenterology
Gastroenterology 医学-胃肠肝病学
CiteScore
45.60
自引率
2.40%
发文量
4366
审稿时长
26 days
期刊介绍: Gastroenterology is the most prominent journal in the field of gastrointestinal disease. It is the flagship journal of the American Gastroenterological Association and delivers authoritative coverage of clinical, translational, and basic studies of all aspects of the digestive system, including the liver and pancreas, as well as nutrition. Some regular features of Gastroenterology include original research studies by leading authorities, comprehensive reviews and perspectives on important topics in adult and pediatric gastroenterology and hepatology. The journal also includes features such as editorials, correspondence, and commentaries, as well as special sections like "Mentoring, Education and Training Corner," "Diversity, Equity and Inclusion in GI," "Gastro Digest," "Gastro Curbside Consult," and "Gastro Grand Rounds." Gastroenterology also provides digital media materials such as videos and "GI Rapid Reel" animations. It is abstracted and indexed in various databases including Scopus, Biological Abstracts, Current Contents, Embase, Nutrition Abstracts, Chemical Abstracts, Current Awareness in Biological Sciences, PubMed/Medline, and the Science Citation Index.
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