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Recompensation of Chronic Hepatitis C-Related Decompensated Cirrhosis Following Direct-Acting Antiviral Therapy: Prospective Cohort Study From a Hepatitis C Virus Elimination Program.
Premkumar, Madhumita; Dhiman, Radha K; Duseja, Ajay; Mehtani, Rohit; Taneja, Sunil; Gupta, Ekta; Gupta, Pankaj; Sandhu, Anchal; Sharma, Prerna; Rathi, Sahaj; Verma, Nipun; Kulkarni, Anand V; Bhujade, Harish; Chaluvashetty, Sreedhara B; Kalra, Naveen; Grover, Gagandeep S; Nain, Jasvinder; Reddy, K Rajender.
Afiliación
  • Premkumar M; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Dhiman RK; Chairman, Technical Resource Group - National Viral Hepatitis Control Program, Government of India, India; Director, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India. Electronic address: rkpsdhiman@hotmail.com.
  • Duseja A; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Mehtani R; Department of Hepatology, Amrita Institute of Medical Sciences and Research Centre, Faridabad, Haryana, India.
  • Taneja S; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Gupta E; Department of Virology, Institute of Liver and Biliary Sciences, New Delhi, India.
  • Gupta P; Department of Radiodiagnosis, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sandhu A; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sharma P; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Rathi S; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Verma N; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kulkarni AV; Department of Hepatology, Asian Institute of Gastroenterology, Hyderabad, India.
  • Bhujade H; Department of Radiodiagnosis, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Chaluvashetty SB; Department of Radiodiagnosis, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kalra N; Department of Radiodiagnosis, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Grover GS; Program Officer, Hepatitis C Virus Infection, Government of Punjab, Punjab, India.
  • Nain J; Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Reddy KR; Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania.
Gastroenterology ; 2024 Aug 23.
Article en En | MEDLINE | ID: mdl-39181168
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 (aHR, 0.6; 95% confidence interval [CI], 0.5-0.8; P < 0.001), INR (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).
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Gastroenterology Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Gastroenterology Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos