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Long-term Effect of the HCV Elimination With Direct-acting Antivirals on the Progression of Gastroesophageal Varices.

Authors :
YUKIHISA YURI
TAKASHI NISHIMURA
NAOTO IKEDA
TOMOYUKI TAKASHIMA
NOBUHIRO AIZAWA
TARO KIMURA
KOHEI YOSHIHARA
RYOTA YOSHIOKA
SHOKI KAWATA
YUTA KAWASE
RYOTA NAKANO
HIDEYUKI SHIOMI
SHINYA FUKUNISHI
SHINICHIRO SHINZAKI
HIRAYUKI ENOMOTO
Source :
In Vivo; Nov/Dec2024, Vol. 38 Issue 6, p2968-2972, 5p
Publication Year :
2024

Abstract

Background/Aim: Gastroesophageal varices (GEV) hemorrhage is a serious complication that can lead to unfavorable outcomes in cirrhotic patients. However, the clinical impact of HCV elimination [sustained viral response (SVR)] by direct-acting antivirals (DAAs), particularly on the long-term effects on the endoscopic findings of GEV have not been sufficiently evaluated. This study aimed to investigate whether HCV elimination with DAA treatment suppresses the progression of GEV. Patients and Methods: The clinical courses of the endoscopic findings of GEV were retrospectively compared between patients without an SVR (non-SVR group: n=71) and those who achieved an SVR with DAAs (DAA-SVR group: n=38). Results: At 1, 3, 5, and 7 years, the cumulative GEV progression rates were 8.7%, 32.8%, 45.6%, and 66.2%, respectively. At 3 years, the cumulative GEV progression rate in the DAA-SVR group was similar to that in the non-SVR group. Beyond 3 years, cases with GEV progression were found in the non-SVR group, but not in the DAA-SVR group. At 7 years, the cumulative GEV progression rate in the DAA-SVR group was significantly lower than that in the non-SVR group (p<0.05, logrank test). Variceal hemorrhage occurred in eight patients in the non-SVR group, while no bleeding events were observed in the DAA-SVR group during the observational period [8/71 (11.3%) vs. 0/38 (0.0%), p<0.05]. Conclusion: DAA treatment suppresses the progression of GEV over the long term. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0258851X
Volume :
38
Issue :
6
Database :
Complementary Index
Journal :
In Vivo
Publication Type :
Academic Journal
Accession number :
181050419
Full Text :
https://doi.org/10.21873/invivo.13779