Evidence map›Paper›PMID 41591519›Full record

ArticleJournal of gastroenterology2026

Continuity of long-term follow-up in patients with chronic hepatitis C after sustained virologic response following direct-acting antiviral therapy: a nationwide real-world multicenter cohort study in Japan.

Masatsugu Ohara, Ritsuzo Kozuka, Yoshihito Uchida, Chikara Iino, Ryo Sasaki, Hiroki Tojima, Kazuhito Kawata, Satoru Kakizaki, Yoshio Tokumoto, Mizuki Endo and 11 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Masatsugu OharaDepartment of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Ritsuzo KozukaDepartment of Hepatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Yoshihito UchidaDepartment of Gastroenterology and Hepatology, Faculty of Medicine, Saitama Medical University, Saitama, Japan.
Chikara IinoDepartment of Gastroenterology, Hematology and Clinical Immunology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Ryo SasakiDepartment of Gastroenterology and Hepatology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Hiroki TojimaDepartment of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Kazuhito KawataHepatology Division, Department of Internal Medicine II, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Satoru KakizakiDepartment of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Yoshio TokumotoDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Mizuki EndoDepartment of Gastroenterology, Oita University, Yufu, Japan.
Akira AsaiMedical Laboratory, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Jun InoueDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kenji NagataDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Hirokazu TakahashiDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Tetsuro ShimakamiDepartment of Gastroenterology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.
Koji OgawaDepartment of Gastroenterology and Hepatology, NTT Medical Center Sapporo, Sapporo, Japan.
Masaru EnomotoDepartment of Hepatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Tadashi IkegamiDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ami, Japan.
Tatsuya IdeDivision of Gastroenterology, Kurume University Medical Center, Kurume, Japan.
Naoya SakamotoDepartment of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Masaaki KorenagaHepatitis Information Center, The Research Center for Hepatitis and Immunology, Japan Institute for Health Security, 1-7-1 Konodai, Ichikawa, Chiba Prefecture, 272-8516, Japan. korenaga.m@jihs.go.jp.ORCID 0000-0002-6360-8297

Funding

Ministry of Health, Labour and Welfare 23HC1001
6 · The paper itself

Abstract

backgroundLong-term follow-up is essential after a sustained virologic response (SVR) to direct-acting antivirals (DAAs) in patients with chronic hepatitis C. However, real-world continuity of care and determinants of disengagement are poorly characterized at the national level. Here, we quantified the follow-up continuity within Japan's government-designated regional core centers and identified independent factors associated with transfer and self-discontinuation.

methodsWe conducted a retrospective multicenter cohort study of 3702 patients with chronic hepatitis C who achieved SVR at 16 regional core centers (2015-2018). Continuation was assessed using Kaplan-Meier analysis and competing-risk analysis, and Fine-Gray regression identified determinants of transfer and discontinuation.

resultsAt 5 years, 56% of the patients were followed up, 24% were transferred, and 18% self-discontinued. Older age was significantly associated with transfer (subdistribution hazard ratio [sHR] 1.41, 95% CI 1.23-1.61), whereas hepatocellular carcinoma (HCC) and other malignancies favored continuous follow-up. Self-discontinuation was more frequent with hepatitis C virus (HCV) serotype 2 (sHR 1.36, 95% CI 1.18-1.57) and less common among patients with advanced disease or prior hospitalization.

conclusionsWithin Japan's core-center network, long-term continuation after SVR is high but not universal. Follow-up was generally maintained for patients with severe comorbidities, while disengagement was more likely among those with lower perceived risk. Strengthening low-intensity, structured support for such patients may improve the continuity and equity of post-SVR care. These findings provide a foundation for optimizing post-SVR care pathways in national liver disease networks.

Indexed as

Antiviral AgentsContinuity of Patient CareHepatitis C, ChronicAgedAge FactorsCohort StudiesFemaleFollow-Up StudiesHumansJapanMaleMiddle AgedRetrospective StudiesSustained Virologic ResponseTime FactorsAntiviral AgentsFollow-up continuityHepatitis C virusRegional core centersSVR

Identifiers

PMID41591519
PMCPMC13048953

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.