Evidence map›Paper›PMID 36852151›Full record

ArticleJGH open : an open access journal of gastroenterology and hepatology2023

Risk factors for loss to follow-up after the start of direct-acting antiviral treatment for hepatitis C virus infection.

Akifumi Kuwano, Masayoshi Yada, Kazuki Kurosaka, Kosuke Tanaka, Akihide Masumoto, Kenta Motomura

Open access · goldAbstract read
In one paragraph

Article in JGH open : an open access journal of gastroenterology and hepatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Akifumi KuwanoDepartment of Hepatology Iizuka Hospital Iizuka Japan.ORCID https://orcid.org/0000-0001-9397-8056
Masayoshi YadaDepartment of Hepatology Iizuka Hospital Iizuka Japan.
Kazuki KurosakaDepartment of Hepatology Iizuka Hospital Iizuka Japan.
Kosuke TanakaDepartment of Hepatology Iizuka Hospital Iizuka Japan.
Akihide MasumotoDepartment of Hepatology Iizuka Hospital Iizuka Japan.
Kenta MotomuraDepartment of Hepatology Iizuka Hospital Iizuka Japan.
Aso Iizuka Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Direct-acting antivirals (DAAs) have recently been developed to treat hepatitis C virus (HCV) infection. Additionally, interferon-free DAA treatment has improved liver function and reduced the risk of hepatocellular carcinoma (HCC) following HCV eradication. Previous studies on HCV have focused mainly on the treatment rate and the risk of developing HCC, and less attention has been given to loss to follow-up (LTFU) after DAA treatment. Therefore, the present study aimed to identify the definitive risk factors for LTFU after the start of DAA treatment. Methods: Between September 2017 and March 2022, 296 patients receiving glecaprevir and pibrentasvir for HCV infection were enrolled in this study. The incidence of LTFU following DAA treatment and the risk factors contributing to LTFU were identified using the patients' clinical characteristics. Results: In the present study, 75 patients (25.3%) interrupted their follow-up visits. Multivariate logistic analysis revealed a history of injection drug use (hazard ratio [HR], 1.81; Conclusion: Young patients and those with injection drug use are likely to discontinue their follow-up visits after the start of DAA treatment for HCV infection. Therefore, these patients require strict supervision.

Indexed as

direct‐acting antiviralsglecaprevir and pibrentasvirhepatitis C virushistory of injection drug useloss to follow‐up

Identifiers

PMID36852151
PMCPMC9958342
OpenAlexW4313401536

What OpenQuestion holds

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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.