Evidence map›Paper›PMID 40251686›Full record

ArticleJournal of pharmaceutical health care and sciences2025

Prescription patterns of comedications associated with drug-drug interactions risk in HCV-infected patients undergoing direct-acting antiviral treatment: an analysis of an administrative claims database in Japan.

Daisuke Nakamoto, Yi Piao, Hajime Mizutani, Ryozo Wakabayashi, Satoshi Otokita, Alice Stead, Candido Hernandez, Masahisa Jinushi

Abstract read
In one paragraph

Article in Journal of pharmaceutical health care and sciences, 2025. 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

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

8 authors.

Daisuke NakamotoGilead Sciences K.K., 1-9-2 Marunochi Gran Tokyo South Tower 16F, Chiyoda-ku, Tokyo, 100-6616, Japan. Daisuke.Nakamoto@gilead.com.
Yi PiaoGilead Sciences K.K., 1-9-2 Marunochi Gran Tokyo South Tower 16F, Chiyoda-ku, Tokyo, 100-6616, Japan.
Hajime MizutaniGilead Sciences K.K., 1-9-2 Marunochi Gran Tokyo South Tower 16F, Chiyoda-ku, Tokyo, 100-6616, Japan.
Ryozo WakabayashiDatack, Inc, 707, 1-8-9, Iidabashi Chiyoda-ku, Tokyo, 102-0072, Japan.
Satoshi OtokitaDatack, Inc, 707, 1-8-9, Iidabashi Chiyoda-ku, Tokyo, 102-0072, Japan.
Alice SteadGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, 94404, USA.
Candido HernandezGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, 94404, USA.
Masahisa JinushiGilead Sciences K.K., 1-9-2 Marunochi Gran Tokyo South Tower 16F, Chiyoda-ku, Tokyo, 100-6616, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWhile direct-acting antivirals (DAA) are effective treatment for hepatitis C virus (HCV) patients, concerns about drug-drug interactions (DDIs) remain a significant challenge. Although there are several studies investigating the risk of DDIs associated with DAA therapy, there is limited research evaluating DDIs of DAA therapy in real-world settings in Japan. We investigated prescription patterns of comedication associated with DDIs risk in HCV patients receiving DAA therapy using a large Japanese database.

methodsThis was a descriptive epidemiological study, using the Japanese administrative claims database provided by DeSC Healthcare, Inc. Patients who initiated sofosbuvir/velpatasvir (SOF/VEL) or glecaprevir/pibrentasvir (GLE/PIB) between April 2017 and August 2023 were identified from the data. The primary outcome was DDIs associated with comedications which were assessed based on both Japanese package inserts and the Liverpool HEP Drug Interaction Checker (Liverpool HEP checker).

resultsPatients included in this study were 7,338, with 467 prescribed SOF/VEL and 6,871 prescribed GLE/PIB. The mean age of the patients was 69.9 years (SD = 13.1), with 50% being male. The median number of comedications was higher in the SOF/VEL group (14.0; IQR = 14.0) than in the GLE/PIB group (9.0; IQR = 12.0) and based on package insert and Liverpool HEP checker, the DDI risk was present in 59.3% (277) of the SOF/VEL group and 51.5% (3,542) of the GLE/PIB group. DDI risk involving two or more medications in combination with a DAA was 14.1% (66) in the SOF/VEL group and 24.0% (1,648) in the GLE/PIB group. In terms of DDI severity, in the SOF/VEL group there were no patients identified under the level "Contraindication (Red)" category, indicating medications that do not co-administered, in contrast with the 1.7% (115) in the GLE/PIB group who were identified as "contraindication (red)".

conclusionA considerable proportion of patients were prescribed medications with DDI risk during DAA treatment. A small but notable proportion of patients were on "Contraindication (Red)" medications. Consideration of the potential DDI risks associated with comedications by healthcare professionals is advised, referring not only to package inserts but also tools such as Liverpool HEP checker to guide safe prescribing when initiating DAA therapy for HCV patients.

Indexed as

Direct-acting antiviral agentsDrug-drug interactionsGlecaprevir/pibrentasvirHepatitis C virusSofosbuvir/velpatasvir

Identifiers

PMID40251686
PMCPMC12008892

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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.