The Efficacy of Glecaprevir/Pibrentasvir in Chronic Hepatitis C Patients and the Impact of the COVID-19 Pandemic: Multicenter Real-Life Data

ArticleAçık Erişim

Özet

Objective: This study aimed to demonstrate the real-life efficacy and safety of glecaprevir / pibrentasvir in the treatment of chronic hepatitis C, as well as to identify the problems caused by the COVID-19 pandemic in the follow-up and treatment of patients. Materials and Methods: The study was conducted retrospectively with the participation of researchers from universities or training and research hospitals. It included patients with chronic hepatitis C who were over 18 years of age, treatment-naïve or treatment-experienced, had detectable HCV RNA and were receiving glecaprevir/pibrentasvir treatment Results: Only 188 of the 385 patients who participated in the study came to the follow-up visit 12 weeks after treatment, and all of them had a sustained virological response. It was thought that a significant portion of the 177 patients who did not come to the follow-up visit at 12 weeks after treatment refrained from coming to the hospital due to the COVID-19 pandemic. None of the patients who attended the follow-up visits required treatment discontinuation due to adverse events. Conclusion: Glecaprevir/pibrentasvir is a highly effective and relatively safe drug in the treatment of chronic hepatitis C. The COVID-19 pandemic has negatively affected the follow-up and treatment processes of patients. New measures are needed for the follow-up and treatment of patients with chronic hepatitis C during pandemics. © 2024, DOC Design and Informatics Co. Ltd.. All rights reserved.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11370Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.36519/idcm.2024.344Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorGürbüz, Yunus
dc.contributor.authorKocagül-çelikbaş, Aysel
dc.contributor.authorÖztoprak, Nefise
dc.contributor.authorAygen, Bilgehan
dc.contributor.authorBatırel, Ayşe
dc.contributor.authorHabiloğlu, Arif Doğan
dc.contributor.authorAktuğ-Demir, Nazlım
dc.contributor.authorÇeken, Sabahat
dc.contributor.authorDemirtürk, Neşe
dc.contributor.authorCeylan, Mehmet Reşat
dc.contributor.authorÜçer, Şengül
dc.contributor.authorKarakeçili, Faruk
dc.contributor.authorAlkan, Sevil
dc.contributor.authorİnce, Nevin
dc.contributor.authorAkça, Anıl
dc.contributor.authorGünay, Veli
dc.contributor.authorMustanoğlu-özatağ, Duru
dc.contributor.authorÇınar, Güle
dc.contributor.authorKınıklı, Sami
dc.contributor.authorYıldız, Orhan
dc.contributor.authorŞarlak-Konya, Petek
dc.contributor.authorSümer, Şua
dc.contributor.authorYekenkurul, Dilek
dc.contributor.authorÇelik, Mehmet
dc.contributor.authorBinay, Umut Devrim
dc.contributor.authorAşık-Otman, Zahide
dc.date.accessioned2026-10-18T20:26:25.882513826Z
dc.date.available2026-10-18T20:26:25.882513826Z
dc.date.issued2024
dc.description.abstractObjective: This study aimed to demonstrate the real-life efficacy and safety of glecaprevir / pibrentasvir in the treatment of chronic hepatitis C, as well as to identify the problems caused by the COVID-19 pandemic in the follow-up and treatment of patients. Materials and Methods: The study was conducted retrospectively with the participation of researchers from universities or training and research hospitals. It included patients with chronic hepatitis C who were over 18 years of age, treatment-naïve or treatment-experienced, had detectable HCV RNA and were receiving glecaprevir/pibrentasvir treatment Results: Only 188 of the 385 patients who participated in the study came to the follow-up visit 12 weeks after treatment, and all of them had a sustained virological response. It was thought that a significant portion of the 177 patients who did not come to the follow-up visit at 12 weeks after treatment refrained from coming to the hospital due to the COVID-19 pandemic. None of the patients who attended the follow-up visits required treatment discontinuation due to adverse events. Conclusion: Glecaprevir/pibrentasvir is a highly effective and relatively safe drug in the treatment of chronic hepatitis C. The COVID-19 pandemic has negatively affected the follow-up and treatment processes of patients. New measures are needed for the follow-up and treatment of patients with chronic hepatitis C during pandemics. © 2024, DOC Design and Informatics Co. Ltd.. All rights reserved.
dc.identifier.doi10.36519/idcm.2024.344
dc.identifier.eissn2667-646X
dc.identifier.endpage224
dc.identifier.issn2667-646X
dc.identifier.issue3
dc.identifier.pmcidPMC11465448
dc.identifier.pmid39399749
dc.identifier.scopus2-s2.0-85211167386
dc.identifier.startpage216
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11370
dc.identifier.volume6
dc.language.isoen
dc.publisherDOC Design and Informatics Co. Ltd.
dc.relation.ispartofInfectious Diseases and Clinical Microbiology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectchronic hepatitis C
dc.subjectCOVID-19
dc.subjectglecaprevir
dc.subjectmulticenter study
dc.subjectpibrentasvir
dc.titleThe Efficacy of Glecaprevir/Pibrentasvir in Chronic Hepatitis C Patients and the Impact of the COVID-19 Pandemic: Multicenter Real-Life Data
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.trdizin0
rdl.departmentHARRAN ÜNİVERSİTESİ
rdl.departmentDÜZCE ÜNİVERSİTESİ
rdl.departmentERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ
rdl.departmentANKARA ÜNİVERSİTESİ
rdl.departmentÇANAKKALE ONSEKİZ MART ÜNİVERSİTESİ
rdl.departmentSELÇUK ÜNİVERSİTESİ
rdl.departmentT.C. SAĞLIK BAKANLIĞI
rdl.departmentKÜTAHYA SAĞLIK BİLİMLERİ ÜNİVERSİTESİ
rdl.departmentAFYONKARAHİSAR SAĞLIK BİLİMLERİ ÜNİVERSİTESİ
rdl.departmentİÇİŞLERİ BAKANLIĞI
rdl.departmentSAĞLIK BİLİMLERİ ÜNİVERSİTESİ
rdl.departmentERCİYES ÜNİVERSİTESİ
rdl.departmentHİTİT ÜNİVERSİTESİ
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexTRDIZIN
rdl.source.indexPUBMED