Evidence map›Paper›PMID 41629822›Full record

ArticleBMC infectious diseases2026

Direct-acting antiviral therapy in HCV patients: a retrospective study of the pre- and post-treatment impact in Saudi Arabia.

Fatimah Salem Alayidh, Alexander Woodman, Nawaf Yahya Zakary, Rehab Yusuf Al-Ansari, Sharjeel Chaudhry, Amal Omar Alsaadi, Khadijah Ahmad Alharbi, Batool Abdullah Alamri, Shahad Mousa Alhomud, Shahad Hassan Albather and 4 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Fatimah Salem AlayidhDepartment of Medical Laboratory, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Saudi Arabia.
Alexander WoodmanScientific Research Department, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Saudi Arabia.
Nawaf Yahya ZakaryDepartment of Internal Medicine, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Kingdom of Saudi Arabia.
Rehab Yusuf Al-AnsariDepartment of Internal Medicine, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Kingdom of Saudi Arabia.
Sharjeel ChaudhryDepartment of Molecular Pathology, Dow University of Health Sciences, Karachi, Pakistan. sharjeel.chaudhry17@didc.duhs.edu.pk.
Amal Omar AlsaadiDepartment of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dhahran, Kingdom of Saudi Arabia.
Khadijah Ahmad AlharbiDepartment of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dhahran, Kingdom of Saudi Arabia.
Batool Abdullah AlamriDepartment of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dhahran, Kingdom of Saudi Arabia.
Shahad Mousa AlhomudDepartment of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dhahran, Kingdom of Saudi Arabia.
Shahad Hassan AlbatherDepartment of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dhahran, Kingdom of Saudi Arabia.
Sarah Abdullah BataweelDepartment of Medical Laboratory, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Saudi Arabia.
Nouf Ahmed MadkhaliDepartment of Medical Laboratory, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Saudi Arabia.
Samira Jamaan AlzahraniDepartment of Medical Laboratory, King Fahad Military Medical Complex, Ministry of Defense Health Services, Dhahran, Saudi Arabia.
Zarmina EhteshamDepartment of Molecular Pathology, Dow University of Health Sciences, Karachi, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough direct-acting antiviral (DAA) therapy revolutionized hepatitis C virus (HCV) treatment, offering high cure rates and improved tolerability compared to previous interferon-based regimens, HCV remains a major global health problem, with a lack of empirical data on HCV in Saudi Arabia. This study aims to investigate the current understanding of the clinical impact of DAA on HCV infection by examining its effectiveness in reducing viral load and achieving sustained virologic response (SVR).

methodsThis retrospective study was conducted in n = 144 Saudi HCV patients, treated in an outpatient clinic and who received DAA treatment between January 2016 and December 2023.

resultsAll included n = 144 (100%) patients achieved SVR and had undetectable viral load after treatment: n = 29 (20.1%) had GT1, n = 9 (6.3%) GT2, n = 8 (5.6%) GT3, n = 56 (38.9%) GT4. It was found that n = 42 (29.2%) had an unknown genotype. While successful completion of the regimen with 100% SVR resulted in a significant reduction in the mean liver enzymes alanine transaminase (ALT), aspartate transaminase (AST), and alkaline phosphate (ALP) (p = 0.000), conjugated bilirubin levels did not change. Between 2016 and 2023, there was a significant decline in HCV incidence of 77%, falling from 0.54% to 0.12% of HCV cases during this period.

conclusionsIn this real-world cohort, direct-acting antiviral (DAA) therapy achieved high sustained virologic response (SVR) rates across all HCV genotypes, with excellent tolerability and minimal adverse events. These findings confirm the effectiveness of DAAs in achieving viral eradication among patients treated at our center. CLINICAL TRIAL: Not applicable. This study was a retrospective observational analysis and was not registered as a clinical trial.

Indexed as

Antiviral AgentsHepacivirusHepatitis CHepatitis C, ChronicAdultAgedFemaleGenotypeHumansMaleMiddle AgedRetrospective StudiesSaudi ArabiaSustained Virologic ResponseTreatment OutcomeViral LoadAntiviral AgentsConjugate bilirubinDirect-acting antiviral treatmentsHepatitis C virusSustained virologic responseUnknown genotype

Identifiers

PMID41629822
PMCPMC12952130

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LicenceCC BY-NC-ND
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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.