Evidence map›Paper›PMID 36157140›Full record

ArticleJournal of clinical and experimental hepatology

Hepatitis B Reactivation Following Eradication of HCV with Direct-Acting Antiviral Drugs (DAAs) in a Cohort of Patients from Different Institutions in Egypt.

Mohamed S Abdelbary, Reham Samir, Saeed M El-Nahaas, Rasha M H Shahin, Mohammad El-Sayed, Yasmine Gaber, Omnia Tantawi, Naglaa A Zayed, Ayman Yosry

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical and experimental hepatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

9 authors at 1 institution in 1 country.

Mohamed S AbdelbaryEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Reham SamirEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Saeed M El-NahaasEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Rasha M H ShahinDepartment of Clinical Pathology, Faculty of Medicine, Cairo University, Egypt.
Mohammad El-SayedEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Yasmine GaberEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Omnia TantawiEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Naglaa A ZayedEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Ayman YosryEndemic Medicine Department and Hepatology Unit, Faculty of Medicine, Cairo University, Egypt.
Cairo University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Concerns about HBV reactivation (HBVr) have been raised with the introduction of DAA for HCV treatment. The aim of the study was to assess the risk of HBVr in chronic HCV patients during or after DAA. Methods: A cohort of 166 chronic HCV patients who were treated with SOF-based DAA regimens and initially positive for HBcAb total were evaluated; 10 HBsAg-positive, 156 had past HBV exposure (HBsAg-negative/HBcAb-positive). Laboratory investigations, including liver functions tests, HBV-DNA, LSM by Transient elastography, and ARFI together with serum markers of fibrosis; APRI and FIB-4 were done at baseline and after 12 weeks of DAAs therapy. HBV-DNA levels and liver functions were monitored for assessment of HBVr. Results: Virological HBVr was diagnosed by ≥ 1 log10 IU/ml HBV-DNA levels in 2/166 patients (1.2%) among the whole HCV cohort, who were initially positive for HBsAg; 20%. Clinical HBVr (>3 folds liver enzyme elevation) was detected in one patient with virological HBVr. Conversely, none of past HBV-infected patients experienced HBVr. All patients achieved SVR12 and had a significant decline in serum transaminases, bilirubin, APRI, and LSM measurements after HCV eradication. Conclusion: HBVr might be considered after successful eradication of HCV following DAAs therapy, especially among patients who are positive for HBsAg, while past HBV infection does not seem to be a predisposing condition to HBVr.

Indexed as

ALT, Alanine AminotransferaseAPASL, Asian Pacific Association for the Study of the LiverAPRI, Aspartate-aminotransferase-to-platelet-ratio indexARFI, Acoustic Radiation Forced ImpulseAST, Aspartate AminotransferaseCUC-HF, Cairo University Center for Hepatic FibrosisDAA, Direct-acting antiviralsDAAsDNA, Deoxyribonucleic acidEASL, European Association for the Study of the LiverFIB-4, Fibrosis-4HBcAb, Hepatitis B core antibody totalHBsAg, Hepatitis B surface antigenHBV-DNAHBV, Hepatitis B virusHBV reactivationHBVr, Hepatitis B virus reactivationHCVHCV, Hepatitis C virusLSM, Liver stiffness measurementMOHP, Ministry of Health and PopulationPCR, Polymerase chain reactionPegINF, Pegylated InterferonULN, upper limit of normal

Identifiers

PMID36157140
PMCPMC9499996
OpenAlexW4229029480

What OpenQuestion holds

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Registered trials

None linked

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.