Evidence map›Paper›PMID 35686236›Full record

ArticleBioMed research international2022

Effectiveness and Safety of Low Dose of Tenofovir Disoproxil Fumarate in Malagasy Patients with Chronic Hepatitis B.

Chantelli Iamblaudiot Razafindrazoto, Tovo Harimanana Rabenjanahary, Andry Lalaina Rinà Rakotozafindrabe, Sedera Radoniaina Rakotondrasoa, Nitah Harivony Randriamifidy, Anjaramalala Sitraka Rasolonjatovo, Soloniaina Hélio Razafimahefa, Rado Manitrala Ramanampamonjy

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. 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
–field-weighted citation impact, top 89% 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, 0 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

8 authors at 2 institutions in 1 country.

Chantelli Iamblaudiot RazafindrazotoDepartment of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.ORCID https://orcid.org/0000-0002-5751-0373
Tovo Harimanana RabenjanaharyDepartment of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.ORCID https://orcid.org/0000-0002-2754-3799
Andry Lalaina Rinà RakotozafindrabeDepartment of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.ORCID https://orcid.org/0000-0002-3667-773X
Sedera Radoniaina RakotondrasoaFaculty of Medicine, University of Antananarivo, Madagascar.ORCID https://orcid.org/0000-0001-9687-9846
Nitah Harivony RandriamifidyDepartment of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.ORCID https://orcid.org/0000-0002-4260-9485
Anjaramalala Sitraka RasolonjatovoDepartment of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.
Soloniaina Hélio RazafimahefaDepartment of Hepato-Gastroenterology, University Hospital Andrainjato, Fianarantsoa, Madagascar.ORCID https://orcid.org/0000-0002-5871-4941
Rado Manitrala RamanampamonjyDepartment of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.
University of Antananarivo · MGUniversité de Fianarantsoa · MG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Accessibility of full dose daily of tenofovir disoproxil fumarate (TDF) is limited in Madagascar with an estimated cost well above the purchasing power of Malagasy population. Objective: The study is aimed at evaluating the efficacy and safety of low-dose tenofovir for the treatment of chronic hepatitis B (CHB). Methods: This prospective cohort study from January 2018 to December 2020 was conducted in the Department of Hepato-Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar. The patients enrolled in the study received low dose of TDF 900 mg/week (300 mg daily, three days per week). Results: A total of 45 patients (male/female: 31/14) were included. The mean age was 45.1 ± 11.5 years. Fifteen patients were nucleos(t)ide (NA)-naïve, and 30 patients had prior NA therapy (NA-experienced). Thirty patients were HBeAg positive. A complete virological response (CVR) was achieved in 36/45 patients (80%) at 3 months, 41/45 (91.1%) at 6 months, and 43/45 (95.6%) at 12 months. High viral load at baseline was negative predictive factor of CVR at 3 months (HR: 0.14; 95% CI: 0.022-0.92; Conclusion: Low dose of tenofovir is effective, safe, and well tolerated in a Malagasy population sample. These results still require verification in a large population.

Indexed as

Hepatitis B, ChronicAdultAntiviral AgentsDNA, ViralFemaleHepatitis B e AntigensHepatitis B virusHumansMaleMiddle AgedProspective StudiesRetrospective StudiesTenofovirTreatment OutcomeAntiviral AgentsDNA, ViralHepatitis B e AntigensTenofovir

Identifiers

PMID35686236
PMCPMC9173890
OpenAlexW4283371199

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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.