Evidence map›Paper›PMID 41724728›Full record

ArticleJournal of viral hepatitis2026

All-Cause Mortality in Persons With HIV-HBV Co-Infection Treated for HBV in Rwanda: A Population-Based Cohort Study.

Jean Damascene Makuza, Michael Law, Joseph Puyat, Alnoor Ramji, Dahn Jeong, Richard L Morrow, Prince Asumadu Adu, Marie Paul Nisingizwe, Alpamys Issanov, Georgine Cua and 4 more

Abstract read
In one paragraph

Article in Journal of viral hepatitis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Jean Damascene MakuzaUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0001-9275-8844
Michael LawUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Joseph PuyatUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Alnoor RamjiDivision of Gastroenterology, University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0003-4059-8767
Dahn JeongUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Richard L MorrowUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Prince Asumadu AduBritish Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0002-3983-0875
Marie Paul NisingizweUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Alpamys IssanovUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Georgine CuaUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.
Héctor Alexander Velásquez GarcíaUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0002-0764-4664
Charles BeraboseRwanda Biomedical Center, Kigali, Rwanda.
Albert TuyishimeRwanda Biomedical Center, Kigali, Rwanda.
Naveed Zafar JanjuaUniversity of British Columbia, School of Population and Public Health, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0001-5681-719X

Funding

Ministry of HealthRwanda Biomedical Centre
6 · The paper itself

Abstract

Chronic hepatitis B virus (HBV) infection increases the risk of cirrhosis, hepatocellular carcinoma and non-liver complications. HIV co-infection accelerates disease progression and increases mortality risk compared to HBV mono-infection, but its impact among treated individuals is not well documented in Sub-Saharan Africa. We evaluated all-cause mortality among people with chronic HBV on treatment and assessed the effect of HIV/HBV co-infection. A retrospective cohort study using data from Rwanda's District Health Information System 2 included individuals aged ≥ 2 years treated for HBV between January 2016 and June 2022. Follow-up began 12 months after treatment initiation until death or 30 June 2023. Crude mortality rates were calculated, and multilevel Cox proportional hazards regression, accounting for hospital clustering, assessed the impact of HIV/HBV co-infection on all-cause mortality. Among 4843 people who received HBV treatment (3905 with HBV mono-infection and 838 with HIV/HBV co-infection), median follow-up was 3.8 (interquartile range 2.8) years. Thirty-four deaths occurred, yielding an overall crude mortality rate of 1.6 per 1000 person-years (PY). Mortality rate was higher among individuals with HIV/HBV co-infection compared to those with HBV mono-infection (3.3 vs. 1.1 per 1000 PY, respectively). HIV/HBV co-infection was associated with increased all-cause mortality (adjusted hazard ratio 4.07, 95% confidence interval: 1.71, 9.69). Mortality was low among HBV-treated individuals in Rwanda. However, HIV co-infection significantly increased mortality risk, highlighting the importance of closer follow-up of individuals with HIV/HBV co-infection and further studies on the role of HIV viral load suppression.

Indexed as

CoinfectionHepatitis B, ChronicHIV InfectionsAdultAntiviral AgentsFemaleHumansMaleMiddle AgedRetrospective StudiesRwandaYoung AdultAntiviral Agentsall‐cause mortalityHBV/HIV‐co‐infectionHBV‐mono‐infectionHBV treatmentpopulation‐based

Identifiers

PMID41724728
PMCPMC12926269

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.