Evidence map›Paper›PMID 32665961›Full record

ArticleOpen forum infectious diseases2020

Decreased All-Cause and Liver-Related Mortality Risk in HIV/Hepatitis B Virus Coinfection Coinciding With the Introduction of Tenofovir-Containing Combination Antiretroviral Therapy.

Berend J van Welzen, Colette Smit, Anders Boyd, Faydra I Lieveld, Tania Mudrikova, Peter Reiss, Annemarie E Brouwer, Andy I M Hoepelman, Joop E Arends

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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.

Berend J van WelzenDepartment of Internal Medicine & Infectious Diseases, University Medical Centre Utrecht, Utrecht, the Netherlands.
Colette SmitStichting HIV Monitoring, Amsterdam, the Netherlands.
Anders BoydStichting HIV Monitoring, Amsterdam, the Netherlands.
Faydra I LieveldDepartment of Internal Medicine & Infectious Diseases, University Medical Centre Utrecht, Utrecht, the Netherlands.
Tania MudrikovaDepartment of Internal Medicine & Infectious Diseases, University Medical Centre Utrecht, Utrecht, the Netherlands.
Peter ReissStichting HIV Monitoring, Amsterdam, the Netherlands.
Annemarie E BrouwerDepartment of Internal Medicine, Elisabeth Tweesteden Hospital, Tilburg, the Netherlands.
Andy I M HoepelmanDepartment of Internal Medicine & Infectious Diseases, University Medical Centre Utrecht, Utrecht, the Netherlands.
Joop E ArendsDepartment of Internal Medicine & Infectious Diseases, University Medical Centre Utrecht, Utrecht, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of efficacious combination antiretroviral therapy (cART) has led to a dramatic decrease in mortality in HIV-positive patients. Specific data on the impact in HIV/hepatitis B virus (HBV)-coinfected patients are lacking. In this study, all-cause and cause-specific mortality risks stratified per era of diagnosis are investigated.

methodsData were analyzed from HIV/HBV-coinfected patients enrolled in the ATHENA cohort between January 1, 1998, and December 31, 2017. Risk for (cause-specific) mortality was calculated using Cox proportional hazard regression analysis, comparing patients diagnosed before 2003 with those diagnosed ≥2003. Risk factors for all-cause and liver-related mortality were also assessed using Cox proportional hazard regression analysis.

resultsA total of 1301 HIV/HBV-coinfected patients were included (14 882 person-years of follow-up). One-hundred ninety-eight patients (15%) died during follow-up. The adjusted hazard ratio (aHR) for all-cause mortality in patients diagnosed in or after 2003 was 0.50 (95% CI, 0.35-0.72) relative to patients diagnosed before 2003. Similar risk reduction was observed for liver-related (aHR, 0.29; 95% CI, 0.11-0.75) and AIDS-related mortality (aHR, 0.44; 95% CI, 0.22-0.87). Use of a tenofovir-containing regimen was independently associated with a reduced risk of all-cause and liver-related mortality. Prior exposure to didanosine/stavudine was strongly associated with liver-related mortality. Ten percent of the population used only lamivudine as treatment for HBV.

conclusionsAll-cause, liver-related, and AIDS-related mortality risk in HIV/HBV-coinfected patients has markedly decreased over the years, coinciding with the introduction of tenofovir. Tenofovir-containing regimens, in absence of major contraindications, should be strongly encouraged in this population.

Indexed as

coinfectionhepatitis B virusHIVliver-related mortalitytenofovir

Identifiers

PMID32665961
PMCPMC7340797

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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.