Evidence map›Paper›PMID 34663473›Full record

ArticleArchives of public health = Archives belges de sante publique2021

The global hepatitis delta virus (HDV) epidemic: what gaps to address in order to mount a public health response?

Tomoyuki Hayashi, Yumie Takeshita, Yvan J-F Hutin, Hande Harmanci, Philippa Easterbrook, Sarah Hess, Judith van Holten, Ena Oghenekaro Oru, Shuichi Kaneko, Cihan Yurdaydin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Archives of public health = Archives belges de sante publique, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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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

11 authors at 3 institutions in 3 countries.

Tomoyuki HayashiGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland. hayasix0917@gmail.com.ORCID http://orcid.org/0000-0002-4416-2912
Yumie TakeshitaGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Yvan J-F HutinGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Hande HarmanciGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Philippa EasterbrookGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Sarah HessGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Judith van HoltenGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Ena Oghenekaro OruGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Shuichi KanekoDepartment of Gastroenterology, Kanazawa University and WHO Collaborating Center for Chronic Hepatitis and Liver Cancer, Kanazawa, Ishikawa, Japan.
Cihan YurdaydinDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkey.
Marc BulterysGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
World Health Organization · CHKanazawa University · JPAnkara University · TR

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundCo-infection between hepatitis B virus (HBV) and hepatitis delta virus (HDV) causes the severest chronic hepatitis and is associated with a high risk of cirrhosis and hepatocellular carcinoma (HCC). The Global Health Sector Strategy on Viral Hepatitis called for the elimination of hepatitis (- 65% mortality and - 90% incidence) by 2030. Our aims were to summarize key points of knowledge and to identify the gaps that need to be addressed to mount a public health response to HDV.

methodsWe performed a current literature review in terms of epidemiology by WHO regions, genotypes distribution and their pathogenicity, factors associated with HDV infection, mortality due to HDV infection, testing strategies and treatment.

resultsPrevalence of infection and genotypes are heterogeneous distributed, with highest prevalence in foci around the Mediterranean, in the Middle East, and in Central, Northern Asia and Eastern Asia. Persons who inject drugs (PWID) and migrants from highly endemic areas are highly affected. While antibody detection tests are available, HDV RNA tests of current infection are not standardized nor widely available. The few therapeutic options, including lofartinib, are not widely available; however several new and promising agents have entered clinical trials.

conclusionHDV infection is an poorly known cause of chronic liver disease. To mount a public health response, we need a better description of the HDV epidemic, standardized testing strategies and better treatment options.

Indexed as

CirrhosisHDVHepatitis B virusHepatitis deltaHepatocellular carcinomaNovel therapeutic strategiesPrevalenceSuperinfection

Identifiers

PMID34663473
PMCPMC8525025
OpenAlexW3205763922

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.