Evidence map›Paper›PMID 26042425›Full record

ArticlePloS one2015

Projections of the current and future disease burden of hepatitis C virus infection in Malaysia.

Scott A McDonald, Maznah Dahlui, Rosmawati Mohamed, Herlianna Naning, Fatiha Hana Shabaruddin, Adeeba Kamarulzaman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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  6. Article
  7. Chronic Viral Hepatitis in Malaysia: "Where are we now?"Euroasian journal of hepato-gastroenterology
    Review
  8. Hepatitis in Malaysia: Past, Present, and Future.Euroasian journal of hepato-gastroenterology
    Review
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

6 authors at 2 institutions in 3 countries.

Scott A McDonaldCentre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia; Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands; School of Health & Life Sciences, Glasgow Caledonian University, Glasgow, Scotland.
Maznah DahluiJulius Centre, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Rosmawati MohamedFaculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Herlianna NaningCentre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia.
Fatiha Hana ShabaruddinJulius Centre, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Adeeba KamarulzamanCentre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia; Julius Centre, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
University of Malaya · MYGlasgow Caledonian University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence of hepatitis C virus (HCV) infection in Malaysia has been estimated at 2.5% of the adult population. Our objective, satisfying one of the directives of the WHO Framework for Global Action on Viral Hepatitis, was to forecast the HCV disease burden in Malaysia using modelling methods.

methodsAn age-structured multi-state Markov model was developed to simulate the natural history of HCV infection. We tested three historical incidence scenarios that would give rise to the estimated prevalence in 2009, and calculated the incidence of cirrhosis, end-stage liver disease, and death, and disability-adjusted life-years (DALYs) under each scenario, to the year 2039. In the baseline scenario, current antiviral treatment levels were extended from 2014 to the end of the simulation period. To estimate the disease burden averted under current sustained virological response rates and treatment levels, the baseline scenario was compared to a counterfactual scenario in which no past or future treatment is assumed.

resultsIn the baseline scenario, the projected disease burden for the year 2039 is 94,900 DALYs/year (95% credible interval (CrI): 77,100 to 124,500), with 2,002 (95% CrI: 1340 to 3040) and 540 (95% CrI: 251 to 1,030) individuals predicted to develop decompensated cirrhosis and hepatocellular carcinoma, respectively, in that year. Although current treatment practice is estimated to avert a cumulative total of 2,200 deaths from DC or HCC, a cumulative total of 63,900 HCV-related deaths is projected by 2039.

conclusionsThe HCV-related disease burden is already high and is forecast to rise steeply over the coming decades under current levels of antiviral treatment. Increased governmental resources to improve HCV screening and treatment rates and to reduce transmission are essential to address the high projected HCV disease burden in Malaysia.

Indexed as

Cost of IllnessAcute DiseaseCalibrationCarcinoma, HepatocellularDisease ProgressionHepacivirusHepatitis CHumansIncidenceMalaysiaModels, BiologicalProbabilitySubstance Abuse, Intravenous

Identifiers

PMID26042425
PMCPMC4456147
OpenAlexW1433757129

What OpenQuestion holds

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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.