Evidence map›Paper›PMID 36119722›Full record

ArticleJHEP reports : innovation in hepatology2022

Trends in decompensated cirrhosis and hepatocellular carcinoma among people with a hepatitis B notification in New South Wales.

Syed Hassan Bin Usman Shah, Maryam Alavi, Behzad Hajarizadeh, Gail V Matthews, Marianne Martinello, Mark Danta, Janaki Amin, Matthew G Law, Jacob George, Heather Valerio and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Syed Hassan Bin Usman ShahThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Maryam AlaviThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Behzad HajarizadehThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Gail V MatthewsThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Marianne MartinelloThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Mark DantaSt Vincent's Hospital, Sydney, Australia.
Janaki AminDepartment of Health Systems and Populations, Macquarie University, Sydney, NSW, Australia.
Matthew G LawThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Jacob GeorgeStorr Liver Centre, Westmead Millennium Institute, University of Sydney and Westmead Hospital, Westmead, Australia.
Heather ValerioThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
Gregory J DoreThe Kirby Institute, University of New South Wales (UNSW), Sydney, NSW, Australia.
UNSW Sydney · AUMacquarie University · AUSt Vincent's Hospital Sydney · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: Population-level trends and factors associated with HBV-related decompensated cirrhosis (DC), hepatocellular carcinoma (HCC), and liver-related mortality are crucial to evaluate the impacts of therapeutic interventions. Methods: Trends in HBV-DC and -HCC diagnoses and liver-related mortality in New South Wales, Australia, were determined through linkage of HBV notifications (1993-2017) to hospital admissions (2001-2018), mortality (1993-2018), and cancer registry (1994-2014) databases. Late HBV notification was defined as notification at or within 2 years of a DC or HCC diagnosis. Cox proportional-hazards regression and multivariable logistic regression analyses were performed to evaluate associated factors. Results: Among 60,660 people with a HBV notification, 1,276 (2.0%) DC and 1,087 (1.8%) HCC diagnoses, and 1,219 (2.0%) liver-related deaths were documented. Since the early 2000s, the number of DC and HCC diagnoses increased; however, age-standardised incidence decreased from 2.64 and 1.95 in 2003 to 1.14 and 1.09 per 1,000 person-years in 2017, respectively. Similarly, age-standardised liver mortality decreased from 2.60 in 2003 to 1.14 per 1,000 person-years in 2017. Among people with DC and HCC diagnoses, late HBV notification declined from 41% and 40% between 2001-2009 to 29% and 25% in 2010-2018, respectively. Predictors of DC diagnosis included older age (birth <1944, adjusted hazard ratio [aHR] 2.06, 95% CI 1.57-2.69), alcohol use disorder (aHR 4.82, 95% CI 3.96-5.87) and HCV co-infection (aHR 1.88, 95% CI 1.53-2.31). Predictors of HCC diagnosis included older age (birth <1944, aHR 3.94, 95% CI 2.91-5.32) and male sex (aHR 3.79, 95% CI 3.05-4.71). Conclusion: In an era of improved antiviral therapies, the risk of HBV-related liver morbidity and mortality has declined. HCV co-infection and alcohol use disorder are key modifiable risk factors associated with the burden of HBV. Lay summary: Rising hepatitis B-related morbidity and mortality is a major public health concern. However, the development of highly effective medicines against hepatitis B virus (HBV) has brought renewed optimism for its elimination by 2030. This study shows a steady decline in HBV-related liver morbidity and mortality in New South Wales, Australia. Moreover, late hepatitis notification has also declined, allowing individuals with HBV to have access to timely antiviral treatment. Despite this, hepatitis C co-infection and alcohol use disorder are key modifiable risk factors associated with HBV disease burden. To attain the desired benefits from highly effective antiviral treatment, managing comorbidities, including hepatitis C and high alcohol use, must improve among individuals with hepatitis B.

Indexed as

APDC, Admitted Patient Data CollectionAUD, alcohol use disordercause of deathCCI, Charlson comorbidity indexDCDC, decompensated cirrhosisESLD, end-stage liver diseaseHCCHCC, hepatocellular carcinomahepatitis Blate HBV notificationLHD, local health districtliver diseaseliver mortalityNCIMS, Notifiable Conditions Information Management SystemNHR, National HIV RegistryNSWCR, NSW Cancer RegistryNSW, New South WalesPBS, Pharmaceutical Benefits Schemepopulation-levelRBDM, Registry of Births, Deaths and Marriagesrecord linkagerisk factorsWHO, World Health Organization

Identifiers

PMID36119722
PMCPMC9478454
OpenAlexW4292791367

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.