Global reporting of progress towards elimination of hepatitis B and hepatitis C.


Journal

The lancet. Gastroenterology & hepatology
ISSN: 2468-1253
Titre abrégé: Lancet Gastroenterol Hepatol
Pays: Netherlands
ID NLM: 101690683

Informations de publication

Date de publication:
04 2023
Historique:
received: 06 09 2022
revised: 01 11 2022
accepted: 02 11 2022
pubmed: 11 2 2023
medline: 15 3 2023
entrez: 10 2 2023
Statut: ppublish

Résumé

The 69th World Health Assembly endorsed the global health sector strategy on viral hepatitis to eliminate viral hepatitis as a public health threat by 2030. Achieving and measuring the 2030 targets requires a substantial increase in the capacity to test and treat viral hepatitis infections and a mechanism to monitor the progress of hepatitis elimination. This study aimed to identify the gaps in data availability or quality and create a new mechanism to monitor the progress of hepatitis elimination. In 2020, using a questionnaire, we collected empirical, systematic, modelled, or surveyed data-reported by WHO country and WHO regional offices-on indicators of progress towards elimination of viral hepatitis, including burden of infection, incidence, mortality, and the cascade of care, and validated these data. WHO received officially validated country-provided data from 130 countries or territories, and used partner-provided data for 70 countries or territories. We estimated that in 2019, globally, 295·9 million (3·8%) people were living with chronic hepatitis B virus (HBV) infection and 57·8 million (0·8%) people were living with chronic hepatitis C virus (HCV) infection. Globally, there were more than 3·0 million new infections with HBV and HCV and more than 1·1 million deaths due to the viruses in 2019. In 2019, 30·4 million (95% CI 24·3-38·0) individuals living with hepatitis B knew their infection status and 6·6 million (5·3-8·3) people diagnosed with hepatitis B received treatment. Among people with HCV infection, 15·2 million (95% CI 12·1-19·0) had been diagnosed between 2015 and 2019, and 9·4 million (7·5-11·7) people diagnosed with hepatitis C infection were treated with direct-acting antiviral drugs between 2015 and 2019. There has been notable global progress towards hepatitis elimination. In 2019, 30·4 million (10·3%) people living with hepatitis B knew their infection status, which was slightly higher than in 2015 (22·0 million; 9·0%), and 6·6 million (22·7%) of those diagnosed with hepatitis B received treatment, compared with 1·7 million (8·0%) in 2015. Mortality from hepatitis C has declined since 2019, driven by an increase in HCV treatment ten times that of the strategy baseline. However, an estimated 89·7% of HBV infections and 78·6% of HCV infections remain undiagnosed. A new global strategy for 2022-30, based on these new estimates, should be implemented urgently to scale up the screening and treatment of viral hepatitis. World Health Organization.

Sections du résumé

BACKGROUND
The 69th World Health Assembly endorsed the global health sector strategy on viral hepatitis to eliminate viral hepatitis as a public health threat by 2030. Achieving and measuring the 2030 targets requires a substantial increase in the capacity to test and treat viral hepatitis infections and a mechanism to monitor the progress of hepatitis elimination. This study aimed to identify the gaps in data availability or quality and create a new mechanism to monitor the progress of hepatitis elimination.
METHODS
In 2020, using a questionnaire, we collected empirical, systematic, modelled, or surveyed data-reported by WHO country and WHO regional offices-on indicators of progress towards elimination of viral hepatitis, including burden of infection, incidence, mortality, and the cascade of care, and validated these data.
FINDINGS
WHO received officially validated country-provided data from 130 countries or territories, and used partner-provided data for 70 countries or territories. We estimated that in 2019, globally, 295·9 million (3·8%) people were living with chronic hepatitis B virus (HBV) infection and 57·8 million (0·8%) people were living with chronic hepatitis C virus (HCV) infection. Globally, there were more than 3·0 million new infections with HBV and HCV and more than 1·1 million deaths due to the viruses in 2019. In 2019, 30·4 million (95% CI 24·3-38·0) individuals living with hepatitis B knew their infection status and 6·6 million (5·3-8·3) people diagnosed with hepatitis B received treatment. Among people with HCV infection, 15·2 million (95% CI 12·1-19·0) had been diagnosed between 2015 and 2019, and 9·4 million (7·5-11·7) people diagnosed with hepatitis C infection were treated with direct-acting antiviral drugs between 2015 and 2019.
INTERPRETATION
There has been notable global progress towards hepatitis elimination. In 2019, 30·4 million (10·3%) people living with hepatitis B knew their infection status, which was slightly higher than in 2015 (22·0 million; 9·0%), and 6·6 million (22·7%) of those diagnosed with hepatitis B received treatment, compared with 1·7 million (8·0%) in 2015. Mortality from hepatitis C has declined since 2019, driven by an increase in HCV treatment ten times that of the strategy baseline. However, an estimated 89·7% of HBV infections and 78·6% of HCV infections remain undiagnosed. A new global strategy for 2022-30, based on these new estimates, should be implemented urgently to scale up the screening and treatment of viral hepatitis.
FUNDING
World Health Organization.

Identifiants

pubmed: 36764320
pii: S2468-1253(22)00386-7
doi: 10.1016/S2468-1253(22)00386-7
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

332-342

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 World Health Organization; licensee Elsevier. This is an Open Access article published under the CC BY 3·0 IGO license which permits users to download and share the article for non-commercial purposes, so long as the article is reproduced in the whole without changes, and provided the original source is properly cited. This article shall not be used or reproduced in association with the promotion of commercial products, services or any entity. There should be no suggestion that WHO endorses any specific organisation, products or services. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL.

Déclaration de conflit d'intérêts

Declaration of interests We declare no competing interests.

Auteurs

Fuqiang Cui (F)

School of Public Health, Peking University, Beijing, China.

Sarah Blach (S)

Center for Disease Analysis Foundation, Lafayette, CO, USA.

Casimir Manzengo Mingiedi (C)

WHO Regional Office for Africa, Brazzaville, Republic of Congo.

Monica Alonso Gonzalez (MA)

WHO Regional Office for the Americas, Washington, DC, USA.

Ahmed Sabry Alaama (A)

WHO Regional Office for the Eastern Mediterranean, Cairo, Egypt.

Antons Mozalevskis (A)

WHO Regional Office for Europe, Copenhagen, Denmark.

Nicole Séguy (N)

WHO Regional Office for Europe, Copenhagen, Denmark.

Bharat Bhushan Rewari (BB)

WHO Regional Office for South- East Asia, New Delhi, India.

Po-Lin Chan (PL)

WHO Regional Office for the Western Pacific, Manila, Philippines.

Linh-Vi Le (LV)

WHO Regional Office for the Western Pacific, Manila, Philippines.

Meg Doherty (M)

WHO Headquarters, Geneva, Switzerland.

Niklas Luhmann (N)

WHO Headquarters, Geneva, Switzerland.

Philippa Easterbrook (P)

WHO Headquarters, Geneva, Switzerland.

Mae Dirac (M)

Institute for Health Metrics and Evaluation, Seattle, WA, USA.

Catherine de Martel (C)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

Shevanthi Nayagam (S)

Faculty of Medicine, School of Public Health, Imperial College London, London, UK.

Timothy B Hallett (TB)

Faculty of Medicine, School of Public Health, Imperial College London, London, UK.

Peter Vickerman (P)

Population Health Sciences, University of Bristol, Bristol, UK.

Homie Razavi (H)

Center for Disease Analysis Foundation, Lafayette, CO, USA.

Olufunmiayo Lesi (O)

WHO Headquarters, Geneva, Switzerland.

Daniel Low-Beer (D)

WHO Headquarters, Geneva, Switzerland. Electronic address: lowbeerd@who.int.

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Classifications MeSH