TREATMENT OF CHRONIC HEPATITIS B VIRUS INFECTION IN RESOURCE-CONSTRAINED SETTINGS: EXPERT PANEL CONSENSUS


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

An estimated 350 million people have chronic hepatitis B virus (HBV) infection and most of them live in resource-constrained settings. Up to 25% of those persons will die prematurely of hepatocellular carcinoma (HCC) or cirrhosis. Universal hepatitis B immunization programmes that target infants will have an impact on HBV-related deaths several decades after their introduction. Treatment of HBV infection in those who need it has been shown to reduce the risk of HCC and death. It is estimated that 20-30% of persons with HBV infection will benefit from treatment. There are antiviral drugs active against HBV; however, they are not widely available or utilized in persons infected with HBV. Currently recommended antiviral agents used for treatment of human immunodeficiency virus (HIV) infection do not adequately suppress HBV replication, which is of great concern for 10% of the HIV-infected persons in Africa who are diagnosed as being co-infected with HBV. Progressive liver disease has been found to occur in co-infected persons who take no drugs to suppress HBV. In view of these problems, an informal World Health Organization (WHO) consultation of experts concluded that: chronic HBV is a major public health problem in developing countries; all HIV-infected persons should be screened for HBV infection; HIV/HBV co-infected persons should be treated with therapies that are active against both viruses and that reduce the risk of resistance; standards for the management of chronic HBV infection should be adapted to resource-constrained settings. In addition, a research agendum has been developed mainly to prevent and treat chronic HBV infection in resource-constrained settings. The WHO is developing guidelines for the management of chronic HBV infection in resource-constrained settings. An informal WHO technical consultation was held to have expert data for next steps to solve the serious public health problem related to HBV infection and its associated disease burden. It was attended by the representatives of professional medical associations dealing with the study of liver diseases, who are well familiar with guidelines for their treatment in resource-constrained setting, as well as by clinicians from resource-constrained countries and by the representatives of affiliated organizations. The conclusions and recommendations made by this consultation are not a portrayal of the official policy of the WHO and its official guidelines; however they will be of importance in meeting the demands of million HBV-infected people worldwide.

Full Text

Restricted Access

About the authors

Steven T. Wiersma

World Health Organization, FCH/IVB

Geneva, Switzerland

Brian McMahon

Alaska Native Medical Center, CDC Arctic Investigations Program

Anchorage, Alaska, USA

Jean-Michel Pawlotsky

Hopital Henri Mondor

Department of Virology Paris, France

Chloe L. Thio

Johns Hopkins University

Department of Medicine Baltimore, Maryland, USA

Mark Thursz

Saint Mary's Hospital Campus, Imperial College

Department of Academic Medicine London, UK

Seng Gee Lim

National University Hospital

Department of Medicine Singapore, Singapore

Ponsiano Ocama

Makerere University, Mulago Hospital

Department of Medicine Kampala, Uganda

Gamal Esmat

Cairo University

Faculty of Medicine Cairo, Egypt

Mendy Maimuna

Medical Research Council

Banjul, Gambia

David Bell

US Centers for Disease Control and Prevention, Division of Viral Hepatitis

Atlanta, USA

Marco Vitoria

World Health Organization, Department of HIV/AIDS

Geneva, Switzerland

Irina Eramova

World Health Organization, EURO Region

Copenhagen, Denmark

Daniel Lavanchy

World Health Organization, HSE

Geneva, Switzerland

Geoff Dusheiko

Royal Free Hospital, School of Medicine

London, UK

References

  1. ВОЗ. Основные факты. Информ. бюл. № 204. http://www.who.int/mediacentre/factsheets/fs204/ru/ (последнее обращение 5 июля 2011 г.).
  2. Goldstein S.T., Zhou F.J., Hadler S.C. et al. A mathematical model to estimate global hepatitis B disease burden and vaccination impact. Int. J. Epidemiol. 2005; 34: 1329-1339.
  3. Perz J.F., Armstrong G.L., Farrington L.A. et al. The contributions of hepatitis B virus and hepatitis C virus infections to cirrhosis and primary liver cancer worldwide. J. Hepatol. 2006; 45: 529-538.
  4. McMahon B.J. The natural history of chronic hepatitis B virus infection. Hepatology 2009; 49: S45- S 55.
  5. Weiss R.A., McMichael A.J. Social and environmental risk factors in the emergence of infectious diseases. Nat. Med. 2004; 10: S70- S76.
  6. Beasley R.P., Hwang L.Y., Lee G.C. et al. Prevention of perinatally transmitted hepatitis B virus infections with hepatitis B virus infections with hepatitis B immune globulin and hepatitis B vaccine. Lancet 1983; 2: 1099-1102.
  7. McMahon B.J., Alward W.L., Hall D.B. et al. Acute hepatitis B virus infection: relation of age to the clinical expression of disease and subsequent development of the carrier state. J. Infect. Dis. 1985; 151: 599-603.
  8. WHO. Hepatitis B Position Statement. WER 2009; 84: 405-420.
  9. Lok AS.F., McMahon B.J. Chronic Hepatitis B: update 2009. Hepatology 2009; 50: 661-662.
  10. Liaw Y.F., Leung N., Kao J.H. et al. Asian-Pacific consensus statement on the management of chronic hepatitis B: a 2008 update. Hepatol. Int. 2008; 2: 263-283.
  11. European Association for the Study of the Liver. EASL clinical practice guidelines: management of chronic hepatitis B. J. Hepatol. 2009; 51: 227-242.
  12. Lin P.F., Nowicka-Sans B., Terry B. et al. Entecavir exhibits inhibitory activity against human immunodeficiency virus under conditions of reduced viral challenge. Antimicrob Agents Chemother. 2008; 52: 1759-1767.
  13. Liaw Y.F., Sung J.J., Chow W.C. et al. Lamivudine for patients with chronic hepatitis B and advanced liver disease. N. Engl. J. Med. 2004; 351: 1521-1531.
  14. Bendavid E., Bhattacharya J. The President’s emergency plan for AIDS relief in Africa: an evaluation of outcomes. Ann. Int. Med. 2009; 150: 688-695.
  15. Modi A.A., Feld J.J. Viral hepatitis and HIV in Africa. AIDS Rev. 2007; 9: 25-39.
  16. Soriano V., Puoti M., Bonacini M. et al. Care of patients with chronic hepatitis B and HIV co-infection: recommendations from an HIV-HBV international panel. AIDS 2005; 19: 221-240.
  17. Alberti A., Clumeck N., Collins S. et al. Short statement of the first European consensus conference on the treatment of chronic hepatitis B and C in HIV co-infected patients. J. Hepatol. 2005; 42: 615-624.
  18. Housset C., Pol S., Carnot F. et al. Interactions between human immunodeficiency virus-1, hepatitis delta virus and hepatitis B virus infections in 260 chronic carriers of hepatitis B virus. Hepatology 1992; 15: 578-583.
  19. Nikolopoulos G.K., Paraskevis D., Hatztheodorou E. et al. Impact of hepatitis B virus infection on the Progression of AIDS and mortality in HIV-infected individuals: a cohort study and metaanalysis. Clin. Infect. Dis. 2009; 48: 1763-1771.
  20. Thio C.L., Seaberg E.C., Skolasky R. et al. HIV-1, hepatitis B virus, and risk of liver-related mortality in the multicenter cohort study (MACS). Lancet 2002; 360: 1921-1926.

Supplementary files

Supplementary Files
Action
1. JATS XML

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies