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Interim effect evaluation of the hepatitis C elimination programme in Georgia: a modelling study.
Walker, Josephine G; Kuchuloria, Tinatin; Sergeenko, David; Fraser, Hannah; Lim, Aaron G; Shadaker, Shaun; Hagan, Liesl; Gamkrelidze, Amiran; Kvaratskhelia, Valeri; Gvinjilia, Lia; Aladashvili, Malvina; Asatiani, Alexander; Baliashvili, Davit; Butsashvili, Maia; Chikovani, Ivdity; Khonelidze, Irma; Kirtadze, Irma; Kuniholm, Mark H; Otiashvili, David; Sharvadze, Lali; Stvilia, Ketevan; Tsertsvadze, Tengiz; Zakalashvili, Mamuka; Hickman, Matthew; Martin, Natasha K; Morgan, Juliette; Nasrullah, Muazzam; Averhoff, Francisco; Vickerman, Peter.
Afiliação
  • Walker JG; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK. Electronic address: j.g.walker@bristol.ac.uk.
  • Kuchuloria T; Centers for Disease Control and Prevention Foundation, Tbilisi, Georgia; TEPHINET, Tbilisi, Georgia.
  • Sergeenko D; Ministry of Labor Health and Social Affairs of Georgia, Tbilisi, Georgia.
  • Fraser H; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Lim AG; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Shadaker S; Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Hagan L; Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Gamkrelidze A; National Center for Disease Control and Public Health of Georgia, Tbilisi, Georgia.
  • Kvaratskhelia V; Ministry of Labor Health and Social Affairs of Georgia, Tbilisi, Georgia.
  • Gvinjilia L; Centers for Disease Control and Prevention Foundation, Tbilisi, Georgia; TEPHINET, Tbilisi, Georgia.
  • Aladashvili M; Infectious Diseases, AIDS and Clinical Immunology Research Center, Tbilisi, Georgia.
  • Asatiani A; National Center for Disease Control and Public Health of Georgia, Tbilisi, Georgia.
  • Baliashvili D; National Center for Disease Control and Public Health of Georgia, Tbilisi, Georgia; Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
  • Butsashvili M; Neolab, Tbilisi, Georgia.
  • Chikovani I; Curatio International Foundation, Tbilisi, Georgia.
  • Khonelidze I; National Center for Disease Control and Public Health of Georgia, Tbilisi, Georgia.
  • Kirtadze I; Addiction Research Center Alternative Georgia, Tbilisi, Georgia; Ilia State University, Faculty of Arts and Sciences, Institute of Addiction Studies, Tbilisi, Georgia.
  • Kuniholm MH; Department of Epidemiology and Biostatistics, University at Albany, State University of New York, Rensselaer, NY, USA.
  • Otiashvili D; Addiction Research Center Alternative Georgia, Tbilisi, Georgia.
  • Sharvadze L; HEPA Clinic, Tbilisi, Georgia.
  • Stvilia K; National Center for Disease Control and Public Health of Georgia, Tbilisi, Georgia.
  • Tsertsvadze T; Infectious Diseases, AIDS and Clinical Immunology Research Center, Tbilisi, Georgia.
  • Zakalashvili M; Medical Center Mrcheveli, Tbilisi, Georgia.
  • Hickman M; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Martin NK; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK; Division of Infectious Diseases and Global Public Health, UC San Diego, California, USA.
  • Morgan J; Division of Global Health Protection, South Caucasus Centers for Disease Control and Prevention Office, Tbilisi, Georgia.
  • Nasrullah M; Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Averhoff F; Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Vickerman P; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Lancet Glob Health ; 8(2): e244-e253, 2020 02.
Article em En | MEDLINE | ID: mdl-31864917
ABSTRACT

BACKGROUND:

Georgia has a high prevalence of hepatitis C, with 5·4% of adults chronically infected. On April 28, 2015, Georgia launched a national programme to eliminate hepatitis C by 2020 (90% reduction in prevalence) through scaled-up treatment and prevention interventions. We evaluated the interim effect of the programme and feasibility of achieving the elimination goal.

METHODS:

We developed a transmission model to capture the hepatitis C epidemic in Georgia, calibrated to data from biobehavioural surveys of people who inject drugs (PWID; 1998-2015) and a national survey (2015). We projected the effect of the administration of direct-acting antiviral treatments until Feb 28, 2019, and the effect of continuing current treatment rates until the end of 2020. Effect was estimated in terms of the relative decrease in hepatitis C incidence, prevalence, and mortality relative to 2015 and of the deaths and infections averted compared with a counterfactual of no treatment over the study period. We also estimated treatment rates needed to reach Georgia's elimination target.

FINDINGS:

From May 1, 2015, to Feb 28, 2019, 54 313 patients were treated, with approximately 1000 patients treated per month since mid 2017. Compared with 2015, our model projects that these treatments have reduced the prevalence of adult chronic hepatitis C by a median 37% (95% credible interval 30-44), the incidence of chronic hepatitis C by 37% (29-44), and chronic hepatitis C mortality by 14% (3-30) and have prevented 3516 (1842-6250) new infections and averted 252 (134-389) deaths related to chronic hepatitis C. Continuing treatment of 1000 patients per month is predicted to reduce prevalence by 51% (42-61) and incidence by 51% (40-62), by the end of 2020. To reach a 90% reduction by 2020, treatment rates must increase to 4144 (2963-5322) patients initiating treatment per month.

INTERPRETATION:

Georgia's hepatitis C elimination programme has achieved substantial treatment scale-up, which has reduced the burden of chronic hepatitis C. However, the country is unlikely to meet its 2020 elimination target unless treatment scales up considerably.

FUNDING:

CDC Foundation, National Institute for Health Research, National Institutes of Health.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite C Crônica / Epidemias / Erradicação de Doenças Tipo de estudo: Incidence_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite C Crônica / Epidemias / Erradicação de Doenças Tipo de estudo: Incidence_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article