Curbing the hepatitis C virus epidemic in Pakistan: the impact of scaling up treatment and prevention for achieving elimination

The World Health Organization (WHO) has developed a global health strategy to eliminate viral hepatitis. We project the treatment and prevention requirements to achieve the WHO HCV elimination target of reducing HCV incidence by 80% and HCV-related mortality by 65% by 2030 in Pakistan, which has the...

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Vydané v:International journal of epidemiology Ročník 47; číslo 2; s. 550
Hlavní autori: Lim, Aaron G, Qureshi, Huma, Mahmood, Hassan, Hamid, Saeed, Davies, Charlotte F, Trickey, Adam, Glass, Nancy, Saeed, Quaid, Fraser, Hannah, Walker, Josephine G, Mukandavire, Christinah, Hickman, Matthew, Martin, Natasha K, May, Margaret T, Averhoff, Francisco, Vickerman, Peter
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England 01.04.2018
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ISSN:1464-3685, 1464-3685
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Abstract The World Health Organization (WHO) has developed a global health strategy to eliminate viral hepatitis. We project the treatment and prevention requirements to achieve the WHO HCV elimination target of reducing HCV incidence by 80% and HCV-related mortality by 65% by 2030 in Pakistan, which has the second largest HCV burden worldwide. We developed an HCV transmission model for Pakistan, and calibrated it to epidemiological data from a national survey (2007), surveys among people who inject drugs (PWID), and blood donor data. Current treatment coverage data came from expert opinion and published reports. The model projected the HCV burden, including incidence, prevalence and deaths through 2030, and estimated the impact of varying prevention and direct-acting antiviral (DAA) treatment interventions necessary for achieving the WHO HCV elimination targets. With no further treatment (currently ∼150 000 treated annually) during 2016-30, chronic HCV prevalence will increase from 3.9% to 5.1%, estimated annual incident infections will increase from 700 000 to 1 100 000, and 1 400 000 HCV-associated deaths will occur. To reach the WHO HCV elimination targets by 2030, 880 000 annual DAA treatments are required if prevention is not scaled up and no treatment prioritization occurs. By targeting treatment toward persons with cirrhosis (80% treated annually) and PWIDs (double the treatment rate of non-PWIDs), the required annual treatment number decreases to 750 000. If prevention activities also halve transmission risk, this treatment number reduces to 525 000 annually. Substantial HCV prevention and treatment interventions are required to reach the WHO HCV elimination targets in Pakistan, without which Pakistan's HCV burden will increase markedly.
AbstractList The World Health Organization (WHO) has developed a global health strategy to eliminate viral hepatitis. We project the treatment and prevention requirements to achieve the WHO HCV elimination target of reducing HCV incidence by 80% and HCV-related mortality by 65% by 2030 in Pakistan, which has the second largest HCV burden worldwide.BackgroundThe World Health Organization (WHO) has developed a global health strategy to eliminate viral hepatitis. We project the treatment and prevention requirements to achieve the WHO HCV elimination target of reducing HCV incidence by 80% and HCV-related mortality by 65% by 2030 in Pakistan, which has the second largest HCV burden worldwide.We developed an HCV transmission model for Pakistan, and calibrated it to epidemiological data from a national survey (2007), surveys among people who inject drugs (PWID), and blood donor data. Current treatment coverage data came from expert opinion and published reports. The model projected the HCV burden, including incidence, prevalence and deaths through 2030, and estimated the impact of varying prevention and direct-acting antiviral (DAA) treatment interventions necessary for achieving the WHO HCV elimination targets.MethodsWe developed an HCV transmission model for Pakistan, and calibrated it to epidemiological data from a national survey (2007), surveys among people who inject drugs (PWID), and blood donor data. Current treatment coverage data came from expert opinion and published reports. The model projected the HCV burden, including incidence, prevalence and deaths through 2030, and estimated the impact of varying prevention and direct-acting antiviral (DAA) treatment interventions necessary for achieving the WHO HCV elimination targets.With no further treatment (currently ∼150 000 treated annually) during 2016-30, chronic HCV prevalence will increase from 3.9% to 5.1%, estimated annual incident infections will increase from 700 000 to 1 100 000, and 1 400 000 HCV-associated deaths will occur. To reach the WHO HCV elimination targets by 2030, 880 000 annual DAA treatments are required if prevention is not scaled up and no treatment prioritization occurs. By targeting treatment toward persons with cirrhosis (80% treated annually) and PWIDs (double the treatment rate of non-PWIDs), the required annual treatment number decreases to 750 000. If prevention activities also halve transmission risk, this treatment number reduces to 525 000 annually.ResultsWith no further treatment (currently ∼150 000 treated annually) during 2016-30, chronic HCV prevalence will increase from 3.9% to 5.1%, estimated annual incident infections will increase from 700 000 to 1 100 000, and 1 400 000 HCV-associated deaths will occur. To reach the WHO HCV elimination targets by 2030, 880 000 annual DAA treatments are required if prevention is not scaled up and no treatment prioritization occurs. By targeting treatment toward persons with cirrhosis (80% treated annually) and PWIDs (double the treatment rate of non-PWIDs), the required annual treatment number decreases to 750 000. If prevention activities also halve transmission risk, this treatment number reduces to 525 000 annually.Substantial HCV prevention and treatment interventions are required to reach the WHO HCV elimination targets in Pakistan, without which Pakistan's HCV burden will increase markedly.ConclusionsSubstantial HCV prevention and treatment interventions are required to reach the WHO HCV elimination targets in Pakistan, without which Pakistan's HCV burden will increase markedly.
The World Health Organization (WHO) has developed a global health strategy to eliminate viral hepatitis. We project the treatment and prevention requirements to achieve the WHO HCV elimination target of reducing HCV incidence by 80% and HCV-related mortality by 65% by 2030 in Pakistan, which has the second largest HCV burden worldwide. We developed an HCV transmission model for Pakistan, and calibrated it to epidemiological data from a national survey (2007), surveys among people who inject drugs (PWID), and blood donor data. Current treatment coverage data came from expert opinion and published reports. The model projected the HCV burden, including incidence, prevalence and deaths through 2030, and estimated the impact of varying prevention and direct-acting antiviral (DAA) treatment interventions necessary for achieving the WHO HCV elimination targets. With no further treatment (currently ∼150 000 treated annually) during 2016-30, chronic HCV prevalence will increase from 3.9% to 5.1%, estimated annual incident infections will increase from 700 000 to 1 100 000, and 1 400 000 HCV-associated deaths will occur. To reach the WHO HCV elimination targets by 2030, 880 000 annual DAA treatments are required if prevention is not scaled up and no treatment prioritization occurs. By targeting treatment toward persons with cirrhosis (80% treated annually) and PWIDs (double the treatment rate of non-PWIDs), the required annual treatment number decreases to 750 000. If prevention activities also halve transmission risk, this treatment number reduces to 525 000 annually. Substantial HCV prevention and treatment interventions are required to reach the WHO HCV elimination targets in Pakistan, without which Pakistan's HCV burden will increase markedly.
Author Fraser, Hannah
Trickey, Adam
Mukandavire, Christinah
Martin, Natasha K
Qureshi, Huma
Hamid, Saeed
Saeed, Quaid
May, Margaret T
Vickerman, Peter
Mahmood, Hassan
Hickman, Matthew
Averhoff, Francisco
Lim, Aaron G
Davies, Charlotte F
Walker, Josephine G
Glass, Nancy
Author_xml – sequence: 1
  givenname: Aaron G
  surname: Lim
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  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
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  surname: Qureshi
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  organization: Pakistan Health Research Council, Islamabad, Pakistan
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  givenname: Hassan
  surname: Mahmood
  fullname: Mahmood, Hassan
  organization: TEPHINET, Centers for Disease Control and Prevention, Atlanta, GA, USA
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  surname: Hamid
  fullname: Hamid, Saeed
  organization: Aga Khan University, Karachi, Pakistan
– sequence: 5
  givenname: Charlotte F
  surname: Davies
  fullname: Davies, Charlotte F
  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
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  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
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  surname: Glass
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  organization: National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA
– sequence: 8
  givenname: Quaid
  surname: Saeed
  fullname: Saeed, Quaid
  organization: National AIDS Control Programme, Islamabad, Pakistan
– sequence: 9
  givenname: Hannah
  surname: Fraser
  fullname: Fraser, Hannah
  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
– sequence: 10
  givenname: Josephine G
  surname: Walker
  fullname: Walker, Josephine G
  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
– sequence: 11
  givenname: Christinah
  surname: Mukandavire
  fullname: Mukandavire, Christinah
  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
– sequence: 12
  givenname: Matthew
  surname: Hickman
  fullname: Hickman, Matthew
  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
– sequence: 13
  givenname: Natasha K
  surname: Martin
  fullname: Martin, Natasha K
  organization: Division of Global Public Health, Department of Medicine, University of California San Diego, CA, USA
– sequence: 14
  givenname: Margaret T
  surname: May
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  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
– sequence: 15
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  organization: National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA
– sequence: 16
  givenname: Peter
  surname: Vickerman
  fullname: Vickerman, Peter
  organization: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
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References 32087161 - Lancet Glob Health. 2020 Mar;8(3):e323-e324. doi: 10.1016/S2214-109X(20)30036-X.
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SubjectTerms Adolescent
Adult
Aged
Aged, 80 and over
Antiviral Agents - therapeutic use
Child
Child, Preschool
Chronic Disease
Developing Countries
Epidemics - prevention & control
Female
Hepatitis C - drug therapy
Hepatitis C - mortality
Hepatitis C - prevention & control
Humans
Infant
Infant, Newborn
Male
Middle Aged
Models, Theoretical
Pakistan - epidemiology
World Health Organization
Young Adult
Title Curbing the hepatitis C virus epidemic in Pakistan: the impact of scaling up treatment and prevention for achieving elimination
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