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Epidemiology of Hepatitis C Infection in Canada

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Hepatitis C Transfusion Working Group, June 1998. Robert S. Hogg, Murray D. Krahn, Robert W.H. Palmer, Jutta K. Preiksaitis, Morris Sherman ... – PowerPoint PPT presentation

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Title: Epidemiology of Hepatitis C Infection in Canada


1
Epidemiology of Hepatitis C Infection in Canada
  • Robert S. Remis MD, MPH, FRCPC
  • Department of Public Health SciencesUniversity
    of Toronto
  • 1st Canadian Conference on Hepatitis CMontreal,
    Quebec
  • May 1-4, 2001

2
Acknowledgements
  • Hepatitis C Transfusion Working Group, June 1998
  • Robert S. Hogg, Murray D. Krahn, Robert W.H.
    Palmer, Jutta K. Preiksaitis, Morris Sherman
  • in collaboration with
  • JoAnne Chiavetta, PhD, Martin Tepper MD, Shimian
    Zou MD and Bob Slinger MD
  • HCV-HIV Study, February 2000-March 2001
  • Marcel DuBois, Chris Archibald, Jennifer Geduld
  • Morris Sherman, Kevin Craib, Shimian Zou
  • Others
  • Michel Alary, Kevin Craib, Elaine Whittingham

3
Background
  • Importance of hepatitis C was underestimated due
    to delay in recognizing infection
  • difficulties in developing diagnostic tools
  • long latency from infection to disease
  • Need to better evaluate extent and distribution
    of HCV infection in Canada
  • develop appropriate guidelines for primary
    prevention
  • develop guidelines for HCV testing
  • assess burden of infection and disease in
    shortand long term
  • plan appropriate health services and support
    programs

4
Overview of presentation
  • 1. Review of literature (published unpublished)
  • 2. Hepatitis C transmitted by blood transfusion
  • 3. Hepatitis C prevalence and incidence in Canada
  • 4. Estimating number of persons in Canada with
    dual HCV-HIV infection
  • 5. Conclusions

5
Selected seroepidemiologic studies among IDUs
6
Selected seroepidemiologic studies among
prisoners
7
Selected seroepidemiologic studies among patient
populations
8
Selected seroepidemiologic studies among
variouspatient populations
9
Hepatitis C infection due to blood transfusion
Methods
  • Model 1 For each year, number of transfused
    units x HCV risk per unit
  • Used survival function to calculate number of
    recipients surviving to July 1998
  • Model 2 Estimated number of HCV-infected persons
    in Canada as of July 1998
  • Calculated proportion and number due to blood
    transfusion
  • Model 3 Estimated number of persons transfused
    in Canada
  • Calculated proportion and number with HCV
    infection

10
Modeled HCV risk and number of HCV-infected
transfusion recipients, 19801991
11
Modeled HCV risk per transfusion episode and
number of HCV-infected transfusion recipients,
1980-1991
12
Modeled number of surviving HCV-infected
transfusion recipients by period of
transfusion,19801992
13
Modeled number of surviving HCV-infected
transfusion recipients by period of transfusion
(n34,800)
14
Modeled number of surviving HCV-infected
transfusion recipients by period of transfusion
19801992
34,790
50
70
420
630
700
900
3,700
5,290
7,660
15,370
15
Hepatitis C prevalence and incidence, 1998
Methods
  • From HCV transfusion Model 2, estimated
    prevalent HCV infections
  • Interpolated to each provinces
  • Using population-based data (limited)
  • Estimating relative population prevalence from
    first-time blood donors

16
Modeled number of HCV-infected persons by
province, 1998 (n240,000)
17
Modeled number of HCV-infected persons by
province (n240,000)
18
Hypothetical number of HCV-infected persons in
Canada by mode of transmission
19
Annual incidence of HCV infection in
CanadaPreliminary perspectives
  • Method 1 Observed incidence among populations in
    sentinel surveillance study projected from
    proportion symptomatic to all HCV infections
  • Method 2 Observed HCV incidence among
    susceptible IDUs in study cohorts projected
    from proportion IDU to all HCV infections
    (90,000 IDU - 68,000 HCV) x 20
  • Preliminary estimate 3,000 - 8,000 new HCV
    infections per year

20
HCV infections in CanadaInterpretation
  • Estimates are subject to considerable uncertainty
    due to very limited Canadian data from
    representative study populations (only one
    study, in Quebec)
  • HCV prevalence appears highest in British
    Columbia, Ontario and Alberta. Four provinces,
    British Columbia, Ontario, Quebec and Alberta
    account for 92 of HCV infections in Canada
  • The majority (gt50) of prevalent HCV infections
    in Canada are among IDUs, where HCV prevalence is
    gt100-fold greater than other Canadians taken as a
    whole

21
Estimating the number of persons in Canada with
dual HCV-HIV infectionMethods
  • 1. Estimate the number of HIV-infected persons by
    HIV-defined exposure category and geographic
    region
  • 2. Estimate HCV prevalence in each group (obtain
    data from available studies and review by expert
    consensus panel)
  • 3. Multiply number by HCV prevalence
  • 4. Plausible limits of outcome using Monte Carlo
    simulation
  • 5. Special analysis for Aboriginal population and
    prisoners to estimate persons in each HIV-defined
    exposure category and then as above

22
Modeled number of HCV-HIV infected persons by
exposure category, 1999
23
Modeled number of HCV-HIV infected persons by
exposure category, 1999 (n11,194)
24
Modeled number of HCV-HIV infected persons by
geographic region, 1999 (n11,194)
25
Modeled number of HCV-HIV infected Aboriginal
people by exposure category, 1999 (n1,477)
26
Modeled number of HCV-HIV infected prisoners by
exposure category, 1999 (n611)
27
Conclusions
  • Current estimates of HCV infections must be
    considered as hypotheses, not as conclusions
    the epidemiology of HCV infection in Canada
    remains largely unknown.
  • Population-based studies are necessary
  • Burden of HCV infection is greatest in four
    provinces which account for most HCV infections
    in Canada
  • Most new HCV infections are probably among IDUs
    but a substantial proprtion, possibility as many
    as 40, are not related to injection
  • Transmission of HCV (probability, determinants)
    in other populations needs further elucidation
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