HIVHEPATITIS C COINFECTION IN A PUERTO RICAN HIVAIDS COHORT - PowerPoint PPT Presentation

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HIVHEPATITIS C COINFECTION IN A PUERTO RICAN HIVAIDS COHORT

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Diana M. Fern ndez, MS, Ed.D. (Candidate) Maria A. G mez, Ph.D. Eddy R os-Olivares, Ph.D., MPH. Robert F. Hunter-Mellado, MD, FACP ... – PowerPoint PPT presentation

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Title: HIVHEPATITIS C COINFECTION IN A PUERTO RICAN HIVAIDS COHORT


1
HIV-HEPATITIS C CO-INFECTION IN A PUERTO RICAN
HIV/AIDS COHORT
  • Angel M. Mayor, MD, MS
  • Diana M. Fernández, MS, Ed.D. (Candidate)
  • Maria A. Gómez, Ph.D.
  • Eddy Ríos-Olivares, Ph.D., MPH
  • Robert F. Hunter-Mellado, MD, FACP
  • Retrovirus Research Center, Universidad Central
    del Caribe, School of Medicine. Hospital Ramón
    Ruiz Arnau, Bayamón, Puerto Rico

2
(No Transcript)
3
HEPATITIS C VIRUS
4
INTRODUCTION
  • Life expectancy of HIV infected persons has
    increase since the introduction of antiretroviral
    therapies.
  • Hepatitis C (HCV) is becoming a great
    contributor for HIV morbidity and mortality.
  • HCV prevalence in USA 2. HCV prevalence in HIV
    infected persons 30-50.
  • HCV transmission Principally by contact with
    infected blood (infected needles) and few by high
    risk sexual behaviors.
  • Injecting drug users (IDUS) have a higher risk of
    harboring HCV co-infected (Prevalence 50-90).
  • 80 of the HCV become a chronic infection, of
    them 75 develop chronic liver disease and 15-20
    develop Liver Cirrhosis.

5
NORMAL LIVER AND CIRRHOTIC LIVER BY HCV INFECTION
6
OBJECTIVES
  • Determine the prevalence of Hepatitis C infection
    in a cohort of Puerto Ricans HIV/AIDS patients.
  • Describe the sociodemographic characteristics,
    risk profile, HIV clinical manifestations, CD4
    and antiretroviral therapy (ART) in the
    co-infected patients.
  • Define the factors that could be associated with
    the HIV-HCV co-infection.
  • Explore the risk factor that increase the
    mortality risk of HIV-HCV patients.

7
METHODS
  • Population 2,996 Puerto Ricans HIV patients,
    followed by the Retrovirus Research Center in the
    Universidad Central del Caribe School of
    Medicine, at Bayamón Puerto Rico, between January
    1992 and December 2001.
  • Sample 592 HIV infected patients with a positive
    ELISA HCV test.
  • Variables Sociodemographic, HIV risk factors,
    HIV clinical manifestations, CD4 cell count ,
    ART and mortality data was explored.
  • Data Analysis Percentage, Fisher, Chi Square and
    Cox Proportional Hazard analysis were performed.

8
HCV PREVALENCE IN THE HIV/AIDS COHORT
N2,996
9
GENDER DISTRIBUTION IN CO-INFECTED CASES
n 592
10
AGE, CD4 COUNT AND AIDS AT HCV INFECTION
11
AIDS DEFINE CONDITION PREVALENCE
n592
12
EMPLOYMENT, EDUCATION LEVEL AND HOUSING
13
INJECTING DRUG USE IN CO-INFECTED CASES
n592
14
CLASS OF DRUG USED BY THE CO-INFECTED IDU
PATIENTS
15
MORTALITY RATE BY THE END OF FOLLOW UP
n592
16
MORTALITY RATE DIFFERENCES
17
MORTALITY RISK FOR HIV-HCV INFECTED CASES
BY COX PROPORTIONAL HAZARD
18
CONCLUSIONS
  • HIV-HCV co-infection prevalence (20) is lower
    than reported in other studies (30-50). An
    underreport of cases could explain this issue,
    HCV screening test was implement in 1998.
  • The co-infection is a potential Public Health
    problem.
  • The IDU risk in HIV-HCV patients (80) was higher
    than the reported in the whole HIV cohort
    (57.2).

19
CONCLUSIONS 2
  • High prevalence of unemployment, low formal
    education and isolation are common in the group.
  • Significant mortality increment in patients with
    high degree of immunological damage and in
    patients with AIDS.
  • Significant mortality decrement in patients with
    Anti Retroviral Treatment.

20
RECOMMENDATIONS
  • Active HCV surveillance in HIV/AIDS patients,
    for early disease diagnosis.
  • Primary prevention strategies to reduce the
    co-infection , specially in IDU persons.
  • Secondary prevention strategies to reduce the
    hepatic damage.
  • Early multi ART will improve the immunological
    system of the patients, reducing their HIV
    morbidity and mortality.

21
ACKNOWLEDGMENTS
  • This study was sponsored by RCMI/NIH Grant number
    G12RR03035, 1U54RR01950701 and CDC/ASD Grant
    number U62/CCU206209
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