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PMTCT in a Brazilian clinic HAART is feasible in a middle income country

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Title: PMTCT in a Brazilian clinic HAART is feasible in a middle income country


1
PMTCT in a Brazilian clinic- HAART is feasible in
a middle income country
  • Breno Riegel Santos, MD
  • Hospital Nossa Senhora da Conceição/GHC
  • Porto Alegre, Brazil
  • IRC session at IMPAACT Leadership retreat,
    October 2007

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Guidelines for ARV therapy/prophylaxis in
pregnancy, adults/adolescents and in children,
Brazilian Ministry of Health
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Unit for Prevention of Vertical Transmission
(UPTV)
  • Hospital based unit (all services free of charge
    at point of delivery- publicly funded)
  • Infectologists Ob/gyns Pediatricians
  • Counseling and adherence nurse
  • Lab tests available at site (routine, CD4, Viral
    Load)
  • Formula provided for 6 months
  • ARV available at site
  • C-section when VLgt1000 or unknown
  • Rapid test when HIV status unk or result gt3 months

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Study objectives
  • To determine the prevalence of HIV-1 infection
    among women receiving pre-natal care at Hospital
    Nossa Senhora da Conceição/GHC
  • To determine HIV-1 MTCT rates among infected
    women attending pre-natal care at our institution
    and women identified as HIV-infected during the
    time of labor and delivery
  • To determine the incidence of HIV-1
    seroconversion during pregnancy and assess MTCT
    risk
  • To assess additional risk factors for MTCT in
    these diverse patient populations

10
Methods
  • Study design retrospective cohort study
    conducted from July/2004 to August/2006.
  • Study population
  • HIV-1 infected pregnant women followed for
    pre-natal care at the UPTV of HNSC receiving
    HAART for PMTCT
  • HIV-1 infected women identified as such by rapid
    HIV-1 testing upon admission for labor and
    delivery with no prior HIV-1 testing during
    pregnancy
  • HIV-1 infected women identified as such by rapid
    HIV-1 testing upon admission for labor and
    delivery with prior HIV-1 negative test results
    obtained during pre-natal care at least 90 days
    before admission (case definition for primary
    HIV-1 infection during pregnancy)
  • Women referred from outside hospitals who did not
    receive prenatal care at our institution and
    received ZDV monotherapy were excluded

11
Methods
  • Assessment of HIV-1 infant infection
  • Presence of 2 detectable HIV-1 virus load
    assessments by bDNA at different timepoints. The
    diagnosis was ruled out in the presence of 2
    negative virus loads with one obtained 5 months
    of life. No mothers breastfed and formula was
    provided according to Brazilian Ministry of
    Health guidelines
  • Data analysis
  • Binomial distribution with 95 CI
  • Chi-square with Yates correction and Fisher test
  • Kruskal Wallis test
  • Analysis of variance (ANOVA)

12
Results
  • In 2 years, deliveries at our institution totaled
    11,241 with 318 (2.9) occuring in HIV-1 infected
    women
  • The incidence of HIV-1 seroconversion was 9 in
    11,241 women or 0.8/1,000 (CI 95 0.4-1.5/1,000)
  • 256 HIV women delivered at our institution
    fulfilling study entry criteria
  • For 212/256 mothers (83) infants outcomes were
    determined
  • Among 70 patients diagnosed at delivered, 61 had
    unknown HIV-1 seroconversion time and 9 had
    proven seroconversion during pregnancy

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Patient population and outcomes (n256)
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HIV-1 MTCT rates by patient group (n212)
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Demographic characteristics of the patient groups
Dados expressos em médiaDP (amplitude) ANOVA
(analysis of variance)
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Comparação entre medianas de carga viral conforme
categorias maternas de uso de ARV e momento da
soroconversão
Kruskall Wallis test
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MTCT risk according to mode of delivery, virus
load and maternal characteristics (ARV use and
timing of seroconversion).
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Conclusions
  • Women who seroconverted during pregnancy had a
    much higer rate of HIV-1 MTCT (33) than women
    with an unknown HIV seroconversion time who did
    not receive ARV therapy (8.2). Women on HAART
    during pregnancy had an MTCT risk of 0.7
  • A prior study in Thailand did not report a higher
    HIV-1 transmission rate among seroconverting
    pregnant women, however ARV therapy was not
    available for any HIV-infected women, including
    those receiving pre-natal care
  • No transmissions ocurred in 122 women with
    undetectable viral load
  • Among 212 women recruited over 2 years, at least
    4.2 (9 women) seroconverted during pregnancy

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Conclusions
  • Demographic parameters were not very helpful in
    the identification of at risk patients
  • The high prevalence of seroconversion in our
    population and the high risk of HIV-1 MTCT under
    these cirsumstances indicates that routine HIV-1
    re-screening of patients during pregnancy and at
    delivery should be implemented in our setting,
    with prompt initiation of ARV treatment upon
    identification of primary infection
  • HIV-1 testing of sexual partners of women in
    prenatal care may be helpful in the
    identification of patients at risk of
    seroconversion and should be considered as a
    public health measure
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