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Part A: Module A3

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Understand the effects of HIV on pregnancy ... Women first diagnosed with HIV infection during pregnancy ... HIV Infection During Pregnancy ... – PowerPoint PPT presentation

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Title: Part A: Module A3


1
  • HIV and Pregnancy
  • Prevention of
  • Mother-to-Child Transmission
  • Part A Module A3
  • Session 1

2
Objectives
  • Understand the effects of HIV on pregnancy
  • Discuss MTCT transmission, factors that may
    increase transmission, and measures that reduce
    transmission
  • Describe how ART is used for the prevention of
    MTCT

3
Objectives, continued
  • Describe the various drug regimens for PMTCT that
    are used during pregnancy, intrapartum, and
    postpartum, including short course ART
  • Discuss issues related to breastfeeding, PMTCT,
    ART and WHO recommendations
  • Discuss national guidelines on infant feeding

4
HIV and Pregnancy Prevention of Mother-to-Child
Transmission
  • Worldwide, each year, two million HIV infected
    women become pregnant, most of them in poor
    countries
  • Between 1/4 and 1/3 transmit the disease to their
    newborns either during labor, during delivery, or
    while breast-feeding (2,000 new AIDS-infected
    infants each day)
  • HIV infected children whose mothers die are left
    orphaned and harder to care for than the HIV
    negative infant

5
HIV and Pregnancy Prevention of Mother-to-Child
Transmission, continued
  • In participants country of women are HIV
    positive. Prevalence is higher in areas
  • HIV presentation is the same in both sexes, but
    the disease has greater implications on a womans
    reproductive health in terms of her ability to
    cope with pregnancy and transmission of the virus
    to her unborn and newborn child
  • During the asymptomatic phase of HIV, most women
    are unaware of their infection until the disease
    is diagnosed in their infants. This may cause
    conflict within the family and the woman might be
    blamed for bringing the infection into the family

6
Effects of HIV on Pregnancy
  • Some studies in Africa suggest that HIV may have
    an adverse affect on fertility in both
    symptomatic and asymptomatic women
  • When comparing changes in CD4 count/percentage
    over time, there is no difference between
    HIV-positive women who are pregnant and
    HIV-positive women who are not pregnant
  • HIV does not seem to significantly cause
    congenital abnormalities or an increase in
    spontaneous abortion

7
Effects of HIV on Pregnancy, continued
  • During the early stages of HIV infection,
    pregnancy does not accelerate disease progression
  • Late HIV disease may affect the outcome of
    pregnancy, i.e., poor fetal growth, preterm
    delivery, low birth weight, prenatal and neonatal
    death
  • With regard to common HIV-related problems, there
    is no difference between pregnant and
    non-pregnant women and they should be managed the
    same (except for drug management)

8
Mother-to-Child Transmission of HIV
  • Transmission
  • Factors which may increase risk of transmission
  • Measures to reduce MTCT
  • ARV Therapy and MTCT
  • Prevention of prenatal transmission
  • Women first diagnosed with HIV infection during
    pregnancy
  • HIV-infected women on ART who become pregnant
  • ART and breastfeeding
  • Treatment postpartum
  • Adherence to therapy
  • Recommendations

9
Transmission
  • HIV may be transmitted to the infant during
    pregnancy, at the time of delivery, and through
    breastfeeding most transmission is thought to
    take place during delivery
  • For a mother known to be HIV-infected prenatally,
    the additional risk of transmission of HIV to her
    infant through breastfeeding has been estimated
    at 14
  • The risk is as high as 29 for mothers who
    acquire HIV post-natally

10
Transmission, continued
  • Many studies indicate that the risk of breast
    milk transmission is higher in the first few
    months of life, with a subsequent tapering off of
    risk
  • The risk persists as long as the infant is
    breastfed
  • HIV transmission is also higher if the mother has
    mastitis

11
Factors Which May Increase the Risk of
Transmission
  • High maternal viral load gt5-10,000 copies/ml
    (e.g., at time of seroconversion and during late
    HIV disease CD4 cell counts lt100 cells/mm)
  • Recurrent STDs
  • Malaria interferes with placental functions and
    eases viral transmission across the placenta
  • Vitamin A deficiency
  • Preterm delivery
  • Infected amniotic fluid (chorioamnionitis)
    (limited data recent studies do not suggest
    increased risk)

12
Factors Which May Increase the Risk of
Transmission, continued
  • Vaginal delivery
  • Duration of rupture of membranes is longer than 4
    hours
  • Placental disruption
  • Invasive procedures during delivery (e.g., vacuum
    extraction, episiotomy, use of forceps, fetal
    scalp monitoring)
  • Mechanical nasal suction after delivery
  • Breastfeeding and especially mixed feeding

13
Measures to Reduce MTCT
  • During pregnancy
  • Provide voluntary counseling and HIV testing plus
    psychosocial support
  • Diagnose and provide aggressive treatment of
    malaria, STDs and other infections as early as
    possible
  • Provide basic antenatal care including
  • Iron Supplementation
  • Education about MTCT and infant feeding options
  • ART for MTCT
  • Risk reduction/safer sex measures

14
Measures to Reduce MTCT
  • During Labor and Delivery
  • Delay rupturing of membranes (ROM)
  • Do only minimal digital examinations after ROM
  • Cleanse the vagina with hibitane or other
    viricides if available
  • Reduce use of assisted delivery with forceps,
  • Reduce use of episiotomy
  • Elective caesarean section has a more protective
    effect against MTCT than vaginal delivery
  • If not already on ART, give NVP

15
Measures to Reduce MTCT
  • After Delivery
  • Avoid mechanical nasal suction
  • Clean the newborn immediately of all maternal
    secretions and blood
  • Support safer infant feeding (according to
    national guidelines re mothers choice to put
    the infant to breast within 30 minutes of birth)
  • If breastfeeding is chosen as an option
    encourage exclusive breastfeeding and advise
    early cessation (up to 6 months) or breast milk
    substitute
  • Advise giving milk substitutes where conditions
    are suitable and no breastfeeding after 6 months

16
Risks and Benefits Breastfeeding vs.
Replacement Feeding
  • Current WHO/UNAIDS/UNICEF guidelines recommend
    that women with HIV infection be fully informed
    of both risks and benefits of breastfeeding and
    be supported in their decision about feeding
    practices
  • Safe alternatives may not be available in some
    resource-limited settings, in which case
    exclusive breastfeeding for the first six months
    of life is recommended

17
Breastfeeding by HIV Positive MothersRisks to
the Infant
  • HIV infection
  • Infection risk persists for as long as the infant
    is breastfeeding
  • Children who receive mixed feeding seem to be at
    higher risk of HIV infection during the first
    months of life than children who receive
    exclusive breastfeeding or exclusive replacement
    feeding
  • Shortening the period of breastfeeding may reduce
    the risk of HIV transmission and mixed feeding
    should be discouraged
  • The alternative of exclusively giving replacement
    feeding also has considerable risks

18
Breastfeeding Benefits to the Infant
  • The immunological, nutritional, psychosocial, and
    child-spacing benefits are well recognized
  • Breast milk plays an important role in preventing
    the infections that accelerate progression of
    HIV-related diseases in already infected children

19
ARV Therapy and MTCT
  • Prevention of Prenatal Transmission
  • ARV therapy can produce a significant reduction
    in mother to child transmission of HIV
  • Studies showed that administration of AZT to
    women from 14th week of pregnancy and during
    labor to the newborn decreased the risk of MTCT
    by nearly 70 in the absence of breastfeeding
  • A shorter AZT alone regimen starting from the
    36th week of pregnancy was shown to reduce the
    risk of transmission of HIV at 6 months by 50 in
    non-breastfeeding population and by 37 in those
    breastfeeding

20
ARV Therapy and MTCT, continued
  • Short course of NVP (HIVNET 012) has been shown
    to reduce the risk of transmission by 47
  • This protocol is the most commonly used one
    because of its
  • demonstrated efficacy in clinical trials in
    reducing MTCT
  • low cost
  • ease of use in MTCT programs
  • Women on treatment with ARVs for HIV infection
    have very low transmission if their viral load is
    lt1000 copies/ml

21
Women First Diagnosed with HIV Infection During
Pregnancy
  • Women in the first trimester may consider
    delaying initiation of ART
  • Consider severity of maternal HIV disease and
    potential benefits and risks of delaying ART
    until after first trimester
  • For women who are severely ill, the benefit of
    early initiation may outweigh theoretical risk to
    fetus in these cases, recommend initiating with
    drugs such as AZT, 3TC, NVP, or NFV

22
HIV-infected Women on ART Who Become Pregnant
  • Options are
  • Suspend therapy temporarily during first
    trimester
  • Continue same therapy
  • Change to a different regimen
  • Issues to consider
  • Gestational stage of the pregnancy
  • Severity of maternal disease
  • Tolerance of regimen in pregnancy
  • Potential for adverse fetal effects

23
ART and Breastfeeding
  • Women who require ART and are breastfeeding
    should continue their ongoing ART regimen
  • Efficacy of a potent ART being given to the
    mother solely to prevent postnatal transmission
    of HIV through breast milk is unknown, but is
    currently being studied

24
Short-Course ARV prophylaxis and Treatment
Postpartum
  • Short-course ARV regimens, that do not fully
    suppress viral replication, may be associated
    with the development of ARV drug resistance
  • The Ugandan HIVNET 012 study of single dose
    intrapartum/newborn NVP for prevention of MTCT
    found that 19 of the women developed resistance
    to the drug. This was associated with delivery,
    HIV viral load and CD4 cell count

25
Short-Course ARV Prophylaxis and Treatment
Postpartum, continued
  • Based on current information (until further
    research is done), prior administration of
    short-course AZT/3TC or single dose NVP for
    prevention of MTCT should not preclude use of
    these agents as part of a combination ARV drug
    regimen initiated for treatment of these women

26
Adherence to Therapy in Pregnancy and Postpartum
  • Difficulty of adherence is greater in pregnant
    and postpartum women
  • Obstacles to adherence morning sickness, GI
    upset, fears about ARV harming the fetus
  • If need to temporarily discontinue therapy during
    pregnancy, stop all drugs and then re-start
    simultaneously
  • This reduces the potential for emergence of
    resistance

27
Adherence to Therapy in Pregnancy and
Postpartum, continued
  • Treatment adherence difficult postpartum
  • Physical changes of postpartum period coupled
    with stresses and demands of caring for a newborn
    infant
  • Important to provide additional supports for
    maintaining adherence to therapy during ante- and
    post-partum periods

28
Recommendations
  • Exclusive breastfeeding for the first 6 months
    generally promoted and supported ---
  • serostatus of most mothers unknown
  • benefits to infants outweigh the risks regardless
    of their HIV status
  • The mother should make final choice about the
    feeding method
  • Whatever her choice may be, health staff should
    provide support to ensure optimal nutrition of
    mother and child
  • Refer to national HIV and infant feeding
    guidelines
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