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Perinatal Infections Fetal Infection

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Title: Perinatal Infections Fetal Infection


1
Perinatal Infections Fetal Infection
  • Nabeel BondagjiConsultant perinatologist
  • KFSHRC Jeddah

2
Infections
  • Toxoplasmosis
  • Rubella
  • Varicella
  • Parvovirus
  • CMV
  • HIV
  • Syphilis

3
Introduction
  • 3 of the perinatal mortalities are related to
    (fetal infection)
  • Fetus can be affected at any gestational age
  • Most severe affection occurs in the first
    trimester
  • Most of the fetal infections are preventable

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Red indicates the most vulnerable period of
development. (Moore 143).
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  • First Trimester
  • Organogenesis
  • Growth restriction
  • Second and Third Trimester
  • Neuological Impairment
  • Growth restriction

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Think of fetal infection
  • I.U.G.R
  • Hepatic Calcification
  • Intracrainal Calcification
  • Hydrocephally, Microcephally
  • Ascits
  • Pericardial,Pleural Effusion
  • Non Immune Hydrops Fetalis

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Toxoplasmosis
  • - Toxoplasmon gondii (intracellular parasite)
  • Trans-placental affect the placenta fetus
  • Transmission Rate
  • - 10 15 1st trimester
  • - 25 2nd trimester
  • - 60 3rd trimester

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Toxoplasmosis
  • Toxoplasmosis
  • - Incidence of congenital toxoplasmosis
  • - 0.07 0.5 1000 London
  • - 2 1000 Brussels
  • - 3.22 1000 Paris

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Risks to the Fetus
  • 1st Trimester
  • - 55 85 will show sequilie
  • - Chrioretinitis severe impairment of vision
  • - Hearing loss
  • - Mental Retardation
  • - Ascits
  • - Periventirecular Calcification
  • - Hydrocephally

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  • Toxoplasmonsis
  • Ultra Sound
  • - Intracranial, hepatic, calcification
  • - Ascitis
  • - Hepatosplenomegally
  • - Microcephally
  • - I.U.G.R
  • Diagnosis Fetal Blood Sampling
  • - IgM
  • - PCR
  • - Culture

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Toxoplasmosis
  • Treatment
  • - Reduce risk of transmission
  • Spiramycin
  • - If fetal infection documented
  • - Pyrimethamine
  • - Sulfadiazine.. Folic acid

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  • Pyron F, Wallonlion C, Goner P,
  • Cochrane Database Review
  • January 2005
  • Objective
  • To assess whether treatment of toxoplasmosis
    reduces the risk of congenital toxoplasmosis
  • Selection Criteria
  • RCT
  • - Antibiotics
  • - No treatment
  • Proven Infection

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  • Look, outcome of the children
  • 3332 Papers identified

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  • NO Trial fulfill the criteria

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  • Conclusion
  • We do not know whether antibiotics Treatment
    reduces the congenital transmission or not.
  • Screening is Expensive
  • Screening is not recommended in countries where
    screening and treatment is not routine.

23
Toxoplasmosis
  • Prevention to Toxoplasmosis Advice to Pregnant
    Women whose Serological Tests are Negative.
  • Cook meat at 60oC (Industrial deep-freezing
    also seems to destroy parasites efficiently).
  • When handling raw meat, do not touch eyes or
    mouth.

24
Cont.. Prevention of Toxoplasmosis
  • Carefully wash hands after handling raw meat,
  • dirt, or vegetables soiled by dirt.
  • Wash fruit and vegetables before eating
  • Wear gloves when gardening
  • Avoid all contacts with things that may have
  • been contaminated by cat feces
  • If the cats litter has to be changed, put on
  • gloves and disinfect often with boiling water.

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Rubella German Measles
  • Rubella
  • - 3rd Disease
  • RNA Virus
  • - Respiratory secretions
  • - 2 3 weeks I.P.

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Rubella
  • - 0.5 2 Non Immune
  • - 0.2 0.5 Congenital Rubella Syndrome
  • Risk of Transmission
  • - 8 12 weeks 90
  • -12 16 weeks 50
  • - 16 20 weeks 17

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Rubella
  • Ultra Sound - I.U.G.R.
  • - Hepto-splenomegally
  • Congenital Rubella syndrome
  • - Eye
  • Cataract, Retinopathy
  • Microphthalmia, glaucoma
  • - Ear
  • Deafness
  • -Heart PDA

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Rubella
  • Diagnosis
  • IgM

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RUBELLA
  • Prevention
  • Active immunization by vaccination is the only
    efficient way of preventing congenital rubella.

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  • Varicella Zoster Virus DNA Herpes
  • - Chickenpox
  • - Herpes Zoster
  • - Incidence in pregnancy 0.4 0.7 1000
  • Maternal
  • - Pneumonia increase mortality
  • Fetal Congenital Varicella Syndrome in 1st tri
    mester
  • - Skin Scar, Limb Hyproplasia
  • - Chrioretinitis, Microcephally

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Varicella
  • Neonatal Infection
  • Increase in Mortality
  • - 5 days before delivery 48 hours post partum
  • - Avoid delivery if possible in this period

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Diagnosis
  • Viral Culture
  • - PCR
  • Presence of infection does not predicate the
    severity of the disease

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VARICELLA
  • Prevention
  • Passive immunization is currently available
  • and should be administered within 24-72
  • hours to sero-negative pregnant patients who
  • have been exposed to varicella.

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Varicella
  • Treatment
  • - Oral cyclovir to improve sysmatic I.V. to
    treat pneumonia
  • - Safe in Pregnancy
  • - Does not prevent or decrease the fetal effect
  • - VZIG to be given to the neonate 5 days before
    delivery 2 days postpartum

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Varicella
  • Screening
  • - Not Recommended

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Parvovirus B.19 the fifth disease
  • Infectious period 5 10 days after exposure
  • Mode of transmission
  • - Transplacental 33 transmission risk
  • - Fetal effect abortion lt20 weeks
  • - Hydrops fetalis 18 of all non immune

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Intrauterine fetal infection
  • Fetal effect of B19 - A symptomatic -
    IUGR - Congenital anomalies - Hydrops
    fetalis - IUFD
  • Parvovirus B 19 pathogenesis a)
    Anemia b) Fetal myocardium and hepatic
    affection c) Vasculitis

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Diagnosis
  • Parpovirus
  • - ELISA
  • -Western blot test
  • IGM Diagnosis of Primary Infection
  • Elect Microscopy
  • - Direct Visualization of the virus or viral
    particles

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Parvovirus
  • Fetal Diagnosis
  • PCR in A.F., Placenta Blood
  • Ultra Sound
  • Hydropy Fetalis

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Parvovirus
  • Prognosis and therapy
  • Survivor recovers normal
  • Fetal Therapy
  • Intravascualr Intrauterine Blood Transfusion

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CMV
  • DNA Herpes Virus
  • Most common perinatal infection
  • 0.2 2 of all newborns
  • Leading cause of hearing loss
  • Mode of transmission
  • Contact with infected
  • -Blood
  • -Urine
  • -Salvia
  • -Sexual contact

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CMV
  • I.P 28 60 days
  • Viremia 2 3 weeks
  • Maternal effect
  • Asympathic, mild fever, malaise myalgia
  • Primary infection 0.7 4
  • Recurrent infection 13.5

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  • Epidimulogical Facts
  • Primary Infection
  • -Risk of Transmission 30 40
  • -10 Seguilie of the infected
  • -30 Prenatal Mortality
  • -Of the survivor 80will have neurological
    damage

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  • Recurrent Infection
  • Transmission 0.1 2 Mostly a symptomatic most
    of the sequilie occurs as hearing loss

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Diagnosis
  • CMV
  • Diagnosis Culture or PCR
  • blood, urine salvia
  • IgG Serial Measurements 3 4 weeks
  • Diagnosis either by seroconversion
  • Or increase titer by more than 4 folds
  • -1 4 1 16
  • -1 16 1 256

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  • IGM is not reliable as it may be negative even in
    the right phase and may persist for months after
    infections

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Diagnosis
  • Fetal Diagnosis Ultra Sound System
  • - Intracrainal or hepatic calcification
  • - Echogenic bowel
  • - Ascits
  • A.F.
  • - Culture
  • - PCR

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  • CMV
  • Treatment
  • - Not available
  • - Neonatal therapy ganciclovir may decrease
    neonatal infections
  • Vaccine
  • - May Reactivate A previous infection
  • CMV
  • Screening
  • Not Recommended

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Human immunodeficiency virus (HIV) Infection
  • This is the major cause of congenital
  • infection in the developing world.
  • Over one million children had been
  • infected from their mother by the end of
    1998.

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  • Mother ? child
  • in utero
  • at birth
  • breast milk
  • Organ/tissue donation
  • Semen
  • Kidneys
  • Skin, bone marrow, corneas, heart valves,
    tendons, etc.

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TO SCREEN OR NOT TO SCREEN?
  • The best defense is a strong offense.
  • The American Academy of Paediatrics and the ACOG
    issued a Joint Statement on HIV Screening in
    Pregnancy (1999) (2001).
  • A pregnant women should receive HIV counseling as
    part of their routine ANC.
  • A pregnant women should have HIV testing with
    their consent.

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PRE-TEST COUNSELING
  • Risks of transmission (including Mode)
  • Risks of perinatal transmission
  • Potential social and psychological implication of
    Positive test.
  • The availability of Agents that may reduce the
    risk of neonatal infection.
  • Clarify the difference between HIV infection and
    disease.

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Timing of Perinatal HIV Transmission
  • Cases documented intrauterine, intrapartum, and
    postpartum by breastfeeding
  • In utero - 25 40 of cases
  • Intrapartum- 60 75 of cases
  • Addition risk with breastfeeding
  • 14 ?risk with established infection
  • 29 ?risk with primary infection
  • Current evidence suggests most transmission
    occurs during the intrapartum period

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Factors Influencing Perinatal Transmission
  • Maternal Factors
  • HIV-1 RNA levels (viral load)
  • Low CD4 lymphocyte count
  • Other infections, Hepatitis C, CMV, bacterial
    vaginosis
  • Maternal infection drug use
  • Lack of ZDV during pregnancy
  • Obstetrical Factors
  • Length of ruptured membranes/chorioamnionitis
  • Vaginal delivery
  • Invasive procedures
  • Infant Factors
  • Prematurity

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Reducing HIV Transmission with Suboptimal
Regimens
  • Partial ZDV regimens ( New York cohort)
  • Transmission rates
  • 6.1 with prenatal, intrapartum, and infant ZDV
  • 10 with only intrapartum ZDV
  • 9.3 if only infant ZDV started within first 48
    hours
  • 26.6 with no ZDV

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Reducing Intrapartum HIV Transmission
Studies of Short Course Therapy
  • Oral ZDV in a non-breastfeeding population
    (Thailand) from 36 weeks and during labor
  • Transmission rate 9.4 ZDV vs. 18.9 placebo
  • PETRA study intrapartum/postpartum oral ZDV/3TC
    in a breast-feeding population (Uganda, S.
    Africa, Tanzania)
  • Transmission rate 10 ZDV/3TC vs. 17 placebo
  • HIV Net 012 intrapartum/postpartum/neonatal
    Nevirapine (NVP) vs. short course/neonatal ZDV in
    a breast-feeding population (Uganda)
  • Transmission rate 12 NVP vs. 21 ZDV

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  • Treatment with zidovudine appears
    to be safe in pregnancy.
  • Elective caesarean section may decrease
    mother-to-child transmission.

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  • HIV
  • Chochrane Database 2002
  • Objective to assess what intervention will
    decrease the risk of mother to children
    transmission of HIV

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  • AZT
  • 4 trials decrease 1585 patients
  • Neviropine compared AZT 626 decrease transmission
  • C/S one trial 436 patients decrease risk of
    transmission
  • Immunoglbullin
  • Does not decrease the risk

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  • Conclusion
  • Zidoridine, Nevirpine
  • C/S decreases the transmission significantly.

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  • Syphilis
  • - T.P.
  • - Increase HIV
  • Transmission all through

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  • Manifestation
  • Ultra Sound
  • Thick Placenta
  • Hydrops fetalis
  • I.U.G.R
  • Hydroamnios Hepato-splenomegaly
  • Risk of Transmission
  • 90 primary
  • 50 secondary
  • 6 14 Latent Syphillis

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  • Diagnosis
  • Screening Non Specific
  • VDAL
  • RPR
  • Specific
  • TPHA
  • F.T.A. becomes ..
  • 3 4 weeks

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  • Treatment
  • - Penicillin
  • - Benzathin Penicillin 2.4 million unit
  • - Erythpromycine

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