Title: Perinatal Infections Fetal Infection
1Perinatal Infections Fetal Infection
- Nabeel BondagjiConsultant perinatologist
- KFSHRC Jeddah
2Infections
- Toxoplasmosis
- Rubella
- Varicella
- Parvovirus
- CMV
- HIV
- Syphilis
3Introduction
- 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
4Red indicates the most vulnerable period of
development. (Moore 143).
5- First Trimester
- Organogenesis
- Growth restriction
- Second and Third Trimester
- Neuological Impairment
- Growth restriction
6Think 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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13Toxoplasmosis
- - 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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15Toxoplasmosis
- Toxoplasmosis
- - Incidence of congenital toxoplasmosis
- - 0.07 0.5 1000 London
- - 2 1000 Brussels
- - 3.22 1000 Paris
16Risks to the Fetus
- 1st Trimester
- - 55 85 will show sequilie
- - Chrioretinitis severe impairment of vision
- - Hearing loss
- - Mental Retardation
- - Ascits
- - Periventirecular Calcification
- - Hydrocephally
17- Toxoplasmonsis
- Ultra Sound
- - Intracranial, hepatic, calcification
- - Ascitis
- - Hepatosplenomegally
- - Microcephally
- - I.U.G.R
- Diagnosis Fetal Blood Sampling
- - IgM
- - PCR
- - Culture
18Toxoplasmosis
- Treatment
- - Reduce risk of transmission
- Spiramycin
- - If fetal infection documented
- - Pyrimethamine
- - Sulfadiazine.. Folic acid
19- 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
20- Look, outcome of the children
- 3332 Papers identified
21- NO Trial fulfill the criteria
22- 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.
23Toxoplasmosis
- 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.
24Cont.. 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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32Rubella German Measles
- Rubella
- - 3rd Disease
- RNA Virus
- - Respiratory secretions
- - 2 3 weeks I.P.
33Rubella
- - 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
34Rubella
- Ultra Sound - I.U.G.R.
- - Hepto-splenomegally
- Congenital Rubella syndrome
- - Eye
- Cataract, Retinopathy
- Microphthalmia, glaucoma
- - Ear
- Deafness
- -Heart PDA
-
35Rubella
36RUBELLA
- Prevention
- Active immunization by vaccination is the only
efficient way of preventing congenital rubella.
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39- 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
-
-
40Varicella
- Neonatal Infection
- Increase in Mortality
- - 5 days before delivery 48 hours post partum
- - Avoid delivery if possible in this period
41Diagnosis
- Viral Culture
- - PCR
- Presence of infection does not predicate the
severity of the disease
42VARICELLA
- 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.
43Varicella
- 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
44Varicella
- Screening
- - Not Recommended
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47Parvovirus 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
-
48Intrauterine 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
49Diagnosis
- Parpovirus
- - ELISA
- -Western blot test
- IGM Diagnosis of Primary Infection
- Elect Microscopy
- - Direct Visualization of the virus or viral
particles -
50Parvovirus
- Fetal Diagnosis
- PCR in A.F., Placenta Blood
- Ultra Sound
- Hydropy Fetalis
51Parvovirus
- Prognosis and therapy
- Survivor recovers normal
- Fetal Therapy
- Intravascualr Intrauterine Blood Transfusion
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55CMV
- 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
-
56CMV
- 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
57- Epidimulogical Facts
- Primary Infection
- -Risk of Transmission 30 40
- -10 Seguilie of the infected
- -30 Prenatal Mortality
- -Of the survivor 80will have neurological
damage
58- Recurrent Infection
- Transmission 0.1 2 Mostly a symptomatic most
of the sequilie occurs as hearing loss
59Diagnosis
- 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
60- IGM is not reliable as it may be negative even in
the right phase and may persist for months after
infections
61Diagnosis
- Fetal Diagnosis Ultra Sound System
- - Intracrainal or hepatic calcification
- - Echogenic bowel
- - Ascits
- A.F.
- - Culture
- - PCR
62- 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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67Human 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.
68- Mother ? child
- in utero
- at birth
- breast milk
- Organ/tissue donation
- Semen
- Kidneys
- Skin, bone marrow, corneas, heart valves,
tendons, etc.
69TO 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.
70PRE-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.
71Timing 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
72Factors 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
73 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
74 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
75- Treatment with zidovudine appears
to be safe in pregnancy. - Elective caesarean section may decrease
mother-to-child transmission.
76- HIV
- Chochrane Database 2002
- Objective to assess what intervention will
decrease the risk of mother to children
transmission of HIV
77- 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
78- Conclusion
- Zidoridine, Nevirpine
- C/S decreases the transmission significantly.
79- Syphilis
- - T.P.
- - Increase HIV
- Transmission all through
80- 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
81- Diagnosis
- Screening Non Specific
- VDAL
- RPR
- Specific
- TPHA
- F.T.A. becomes ..
- 3 4 weeks
82- Treatment
- - Penicillin
- - Benzathin Penicillin 2.4 million unit
- - Erythpromycine
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