Perinatal Infections Fetal Infection - PowerPoint PPT Presentation

About This Presentation
Title:

Perinatal Infections Fetal Infection

Description:

Perinatal Infections Fetal Infection Nabeel Bondagji Consultant perinatologist KFSH&RC Jeddah – PowerPoint PPT presentation

Number of Views:556
Avg rating:5.0/5.0
Slides: 90
Provided by: kfs7
Category:

less

Transcript and Presenter's Notes

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

4
Red indicates the most vulnerable period of
development. (Moore 143).
5
  • First Trimester
  • Organogenesis
  • Growth restriction
  • Second and Third Trimester
  • Neuological Impairment
  • Growth restriction

6
Think of fetal infection
  • I.U.G.R
  • Hepatic Calcification
  • Intracrainal Calcification
  • Hydrocephally, Microcephally
  • Ascits
  • Pericardial,Pleural Effusion
  • Non Immune Hydrops Fetalis

7
(No Transcript)
8
(No Transcript)
9
(No Transcript)
10
(No Transcript)
11
(No Transcript)
12
(No Transcript)
13
Toxoplasmosis
  • - Toxoplasmon gondii (intracellular parasite)
  • Trans-placental affect the placenta fetus
  • Transmission Rate
  • - 10 15 1st trimester
  • - 25 2nd trimester
  • - 60 3rd trimester

14
(No Transcript)
15
Toxoplasmosis
  • Toxoplasmosis
  • - Incidence of congenital toxoplasmosis
  • - 0.07 0.5 1000 London
  • - 2 1000 Brussels
  • - 3.22 1000 Paris

16
Risks 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

18
Toxoplasmosis
  • 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.

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.

25
(No Transcript)
26
(No Transcript)
27
(No Transcript)
28
(No Transcript)
29
(No Transcript)
30
(No Transcript)
31
(No Transcript)
32
Rubella German Measles
  • Rubella
  • - 3rd Disease
  • RNA Virus
  • - Respiratory secretions
  • - 2 3 weeks I.P.

33
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

34
Rubella
  • Ultra Sound - I.U.G.R.
  • - Hepto-splenomegally
  • Congenital Rubella syndrome
  • - Eye
  • Cataract, Retinopathy
  • Microphthalmia, glaucoma
  • - Ear
  • Deafness
  • -Heart PDA

35
Rubella
  • Diagnosis
  • IgM

36
RUBELLA
  • Prevention
  • Active immunization by vaccination is the only
    efficient way of preventing congenital rubella.

37
(No Transcript)
38
(No Transcript)
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

40
Varicella
  • Neonatal Infection
  • Increase in Mortality
  • - 5 days before delivery 48 hours post partum
  • - Avoid delivery if possible in this period

41
Diagnosis
  • Viral Culture
  • - PCR
  • Presence of infection does not predicate the
    severity of the disease

42
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.

43
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

44
Varicella
  • Screening
  • - Not Recommended

45
(No Transcript)
46
(No Transcript)
47
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

48
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

49
Diagnosis
  • Parpovirus
  • - ELISA
  • -Western blot test
  • IGM Diagnosis of Primary Infection
  • Elect Microscopy
  • - Direct Visualization of the virus or viral
    particles

50
Parvovirus
  • Fetal Diagnosis
  • PCR in A.F., Placenta Blood
  • Ultra Sound
  • Hydropy Fetalis

51
Parvovirus
  • Prognosis and therapy
  • Survivor recovers normal
  • Fetal Therapy
  • Intravascualr Intrauterine Blood Transfusion

52
(No Transcript)
53
(No Transcript)
54
(No Transcript)
55
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

56
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

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

59
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

60
  • IGM is not reliable as it may be negative even in
    the right phase and may persist for months after
    infections

61
Diagnosis
  • 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

63
(No Transcript)
64
(No Transcript)
65
(No Transcript)
66
(No Transcript)
67
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.

68
  • Mother ? child
  • in utero
  • at birth
  • breast milk
  • Organ/tissue donation
  • Semen
  • Kidneys
  • Skin, bone marrow, corneas, heart valves,
    tendons, etc.

69
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.

70
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.

71
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

72
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

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

83
(No Transcript)
84
(No Transcript)
85
(No Transcript)
86
(No Transcript)
87
(No Transcript)
88
(No Transcript)
89
(No Transcript)
Write a Comment
User Comments (0)
About PowerShow.com