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Group B Streptococcus

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Group B Streptococcus Adunni Morohunfola, M.D. Dept. of Pediatrics, Texas Tech * * * one way * Incidence for year 2000 was 0.57/1000 live birth at Thomason, which is ... – PowerPoint PPT presentation

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Title: Group B Streptococcus


1
Group B Streptococcus
  • Adunni Morohunfola, M.D.
  • Dept. of Pediatrics, Texas Tech

2
Etiolgy
  • Group B streptococcus(Strep.agalactiae)
  • Facultative encapsulated gram-positive
    diplococcus
  • Produces a narrow zone of beta hemolysis on
    blood agar.
  • Most strains are resistant to bacitracin and
    septrin
  • Positive CAMP

3
Etiology
  • Divided into the following serotypes based on
    capsular polysacch. types Ia, Ib,II and III
    through VII.
  • All serotypes can cause infections in newborns
    but Ia,II,III,V account for 90.
  • Late onset dx and early-onset meningitis is due
    to type III.

4
Epidemiology
  • Approx. 10-35 of pregnant women are
    asymptomatic carriers of GBS in the genital and
    G. Intestinal tract.
  • At birth 1 in 2 infants born to colonized mothers
    are colonized.
  • 98 of colonized infants are without symptoms,
    but 1-2 developed GBS.
  • Nearly 50 of sexual partners of colonized women
    are colonized themselves.

5
Epidemiology
  • Incidence rate of 0.2 3.7/1000 live births.
  • Mortality rate of 5-15/1000 live births.
  • More recent surveillance shows a decrease in I.R
    to 0.8 per 1000 live births-reflection of use of
    maternal antibiotic prophylaxis.
  • Incidence rate at Thomason
    - 0.57
    /1000 live births in 2000
    - 0.40/1000 live births in 2001.

6
Incidence per 1000 live births of early-onset GBS
disease at Thomason Hospital
  • Data Source Dept. of Pediatrics, Texas Tech







7
Epidemiology
  • Direct cost of treating neonate with proven GBS
    300 million dollars/year.
  • Indirect costs
  • Mothers prophylaxis?
  • Babys treatment for suspected sepsis?

8
Transmission/ Incubation period.
  • Vertical transmission From mother to infant
    occurs shortly before or during delivery.
  • After delivery, person-to-person transmission
    can occur via hand contamination.
  • Incubation Period
  • early onset disease is less than 6 days
  • late onset disease is unknown.

9
Risk factors for Colonization
  • Infants born lt 37weeks
  • Heavily colonized mothers
  • PROM gt 18 hrs.
  • Intrapartum fever 100.4 F
  • Maternal chorioamnionitis
  • GBS bacteruria
  • Maternal age lt 20yrs
  • African American ethnicity

10
Early onset vs. Late onset
  • Occurs in 1st week. Usually before 72hrs
  • Pathophysiology.
    -Colonization.




  • -Immature host defense mech particularly among
    low birth wt infants.
  • 1week to 6months. Usually at 3-4 weeks.
  • Pathopysiology. -Related to
    initial colonization. -Alteration of the mucosa
    barrier by a viral resp tract inf.,weakened host
    defense,decrease amt of maternal antibodies.

11
Early Onset Vs Late Onset
  • Transmission

    -aquired thru vertical transmission.

  • -ascending infection, duration of rupture of
    memb. directly proportional to I.R.


  • -during passage thru a colonized birth
    canal.
  • Transmission -aquired
    thru horizontal transmission
    -nurseries -hospital
    personnel -community

12
Early Onset Vs Late onset
  • Clinical Manifestation

    -Pneumoniarespiratory distress, tachypnea
    cyanosis,hypoxaemia apnea
    -Pulmonary HTN
    -Shock -Poor feeding
    -Abnormal temperature
    -Less often meningitis
  • Clinical manifestation
  • Occult bacteremia, meningitis, ventriculitis, and
    other focal infections, e.g. septic arthritis,
    osteomyelitis.

13
Laboratory Findings
  • Identification of Gm ve cocci in pairs and in
    chains in fluids that are sterile indicate
    invasive disease.

    -CSF,Blood,Pleural
    Fluid,Joint Fluid.
  • Gm ve cocci in gastric or tracheal aspirate,skin
    and mucous memb indicate colonization.
  • Rapid antigen test in CSF.
    -rapid test that identify GBS
    antigen In other body fluids not recommended.

14
LABORATORY fINDINGS
  • Non specific tests
    -CBC Leukocytosis, Lt
    shift, increased band count, Increase I.T ratio
    gt0.20,neutropenia, thrombocytopenia
    . -Incr.
    CRP.
    -Cxray showing
    pneumonia, atelectasis.

15
Differential Diagnosis
  • Sepsis
  • Aspiration pneumonia(meconium)
  • HMD
  • Wet lung(TTNB)
  • Total anomalous pulmonary venous return
  • Poor inspiration film

16
Treatment of GBS
  • Drug of choice when organism has been identified
    is Pen G. 200,000U/kg/day.
  • Empirical Rx Ampicillin Gent.
    -used until GBS has been
    cultured.
  • Also susceptible to
    -Vancomycin

    -Cefotaxime
    -Ceftriaxone

    -Chloramphenicol

17
Treatment
  • Supportive care
    hypoxia- mechanical ventilation

    DIC-Fresh frozen plasma

    Seizures-antiseizure
    medication
    -Increased
    ICP
    SIADH-Fluid restriction

18
Treatment of GBS Meningitis
  • I.V Penicillin G
    -Infants lt7 days 250-300,000U/kg/day.
    -Infants gt 7days 300,000U/kg/day.
  • I.V Ampicillin
    -Infantslt 7days 200-300mg/kg/day.
    -Infants gt7days 300mg/kg/day.

19
Treatment of GBS Meningitis
  • Repeat lumbar puncture 24-48 hrs after
    initiation of Rx.
  • Consultation with a specialist in pediatric I.D
    may be useful.

20
Duration of Rx of GBS
  • Bacteremia 10days.
  • Uncomplicated meningitis 14days.
  • Complicated meningitis
    -Requires prolonged course,guided by
    bacteriologic report.
  • Osteomyelitis,ventriculitis-4weeks.

21
Complications of GBS
  • Mortality rate ranges 5-15 highest in
  • very low birth wt infants
  • Septic shock
  • Delay in instituting antimicrobial Rx.

22
Complications of GBS
  • Neurological sequelae
  • Mental retardation
  • Quadriplegia
  • Hemiplegia
  • Seizures
  • Cortical blindness
  • Bilateral deafness
  • Hydrocephalus
  • SIADH

23
Control Measures
  • Screening based Strategy
  • -All pregnant women _at_35-37weeks,
    Offer prophylaxis to GBS carriers.
    If GBS unknown _at_ onset of
    labor or ROM Rx .
  • Risk factor based strategy
    -Prevention based on presence of
    intrapartum risk factor without screening.

24
Control Measures
  • Important factors of maternal prophylaxis
  • Administer intrapartum antibiotics 4 or more hrs
    before delivery
  • 2 or more doses of Pen.G or Ampicillin.

25
Guidelines
  • Empiric mgt of asymptomatic infants
  • lt35wks whose mom received antibiotic 2 or more
    doses
  • CBC,Bld Cx
  • Observe for 48hrs without antibiotics.

  • gt35wks whose mom received antibiotic 2 or more
    doses
  • No lab eval required
  • Observe for 48hrs without antibiotics.


26
Guidelines
  • Empiric Mgt. (Contd.)
  • For infants gt 35wks whose moms received 1 dose
  • May include CBC,CRP,Bld Cx
  • Observe for 48hrs.

27
Incidence rate (per 1000 live births) of
early-onset GBS disease prior to use of IPC
  • Data Source CDC Publications/Thomason


28
Incidence rate (per 1000 live births) of
early-onset GBS disease by year and site
  • Data Source CDC Publications/Thomason


29
Incidence rate (per 1000 live births) of
early-onset GBS disease at Thomason
  • Data Source Dept. of Pediatrics, Texas tech







30
Incidence Rate of EOGBS Disease vs. of
Hospitals with DX Prevention Policy
31
Prognosis
  • Of all survivors of early or late onset GBS
    meningitis
  • 25-50 have permanent neurological sequelae
  • 1/3 of these patients will have severe blindness,
    deafness,and/or global developmental delay.

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