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Neonatal Sepsis
Davie Kazumba/ Medical
Licentiate practioner
2020
Kazumba 1
Definition & Incidence
 Clinical syndrome of systemic illness
accompanied by bacteremia occurring in
the first month of life
 Incidence
 1-8/1000 live births
 13-27/1000 live births for infants < 1500g
 Mortality rate is 13-25%
 Higher rates in premature infants and those
with early fulminant disease
Kazumba 2
Early Onset
 First 5-7 days of life
 Usually multisystem fulminant illness with
prominent respiratory symptoms (probably due
to aspiration of infected amniotic fluid)
 High mortality rate
 5-20%
 Typically acquired during intrapartum period
from maternal genital tract
 Associated with maternal chorioamnionitis
Kazumba 3
Late Onset
 May occur as early as 5 days but is most
common after the first week of life
 Less association with obstetric
complications
 Usually have an identifiable focus
 Most often meningitis or sepsis
 Acquired from maternal genital tract or
human contact
Kazumba 4
Nosocomial sepsis
 Occurs in high-risk newborns
 Pathogenesis is related to
 the underlying illness of the infant
 the flora in the NICU environment
 invasive monitoring
 Breaks in the barrier function of the skin
and intestine allow for opportunistic
infection
Kazumba 5
Causative organisms
 Primary sepsis
 Group B streptococcus
 Gram-negative enterics (esp. E. coli)
 Listeria monocytogenes, Staphylococcus, other
streptococci (entercocci), anaerobes, H. flu
 Nosocomial sepsis
 Varies by nursery
 Staphylococcus epidermidis, Pseudomonas,
Klebsiella, Serratia, Proteus, and yeast are most
common
Kazumba 6
Risk factors
 Prematurity and low birth weight
 Premature and prolonged rupture of membranes
 Maternal peripartum fever
 Amniotic fluid problems (i.e. mec, chorio)
 Resuscitation at birth, fetal distress
 Multiple gestation
 Invasive procedures
 Galactosemia
 Other factors: sex, race, variations in immune
function, hand washing in the NICU
Kazumba 7
Clinical presentation
 Clinical signs and symptoms are
nonspecific
 Differential diagnosis
 RDS
 Metabolic disease
 Hematologic disease
 CNS disease
 Cardiac disease
 Other infectious processes (i.e. TORCH)
Kazumba 8
Clinical presentation
 Temperature irregularity (high or low)
 Change in behavior
 Lethargy, irritability, changes in tone
 Skin changes
 Poor perfusion, mottling, cyanosis, pallor, petechiae, rashes,
jaundice
 Feeding problems
 Intolerance, vomiting, diarrhea, abdominal distension
 Cardiopulmonary
 Tachypnea, grunting, flaring, retractions, apnea, tachycardia,
hypotension
 Metabolic
 Hypo or hyperglycemia, metabolic acidosis
Kazumba 9
Diagnosis
 Cultures
 Blood
 Confirms sepsis
 94% grow by 48 hours of age
 Urine
 Don’t need in infants <24 hours old because UTIs are
exceedingly rare in this age group
 CSF
 Controversial
 May be useful in clinically ill newborns or those with positive
blood cultures
Kazumba 10
Adjunctive lab tests
 White blood cell count and differential
 Neutropenia can be an ominous sign
 I:T ratio > 0.2 is of good predictive value
 Serial values can establish a trend
 Platelet count
 Late sign and very nonspecific
 Acute phase reactants
 CRP rises early, monitor serial values
 ESR rises late
 Other tests: bilirubin, glucose, sodium
Kazumba 11
Radiology
 CXR
 Obtain in infants with respiratory symptoms
 Difficult to distinguish GBS or Listeria
pneumonia from uncomplicated RDS
 Renal ultrasound and/or VCUG in infants
with accompanying UTI
Kazumba 12
RDS vs. GBS pneumonia???
QuickTime™ and a
TIFF (Uncompressed) decompressor
are needed to see this picture.
Kazumba 13
Maternal studies
 Examination of the placenta and fetal
membranes for evidence of
chorioamnionitis
Kazumba 14
Management
 Antibiotics
 Primary sepsis: ampicillin and gentamicin
 Nosocomial sepsis: vancomycin and
gentamicin or cefotaxime
 Change based on culture sensitivities
 Don’t forget to check levels
Kazumba 15
Supportive therapy
 Respiratory
 Oxygen and ventilation as necessary
 Cardiovascular
 Support blood pressure with volume expanders and/or
pressors
 Hematologic
 Treat DIC with FFP and/or cryo
 CNS
 Treat seizures with phenobarbital
 Watch for signs of SIADH (decreased UOP, hyponatremia)
and treat with fluid restriction
 Metabolic
 Treat hypoglycemia/hyperglycemia and metabolic acidosis
Kazumba 16
GBS Prophylaxis
 GBS is the most common cause of early-
onset sepsis
 0.8-5.5/1000 live births
 Fatality rate of 5-15%
 10-30% of women are colonized in the
vaginal and rectal areas
 Most mothers are screened at 35-37
weeks gestation
Kazumba 17
QuickTime™ and a
TIFF (Uncompressed) decompressor
are needed to see this picture.
Kazumba 18

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Neonatal-Sepsis.ppt

  • 1. Neonatal Sepsis Davie Kazumba/ Medical Licentiate practioner 2020 Kazumba 1
  • 2. Definition & Incidence  Clinical syndrome of systemic illness accompanied by bacteremia occurring in the first month of life  Incidence  1-8/1000 live births  13-27/1000 live births for infants < 1500g  Mortality rate is 13-25%  Higher rates in premature infants and those with early fulminant disease Kazumba 2
  • 3. Early Onset  First 5-7 days of life  Usually multisystem fulminant illness with prominent respiratory symptoms (probably due to aspiration of infected amniotic fluid)  High mortality rate  5-20%  Typically acquired during intrapartum period from maternal genital tract  Associated with maternal chorioamnionitis Kazumba 3
  • 4. Late Onset  May occur as early as 5 days but is most common after the first week of life  Less association with obstetric complications  Usually have an identifiable focus  Most often meningitis or sepsis  Acquired from maternal genital tract or human contact Kazumba 4
  • 5. Nosocomial sepsis  Occurs in high-risk newborns  Pathogenesis is related to  the underlying illness of the infant  the flora in the NICU environment  invasive monitoring  Breaks in the barrier function of the skin and intestine allow for opportunistic infection Kazumba 5
  • 6. Causative organisms  Primary sepsis  Group B streptococcus  Gram-negative enterics (esp. E. coli)  Listeria monocytogenes, Staphylococcus, other streptococci (entercocci), anaerobes, H. flu  Nosocomial sepsis  Varies by nursery  Staphylococcus epidermidis, Pseudomonas, Klebsiella, Serratia, Proteus, and yeast are most common Kazumba 6
  • 7. Risk factors  Prematurity and low birth weight  Premature and prolonged rupture of membranes  Maternal peripartum fever  Amniotic fluid problems (i.e. mec, chorio)  Resuscitation at birth, fetal distress  Multiple gestation  Invasive procedures  Galactosemia  Other factors: sex, race, variations in immune function, hand washing in the NICU Kazumba 7
  • 8. Clinical presentation  Clinical signs and symptoms are nonspecific  Differential diagnosis  RDS  Metabolic disease  Hematologic disease  CNS disease  Cardiac disease  Other infectious processes (i.e. TORCH) Kazumba 8
  • 9. Clinical presentation  Temperature irregularity (high or low)  Change in behavior  Lethargy, irritability, changes in tone  Skin changes  Poor perfusion, mottling, cyanosis, pallor, petechiae, rashes, jaundice  Feeding problems  Intolerance, vomiting, diarrhea, abdominal distension  Cardiopulmonary  Tachypnea, grunting, flaring, retractions, apnea, tachycardia, hypotension  Metabolic  Hypo or hyperglycemia, metabolic acidosis Kazumba 9
  • 10. Diagnosis  Cultures  Blood  Confirms sepsis  94% grow by 48 hours of age  Urine  Don’t need in infants <24 hours old because UTIs are exceedingly rare in this age group  CSF  Controversial  May be useful in clinically ill newborns or those with positive blood cultures Kazumba 10
  • 11. Adjunctive lab tests  White blood cell count and differential  Neutropenia can be an ominous sign  I:T ratio > 0.2 is of good predictive value  Serial values can establish a trend  Platelet count  Late sign and very nonspecific  Acute phase reactants  CRP rises early, monitor serial values  ESR rises late  Other tests: bilirubin, glucose, sodium Kazumba 11
  • 12. Radiology  CXR  Obtain in infants with respiratory symptoms  Difficult to distinguish GBS or Listeria pneumonia from uncomplicated RDS  Renal ultrasound and/or VCUG in infants with accompanying UTI Kazumba 12
  • 13. RDS vs. GBS pneumonia??? QuickTime™ and a TIFF (Uncompressed) decompressor are needed to see this picture. Kazumba 13
  • 14. Maternal studies  Examination of the placenta and fetal membranes for evidence of chorioamnionitis Kazumba 14
  • 15. Management  Antibiotics  Primary sepsis: ampicillin and gentamicin  Nosocomial sepsis: vancomycin and gentamicin or cefotaxime  Change based on culture sensitivities  Don’t forget to check levels Kazumba 15
  • 16. Supportive therapy  Respiratory  Oxygen and ventilation as necessary  Cardiovascular  Support blood pressure with volume expanders and/or pressors  Hematologic  Treat DIC with FFP and/or cryo  CNS  Treat seizures with phenobarbital  Watch for signs of SIADH (decreased UOP, hyponatremia) and treat with fluid restriction  Metabolic  Treat hypoglycemia/hyperglycemia and metabolic acidosis Kazumba 16
  • 17. GBS Prophylaxis  GBS is the most common cause of early- onset sepsis  0.8-5.5/1000 live births  Fatality rate of 5-15%  10-30% of women are colonized in the vaginal and rectal areas  Most mothers are screened at 35-37 weeks gestation Kazumba 17
  • 18. QuickTime™ and a TIFF (Uncompressed) decompressor are needed to see this picture. Kazumba 18