Neonatal sepsis (NS)

• Neonatal sepsis (NS) is defined as clinical

syndrome of bacteremia with systemic signs
and symptoms of infection in the first four
weeks of life.
 ETIOLOGY
• Common organisms identified:
• 1. Escherichia coli.
• 2. Group B Streptococci.
• 3. Listeria monocytogenes.
 4.Others:
 Coagulase negative staphylococci.
 Streptococcus pneumoniae.
 Klebsiella pneumoniae.
 Acinetobacter species.
 Pseudomonas aeruginosa.
 Candida.
 EPIDEMIOLOGY
• Incidence: 1-8 cases per 1,000 live births.
• Mortality: 13-70% world wide.
• 13-15% of all neonatal deaths (USA) (8 th
cause).
• Sex: Males > Females.
• Age: premature infants
 Pathogenesis
• Neonatal infections are unique in several ways:
1. Infectious agents can be transmitted from the mother to the fetus or newborn infant by
diverse modes.
2. Newborn infants are less capable of responding to infection because of 1 or more
immunologic deficiencies.
3. Coexisting conditions often complicate the diagnosis and management of neonatal
infections.
4. The clinical manifestations of newborn infections vary and include subclinical infection,
mild to severe manifestations of focal or systemic infection, and, rarely, congenital
syndromes resulting from in utero infection. The timing of exposure, inoculum size, immune
status, and virulence of the etiologic agent influence the expression of disease.
5. Maternal infection that is the source of transplacental fetal infection is often undiagnosed
during pregnancy because the mother was either asymptomatic or had nonspecific signs
and symptoms at the time of acute infection.
6. A wide variety of etiologic agents infect the newborn, including bacteria, viruses, fungi,
protozoa, and mycoplasmas.
7. Immature, very low birthweight (VLBW) newborns have improved survival but remain in the
hospital for a long time in an environment that puts them at continuous risk for acquired
infections.
 Classification
• Neonatal sepsis include the following:
• Congenital infection —major risk factor is maternal
infection.
 Early-onset sepsis (birth to 7 days)—transplacental,
ascending, or intrapartum.
 manifests as: 1. Pneumonia (Frequently) 2. Less commonly
as: • Septicemia. • Meningitis.
 Late-onset sepsis (8 to 28 days)—acquired in hospital,
home, or community
 manifests as: 1.Septicemia. 2.hematogenous seeding may
result in focal infections, such as meningitis (in 75% of
cases), osteomyelitis (group B streptococci, S. aureus),
arthritis (gonococcus, S. aureus, Candida albicans, gram-
negative bacteria), and urinary tract infection (gram-
negative bacteria).
 Early Versus Late Neonatal Sepsis

Risk Factors Pathogens Symptoms Treatment

Prematurity #1 Most commonly: 95% show symptoms within Ampicillin and gentamicin ×
Chorioamnionitis Escherichia coli and GBS first 72 h of life 48–72 h for rule out, 7–10 d
Prolonged rupture Also, Streptococcus sp., Bacteremia in 80% if positive cultures or high
of membranes Listeria monocytogenes, Pneumonia in 7%–10% degree of suspicion
(>18 h) and nontypeable If bacteremia, meningitis in Treat meningitis × 14–21 d
Maternal Haemophilus influenzae 5%–15% Mortality 5%–20%
Early onset
colonization with Nonspecific symptoms most
known pathogens common—in severe cases,
(e.g., GBS) apnea, hypotension, DIC

Prematurity Coagulase negative Onset more insidious, fever Treatment based on

Invasive Staphylococcus aureus frequent culture-proven or
procedures and most common (CONS) 66% have bacteremia, suspected pathogen
Late onset devices (e.g. Others: S. aureus, GBS, 20%–30% have meningitis Handwashing most
catheters, Enterococcus, Candida, E. effective intervention to
ventilators, VP Coli decrease nosocomial
shunts) infection rate
DIC, disseminated intravascular coagulation; GBS, group B Streptococcus; VP, ventriculoperitoneal.
 CLINICAL FEATURES
• Manifestations of neonatal sepsis are usually VAGUE and
demand A HIGH INDEX OF SUSPICION for early diagnosis.
• Most common manifestations include:
• 1. Respiratory distress in early onset NS.
• 2. Altered feeding behavior in a well established feeding
newborn (aspiration, vomiting, etc).
• 3. Baby who was active, suddenly or gradually becomes
lethargic, inactive or unresponsive and refuses to suckle.
• 4. Temperature instability: Hypo- or hyperthermia.
• 5. Skin: Poor peripheral perfusion, cyanosis, pallor,
petechiae, rashes, or jaundice.
• 6. Metabolic:Hypo- or hyperglycemia or metabolic acidosis.
 Diagnosis
 A. Non-specific:
• White blood cell count and
differential:
 Neutropenia can be a threatening
sign (< 1,800/cmm).
 Immature to Total neutrophil (I:T)
ratio ≥ 0.2 is predictive (Normal: ˂
0.16).
• Acute phase reactants:
 C-Reactive Protein (CRP): rises
early.
 ESR rises > 15 mm 1 st hr.
• Platelet count:
 Decreases, a late sign and non-
specific.
• Others: – Bilirubin, glucose,
sodium.
 B. Definitive, specific:
Cultures:
• Blood: Confirms sepsis.
• Urine:
• CSF: May be useful in clinically
ill newborns or those with
positive blood cultures.
 C: Radiology
• Chest X-Ray: – For infants
with respiratory symptoms.
• Renal ultrasound: – For
infants with accompanying
UTI.
• CT scan: – For infants with
probable meningitis or
seizures.
 Differential Diagnosis
• Respiratory distress syndrome (RDS).
• Metabolic diseases.
• Hematologic diseases.
• CNS diseases.
• Cardiac diseases.
• Other infections (e.g. ToRCH infections).
 TREATMENT
• 1. Antibiotics:
 Should be based on culture & sensitivity
 Antibiotics are used to suppress bacterial growth,
allowing the infant's defense mechanisms time to
respond.
• 2. Supportive therapy
 In addition, support measures, such as assisted
ventilation and cardiovascular support, are
equally important to the management of the
infant.
• 1. Antibiotics:
• A combination of ampicillin and an
aminoglycoside (usually gentamicin) for 10 to 14
days is effective treatment against most
organisms responsible for early-onset sepsis.
• The combination of ampicillin and cefotaxime
also is proposed as an alternative method of
treatment.
• If meningitis is present, the treatment should be
extended to 21 days or 14 days after a negative
result from a CSF culture.
• 2. Supportive therapy
• Respiratory: Oxygen and ventilation as necessary.
• Cardiovascular: Support blood pressure with
volume expanders.
• Hematologic: Treat DIC.
• CNS: Treat seizures with phenobarbital.
• Metabolic: Correct hypo-/hyperglycemia and
metabolic acidosis.
 PREVENTION
• Good antenatal care.
• Maternal infections diagnosed and treated
early.
• Babies should be breastfed early.
• Infection control policies applied in the unit
THANKS FOR YOUR
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