Neonatal Sepsis and Meningitis Flashcards
Neonatal sepsis
is a clinical syndrome of
systemic illness accompanied by bacteremia occurring in the first month of life.
Early sepsis Pattern
Onset
🧿Acquired before or during delivery (vertical
mother-to-child transmission)
In the 1 st week (usually <72 hr)
Risk factors for early onset sepsis
y Prematurity
y Premature rupture of membranes > 18 hr.
y Chorioamnionitis
y Maternal intrapartum fever ’ y Maternal bacteruria.
-General – socioeconomic status, poor prenatal care,
Organisms of early onset sepsis
y 😱😱😱Group B streptococci (GBS)
😱😱😱y E.Coli
y Listeria monocytogenes
Late and nosocomial sepsis- general
-Develop after delivery from
organisms acquired in the
hospital or the community
After the 1 st week
Late and nosocomial sepsis-risk factor
-y Prematurity.
y Hospitalization
y Umbilical catheterization ,
or poor cord care
y Endotracheal intubation y Mechanical ventilation.
-General – socioeconomic status, poor prenatal care,
Late and nosocomial sepsis -organism
-y 😱😱😱Staphylococcus Aureus.
y Hemophilus influenza
y Klebsiella.
y Pseudomonas.
y Viral or candida
Early-onset sepsis clinical manifestations
🧿frequently manifested as respiratory failure, shock, meningitis (in 30% of cases), disseminated intravascular coagulation, acute tubular necrosis, and symmetrical peripheral gangrene.
🧿Early manifestations—grunting, poor feeding, pallor, apnea, lethargy, hypothermia, or an abnormal cry—may be nonspecific.
🧿Profound neutropenia, hypoxia, and hypotension may be refractory to treatment with broad-spectrum antibiotics, mechanical ventilation, and vasopressors such as dopamine.
🧿Poor Moro and suckling reflexes
Late manifestations
🧿Early manifestations plus more focal infections
🧿Meningitis
🧿Hepatitis Direct hyperbilirubinemia Hepatosplenomegaly
🧿Necrotizing enterocolitis
🧿Sclerema = hardening of the skin ( poor prognostic sign)
🧿Pneumonia
🧿Septic shock / Septic renal failure with oligoanuria and metabolic acidosis
🧿Purpura / DIC
Diagnosis of sepsis
- History : for risk factors
- Clinical picture
- Investigations
a. 😷Sepsis screen: Septicemia is suggested when:
CBC findings
- Leucopenia < 5000/mm 3 (with severe sepsis)
- Toxic granulations in neutrophils.
- Bandemia: Band cells (immature) >20% of total neutrophil count.
- Less commonly leucocytosis (> 30.000 / mm3 )
- Thrombocytopenia Markers of inflammation
- Serial determination of C-reactive protein (CRP)
- ESR
b. 😷Detect causative organism by - Cultures of Blood, CSF, urine, and endotracheal aspirate.
c. 😷Evidence of Multiorgan System Disease
1- Pulmonary: Chest x ray for pneumonia, blood gases
2- CSF analysis, culture and gram stain for meningitis
3- Liver enzymes, bilirubin, ammonia, prothrombin time, PTT
4- Serum urea and electrolytes, blood glucose
False negative Blood Culture
Maternal antibiotics
Small blood sample
Bacteria load, timing of sampling
Antibiotics For early onset sepsis:
🧿Ampicillin plus Gentamicin
🧿Third-generation cephalosporins such as cefotaxime or ceftazidime are valuable additions for treating documented neonatal sepsis and meningitis
🧿-All antibiotics should be given for 10-14 days (21d for meningitis).
Antibiotics For late onset sepsis:
- Vancomycin(as the causetive is staph MRSA) plus Gentamicin
- Third-generation cephalosporins such as cefotaxime or ceftazidime are valuable additions for treating documented neonatal sepsis and meningitis
- All antibiotics should be given for 10-14 days (21d for meningitis).
A. Prophylaxis of sepsis
Maternal intrapartum ampicillin prevent perinatal transmission of GBS
Curative of sepsis
- Incubator care in neonatal intensive care unit (NICU) (See before)
- Specific treatment y Immediate parenteral antibiotics are initiated after taking appropriate cultures.
y Antibiotics are given according to culture and sensitivity(C/S) y While waiting for C/S ; empiric antibiotic combinations is given:
o For early onset sepsis: Ampicillin plus Gentamicin o For late onset sepsis: Vancomycin(or oxacillin) plus Gentamicin o Some experts recommend antifungal prophylaxis with fluconazole for particularly high-risk newborns—that is, those of extremely LBW (<1000 g) and low gestational age (<27 wk).
o Third-generation cephalosporins such as cefotaxime or ceftazidime are valuable additions for treating documented neonatal sepsis and meningitis
2- tx of the complications