Other Pediatric Bacterial Infections

Chlamydia trachomatis

  • Chlamydia trachomatis is an obligate intracellular bacteria.
  • Transmission: Perinatal transmission (most important in pediatrics) occurs when an infected mother transmits bacteria to the infant during passage through birth canal. Risk: 30–50% of exposed infants. Rarely: postnatal transmission via caregivers.

Manifestations

  1. Ophthalmia neonatorum (Neonatal conjunctivitis):
    • Onset: 5–14 days after birth (later than gonococcal).
    • Symptoms: eye discharge (watery to mucopurulent), eyelid swelling, conjunctival hyperemia. If untreated → risk of corneal damage and scarring.
  2. Chlamydial pneumonia:
    • Onset: 2–12 weeks of age.
    • Features: Afebrile pneumonia with staccato cough, tachypnea, nasal congestion. Inspiratory crackles, hyperinflated chest. Often associated with conjunctivitis history.
    • Labs: eosinophilia (up to 400–500 cells/μL).
  3. Other: Otitis media, pharyngitis, though less common.

Diagnosis and Treatment

  • Diagnosis: Conjunctival / nasopharyngeal swabs → Nucleic acid amplification test (NAAT) (gold standard). Culture (less used now). Chest X-ray in pneumonia: hyperinflation, bilateral interstitial infiltrates.
  • Treatment: Oral erythromycin (50 mg/kg/day divided 6 hourly for 14 days). Alternative: Oral azithromycin (20 mg/kg once daily for 3 days). Topical therapy alone is not sufficient.
  • Prevention: Screening and treatment of pregnant women. Prophylactic eye drops at birth do not prevent chlamydial conjunctivitis (they mainly prevent gonococcal infection).

Gonococcal

Chlamydia Trachomatis

Neisseria Gonorrhoeae

  • N. gonorrhoeae infection in a newborn usually involves the eyes (Gonococcal Ophthalmia Neonatorum).
  • Transmission: During passage through the birth canal.
  • Features: Usually present within the first 5 days (2 – 5 days) of life. Characterized initially by a clear, watery discharge, which rapidly becomes purulent. Marked conjunctival hyperemia and eye swelling.
  • Complications: Untreated infections can spread to the cornea (keratitis) and anterior chamber of the eye causing corneal perforation and blindness.
  • First line treatment is ceftriaxone 25-50 mg/kg single dose IV or IM.
  • Infants with gonococcal ophthalmia should receive eye irrigations with saline solution at frequent intervals.
  • Infants should be hospitalized and evaluated for disseminated disease (sepsis, arthritis, meningitis and others sexually transmitted diseases).
  • Prevention: Topical prophylaxis (Ophthalmic ointment) with erythromycin or tetracycline is recommended for all newborns.

Neonatal Sepsis

Classification by Age of Onset

  1. Early-onset sepsis: usually acquired before or during delivery usually within the first 72 hr (up to the end of the 1st wk). Source is usually maternal. Usually multisystemic.
  2. Late-onset sepsis: after 72 hr (4 - 28) of life. Usually due to either nosocomial or community-acquired infection. Multisystemic or localized.
  3. Very-late-onset sepsis: after (>28 days in preterm/VLBW infants still in NICU). Organisms are usually multidrug resistant.

Risk Factors for Early-Onset Sepsis (within 72 hr)

  • Maternal: Maternal features of sepsis or chorioamnionitis; Prolonged rupture of the membrane (> 18 hr); Prolonged labor(more than 12 hours); Frequent vaginal examinations; GBS colonization; Previous infant with early onset GBS disease; Inadequate antibiotic administration before delivery.
  • Neonatal: Prematurity and LBW; infants that need resuscitation at birth; Invasive procedures (monitoring, respiratory support); Males > 4 times than females; black infants > white; Improper hand washing. (doctors ,nurses family members ..etc).

Clinical Features

Neonates may have nonspecific signs or focal signs initially.

  • General: “not doing well”, temperature instability (fever or hypothermia), poor feeding and edema.
  • Respiratory: Apnea, dyspnea, tachypnea, retractions, flaring, grunting, cyanosis.
  • CVS: Pallor, mottling, cold, clammy skin, tachycardia, bradycardia, hypotension.
  • GIT: Abdominal distention, vomiting, diarrhea, HSM.
  • CNS: Irritability, lethargy, tremors, seizures, hyporeflexia, hypotonia, abnormal Moro reflex, bulging fontanel.
  • Hematologic: Jaundice, splenomegaly, pallor, petechiae, purpura, bleeding.
  • Renal: Oliguria.

Organisms

  • Early Onset: GBS, E.coli, Listeria monocytogenes, HSV, Chlamydia trachomatis.
  • Late Onset: Coagulase negative staphylococci, Pseudomonas, Klebsiella, Fungal infections (e.g. candida albicans).
  • Late-Onset Presentations: Meningitis, Lower respiratory tract infection, UTI, Skin infection, Gastroenteritis, Osteomylitis, Systemic candidates.

Investigations (Septic Screen)

  1. CBP & Blood film.
  2. CRP & ESR.
  3. Blood culture (obtain before antibiotics).
  4. CSF exam & culture (important if meningitis suspected).
  5. GUE & culture.
  6. CXR, if pneumonia is suspected.
  7. PCR or DNA testing for specific infections.

Management

It is generally involve parenteral antibiotics & supportive care:-

  • Antibiotics: Given IV immediately after blood culture.
    • Empirical: Ampicillin + Aminoglycoside (gentamycin) or 3rd generation Cephalosporins.
    • Staph: anti-staphylococcal penicillin or Vancomycin.
    • Anaerobic: metronidazole or clindamycin.
  • Supportive: Fluids & electrolytes, correction of hypoglycemia & acidosis. Ventilatory support (O₂ & humidification). Management of seizure, jaundice, & DIC. Trial of IVIG, Granulocyte transfusion. (to abolish sepsis induced neutropenia ) .

Complications

  • Systemic: Shock. HF, respiratory failure, pulmonary hypertension, ARF, liver dysfunction, cerebral edema & thrombosis, adrenal hemorrhage, BM dysfunction, and DIC.
  • Meningitis: ventriculitis, cerebritis, and brain abscess.
  • Bacteremia: endocarditis, septic emboli, abscess formation, septic arthritis, and osteomyelitis.
  • Candidemia: vasculitis, endocarditis, endophthalmitis, abscesses in kidneys/liver/lungs/brain.

Prevention

  • Maternal immunization against preventable intrauterine infections .
  • Intrapartum penicillin to the mother can prevent perinatal and postnatal GBS infections .
  • Aggressive treatment of chorioamnionites .
  • Prevention of nosocomial infection .
  • Prophylactic administration of fluconazole during the first six weeks of life