Neonatal Infections

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These include:

Syphyllis

Ophthalmia Neonatorum

Neonatal Sepsis

 

Congenital Infections

Syphilis

Description

Most common congenital infection in our setting. Two thirds of affected infants have no clinical signs of congenital syphilis

Signs and Symptoms

• Persistent snuffles
• Erythematous rash, which may be macular or popular and affects the palms and soles
• Osteoporosis and periostitis on x-ray

Investigations

• TPHA
• RPR/VDRL

Treatment

Symptomatic baby 10-day course
Benzyl Penicillin IV 50, 000 U/kg/dose twice a day
Asymptomatic baby + partially or
untreated mother
Single dose Benzathine Penicillin (IM) 50, 000 U/kg
Ophthalmia Neonatorum

Description

Ophthalmia Neonatorum is inflammation of the conjunctiva in the neonatal period due to infection with Neisseria gonorrhoeae. Non-gonococcal conjunctivitis is due to Chlamydia trachomatis, Staphylococcus aureus and Streptococcus pneumoniae.

Signs and Symptoms

• Purulent, copious eye discharge usually in both eyes
• Itching and redness are also present
• The neonate may also present with septicaemia with fever, rash and joint swelling.

Investigations

This is confirmed by taking an eye swab for culturing for Gonorrhoea.

Treatment

Refer to the Table 129 under adult genito-urinary conditions.

Note: The use of antibiotic eye ointments in gonococcal conjunctivitis is of no documented benefit. Systemic treatment is recommended for all symptomatic cases. The baby’s mother and partner(s) should receive syndromic treatment for Gonorrhea and Chlamydia. Breastfeeding mothers should be given Gentamicin and not Ciprofloxacin for gonorrhoea but for Chlamydia give Erythromycin

Neonatal Sepsis

Description

Neonates are particularly susceptible to bacterial sepsis. The highest incidence being in the very low birth weight infants.

Early-onset sepsis
• < 72 hours after birth
• Results from vertical exposure to bacteria before and during birth

Late-onset sepsis
• > 72 hours after birth
• Mostly from organisms acquired by nosocomial transmission
• May also be caused by community acquired organisms

Risk factors

Early-onset sepsis

• Preterm infant
• Prolonged rupture of membranes > 18 hours
• Maternal fever in labour (>38 C)
• Chorioamnionitis
• Maternal colonization with Group B Streptococcus

Late-onset sepsis
• Preterm infant
• Indwelling catheters or tracheal tube
• Prolonged antibiotics
• Damage to skin

Signs and Symptoms

• Usually, non-specific
• Altered behaviour or responsiveness

• Apnoea and bradycardia
• Respiratory distress – increase in oxygen requirement/respiratory support
• Poor feeding, poor suck, vomiting, abdominal distension
• Hypoglycaemia or hyperglycaemia
• Fever, hypothermia, or temperature instability
• Cyanosis or poor colour
• Poor perfusion (CRT>3sec; mottling)
• Hypotension
• Tachycardia
• Circulatory collapse or shock
• Irritability, inactivity, lethargy
• Seizures
• Hypotonia
• Jaundice
• Rash
• Meningitis
• Tense or bulging fontanelle
• Head retraction (Opisthotonus)

Investigations

• Full Blood count
• C-reactive protein
• Blood culture
• Lumbar puncture – if blood culture positive or clinical features of meningitis
• CXR – if indicated
• Tracheal aspirate
• Coagulation screen
• Blood gas
• Placental tissue culture and histopathology
Interpretation of laboratory investigations
Features suggestive of sepsis
• Neutropenia or neutrophilia
• Increased ratio of immature(bands): total neutrophils
• Thrombocytopaenia
• Positive blood culture
• Raised CRP (>10 mg/L)

Treatment

• Supportive care
• Start antibiotics – antibiotic choice depends on local incidence, practice and antibiogram
Duration of Antibiotics
• Blood culture negative, CRP remains normal and no clinical signs of infection – Stop antibiotics at 36-48
hours
• Blood culture negative but CRP raised – treat as infected
• Blood culture positive – treat until clinical improvement and CRP has returned to normal (7-10 days)
• Meningitis – 14-21 days


Antibiotic policy for suspected sepsis
Antibiotics policy is determined by considering the organism known to have caused infection in the neonatal unit/nursery in the last 6 months. This policy should be regularly reviewed and revised as necessary. A disciplined and consistent approach to antibiotic usage is necessary to provide optimal broad-spectrum cover in suspected sepsis and to limit the emergence of resistant organisms in areas of high usage.

Proposed antibiotics
• Decide according to unit cultures and sensitivities
• Early onset sepsis (< 72hrs of age): Benzyl Penicillin and Gentamicin
o Benzyl Penicillin IV 50, 000 U/kg/dose twice a day, increased if necessary to 50, 000 U/kg/dose every
8 hours
AND
o Gentamicin IV 5 mg/kg every 24 hours.
• Late onset sepsis (> 72hrs of age):
o First line: Benzyl Penicillin IV 50, 000 U/kg/dose twice a day, increased if necessary to 50, 000 U/kg/
dose every 8 hours
OR
Cloxacillin IV 50 mg/kg every 12 hours
PLUS
Gentamicin IV 5 mg/kg every 24 hours.
o Second line Antibiotics: Cefotaxime IV 25mg/kg every 12 hours
PLUS
Cloxacillin IV 50 mg/kg every 12 hours
OR
Ciprofloxacin IV 15 mg/kg loading dose then 7.5 mg/kg 1 hourly.
o Third line: Should be guided by blood culture report

Once started, the duration of treatment should be tailored to clinical circumstances. If cultures come back to normal, laboratory indices are normal and the patient no longer shows signs of sepsis, stop antibiotics after 36– 48 hours.In the absence of proven sepsis there is no place for “a course” of prophylactic antibiotics.

Criteria for Commencing Antibiotics in a Baby with Risk of Having an Early Onset Infection

1. Absolute indication for empiric antibiotic treatment
• Maternal invasive bacterial infection requiring antibiotics (eg: septicaemia) – suspected or confirmed (NB: Not prophylaxis)
• Confirmed or suspected infection in twin
• Respiratory distress starting more than 4 hrs after birth
• Mechanical ventilation in a term baby
• Seizures
• Signs of shock
• Home delivery
2. Start antibiotics if two or more are present of:
Antenatal
• Preterm birth following spontaneous labour <37 weeks or Prelabour ROM
• ROM ≥18 hours
• Maternal fever ≥ 38ºC or chorioamnionitis
Postnatal
• Altered behaviour/tone/responsiveness
• Feeding difficulties (e.g. Poor feeding in a term baby) or intolerance
• Respiratory distress
• Apnoea
• Abnormal heart rate (bradycardia or tachycardia)
• Altered glucose homeostasis (hypo/hyperglycaemia)
• Metabolic acidosis
• Temperature abnormality >38º or < 36º not explained by environmental factors

If only one risk factor is present, consider observation for 24 hrs