Need to distinguish between benign conditions/normal variants and critical neonatal illness
Signs and symptoms of critical neonatal illness often nonspecific
Red flags: poor feeding, vomiting, lethargy, cyanosis, apnea, seizures, hypo/hyperthermia, excessive weight loss
Table 11.1 Normal Variants | ||||||||
---|---|---|---|---|---|---|---|---|
|
Table 11.2 Benign Conditions | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
|
Table 11.3 Transient Benign Cutaneous Lesions | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Due to Staphylococcus aureus colonization in first few weeks of life
Vesicles, pustules, and bullae arising on normal or slightly erythematous skin; bullae rupture easily to leave superficial erosion with a collarette of scale
Common sites: periumbilical region, neck folds, axillae, and diaper area
Diagnosis: Gram stain and culture of contents of bullae or pustule
Treatment: topical antibiotic ointment if localized, but most infants require oral therapy with cloxacillin or a cephalosporin
Due to endotoxin from certain Staphylococcus aureus strains
Onset between 3-7 days with fever, irritability, cutaneous tenderness and erythema; flaccid bullae that rapidly denude on erythematous base
Nikolsky sign: rubbing of skin causes skin separation
Treatment: intravenous cloxacillin
Due to C. albicans often in first weeks of life; often involves diaper area and oral mucosa (thrush)
Erythematous scaly patches with characteristic satellite papules and pustules
Topical therapy with an imidazole cream for skin rash
HSV 1 or 2; 80% due to HSV 2—poorer prognosis
Route of transmission usually occurs during delivery (85%), but may occur in utero (5%) or postnatally (10%)
Highest risk of transmission in pregnant women with primary infection in third trimester (50%)
May occur in absence of skin lesions; need high index of suspicion
60-80% of infected infants born to mothers with no history of genital herpes
Presents at ˜ day 10-11
Discrete vesicles and keratoconjunctivitis
Risk of neurologic impairment 30-40% if do not receive antiviral therapy
75% progress to either CNS or disseminated disease without antiviral treatment; therefore, all require aggressive treatment
May present with seizures (50%), lethargy, irritability, tremors, poor feeding, temperature instability, bulging fontanelle, and pyramidal tract signs
CSF culture positive in 25-40%; generally have proteinosis and pleocytosis (50-100 WBC/mm3) with predominantly mononuclear cells
40% do not have cutaneous vesicles at presentation
High incidence of morbidity and mortality despite treatment
Present generally at day 9-11 of life
Multiple organ involvement and signs: irritability, seizures, respiratory distress, jaundice, bleeding diatheses, shock, and often vesicular rash
22% of HSV-infected neonates
70% survival with treatment; 15% neurologic abnormalities
Intravenous acyclovir for 14-21 days (21 days if CNS involvement or disseminated disease)
Monitor neutrophil count if receiving IV acyclovir (neutropenia)
Self-limited inflammatory condition, usually appears within 3-8 weeks of life
Well-demarcated areas of erythema covered by greasy scale over scalp (cradle cap), face, diaper area, trunk, and proximal flexures
Treatment: olive oil to loosen scales on scalp and mild topical hydrocortisone cream or ointment to involved areas
Imbalance between production and elimination of bilirubin
Occurs in 60-70% of term infants and most premature infants
Visual estimation of degree of jaundice poor
Severe jaundice and kernicterus can occur in full-term healthy newborns with no apparent hemolysis or any cause other than breastfeeding
Increased risk of kernicterus with G6PD deficiency
Assess adequacy of breastfeeding
Weight loss (average 6.1% by day 3)
Urine output (4-6 wet diapers) and 3-4 stools/day
Acute bilirubin encephalopathy
Clinical neurologic findings caused by bilirubin toxicity
Early phase: lethargy, hypotonia, poor feeding
Intermediate phase: stupor, irritability, and hypertonia; fever, high-pitched cry; may alternate with drowsiness and hypotonia
Late phase: pronounced retrocollis-opisthotonos, shrill cry, no feeding, apnea, fever, deep stupor to coma, seizures → death
Predischarge total serum bilirubin in high-risk zone
Jaundice in first 24 hours
Gestational age 35-36 weeks
Previous sibling requiring phototherapy
ABO incompatibility with positive Coombs or other hemolytic disease
Cephalohematoma or significant bruising
Adequacy of breastfeedingFull access? Get Clinical Tree