Fetal and Neonatal Care
Birth injuries: brachial plexus palsy, cephalohematoma, caput succedaneum
Birth injuries encompass mechanical trauma sustained during labor and delivery. Three high-yield entities for the ABP exam are brachial plexus palsy (BPP), cephalohematoma, and caput succedaneum.
— Macrosomia (birth weight >4,000 g, especially >4,500 g)
— Shoulder dystocia
— Prolonged or difficult labor
— Instrumental delivery (vacuum, forceps)
— Breech presentation (especially BPP)

A detailed birth history is essential when evaluating any suspected birth injury:
— Shoulder dystocia: documented? Maneuvers used (McRoberts, suprapubic pressure, delivery of posterior arm)?
— Instrumentation: vacuum (associated with cephalohematoma, subgaleal hemorrhage), forceps (bruising, facial nerve palsy, cephalohematoma)

— Soft, boggy, superficial swelling of the scalp
— Located ABOVE the periosteum in the subcutaneous tissue
— CROSSES suture lines — this is the defining feature
— Present at birth, often over the presenting part
— May have overlying ecchymosis or petechiae
— Resolves spontaneously within 24–48 hours
— Subperiosteal hemorrhage — blood collects between periosteum and skull bone
— Does NOT cross suture lines — confined to one cranial bone (most commonly parietal)
— May NOT be present at birth — appears hours after delivery and enlarges over first 24–48 hours
— Firm, fluctuant, well-circumscribed
— Can calcify if large; may take weeks to months to resolve
— Asymmetric posture/movement of the upper extremities
— Erb palsy (C5–C6): "waiter's tip" — arm adducted, internally rotated, forearm pronated, wrist flexed; absent Moro on affected side
— Klumpke palsy (C8–T1): rare; "claw hand," absent grasp reflex, ± ipsilateral Horner syndrome
— Total plexus palsy (C5–T1): flaccid arm, no movement
Board pearl: Asymmetric Moro reflex is the classic exam clue for BPP on board questions

— Diagnosis is CLINICAL — no imaging or labs needed
— If extensive bruising → monitor for indirect hyperbilirubinemia (↑ bilirubin from resorption of extravasated blood)
— Diagnosis is usually clinical based on characteristic exam (does not cross sutures, appears after birth)
— Imaging: skull radiograph or CT ONLY if fracture suspected (underlying linear skull fracture present in ~5–18% of cephalohematomas)
— Labs: monitor transcutaneous or serum bilirubin — cephalohematomas are a significant risk factor for neonatal hyperbilirubinemia
— CBC if very large → may contribute to anemia
— Board pearl: Do NOT aspirate a cephalohematoma — risk of introducing infection far outweighs any benefit; allow spontaneous resorption
— Subgaleal hemorrhage: blood beneath the aponeurosis → diffuse, fluctuant swelling that CROSSES suture lines AND increases in size
— Unlike caput, subgaleal hemorrhage is progressive and can cause hypovolemic shock
— Associated with vacuum-assisted delivery
— Requires urgent volume resuscitation and monitoring

— Test each muscle group: deltoid (C5), biceps (C5–C6), wrist extensors (C6–C7), finger extensors (C7), hand intrinsics (C8–T1)
— Check Moro, biceps, grasp reflexes bilaterally
— Assess for Horner syndrome (ptosis, miosis, anhidrosis) → suggests C8–T1 involvement or avulsion
— Ipsilateral clavicle fracture (palpate for crepitus, tenderness, step-off) — most commonly associated fracture
— Humeral fracture — swelling, pseudoparalysis
— Phrenic nerve palsy (C3–C5) → ipsilateral diaphragm paralysis → tachypnea, asymmetric chest rise
— X-ray of clavicle and humerus to exclude fracture
— Chest X-ray if respiratory distress → elevated hemidiaphragm suggests phrenic nerve injury
— MRI of brachial plexus if no improvement by 1–3 months → evaluate for nerve root avulsion
— EMG/nerve conduction studies at 3–4 weeks if needed to assess severity (denervation potentials)

— Reassurance — resolves within 24–72 hours
— No intervention needed
— Monitor bilirubin only if significant bruising coexists
— Observation — most resolve over 2 weeks to 3 months
— Do NOT aspirate, incise, or apply pressure bandages
— Monitor for jaundice: bilirubin check per hour-specific nomogram; earlier phototherapy threshold may apply because cephalohematoma is a risk factor for significant hyperbilirubinemia
— Monitor head circumference serially — enlarging swelling raises concern for re-bleeding or underlying fracture
— Large cephalohematomas → CBC to assess for anemia; rare need for transfusion
— Calcification may occur, creating a hard, bony ridge that can persist for months but eventually remodels
— Board pearl: The ABP frequently tests that cephalohematoma is a risk factor for hyperbilirubinemia requiring phototherapy — especially in combination with other risk factors (prematurity, ABO incompatibility, G6PD deficiency)

— Gentle handling of the affected arm
— Avoid traction on the limb
— Pin the sleeve to the shirt or gentle immobilization in a neutral position for the first 1–2 weeks to reduce pain and further stretching
— Parents should be taught passive range-of-motion (ROM) exercises starting at ~2–3 weeks of age to prevent joint contractures
— Begin formal PT by 2–4 weeks of life
— Focus on passive ROM (shoulder abduction, external rotation, forearm supination) to maintain joint mobility
— Active-assisted exercises as reinnervation occurs
— Frequent reassessment in first 3 months: serial exam tracking biceps function recovery
— If biceps function does not recover by 3–6 months → refer to a pediatric nerve/hand surgeon for consideration of microsurgical repair

— No biceps recovery by 3–6 months (depending on center)
— Total plexus palsy with Horner syndrome (suggests root avulsion → less likely to recover spontaneously)
— Evidence of nerve root avulsion on MRI
— Nerve grafting (sural nerve graft to bridge gap)
— Neurolysis (release of scar tissue)
— Nerve transfer (redirect functioning nerve to denervated muscle)
— Secondary procedures: tendon transfers, osteotomies for persistent contractures or skeletal deformity (posterior shoulder subluxation)
— Shoulder dysplasia and posterior subluxation/dislocation (from muscle imbalance → internal rotation contracture)
— Limb-length discrepancy (affected arm shorter)
— Reduced strength and ROM even after recovery
— Psychosocial impact: body image, functional limitations in childhood activities

— Bilirubin risk peaks at 3–5 days as the hematoma is resorbed → ensure close outpatient follow-up for jaundice if early discharge
— Newborn exam: asymmetric Moro is the most reliable clue; asymmetric tonic neck reflex may also be absent
— Pain may cause pseudoparalysis → differentiate from true nerve injury by observing over days as pain subsides
— Must rule out clavicle and humeral fractures in the first 24–48 hours
— Early parental counseling is essential: most cases recover, but set expectations for close follow-up

— By 2–4 weeks: may feel firm/calcified at edges with soft center → parents may worry about a "dent" in the skull → reassure that this is normal remodeling and resolves by 3–6 months
— Rarely: organized cephalohematoma persists → may require surgical correction for cosmesis if very large, though this is uncommon
— Late-presenting anemia or prolonged jaundice → consider unresolved cephalohematoma or coagulopathy
— 1–3 months: most upper trunk injuries show progressive recovery; absence of biceps function is concerning
— 3–6 months: decision window for surgical referral
— 6–12 months: secondary shoulder contractures may begin → monitor with serial ROM measurement
— Toddler/preschool: children adapt remarkably; occupational therapy focuses on functional activities, fine motor, and bilateral coordination
— School age: may have persistent internal rotation contracture, supination deficit → affects activities (reaching overhead, carrying, sports)

— Rarely significant; overlying skin breakdown (from prolonged pressure or vacuum) → infection risk
— Extensive caput with ecchymosis → ↑ bilirubin load → watch for severe hyperbilirubinemia
— Hyperbilirubinemia: the most common and testable complication; breakdown of trapped RBCs → ↑ unconjugated bilirubin
— Anemia: large hematomas can sequester significant blood volume
— Infection: extremely rare but can occur → presents as enlarging, warm, erythematous swelling with fever → aspirate ONLY if infection suspected, send for culture
— Underlying skull fracture: typically linear, non-displaced → usually no treatment needed; depressed fractures rare
— Calcification: cosmetic concern; remodels over months
— This is the emergency that must NOT be missed
— Blood accumulates in the potential space beneath the galea aponeurotica → can hold the neonate's ENTIRE blood volume
— Signs: progressive, fluctuant boggy swelling crossing sutures, ↑ head circumference, pallor, tachycardia, hypotension
— Management: emergent volume resuscitation, blood products, NICU admission
— Board pearl: Vacuum delivery + progressive scalp swelling + hemodynamic instability = subgaleal hemorrhage until proven otherwise

— Clavicle fracture (most common associated injury, ~10% of BPP)
— Humeral fracture (less common)
— Phrenic nerve palsy (C3–C5): diaphragm paralysis → respiratory distress, elevated hemidiaphragm on CXR; occurs in ~5% of BPP cases
— Facial nerve palsy: may coexist with difficult delivery
— Cervical spinal cord injury (very rare): suspect if bilateral upper extremity weakness or lower extremity involvement
— Respiratory distress with ipsilateral BPP → evaluate for phrenic nerve palsy (CXR → fluoroscopy/ultrasound of diaphragm)
— No improvement or worsening at 4–6 weeks → ensure correct diagnosis; consider alternative etiologies (fracture, CNS lesion)
— Total plexus palsy with Horner syndrome at birth → early neurosurgical/nerve specialist referral (high likelihood of avulsion)

| • The ABP expects you to distinguish these entities by anatomy and clinical features: | |||
| Feature | Caput | Cephalohematoma | Subgaleal hemorrhage |
| • Layer: Caput → subcutaneous/above periosteum; Cephalohematoma → subperiosteal; Subgaleal → sub-aponeurotic | |||
| • Crosses sutures: Caput → YES; Cephalohematoma → NO; Subgaleal → YES | |||
| • Timing: Caput → present at birth, resolves quickly; Cephalohematoma → appears after birth, enlarges over hours; Subgaleal → progressive, relentless | |||
| • Consistency: Caput → soft, pitting; Cephalohematoma → firm, fluctuant; Subgaleal → boggy, diffuse, ballotable | |||
| • Hemodynamic impact: Caput → none; Cephalohematoma → rare mild anemia; Subgaleal → potentially catastrophic hemorrhage | |||
| • Other differentials for scalp swelling: | |||
| — Craniosynostosis (ridging along sutures, abnormal head shape) | |||
| — Dermoid cyst (midline or lateral, non-tender, present from birth but doesn't change rapidly) | |||
| — Encephalocele (midline defect, transilluminates, covered by skin) | |||
| • Board pearl: If a scalp swelling crosses suture lines AND is getting bigger → it is NOT a cephalohematoma; consider caput (resolving) vs subgaleal hemorrhage (expanding → emergency) |

— Pseudoparalysis from pain → infant does not move arm
— Moro reflex: typically INTACT once pain subsides (vs absent in BPP)
— Palpable crepitus/irregularity over clavicle
— X-ray confirms fracture; greenstick fractures may be subtle initially
— Swelling, tenderness of the arm
— Moro reflex absent on affected side (similar to BPP)
— X-ray differentiates
— Onset typically after first 48 hours (not immediately at birth)
— Fever, irritability, swelling, erythema around joint
— Labs: ↑ CRP, ↑ WBC; blood culture, joint aspiration
— Usually bilateral or involves lower extremities as well
— Altered sensorium, seizures may be present
— Tone abnormalities beyond a single nerve distribution

— Accurate estimation of fetal weight (clinical + ultrasound)
— Planned cesarean delivery may be discussed for estimated fetal weight >5,000 g (non-diabetic) or >4,500 g (diabetic mother)
— Appropriate management of shoulder dystocia with established maneuvers
— ALL newborns should have a complete physical exam within 24 hours including assessment of clavicles, extremity movement, Moro reflex symmetry, and scalp/head exam
— Document head circumference and scalp findings — repeat measurement before discharge if cephalohematoma present
— Universal pre-discharge bilirubin screening (transcutaneous or serum) — cephalohematoma is a recognized risk factor that lowers the threshold for follow-up
— Plot on hour-specific nomogram
— Ensure outpatient follow-up within 24–48 hours of discharge for bilirubin recheck if in intermediate or high-risk zone

— No specific follow-up needed beyond routine newborn care
— Reassure parents it is temporary and benign
— Outpatient bilirubin recheck within 24–48 hours of discharge
— Recheck head circumference at 2-week well visit — should be stable or decreasing
— Counsel parents: the mass may feel firm/calcified at 2–4 weeks → this is normal; it will remodel and flatten over weeks to months
— If swelling increases or new symptoms develop (fever, expanding mass, increasing pallor) → return immediately
— 2-week visit: reassess motor function, start gentle ROM exercises at home
— Monthly neurovascular reassessment for first 3 months
— PT referral by 2–4 weeks
— Critical milestone: biceps function recovery by 3 months → if absent, refer to specialist
— Educate parents on home ROM exercises: passive shoulder abduction, external rotation, elbow flexion/extension, forearm supination — performed gently during diaper changes and play

— Parents may feel the injury was preventable or someone is "at fault"
— Provide empathetic, honest counseling: explain that birth injuries can occur even with optimal obstetric care
— Use clear language: avoid jargon; explain anatomy simply ("a collection of blood between the bone and its covering")
— Emphasize the favorable prognosis: >80% of Erb palsies recover fully or near-fully by 3–6 months
— Set realistic expectations: recovery is gradual; some infants recover in weeks, others in months
— Acknowledge parental frustration with the "wait and see" approach — frame it as active monitoring, not passive neglect
— Discuss that surgical options exist if recovery does not occur, and the timeline for those decisions
— Connect families with support groups (e.g., United Brachial Plexus Network)
— Reassure about the benign natural history
— Explain the jaundice risk and importance of bilirubin follow-up
— Warn about calcification phase so parents are not alarmed by the changing texture of the lump




