Birth Trauma

Birth trauma (also called birth injury) refers to physical injury sustained by a newborn during the labour and delivery process. Most injuries are minor and resolve spontaneously, but some can lead to significant morbidity.

Overview

Incidence:
  • Occurs in approximately 2-7 per 1,000 live births
  • Higher rates with:
    • Instrumental deliveries (forceps, vacuum)
    • Macrosomia (birth weight >4,000 g)
    • Prematurity (fragile tissues)
    • Abnormal presentations (breech, face)
    • Prolonged or precipitous labour
    • First vaginal delivery
Most birth injuries are preventable with appropriate obstetric management and timely intervention.

Risk Factors

Maternal factors:
  • Primiparity
  • Short stature, small pelvis
  • Maternal diabetes (macrosomia)
  • Obesity
  • Prolonged or precipitous labour
  • Abnormal uterine contractions
Fetal factors:
  • Macrosomia (>4,000 g)
  • Prematurity (<37 weeks)
  • Abnormal presentation (breech, transverse lie)
  • Multiple gestation
  • Congenital anomalies
Delivery factors:
  • Instrumental delivery (forceps, vacuum)
  • Shoulder dystocia
  • Emergency caesarean section
  • Difficult or traumatic delivery
  • Inappropriate use of fundal pressure

Types of Birth Trauma

1. Soft Tissue Injuries

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Caput Succedaneum

Definition: Oedema of the scalp overlying the presenting part.
Pathophysiology:
  • Pressure of the presenting part against the cervix during labour
  • Fluid accumulation in subcutaneous tissue
  • Crosses suture lines
Clinical features:
  • Soft, pitting oedema on scalp
  • Present at birth
  • Crosses suture lines (unlike cephalhaematoma)
  • May have bruising or abrasions
  • Not fluctuant
Management:
  • No treatment required
  • Resolves spontaneously within 2-3 days
  • Reassure parents
Complications:
  • Usually none
  • Rarely contributes to hyperbilirubinaemia

Cephalhaematoma

Definition: Subperiosteal haemorrhage (blood collection between skull bone and periosteum).
Pathophysiology:
  • Rupture of blood vessels between skull and periosteum during delivery
  • Common with instrumental deliveries
  • Accumulates over hours after birth
Clinical features:
  • Firm, fluctuant swelling on scalp
  • Appears several hours after birth (not immediately)
  • Does NOT cross suture lines (limited by periosteal attachments)
  • Most common over parietal bones (unilateral or bilateral)
  • No discolouration initially
  • Well-demarcated edges
Natural history:
  • Enlarges over first 24-48 hours
  • Resolves over 6-8 weeks (up to 3 months)
  • May leave calcified rim that eventually remodels
Management:
  • No aspiration or drainage (risk of infection, rebleeding)
  • Observation
  • Monitor for jaundice (breakdown of blood)
  • Rarely needs phototherapy for jaundice
Complications:
  • Hyperbilirubinaemia (as blood breaks down)
  • Anaemia (if large)
  • Infection (rare, if aspirated)
  • Underlying skull fracture (10-25% of cases)
  • Calcification (benign, remodels over time)
Investigations:
  • Usually none needed
  • Skull X-ray or CT if concerned about fracture (not routine)
  • Monitor bilirubin if jaundice develops

Subgaleal (Subaponeurotic) Haemorrhage

Definition: Bleeding into the potential space between the scalp aponeurosis and periosteum.
⚠️ SERIOUS - Can be life-threatening
Pathophysiology:
  • Large potential space (extends from orbital ridges to nape of neck)
  • Can accumulate large volumes of blood (up to 260 mL - 80% of newborn blood volume)
  • Associated with vacuum extraction, coagulopathy
Clinical features:
  • Diffuse, fluctuant scalp swelling
  • Crosses suture lines (unlike cephalhaematoma)
  • Appears hours after delivery and progressively enlarges
  • Boggy, shifting fluid wave
  • Signs of hypovolaemia:
    • Pallor
    • Tachycardia
    • Hypotension
    • Shock
  • May have bruising around ears and eyes as blood tracks down
Management:
  • Emergency management:
    • Immediate resuscitation
    • IV access
    • Volume replacement (crystalloid, blood transfusion)
    • Monitor vital signs closely
  • Investigations:
    • Serial haemoglobin/haematocrit
    • Coagulation screen
    • Cross-match blood
    • Serial head circumference measurements
  • Supportive care:
    • NICU admission
    • Avoid procedures increasing intracranial pressure
    • Monitor for complications
Complications:
  • Hypovolaemic shock (life-threatening)
  • Severe anaemia
  • Hyperbilirubinaemia
  • Disseminated intravascular coagulation (DIC)
  • Death (if not recognized and treated)
Prognosis:
  • High mortality if not promptly recognized
  • Resolves over 2-3 weeks with appropriate management

Facial and Scalp Injuries

Bruising and petechiae:
  • Common after face or breech presentation
  • Resolves spontaneously
  • May contribute to jaundice
Lacerations:
  • From scalpel during caesarean section
  • Forceps or other instruments
  • Usually superficial
  • May need suturing if deep
Forceps marks:
  • Linear bruising or abrasions from forceps blades
  • Resolve within days
  • Usually no treatment needed
Fat necrosis:
  • Firm subcutaneous nodules (cheeks, buttocks)
  • From pressure or trauma
  • Resolve spontaneously over weeks-months

2. Skeletal Injuries

Clavicular Fracture

Most common birth fracture (0.5-1% of all deliveries)
Risk factors:
  • Macrosomia
  • Shoulder dystocia
  • Difficult delivery
  • Instrumental delivery
Clinical features:
  • May be asymptomatic
  • Decreased movement of affected arm
  • Crepitus over clavicle
  • Asymmetric Moro reflex
  • Tenderness, swelling over clavicle
  • Palpable deformity or irregularity
  • Callus formation evident at 1-2 weeks (healing sign)
Diagnosis:
  • Clinical examination
  • X-ray (if diagnosis uncertain, but often not needed)
Management:
  • Usually no treatment required
  • Gentle handling
  • Pin sleeve to shirt to limit arm movement (optional)
  • Analgesics if needed
  • Heals spontaneously within 2-3 weeks
Prognosis:
  • Excellent
  • Complete healing without complications
  • Remodelling of callus over months

Skull Fractures

Types:
  • Linear fractures (most common) - usually benign
  • Depressed fractures ("ping-pong ball" deformity)
  • Occipital osteodiastasis (separation of occipital bone)
Risk factors:
  • Forceps delivery
  • Difficult labour
  • Underlying cephalhaematoma
Clinical features:
  • Often asymptomatic
  • May have overlying swelling (cephalhaematoma)
  • Visible or palpable depression (depressed fracture)
  • Rarely signs of intracranial injury
Investigations:
  • Skull X-ray or CT scan
  • MRI/CT if neurological signs
Management:
  • Linear fractures: Observation, heal spontaneously
  • Depressed fractures:
    • May require neurosurgical elevation if significant
    • Many resolve spontaneously
  • Monitor for complications
Complications:
  • Usually none
  • Rarely: intracranial haemorrhage, growing fracture

Long Bone Fractures

Humerus and femur fractures (rare)
Risk factors:
  • Breech delivery
  • Macrosomia
  • Difficult extraction
Clinical features:
  • Decreased or absent movement of limb
  • Swelling, tenderness, deformity
  • Crepitus
  • Pseudoparalysis (refusal to move limb)
Diagnosis:
  • X-ray
Management:
  • Immobilization (splinting)
  • Analgesics
  • Orthopaedic referral if needed
  • Heals within 2-3 weeks (newborn bones heal quickly)
Prognosis:
  • Excellent with appropriate treatment
  • Complete remodelling

3. Nerve Injuries

Brachial Plexus Injury (Erb's Palsy, Klumpke's Palsy)

Incidence: 0.4-2 per 1,000 live births
Pathophysiology:
  • Stretching or tearing of brachial plexus nerve roots (C5-T1)
  • Associated with shoulder dystocia, difficult delivery, macrosomia
Types:
Erb's Palsy (most common, 90%):
  • Injury to upper roots C5-C6 (± C7)
  • From lateral traction on head during shoulder dystocia
Klumpke's Palsy (rare):
  • Injury to lower roots C8-T1
  • From hyperabduction of arm during breech delivery
Clinical features:
Erb's Palsy:
  • "Waiter's tip" position:
    • Shoulder adducted and internally rotated
    • Elbow extended
    • Forearm pronated
    • Wrist flexed
  • Absent Moro reflex on affected side
  • Absent biceps reflex
  • Preserved grasp reflex
  • May have associated phrenic nerve palsy (C3-C5) → elevated hemidiaphragm
  • May have Horner's syndrome (ptosis, miosis, anhidrosis) if severe
Klumpke's Palsy:
  • "Claw hand" deformity
  • Paralysis of hand muscles
  • Absent grasp reflex
  • Preserved Moro reflex
  • Often associated with Horner's syndrome (T1 involvement)
Investigations:
  • Clinical diagnosis
  • X-ray to rule out associated fractures (clavicle, humerus)
  • Chest X-ray if concerned about phrenic nerve palsy
  • EMG/nerve conduction studies (at 3-4 weeks if not improving)
  • MRI (if considering surgery)
Management:
Conservative (most cases):
  • Gentle range of motion exercises (start at 7-10 days)
  • Physiotherapy
  • Avoid immobilization (promotes contractures)
  • Regular follow-up
Surgical:
  • Consider if no improvement by 3-6 months
  • Nerve grafting, nerve transfer, neurolysis
Prognosis:
  • 70-90% recover fully by 12 months (neurapraxia)
  • Earlier recovery (within 2 weeks) predicts better outcome
  • Poor prognostic signs:
    • No recovery by 3 months
    • Horner's syndrome
    • Complete plexus injury
    • Nerve root avulsion (on MRI)
  • Persistent weakness may require ongoing therapy, orthoses, or surgery

Phrenic Nerve Palsy

Pathophysiology:
  • Injury to phrenic nerve (C3-C5)
  • Often associated with Erb's palsy (same nerve roots)
Clinical features:
  • Respiratory distress
  • Reduced breath sounds on affected side
  • Asymmetric chest movement
  • Paradoxical breathing
Investigations:
  • Chest X-ray: elevated hemidiaphragm
  • Ultrasound: reduced or paradoxical diaphragm movement
Management:
  • Supportive care
  • Oxygen, respiratory support if needed
  • Position on affected side (improves ventilation)
  • Usually resolves spontaneously within weeks-months
  • Surgical plication if persistent and symptomatic

Facial Nerve Palsy

Incidence: 0.3-7 per 1,000 live births
Pathophysiology:
  • Compression of facial nerve (CN VII)
  • Usually from forceps blade pressure
  • Can also occur from intrauterine positioning
Clinical features:
  • Asymmetry when crying:
    • Affected side remains smooth
    • Unaffected side shows normal movement
    • Mouth deviates to unaffected side
  • Eye remains open on affected side
  • Absent nasolabial fold on affected side
  • Difficulty feeding (weak suck)
Differential diagnosis:
  • Central vs peripheral palsy:
    • Peripheral: involves entire half of face (including forehead)
    • Central: spares forehead (unlikely in newborn)
  • Asymmetric crying facies (congenital absence of depressor anguli oris muscle) - affects only lower face, eye closure normal
  • Möbius syndrome (congenital bilateral facial palsy)
Management:
  • Usually none required
  • Eye care if lagophthalmos (inability to close eye):
    • Artificial tears
    • Eye patching
  • Spontaneous recovery in 90% within weeks to months
Prognosis:
  • Excellent in most cases
  • Persistent palsy suggests nerve division (rare)

4. Intracranial Haemorrhage

Subdural Haemorrhage

Pathophysiology:
  • Rupture of bridging veins or dural sinuses
  • Associated with difficult delivery, rapid moulding, instrumental delivery
  • More common in large babies or precipitous delivery
Clinical features:
  • May be asymptomatic
  • Seizures (focal or generalized)
  • Lethargy, irritability
  • Full fontanelle
  • Altered consciousness
  • Focal neurological signs
  • Anaemia if large bleed
Investigations:
  • Cranial ultrasound (screening)
  • CT or MRI brain (diagnostic)
  • Coagulation screen
Management:
  • Supportive care
  • Seizure management if needed
  • Most small bleeds resolve spontaneously
  • Neurosurgical drainage rarely needed (if large, symptomatic)
Prognosis:
  • Small bleeds: good outcome
  • Large bleeds: risk of neurological sequelae

Subarachnoid Haemorrhage

Most common type of intracranial haemorrhage in term infants.
Pathophysiology:
  • Rupture of small bridging veins
  • Associated with trauma or hypoxia
Clinical features:
  • Often asymptomatic (incidental finding)
  • May have seizures (typically on day 2 of life)
  • Well between seizures
  • No focal neurological signs
Investigations:
  • Lumbar puncture: bloody or xanthochromic CSF
  • CT or MRI brain
Management:
  • Supportive
  • Anticonvulsants if seizures
Prognosis:
  • Usually excellent
  • Most have no long-term sequelae

Intraventricular Haemorrhage (IVH)

More common in preterm infants. (Covered in detail in
Intraventricular Haemorrhage
)

5. Visceral Injuries

Hepatic Rupture/Subcapsular Haematoma

Rare but life-threatening
Risk factors:
  • Macrosomia
  • Difficult delivery
  • Breech extraction
  • Hepatomegaly
Clinical features:
  • May be asymptomatic initially
  • Delayed presentation (hours to days):
    • Sudden deterioration
    • Pallor, shock
    • Abdominal distension
    • Anaemia
    • Bluish discolouration of abdomen
Investigations:
  • Ultrasound abdomen
  • CT abdomen
  • Serial haemoglobin
Management:
  • Emergency resuscitation:
    • Volume replacement
    • Blood transfusion
  • Surgical exploration if ongoing bleeding or unstable
  • Conservative management if stable
Prognosis:
  • High mortality if ruptured
  • Better outcome if detected early

Splenic Rupture

Very rare
  • Similar presentation to hepatic rupture
  • Management similar (resuscitation, possible splenectomy)

Adrenal Haemorrhage

Pathophysiology:
  • Adrenal glands vulnerable to trauma during delivery
  • Associated with macrosomia, difficult delivery, birth asphyxia
Clinical features:
  • Often asymptomatic
  • Abdominal mass (flank)
  • Jaundice (from blood breakdown)
  • Rarely adrenal insufficiency (if bilateral and severe)
Investigations:
  • Ultrasound abdomen: adrenal mass
  • Serial imaging (may enlarge then resolve)
  • Monitor for adrenal insufficiency if bilateral
Management:
  • Usually observation
  • Rarely requires intervention
  • Monitor for adrenal insufficiency
  • Follow-up imaging (may calcify)
Prognosis:
  • Usually benign
  • Resolves spontaneously

6. Spinal Cord Injury

Rare but devastating
Pathophysiology:
  • Excessive longitudinal traction or rotation during delivery
  • Associated with breech delivery, hyperextension of neck, difficult extraction
Clinical features:
  • Hypotonia, flaccid paralysis below level of injury
  • Respiratory distress (if high cervical injury)
  • Absent deep tendon reflexes
  • Bladder dysfunction
  • Sensory loss
  • May have concurrent brachial plexus injury
Investigations:
  • MRI spine (imaging of choice)
  • X-ray spine
Management:
  • Supportive care
  • Respiratory support
  • Bladder catheterization
  • Multidisciplinary management
  • Prognosis generally poor
Outcome:
  • High mortality
  • Survivors have permanent neurological disability

General Management Principles

Assessment:
  • Thorough physical examination of all newborns
  • Document any injuries
  • Assess severity and need for intervention
Investigations:
  • Guided by clinical findings
  • Imaging as appropriate (X-ray, ultrasound, CT, MRI)
  • Rule out associated injuries
Treatment:
  • Most injuries require observation only
  • Supportive care
  • Analgesia if painful
  • Physiotherapy for nerve injuries
  • Surgical intervention rarely needed
Parent education:
  • Explain nature of injury
  • Reassure about prognosis (most injuries resolve)
  • Provide guidance on handling and care
  • Arrange follow-up
Documentation:
  • Detailed documentation in medical records
  • Inform paediatrician and GP
Follow-up:
  • Ensure appropriate follow-up appointments
  • Monitor for complications
  • Early intervention if delays in recovery

Prevention

Antenatal:
  • Good glycaemic control in diabetic mothers (prevent macrosomia)
  • Accurate estimation of fetal weight
  • Consider elective caesarean for significant macrosomia or high-risk factors
Intrapartum:
  • Careful obstetric technique
  • Appropriate management of shoulder dystocia (McRoberts manoeuvre, suprapubic pressure)
  • Avoid excessive traction or rotation
  • Judicious use of instrumental delivery
  • Avoid fundal pressure
  • Timely caesarean section when indicated
Delivery planning:
  • Discuss mode of delivery for high-risk cases
  • Experienced obstetrician for anticipated difficult deliveries
  • Neonatal team available for high-risk deliveries

Key Points: Most birth injuries are minor and resolve spontaneously. Clavicular fracture is the most common skeletal injury. Erb's palsy (70-90% recovery) is more common than Klumpke's palsy. Subgaleal haemorrhage can be life-threatening. Early recognition and appropriate management improve outcomes. Most injuries are preventable with good obstetric practice.