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

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.