Intraventricular Haemorrhage (IVH)
Why is this topic important?
Intraventricular haemorrhage is one of the most important neurological complications of prematurity. It is a high-yield MRCPCH topic because candidates must understand risk factors, cranial ultrasound findings, grading, complications and neurodevelopmental implications.
Definition
Intraventricular haemorrhage is bleeding into the germinal matrix and ventricular system of the brain, most commonly seen in very preterm infants.
The germinal matrix is fragile and highly vascular, making it vulnerable to bleeding.
Key MRCPCH Facts
- Most common in very preterm and extremely low birth weight infants.
- Highest risk is in the first week of life.
- Cranial ultrasound is the main screening investigation.
- Severe IVH is associated with worse neurodevelopmental outcome.
- Post-haemorrhagic ventricular dilatation is an important complication.
Pathophysiology
The germinal matrix in preterm infants is fragile.
Bleeding may occur due to:
- Fluctuating cerebral blood flow
- Respiratory instability
- Hypotension
- Sepsis
- Coagulopathy
- Rapid changes in carbon dioxide
Once bleeding occurs, it may extend:
- Within germinal matrix
- Into ventricles
- Into brain parenchyma
- Causing ventricular dilatation
Risk Factors
Infant Factors
- Extreme prematurity
- Very low birth weight
- Respiratory distress
- Hypotension
- Sepsis
- Coagulopathy
Perinatal Factors
- Lack of antenatal steroids
- Difficult resuscitation
- Hypoxia
- Acidosis
Clinical Features
Many babies are asymptomatic.
Possible features include:
- Apnoea
- Bradycardia
- Desaturation
- Hypotension
- Seizures
- Bulging fontanelle
- Sudden fall in haemoglobin
- Reduced tone or activity
Investigations
Cranial Ultrasound
Main bedside investigation.
Advantages:
- Safe
- Portable
- Repeatable
- No radiation
MRI Brain
Useful for:
- Defining extent of injury
- Prognosis
- Follow-up planning
Other Tests
If clinically indicated:
- FBC
- Coagulation profile
- Blood gas
- Infection screen
Grading
Common grading concept:
Grade I
Bleeding limited to germinal matrix.
Grade II
Blood in ventricles without ventricular dilatation.
Grade III
Blood in ventricles with ventricular dilatation.
Grade IV
Parenchymal haemorrhagic infarction.
Higher grades are associated with poorer outcomes.
Management
Supportive Care
- Optimise ventilation
- Avoid hypoxia and hyperoxia
- Maintain stable blood pressure
- Correct coagulopathy
- Treat sepsis
Monitoring
- Serial cranial ultrasound
- Head circumference
- Fontanelle assessment
- Neurological examination
Post-Haemorrhagic Ventricular Dilatation
May require:
- Neurosurgical discussion
- CSF drainage procedures
- Ventricular reservoir or shunt in selected cases
Complications
Short-Term
- Ventricular dilatation
- Hydrocephalus
- Seizures
- Anaemia
Long-Term
- Cerebral palsy
- Developmental delay
- Learning difficulties
- Epilepsy
- Visual impairment
Common Exam Traps
Trap 1
Many IVHs are clinically silent.
Trap 2
Cranial ultrasound is first-line, not CT.
Trap 3
Severe IVH with ventricular dilatation has higher risk of adverse outcome.
Trap 4
Grade I and II IVH usually have better prognosis than severe IVH.
One Minute Revision
- IVH = complication of prematurity.
- Germinal matrix is fragile.
- Screen with cranial ultrasound.
- Severe IVH + ventricular dilatation = poor prognostic marker.
- Monitor head circumference and ventricular size.
Related Question of the Day
What is the routine bedside screening investigation for IVH in very preterm infants?
A. CT brain
B. MRI brain
C. Cranial ultrasound
D. Skull X-ray
E. EEG
Answer
C. Cranial ultrasound
Explanation
Cranial ultrasound is portable, safe and widely used for IVH screening in preterm infants.
Related Topics
- HIE
- RDS
- PDA
- Apnoea of Prematurity
- Neurodevelopmental Follow-up
Suggested References
- BAPM Guidance
- RCPCH Guidance
- Nelson Textbook of Pediatrics
- Rennie & Roberton’s Textbook of Neonatology
- Volpe’s Neurology of the Newborn
Disclaimer
These notes are intended for MRCPCH revision and educational purposes only. They do not replace local, national or institutional guidelines. Clinical decisions should always be based on current guidance, senior advice and individual patient circumstances.
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