Sudural Haemorrhage Flashcards

1
Q

Definition of SDH

A

A collection of blood between the dural and arachnoid layers of the brain

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2
Q

Aetiology of SDH

A

• The primary cause for both acute and chronic SDH is TRAUMA
◦ Less commonly, they’re associated with rupture of cerebral aneurysm or vascular malformation

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3
Q

Pathophysiology of SDH

A

• Typically result from torsional or shear forces that disrupt the cortical veins. Venous= low pressure
• As the volume of the haematoma increases, the brain parenchyma is compressed and a midline shift may occur.
• The raised ICP can cause herniation and coning if not treated.
◦ The raised ICP can also limit cerebral blood flow and hence ischaemic injury would occur

• Chronic SDH take longer to display symptoms due to brain atrophy allowing for the haematoma to grow more before causing symptoms

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4
Q

History and Examination of SDH

A

• Evidence of trauma: scalp and face abrasions, lacerations, ecchymosis etc
• Headache: can be a sign of increased ICP
• Confusion: may be a sign of raised ICP
• Loss of consciousness/decreased alertness: sign of midline shift
• Fluctuating consciousness/Insidious neurological deficit: can indicate growing of haematoma
• Diminished eye, verbal and/or motor response
• Nausea/vomiting
• Occurs late, often >1 month after injury
• Hemiparesis
• Seizures

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5
Q

Risk factors of SDH

A

• Recent trauma
• Coagulopathy and anticoagulant use
• Advanced age

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6
Q

Investigations for SDH

A

• Non-contrast CT scan: can show the fluid collection and maybe midline shift (compresses ventricles). Would have a ‘crescent’ shape
• May do MRI

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7
Q

Treatment for SDH if ‘<10mm size, midline shift <5mm non-expansile without significant neuro dysfunction’:

A

1) Observation, monitoring and follow up imaging: Monitor GCS, pupils and ICP. Follow up CT 2-3 weeks after discharge

+Prophylactic Antiepileptics: Phenytoin generally given for 7 days

+Correct coagulopathy: Stop anticoagulation

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8
Q

Treatment for SDH if ‘
>10mm size or midline shift, >5mm or expansile or significant neuro dysfunction’:

A

1) Surgery: Is indicated for expanding haematoma and/or if causing neuro deficit. May need burr hole craniotomy with irrigation
+ Monitoring: GCS, ICP

+ Prophylactic antiepileptics: Given for 7 days

+ Stop anti-coagulation

+address cause of the trauma (e.g falls, abuse etc)

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9
Q

Prevention of SDH

A

Seatbelts and helmets should be used. Patients on anticoagulation should use walking aids if required
After SDH, patients should avoid antithrombotics or anticoagulants unless very much needed

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10
Q

Complications of SDH

A

• Epilepsy: high risk of post-traumatic epilepsy
• Neurological deficits

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11
Q

Prognosis of SDH

A

Poor prognostic outcomes if older age, greater severity, low GCS, midline shift, raised ICP.

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