Subdural haemorrhage/haematoma (SDH) is a collection of blood accumulating in the subdural space. Subdural haemorrhage can happen in any age group, is mainly due to head trauma and CT scans are usually sufficient to make the diagnosis. Prognosis varies widely depending on the size and chronicity of the haemorrhage.
On this page:
Epidemiology
Subdural haematomas, most frequently due to trauma, are seen in all age groups although aetiology will vary 4,5:
infants: non-accidental injury
young adults: motor vehicle accidents, vascular lesions
elderly: falls (although a definite history of trauma may be lacking)
They are present in ~15% (range 10-20%) of all head trauma cases and occur in up to 30% of fatal injuries.
In addition to trauma, there are numerous other far less common causes:
glutaric aciduria type 1 13 (infants and children, rare)
vascular malformations (all ages) and intracranial aneurysms 15
Clinical presentation
Acute subdural haemorrhages usually present in the setting of head trauma. This is especially the case in young patients, where they commonly coexist with cerebral contusions.
Most patients (65-80%) present with a severely depressed conscious state and pupillary abnormalities are seen in ~40% (range 30-50%) of cases 5.
Occasionally spontaneous acute subdural haematomas are seen with an underlying bleeding disorder (e.g. anticoagulation medication, thrombocytopenia) or structural abnormality (e.g. dural arteriovenous fistula).
Clinical presentation of subacute/chronic subdural in the elderly is often vague and is one of the classic causes of pseudodementia. A history of head trauma is often absent or very minor.
See the article: EDH vs SDH
Pathology
Subdural haemorrhages are believed to be due to stretching and tearing of bridging cortical veins as they cross the subdural space to drain into an adjacent dural sinus. These veins rupture due to shearing forces when there is a sudden change in the velocity of the head. The arachnoid may also be torn, creating a mixture of blood and CSF in the subdural space.
10 to 30% of chronic subdural haematomas show evidence of repeated haemorrhage. Rebleeding usually occurs from the rupture of stretched cortical veins as they cross the enlarged fluid-filled subdural space or from the vascularised neomembrane on the outer (calvarial) side of the fluid collection.
Subdural haematomas are interposed between the dura and arachnoid. Typically crescent-shaped, they are usually more extensive than extradural haematomas. In contrast to extradural haemorrhage, subdural haemorrhage is not limited by sutures but is limited by dural reflections, such as the falx cerebri, tentorium, and falx cerebelli.
Some controversy, albeit of academic interest only, exists as to the exact location of a subdural haematoma. Classical teaching is that it is located in the potential space between the arachnoid layer and inner layer of the dura; however, no such space really exists. Rather the arachnoid-dura junction is composed of "avascular tissue with flake-like [...] cells stacked in several layers with narrow intercellular clefts" 10. Bleeding occurs within this multicellular layer, with these cells located on both sides of the haematoma 9,10. This possibly accounts for why some acute haematomas appear to have multiple compartments, usually ascribed to intermittent bleeding ref required.
Radiographic features
Overall 85% of subdural haematomas are unilateral in adults. However, 75-85% are bilateral in infants. Common sites for subdural haematomas are frontoparietal convexities and the middle cranial fossa. Isolated interhemispheric/parafalcine subdural haematomas are seen more frequently in children and are common in cases of non-accidental trauma.
In the vast majority of cases, CT scans are sufficient to make the diagnosis and manage these patients. Contrast is sometimes helpful if there is a concern of subdural empyema, of the presence of a small isodense subdural, or to try and distinguish enlargement of the extra-axial CSF space from a chronic subdural haematoma. Routine use of intermediate (subdural) windows in all imaging planes is highly recommended to detect discrete subdural bleeds that blend in with the adjacent calvarium due to blooming in standard brain window images 12.
CT
The appearance of SDHs on CT varies with clot age and organisation.
Hyperacute
In most instances, patients are not imaged in the hyperacute phase (first hour or so), but on occasion when this is performed they appear relatively isodense to the adjacent cortex, with a swirled appearance due to a mixture of the clot, serum and ongoing unclotted blood 4. There is often a degree of underlying cerebral swelling (especially in young patients where head trauma is often more severe) which accentuates the mass-effect created by the collection 4.
Acute
The classic appearance of an acute subdural haematoma is a crescent-shaped homogeneously hyperdense extra-axial collection that spreads diffusely over the affected hemisphere. As the clot starts to retract the density increases typically to >50-60 HU and is thus hyperdense relative to the cortex 4.
Up to 40% of SDHs have mixed hyper- or hypodense areas that reflect unclotted blood, serum extruded during clot retraction, or CSF within the subdural haematoma due to an arachnoid laceration.
Rarely, acute subdural haemorrhages may be nearly isodense with the adjacent cerebral cortex. This occurs with anticoagulation, coagulopathies, or severe anaemia when the haemoglobin concentration drops to 8 to 10 g/dL. Patients with deficient coagulation can also demonstrate a haematocrit fluid-fluid level as the blood does not form a clot and red cells have time to drift dependently 4.
In patients with underlying low haemoglobin and platelet conditions such as sickle cell anaemia, acute subdural haemorrhage may be hypodense even in the acute phase 11.
Subacute
As the clot ages and protein degradation occurs, the density of the subdural haemorrhage starts to drop. At some point between 3 and 21 days (typically 10-14 days), the density will drop to ~ 35-40 HU and become isodense to the adjacent cortex, making identification potentially tricky, especially if subdural collections are bilateral 4. Contrast-enhanced CT is often useful in this instance if MRI is unavailable. The key to identification is visualising a number of indirect signs, including:
CSF-filled sulci do not reach the skull but rather fade out into the subdural
mass-effect including sulcal effacement (distortion) and midline shift
apparent thickening of the cortex
Chronic
By definition, the subdural haemorrhage is at least 3 weeks old.
The subdural collection becomes hypodense to the adjacent cortex and can reach ~0 HU and be isodense to CSF, and mimic a subdural hygroma.
A crescentic shape may change to a biconvex one.
Rarely, the periphery of the SDH may calcify, see calcified chronic subdural haematoma for an in-depth discussion regarding the CT appearance of this entity.
Acute on chronic
Acute on chronic subdural haematomas refers to a second episode of acute haemorrhage into a pre-existing chronic subdural haematoma. It typically appears as a hypodense collection with a haematocrit level (located posteriorly). A similar appearance can be seen in patients with clotting disorders or on anticoagulants 4.
MRI
The appearance of a subdural haemorrhage varies with the biochemical state of haemoglobin which varies with the age of the haematoma. The most sensitive standard sequence is FLAIR.
Hyperacute
T1: isointense to grey matter
T2: iso- to hyperintense
FLAIR: hyperintense to CSF
Acute
T1: iso- to hypointense to grey matter
T2: hypointense to grey matter
FLAIR: hyperintense to CSF
Subacute
Subacute subdural haemorrhages may appear biconvex-shaped on the coronal plane rather than crescent-shaped which is a typical appearance on the axial plane
T1: typically hyperintense due to the presence of methaemoglobin
T2: variable appearance, usually hyperintense
FLAIR: hyperintense
Chronic
T1: if the haematoma is stable it appears isointense to CSF, it can appear hyperintense to CSF if there is a rebleed or infection.
T2: if the haematoma is stable it appears isointense to CSF if there is rebleed the haematoma appears hypointense
FLAIR: hyperintense to CSF
Rarely, the periphery of the subdural haemorrhage may calcify, see calcified chronic subdural haematoma for an in-depth discussion regarding the MRI signal characteristics of this entity.
Treatment and prognosis
Treatment depends primarily on the amount of mass-effect and neurological impairment caused by the collection, and thus correlates with the size of the subdural haemorrhage.
Small collections – so-called 'smear subdurals' – especially those which are chronic and are not causing symptoms can be observed with serial CT scans.
Symptomatic collections need to be surgically evacuated. In the acute setting, this should be performed rapidly (within 4 hours) 3 and usually requires a craniotomy as the clot is not easily evacuated via burr holes.
Care must be taken to evaluate whether the resultant subfalcine herniation (if there is any) is in proportion with the extent of the haematoma on imaging. If the difference between the width of the haematoma and the midline shift exceeds 3 mm it signals a significant concurrent cerebral oedema, carrying a dismal prognosis. These patients require early aggressive treatment against cerebral swelling 12.
Symptomatic subacute/chronic subdural haematomas are often treated via one or more burr holes as the blood clot has liquefied and can be washed out more easily. The compressed brain can take some time to re-expand, and subdural collections may re-accumulate. Middle meningeal artery embolisation is a promising and less invasive technique to treat chronic SDH in selected patient groups 14.
Although subdural haematomas are often thought of as relatively benign entities it should be noted that the mortality in acute subdural haematomas requiring surgery is very high (50-90%), particularly in patients who are anticoagulated, and that only 20% fully recover 2,3,5.
Differential diagnosis
General imaging differential considerations include 1-4:
-
prominent subarachnoid space due to cerebral atrophy or benign enlargement of the subarachnoid space in infancy
can look similar
lack of mass effect
vessels course through space rather than displaced towards the brain
CT contrast, therefore, helps (in adults) by delineating the vessels (cortical vein sign) as well as demonstrating an enhancing 'capsule' of a subdural haematoma/empyema
ultrasound and MRI are useful in infancy
-
similar appearance on non-contrast scans
different clinical context (patients usually unwell and febrile)
prominent marginal enhancement
associated cerebral abscess/infarction
-
sometimes difficult to differentiate if small
biconvex in shape (lentiform) rather than crescentic
limited by sutures
may displace dural venous sinuses
usually associated with fractures
-
on CT can be indistinguishable from a chronic subdural haematoma
near CSF density
-
no evidence of prior haemorrhage
but may coexist with subdural haemorrhage
-
artifact
patient-based e.g. motion artifact
physics-based e.g. beam hardening
cortical veins
Unable to process the form. Check for errors and try again.