ABSTRACT

Grossman & Yousem (2003), 153-6; Brant & Helms (2007), 133.

4) e. Cerebral perfusion CT can distinguish viable but ischaemic tissue (the penumbra) from tissue that is beyond recovery. Other uses include evaluation of vasospasm after subarachnoid haemorrhage, assessment of cerebrovascular reserve with acetazolamide (cerebral arteriole vasodilator) in cases of vascular stenosis, evaluation of collateral flow and cerebrovascular reserve in patients having temporary balloon occlusion and assessment of microvascular permeability of intracranial neoplasms. Cerebral perfusion CTutilizes the central volume principle. This states that CBF¼CBV/MTT, where CBF is cerebral blood flow, CBV is cerebral blood volume and MTT is mean transit time. In practice, two CT perfusion techniques can be used. One is perfused-bloodvolume mapping, in which a quantity is assigned to cerebral blood volume by subtracting unenhanced CT data from CTangiographic data. It has the advantage of imaging the whole brain. The second technique is a dynamic, contrast-enhanced technique that acquires data from a limited number of axial slices, and monitors the first pass of an iodinated contrast agent bolus through the cerebral circulation. This requires an unenhanced CT brain, followed by a dynamic CT performed during injection of 50 ml of iodinated contrast (300 mg I/ml) at 4 ml/s. The first pass of contrast is observed in the brain. Cerebral perfusion is related to the concentration of iodinated contrast, which is directly related to the attenuation measured. Several maps are produced, including the CBV, CBF and MTT. MTT is derived from arterial and venous enhancement curves, measured by using regions of interest placed on an artery (one that is not occluded as part of an acute event) and a venous sinus. CBV is the area under the enhancement curves, and CBF is obtained from the central volume equation. Differentiation of infarcted brain from penumbra is important because, while penumbra can be saved by timely thrombolysis, infarcted tissue has an increased risk of bleeding from thrombolysis with no chance of recovery. CBF is decreased in both ischaemia and infarction, MTT is longer (.6 s) in both, while CBV is decreased in infarct but increased (or normal) in the penumbra due to cerebral autoregulatory mechanisms. MTT is the most sensitive for stroke. So this or CBF can be used to detect stroke while CBV is used to determine whether there is infarct or reversible ischaemia.