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http://brain.oxfordjournals.org/content/138/7/1768
This
scientific commentary refers to ‘Perfusion computed tomography to
assist decision making for stroke thrombolysis’, by Bivard et al. (doi:10.1093/brain/awv071).
The
ischaemic penumbra, defined as severely hypoperfused, functionally
impaired yet salvageable tissue, has been established as the key target
for acute stroke therapy for more than three decades (Muir et al., 2006).
However, the penumbra has a limited lifespan and, unless reperfused
early, it progresses to become part of the irreversibly damaged tissue
referred to as the ‘core’. The core therefore grows over time,
incorporating first the most hypoperfused portions of the penumbra, and
then progressively less hypoperfused portions, until none remains. How
fast this process occurs varies greatly from subject to subject, mainly
because of variable pial collaterals and the occurrence of spontaneous
reperfusion (Fig. 1). On a mechanistic basis, reperfusion therapy—such
as with intravenous thrombolysis using recombinant tissue plasminogen
activator (rt-PA)—would be expected to be of no benefit, and potentially
harmful, in cases with large core or no penumbra (Marchal et al., 1993).
Figure 1
The three main pathophysiological profiles used by Bivard et al. to categorize acute stroke patients, as originally defined using PET with 15oxygen-labelled compounds to generate quantitative maps of cerebral blood flow (CBF, left column) and the cerebral oxygen metabolic rate (CMRO2, right). Validated tissue compartments including penumbra (reduced cerebral blood flow but relatively preserved CMRO2) and core (markedly reduced CMRO2) were used to characterize the three profiles of ‘target mismatch', ‘large core' and ‘no mismatch' (Muir et al., 2006). Consistent with the strikingly distinct spontaneous outcomes associated with these profiles (Marchal et al., 1993), Bivard et al.
provide evidence from their cohort that the target mismatch group, i.e.
patients with significant penumbral tissue and a small core, benefit
the most from intravenous …
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