5 Stages of Intraparenchymal Hemorrhage
Stage Time (Range) Blood Products T1 T2
Hyperacute < 24 hours Oxyhemoglobin Isointense Bright
Acute 1-3 days (hours to days) Deoxyhemoglobin Isointense Dark
Early subacute > 3 days (days to 1 week) Intracellular methemoglobin Bright Dark
Late subacute > 7 days (1 week to months) Extracellular methemoglobin Bright Bright
Chronic > 14 days (≥ months) Hemosiderin Dark Dark
The effective therapeutic window for the posterior circulation
is thought to be longer than the 3-6-hour window, but the
exact time is variable and depends on collateral circulation.
Therefore, patients with vertebrobasilar thrombosis are
evaluated individually for risk vs. benefit of IA thrombolysis or
Ischemic stroke results in a core of tissue that has undergone
irreversible injury. The ischemic penumbra is the area of brain
that may be salvageable with appropriate therapy. The
penumbra typically surrounds the ischemic core and is
supported by collateral circulation.
The ischemic penumbra can be identified by a combination of
MR diffusion (DWI) and perfusion (PWI). DWI is the most
reliable estimate of the ischemic core and generally correlates
with irreversible injury. However, with early reperfusion
following thrombolysis, some reversal of DWI can be
observed. PWI evaluates the presence of a penumbra. With
MR, the mismatch between the DWI and PWI defines the
penumbra. This model provides a practical means to estimate
the ischemic penumbra. In general, if there is no
diffusion/perfusion mismatch, therapy may be ineffective.
With the newer CT perfusion techniques, an ischemic
penumbra may also be measured with CT.
With the urgency of acute stroke, MR may be impractical.
However, with new faster MR protocols and the superiority of
MR to CT in detecting small vessel ischemia and brainstem
ischemia, MR may be a preferred technique.
Cerebral perfusion refers to the tissue-level blood flow in the
brain. This flow is evaluated by 3 main parameters at CT
perfusion (pCT): Cerebral blood flow (CBF), cerebral blood
volume (CBV), and mean transit time (MTT).
CBF is defined as the volume of blood moving through a given
unit of volume of brain per unit time. CBF uses units of
milliliters of blood per 100 g of brain tissue per minute.
Studies suggest that CBF is a reasonable marker for the
CBV is defined as the total volume of blood in a given unit of
volume of brain. This includes blood in the tissues as well as
blood in the large-capacitance vessels, such as arteries,
arterioles, capillaries, venules, and veins. CBV uses units of
milliliters of blood per 100 g of brain tissue. Some studies
suggest that pCT-acquired CBV is a reasonably reliable marker
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