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Fluid-Attenuated Inversion Recovery May Serve As a Tissue Clock in Patients Treated With Endovascular Thrombectomy
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Background and Purpose:
We investigated whether the signal change on fluid-attenuated inversion recovery (FLAIR) can serve as a tissue clock that predicts the clinical outcome after endovascular thrombectomy (EVT), independently of the onset-to-admission time.
Methods:
Consecutive patients with acute stroke treated with EVT between September 2014 and December 2018 were enrolled. Based on the parenchymal signal change on FLAIR, patients were classified into FLAIR-negative and FLAIR-positive groups. The clinical characteristics, imaging findings, EVT parameters, and the intracranial hemorrhage defined as Heidelberg Bleeding Classification ≥1c hemorrhage (parenchymal hemorrhage, intraventricular hemorrhage, subarachnoid hemorrhage, and/or subdural hemorrhage) were compared between the 2 groups. A modified Rankin Scale score 0 to 1 at 3 months was considered to represent a good outcome.
Results:
Of the 227 patients with EVT during the study period, 140 patients (62%) were classified into the FLAIR-negative group and 87 (38%) were classified into the FLAIR-positive group. In the FLAIR-negative group, the patients were older (
P
=0.011), the onset-to-image time was shorter (
P
<0.001), the frequency of cardioembolic stroke was higher (
P
=0.006), and the rate of intravenous thrombolysis was higher (
P
<0.001) in comparison to the FLAIR-positive group. Although the rate of complete recanalization after EVT did not differ between the 2 groups (
P
=0.173), the frequency of both any-intracranial hemorrhage and Heidelberg Bleeding Classification ≥1c hemorrhage were higher in the FLAIR-positive group (
P
=0.004 and 0.011). At 3 months, the percentage of patients with a good outcome (FLAIR-negative, 41%; FLAIR-positive, 27%) was significantly related to the FLAIR signal change (
P
=0.047), while the onset-to-image time was not significant (
P
=0.271). A multivariate regression analysis showed that a FLAIR-negative status was independently associated with a good outcome (odds ratio, 2.10 [95% CI, 1.02–4.31],
P
=0.044).
Conclusions:
A FLAIR-negative status may predict the clinical outcome more accurately than the onset-to-admission time, which may support the role of FLAIR as a tissue clock.
Ovid Technologies (Wolters Kluwer Health)
Title: Fluid-Attenuated Inversion Recovery May Serve As a Tissue Clock in Patients Treated With Endovascular Thrombectomy
Description:
Background and Purpose:
We investigated whether the signal change on fluid-attenuated inversion recovery (FLAIR) can serve as a tissue clock that predicts the clinical outcome after endovascular thrombectomy (EVT), independently of the onset-to-admission time.
Methods:
Consecutive patients with acute stroke treated with EVT between September 2014 and December 2018 were enrolled.
Based on the parenchymal signal change on FLAIR, patients were classified into FLAIR-negative and FLAIR-positive groups.
The clinical characteristics, imaging findings, EVT parameters, and the intracranial hemorrhage defined as Heidelberg Bleeding Classification ≥1c hemorrhage (parenchymal hemorrhage, intraventricular hemorrhage, subarachnoid hemorrhage, and/or subdural hemorrhage) were compared between the 2 groups.
A modified Rankin Scale score 0 to 1 at 3 months was considered to represent a good outcome.
Results:
Of the 227 patients with EVT during the study period, 140 patients (62%) were classified into the FLAIR-negative group and 87 (38%) were classified into the FLAIR-positive group.
In the FLAIR-negative group, the patients were older (
P
=0.
011), the onset-to-image time was shorter (
P
<0.
001), the frequency of cardioembolic stroke was higher (
P
=0.
006), and the rate of intravenous thrombolysis was higher (
P
<0.
001) in comparison to the FLAIR-positive group.
Although the rate of complete recanalization after EVT did not differ between the 2 groups (
P
=0.
173), the frequency of both any-intracranial hemorrhage and Heidelberg Bleeding Classification ≥1c hemorrhage were higher in the FLAIR-positive group (
P
=0.
004 and 0.
011).
At 3 months, the percentage of patients with a good outcome (FLAIR-negative, 41%; FLAIR-positive, 27%) was significantly related to the FLAIR signal change (
P
=0.
047), while the onset-to-image time was not significant (
P
=0.
271).
A multivariate regression analysis showed that a FLAIR-negative status was independently associated with a good outcome (odds ratio, 2.
10 [95% CI, 1.
02–4.
31],
P
=0.
044).
Conclusions:
A FLAIR-negative status may predict the clinical outcome more accurately than the onset-to-admission time, which may support the role of FLAIR as a tissue clock.
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