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Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Late endovascular revascularization in acute ischemic stroke based on clinical-diffusion mismatch
N Janjua1, A El-Gengaihy, J Pile-Spellman
1Department of Neurology, Division of Interventional and Critical Care Neurology, Long Island College Hospital, Brooklyn, NY 11201, USA. NJanjua@chpnet.org
AJNR. American Journal of Neuroradiology
|February 6, 2009
Summary
Reperfusion therapy for acute ischemic stroke beyond 8 hours is feasible and safe in select patients. This treatment may prevent early neurologic deterioration and promote improvement in stroke patients with a clinical-diffusion mismatch.
Area of Science:
- Neurology
- Interventional Radiology
- Emergency Medicine
Background:
- A clinical-diffusion mismatch (CDM) in stroke patients presenting within 12-24 hours is linked to worsening symptoms and larger infarcts.
- Identifying suitable candidates for reperfusion therapy is crucial for improving outcomes.
Purpose of the Study:
- To assess the feasibility and safety of reperfusion therapy in stroke patients with a clinical-diffusion mismatch presenting beyond 8 hours.
- To evaluate the impact of endovascular treatment on neurologic status and intracranial hemorrhage.
Main Methods:
- Eleven patients with large vessel syndromes, NIHSS score >=8, and limited diffusion abnormalities on MRI beyond 8 hours were included.
- Revascularization therapy was considered. Early neurologic deterioration (END) and early neurologic improvement (ENI) were assessed using NIHSS scores at 1 and 7 days.
- Follow-up imaging evaluated for intracranial hemorrhage (ICH).
Main Results:
- Eight of eleven patients (72%) were successfully revascularized.
- Successfully revascularized patients showed significant improvement in NIHSS scores at 24 hours and 1 week.
- Eight treated patients (100% of those revascularized) experienced ENI; no patients had END or ICH.
Conclusions:
- Endovascular treatment for acute ischemic stroke beyond 8 hours is feasible and safe in patients meeting CDM criteria.
- This therapy may prevent early neurologic deterioration and promote early neurologic improvement.
- A prospective study is planned to further validate these findings.
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