Mechanical thrombectomy of acute ischemic stroke of Medium Sized Vessels (M2 segment of middle cerebral artery occlusion)
Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Background Data on mechanical thrombectomy (MT) to treat M2 occlusions of the middle cerebral artery (MCA) are sparse. We report the outcome and safety of MT versus intravenous recombinant tissue plasminogen activator (IV rTPA) versus conventional medical treatment of acute ischemic stroke (AIS) due to occlusion of the M2 segment of the MCA. This prospective study compared the outcomes and safety of MT, rTPA, and conventional medical treatment in M2 occlusion AIS patients. National Institutes of Health Stroke Scale (NIHSS), Modified Rankin Scale (mRS), and recanalization rate assessed outcomes. Results 74 AIS patients were recruited (23 MT, 23 rTPA, 28 conventional treatments). MT group had significantly higher admission NIHSS (p = 0.037). At 24 hours, NIHSS improved more with MT and rTPA than conventional treatment (p < 0.0001). At 3 months, mRS were better with MT and rTPA versus conventional treatment (p < 0.0001). Successful recanalization occurred in 73.9% of the MT group. 69% of the MT group required stent retrieval plus aspiration thrombectomy and 60.9% required ≥ 3 trials, but outcomes did not differ by technique or number of trials. A good outcome (mRS 0–2) at 3 months was achieved in 69.6% MT versus 65.2% rTPA versus 7.1% conventional treatment (p < 0.0001). Symptomatic intracranial hemorrhage (sICH) rates were slightly, but insignificantly, higher with conventional treatment. Mortality did not significantly differ between groups. Conclusions For M2 occlusions, MT and rTPA achieved better early and 3-month outcomes than conventional management, however, MT was not superior to rTPA. MT of M2 is feasible and effective, with a lower hemorrhage rate than rTPA and conventional treatment. Trial registration This study was prospectively registered in the clinical trial with ClinicalTrials.gov ID (NCT05091320). The link https//clinicaltrials.gov/study/NCT05091320