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Updated: Jul 16, 2026

The Stroke Preclinical Assessment Network Multi-Laboratory Model of Thromboembolic Stroke with Thrombolysis: TE-MCAo
Published on: December 19, 2025
Large bore versus super large bore aspiration catheters in mechanical thrombectomy: a systematic review and
Ariana Chacon1, Layth Jm Saada1, Dareen Hijazi1
1Neurosurgery, Emory University School of Medicine, Atlanta, Georgia, USA.
Background:
Endovascular thrombectomy (EVT) is a cornerstone treatment for acute ischemic stroke (AIS) due to large vessel occlusion (LVO). Super large bore (SLB) catheters represent the latest evolution in device design for aspiration technology; however, their benefit over standard large bore (LB) catheters remains uncertain.
Methods:
A systematic literature search and proportional meta-analysis were conducted on studies reporting EVT outcomes with LB and SLB aspiration catheters. Both single-arm and comparative studies were included. The primary outcome was first-pass modified treatment in cerebral infarction (mTICI) score ≥2C (FPE2C). Secondary outcomes included safety and procedural measures. Random-effects models generated pooled estimates, with subgroup comparisons between LB and SLB and sensitivity analyses using leave-one-out and outlier exclusion.
Results:
A total of 3966 patients (39 studies) were included in the primary analyses (SLB n=376; LB n=3590). FPE2C rates were similar between SLB and LB catheters (56% vs 50%; P=0.4). Final successful recanalization rates were high and similar in both groups (92% vs 92%; P=0.9). Procedural time did not differ, with pooled mean times of 27.03 min for SLB and 26.97 min for LB catheters. The need for rescue therapy showed a trend toward lower use with SLB compared with LB catheters (11% vs 20%; P=0.06). Rates of failure to reach the target clot showed a trend toward higher rates in the SLB group (10% vs 5%; P=0.11). Safety outcomes did not differ significantly (P>0.2).
Conclusion:
SLB catheters did not demonstrate a clear advantage over LB catheters in reperfusion outcomes. Limited clinical data prevent conclusions on functional benefit, and further prospective studies are needed.
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