» Articles » PMID: 34003709

Direct Mechanical Thrombectomy Without Intravenous Thrombolysis Versus Bridging Therapy for Acute Ischemic Stroke: A Meta-analysis of Randomized Controlled Trials

Overview
Journal Int J Stroke
Publisher Sage Publications
Date 2021 May 18
PMID 34003709
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Direct mechanical thrombectomy may result in similar outcomes compared to a bridging approach with intravenous thrombolysis (IVT + MT) in acute ischemic stroke. Recent randomized controlled trials have varied in their design and noninferiority margin.

Aim: We sought to meta-analyze accumulated trial data to assess the difference and non-inferiority in clinical and procedural outcomes between direct mechanical thrombectomy and bridging therapy.

Summary Of Review: We conducted a systematic review of electronic databases following the preferred reporting items for systematic reviews and meta-analyses guidelines. Random effects meta-analyses were conducted for the pooled data. The primary outcome was good functional outcome at 90 days (modified Rankin scale (mRS) ≤ 2). Secondary outcomes included excellent functional outcome (mRS ≤ 1), mortality, any intracranial hemorrhage, symptomatic intracranial hemorrhage, successful reperfusion (thrombolysis in cerebral infarction ≥ 2 b), and procedure-related complications. Four randomized controlled trials comprising 1633 patients (817 direct mechanical thrombectomy, 816 bridging therapy) were included. There were no statistical differences for the 90-day good functional outcome (OR = 1.02, 95% CI 0.84-1.25,  = 0.54, = 0%), and the absolute risk difference was 1% (95% CI: -4% to 5%). The lower 95% CI falls within the strictest noninferiority margin of -10% among included randomized control trials. Direct mechanical thrombectomy reduced the odds of successful reperfusion (OR = 0.76, 95% CI: 0.60-0.97,  = 0.03, = 0%) and any intracranial hemorrhage (OR = 0.65, 95% CI: 0.49-0.86,  = 0.003, I= 38%). There was no difference in the remaining secondary outcomes. The risk of bias for all studies was low.

Conclusion: The combined trial data assessing direct mechanical thrombectomy versus bridging therapy showed no difference in improving good functional outcome. The wide noninferiority thresholds set by individual trials are in contrast with the clinical consensus on minimally important differences. However, our pooled analysis indicates noninferiority of direct mechanical thrombectomy with a 4% margin of confidence. The application of these findings is limited to patients presenting directly to mechanical thrombectomy-capable centers and real-world workflow times may differ against those achieved in a trial setting.

Citing Articles

Hyperdense Middle Cerebral Artery Sign as a Predictor of First-Pass Recanalization and Favorable Outcomes in Direct Thrombectomy Patients.

Sun Y, Sun D, Jia B, Huo X, Tong X, Wang A Clin Neuroradiol. 2024; .

PMID: 39704829 DOI: 10.1007/s00062-024-01484-2.


Safety and efficacy of bridging intravenous thrombolysis plus mechanical thrombectomy versus direct mechanical thrombectomy in different age groups of acute ischemic stroke patients.

Marrama F, Mascolo A, Sallustio F, Bovino M, Rocco A, DAgostino F Acta Neurol Belg. 2024; 125(1):141-148.

PMID: 39436555 DOI: 10.1007/s13760-024-02672-0.


A Short Review on Advances in Early Diagnosis and Treatment of Ischemic Stroke.

Sun B, Wang Z Galen Med J. 2024; 12:e2993.

PMID: 39430040 PMC: 11491119. DOI: 10.31661/gmj.v12i0.2993.


Assessment of Thrombectomy versus Combined Thrombolysis and Thrombectomy in Patients with Acute Ischemic Stroke and Medium Vessel Occlusion.

Dmytriw A, Ghozy S, Salim H, Musmar B, Siegler J, Kobeissi H Radiology. 2024; 312(2):e233041.

PMID: 39105645 PMC: 11366672. DOI: 10.1148/radiol.233041.


Real-world setting comparison of bridging therapy versus direct mechanical thrombectomy for acute ischemic stroke: A meta-analysis.

Qin B, Wei T, Gao W, Qin H, Liang Y, Qin C Clinics (Sao Paulo). 2024; 79:100394.

PMID: 38820696 PMC: 11177057. DOI: 10.1016/j.clinsp.2024.100394.