Recombinant Tissue Plasminogen Activator for Acute Ischaemic Stroke: an Updated Systematic Review and Meta-analysis
Overview
Authors
Affiliations
Background: Recombinant tissue plasminogen activator (rt-PA, alteplase) improved functional outcome in patients treated soon after acute ischaemic stroke in randomised trials, but licensing is restrictive and use varies widely. The IST-3 trial adds substantial new data. We therefore assessed all the evidence from randomised trials for rt-PA in acute ischaemic stroke in an updated systematic review and meta-analysis.
Methods: We searched for randomised trials of intravenous rt-PA versus control given within 6 h of onset of acute ischaemic stroke up to March 30, 2012. We estimated summary odds ratios (ORs) and 95% CI in the primary analysis for prespecified outcomes within 7 days and at the final follow-up of all patients treated up to 6 h after stroke.
Findings: In up to 12 trials (7012 patients), rt-PA given within 6 h of stroke significantly increased the odds of being alive and independent (modified Rankin Scale, mRS 0-2) at final follow-up (1611/3483 [46·3%] vs 1434/3404 [42·1%], OR 1·17, 95% CI 1·06-1·29; p=0·001), absolute increase of 42 (19-66) per 1000 people treated, and favourable outcome (mRS 0-1) absolute increase of 55 (95% CI 33-77) per 1000. The benefit of rt-PA was greatest in patients treated within 3 h (mRS 0-2, 365/896 [40·7%] vs 280/883 [31·7%], 1·53, 1·26-1·86, p<0·0001), absolute benefit of 90 (46-135) per 1000 people treated, and mRS 0-1 (283/896 [31·6%] vs 202/883 [22·9%], 1·61, 1·30-1·90; p<0·0001), absolute benefit 87 (46-128) per 1000 treated. Numbers of deaths within 7 days were increased (250/2807 [8·9%] vs 174/2728 [6·4%], 1·44, 1·18-1·76; p=0·0003), but by final follow-up the excess was no longer significant (679/3548 [19·1%] vs 640/3464 [18·5%], 1·06, 0·94-1·20; p=0·33). Symptomatic intracranial haemorrhage (272/3548 [7·7%] vs 63/3463 [1·8%], 3·72, 2·98-4·64; p<0·0001) accounted for most of the early excess deaths. Patients older than 80 years achieved similar benefit to those aged 80 years or younger, particularly when treated early.
Interpretation: The evidence indicates that intravenous rt-PA increased the proportion of patients who were alive with favourable outcome and alive and independent at final follow-up. The data strengthen previous evidence to treat patients as early as possible after acute ischaemic stroke, although some patients might benefit up to 6 h after stroke.
Funding: UK Medical Research Council, Stroke Association, University of Edinburgh, National Health Service Health Technology Assessment Programme, Swedish Heart-Lung Fund, AFA Insurances Stockholm (Arbetsmarknadens Partners Forsakringsbolag), Karolinska Institute, Marianne and Marcus Wallenberg Foundation, Research Council of Norway, Oslo University Hospital.
Emerging Elastic Micro-Nano Materials for Diagnosis and Treatment of Thrombosis.
Lu C, Li C, Gu N, Yang F Research (Wash D C). 2025; 8:0614.
PMID: 40028043 PMC: 11868703. DOI: 10.34133/research.0614.
Damen F, Su C, Tsuruda J, Anderson T, Valyi-Nagy T, Li W Magn Reson Imaging. 2024; 117:110294.
PMID: 39638136 PMC: 11807747. DOI: 10.1016/j.mri.2024.110294.
Luo L, Hu Q, Yan R, Gao X, Zhang D, Yan Y Mol Neurobiol. 2024; 62(4):5252-5272.
PMID: 39531192 DOI: 10.1007/s12035-024-04596-5.
Botezat M, Caragea A, Popescu G, Rosu G, Zorila M, tenea-Cojan T Rom J Morphol Embryol. 2024; 65(3):449-455.
PMID: 39529338 PMC: 11657329. DOI: 10.47162/RJME.65.3.07.
Xiang H, Ma Y, Luo X, Guo J, Yao M, Liu Y Neurotherapeutics. 2024; 22(1):e00474.
PMID: 39482180 PMC: 11742624. DOI: 10.1016/j.neurot.2024.e00474.