• Werner Hacke, Geoffrey Donnan, Cesare Fieschi, Markku Kaste, Rüdiger von Kummer, Joseph P Broderick, Thomas Brott, Michael Frankel, James C Grotta, E Clarke Haley, Thomas Kwiatkowski, Steven R Levine, Chris Lewandowski, Mei Lu, Patrick Lyden, John R Marler, Suresh Patel, Barbara C Tilley, Gregory Albers, Erich Bluhmki, Manfred Wilhelm, Scott Hamilton, ATLANTIS Trials Investigators, ECASS Trials Investigators, and NINDS rt-PA Study Group Investigators.
• Medical University at Heidelberg, Germany.
• Lancet. 2004 Mar 6; 363 (9411): 768774768-74.

BackgroundQuick administration of intravenous recombinant tissue plasminogen activator (rt-PA) after stroke improved outcomes in previous trials. We aimed to analyse combined data for individual patients to confirm the importance of rapid treatment.MethodsWe pooled common data elements from six randomised placebo-controlled trials of intravenous rt-PA. Using multivariable logistic regression we assessed the relation of the interval from stroke onset to start of treatment (OTT) on favourable 3-month outcome and on the occurrence of clinically relevant parenchymal haemorrhage.FindingsTreatment was started within 360 min of onset of stroke in 2775 patients randomly allocated to rt-PA or placebo. Median age was 68 years, median baseline National Institute of Health Stroke Scale (NIHSS) 11, and median OTT 243 min. Odds of a favourable 3-month outcome increased as OTT decreased (p=0.005). Odds were 2.8 (95% CI 1.8-4.5) for 0-90 min, 1.6 (1.1-2.2) for 91-180 min, 1.4 (1.1-1.9) for 181-270 min, and 1.2 (0.9-1.5) for 271-360 min in favour of the rt-PA group. The hazard ratio for death adjusted for baseline NIHSS was not different from 1.0 for the 0-90, 91-180, and 181-270 min intervals; for 271-360 min it was 1.45 (1.02-2.07). Haemorrhage was seen in 82 (5.9%) rt-PA patients and 15 (1.1%) controls (p<0.0001). Haemorrhage was not associated with OTT but was with rt-PA treatment (p=0.0001) and age (p=0.0002).InterpretationThe sooner that rt-PA is given to stroke patients, the greater the benefit, especially if started within 90 min. Our results suggest a potential benefit beyond 3 h, but this potential might come with some risks.

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