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  Time to treatment with intravenous alteplase and outcome in stroke: An updated pooled analysis of ECASS, ATLANTIS, NINDS, and EPITHET trials

Lees, K. R., Bluhmki, E., von Kummer, R., Brott, T. G., Toni, D., Grotta, J. C., et al. (2010). Time to treatment with intravenous alteplase and outcome in stroke: An updated pooled analysis of ECASS, ATLANTIS, NINDS, and EPITHET trials. The Lancet, 375(9727), 1695-1703. doi:10.1016/S0140-6736(10)60491-6.

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Lees, Kennedy R.1, Author
Bluhmki, Erich1, Author
von Kummer, Rüdiger1, Author
Brott, Thomas G.1, Author
Toni, Danilo1, Author
Grotta, James C.1, Author
Albers, Gregory W.1, Author
Kaste, Markku1, Author
Marler, John R.1, Author
Hamilton, Scott A.1, Author
Tilley, Barbara C.1, Author
Davis, Stephen M.1, Author
Donnan, Geoffrey A.1, Author
Hacke, Werner1, Author
ECASS, ATLANTIS, NINDS and EPITHET rt-PA Study Group, Author              
Villringer, Arno2, Author                 
Allen, Kathryn, Author
Mau, Jochen, Author
Meier, Dieter, Author
del Zoppo, Gregory, Author
De Silva, D. A., AuthorButcher, K. S., AuthorParsons, M. W., AuthorBarber, P. A., AuthorLevi, C., AuthorBladin, C., AuthorByrnes, G., Author more..
Affiliations:
1External Organizations, ou_persistent22              
2Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              

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 Abstract: Background: Early administration of intravenous recombinant tissue plasminogen activator (rt-PA) after ischaemic stroke improves outcome. Previous analysis of combined data from individual patients suggested potential benefit beyond 3 h from stroke onset. We re-examined the effect of time to treatment with intravenous rt-PA (alteplase) on therapeutic benefit and clinical risk by adding recent trial data to the analysis.

Methods: We added data from ECASS III (821 patients) and EPITHET (100 patients) to a pool of common data elements from six other trials of alteplase for acute stroke (2775 patients). We used multivariate logistic regression to assess the relation of stroke onset to start of treatment (OTT) with treatment on favourable 3-month outcome (defined as modified Rankin score 0-1), mortality, and occurrence and outcome of clinically relevant parenchymal haemorrhage. The presence of an arterial occlusion was inferred from the patient's symptoms and absence of haemorrhage or other causes of ischaemic stroke. Vascular imaging was not a requirement in the trials. All patients with confirmed OTT within 360 min were included in the analysis.

Findings: Treatment was started within 360 min of stroke onset in 3670 patients randomly allocated to alteplase (n=1850) or to placebo (n=1820). Odds of a favourable 3-month outcome increased as OTT decreased (p=0.0269) and no benefit of alteplase treatment was seen after around 270 min. Adjusted odds of a favourable 3-month outcome were 2.55 (95% CI 1.44-4.52) for 0-90 min, 1.64 (1.12-2.40) for 91-180 min, 1.34 (1.06-1.68) for 181-270 min, and 1.22 (0.92-1.61) for 271-360 min in favour of the alteplase group. Large parenchymal haemorrhage was seen in 96 (5.2%) of 1850 patients assigned to alteplase and 18 (1.0%) of 1820 controls, with no clear relation to OTT (p=0.4140). Adjusted odds of mortality increased with OTT (p=0.0444) and were 0.78 (0.41-1.48) for 0-90 min, 1.13 (0.70-1.82) for 91-180 min, 1.22 (0.87-1.71) for 181-270 min, and 1.49 (1.00-2.21) for 271-360 min.

Interpretation: Patients with ischaemic stroke selected by clinical symptoms and CT benefit from intravenous alteplase when treated up to 4.5 h. To increase benefit to a maximum, every effort should be taken to shorten delay in initiation of treatment. Beyond 4.5 h, risk might outweigh benefit.

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Language(s): eng - English
 Dates: 2010-05-132010-05-15
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1016/S0140-6736(10)60491-6
PMID: 20472172
 Degree: -

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Title: The Lancet
Source Genre: Journal
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Publ. Info: New York : J.B. Flint & Co.
Pages: - Volume / Issue: 375 (9727) Sequence Number: - Start / End Page: 1695 - 1703 Identifier: ISSN: 1050-5911
CoNE: https://pure.mpg.de/cone/journals/resource/954925470330