Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/12100
Title: Recruitment to trials of late thrombolysis: lessons from the EXTEND study.
Authors: Dagonnier, Marie;Howells, David William;Donnan, Geoffrey A;Dewey, Helen M
Affiliation: National Stroke Research Institute, The Florey Institute for Neurosciences and Mental Health, Melbourne Brain Centre, Austin Campus, 245 Burgundy Street, Heidelberg, VIC 3084, Australia; University of Melbourne, Melbourne, VIC, Australia. Electronic address: marie.dagonnier@unimelb.edu.au.
National Stroke Research Institute, The Florey Institute for Neurosciences and Mental Health, Melbourne Brain Centre, Austin Campus, 245 Burgundy Street, Heidelberg, VIC 3084, Australia.
National Stroke Research Institute, The Florey Institute for Neurosciences and Mental Health, Melbourne Brain Centre, Austin Campus, 245 Burgundy Street, Heidelberg, VIC 3084, Australia; University of Melbourne, Melbourne, VIC, Australia; Department of Neurology, Austin Health, Heidelberg, VIC, Australia.
Issue Date: 29-Jan-2014
Citation: Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia 2014; 21(7): 1215-9
Abstract: To increase the percentage of acute stroke patients benefiting from thrombolysis, the utility of expanding the time window of treatment beyond 4.5 hours after stroke onset needs to be investigated. We aimed to identify the target population and the challenges of recruitment of patients for the time window beyond 4.5 hours. Extending the time for Thrombolysis in Emergency Neurological Deficits (EXTEND), a multicentre randomised controlled trial testing the efficacy of thrombolytic therapy in patients with clinically significant ischaemic penumbra between 4.5 to 9 hours after stroke onset, was used as a model to evaluate inclusion and exclusion criteria for late thrombolysis trials. Data from all stroke patients admitted to Austin Health over a 1 year period were retrospectively analysed. Case notes were examined to determine potential trial eligibility. Of 556 patients assessed, 95 (17%) presented during the EXTEND time window. Sixty-seven of these (70.5%) were wake-up strokes (WUS) and 28 (29.5%) arrived between 4.5 and 9 hours after symptoms onset. At least one exclusion criterion was found for 78 (82%) of them. Hence, 17 (3%) patients arrived within an appropriate time frame for the study without any exclusion criteria. Most of these (13) arrived outside routine MRI hours. The number of patients recruited would have increased more than three-fold if imaging had been available 24 hours, 7 days a week. A significant proportion (17%) of ischaemic stroke patients presented between 4.5 and 9 hours after stroke onset. The majority of these were WUS. The major challenge identified for patient recruitment was imaging availability.
Internal ID Number: 24583057
URI: http://ahro.austin.org.au/austinjspui/handle/1/12100
DOI: 10.1016/j.jocn.2013.10.033
URL: http://www.ncbi.nlm.nih.gov/pubmed/24583057
Type: Journal Article
Subjects: Clinical trials
Imaging
Recruitment
Stroke
Thrombolysis
Female
Humans
Male
Nervous System Diseases.drug therapy.etiology
Patient Selection
Randomized Controlled Trials as Topic
Retrospective Studies
Stroke.complications.drug therapy
Thrombolytic Therapy.methods
Time Factors
Tissue Plasminogen Activator.therapeutic use
Appears in Collections:Journal articles

Files in This Item:
There are no files associated with this item.


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.