2006
DOI: 10.1007/s10072-006-0632-9
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The SITS-MOST registry

Abstract: In September 2002 the European Medicines Evaluation Agency (EMEA) approved a licence for alteplase (rt-PA) in the treatment of ischaemic stroke within 3 h of symptom onset. One of the conditions required by the EU regulatory authorities for the official definitive approval of thrombolytic therapy was that treatment safety should be monitored over a period of three years by entering all treated patients in the SITS-ISTR (Safe Implementation of Thrombolysis in Stroke -Thrombolysis Register) web register, in acco… Show more

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Cited by 43 publications
(32 citation statements)
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“…The inclusion criteria, according to criteria as published by Toni and colleagues, 13 for the present study were as follows:…”
Section: Patient Selectionmentioning
confidence: 99%
See 1 more Smart Citation
“…The inclusion criteria, according to criteria as published by Toni and colleagues, 13 for the present study were as follows:…”
Section: Patient Selectionmentioning
confidence: 99%
“…Completed treatment with a full dose of IVT according to a previously published protocol. 13 Complete documentation of the clinical course, including the initial National Institutes of Health Stroke Scale (NIHSS) score, NIHSS score at 7 days, and modified Rankin Scale (mRS) score at 90 days (90d-mRS). No additional vasculopathy in either a different intracranial territory or the cervical vessels (especially no relevant preceding stenosis).…”
Section: Patient Selectionmentioning
confidence: 99%
“…Finally, insights from audit data are dependent on the extent, level of detail and completeness of the data set and may not be fit for purpose, and they cannot address the nuances of decision-making. For instance, the SITS-MOST database 36 is limited to thrombolysed cases only and SSNAP does not collect information on all patient and clinician factors that could influence clinical decision-making.…”
Section: Chapter 3 Research Methodologymentioning
confidence: 99%
“…The ECASS-III 35 trial supported extension of the time window for treatment from 3 to 4.5 hours and the European licence time window was extended. 3 However, according to the Safe Implementation of Thrombolysis in Stroke-Monitoring (SITS-MOST) study, it is common for patients outside the licensing criteria to be treated, 36 suggesting that different clinicians are satisfied with different levels of evidence and/or vary in their decision-making process regarding patient eligibility given the same evidence. Yet little is known about the source or drivers of this variation.…”
mentioning
confidence: 99%
“…26 All patients who fulfilled the Safe Implementation of Thrombolysis in Stroke-Monitoring Study criteria for IV thrombolysis were treated by using rtPA (0.9 mg/kg) within 4.5 hours after ischemic stroke onset. 26,27 Anticoagulation therapy (oral, subcutaneous, or intravenous) and oral administration of acetylsalicylic acid or other antiplatelet agents were used as standard treatment for patients 24 hours after ischemic stroke onset according to guidelines set by the European Stroke Organization.…”
Section: Treatmentmentioning
confidence: 99%