التفاصيل البيبلوغرافية
| العنوان: |
A Reduction in Time with Electronic Monitoring In Stroke (ARTEMIS): study protocol for a randomised multicentre trial. |
| المؤلفون: |
Koster, Gaia T., T. Truc My Nguyen, Groot, Adrien E. D., Coutinho, Jonathan M., Bosch, Jan, den Hertog, Heleen M., van Walderveen, Marianne A. A., Algra, Ale, Wermer, Marieke J. H., Roos, Yvo B., Kruyt, Nyika D. |
| المصدر: |
BMJ Open; Jun2018, Vol. 8 Issue 6, p1-7, 7p |
| مستخلص: |
Introduction Time is the most crucial factor limiting efficacy of intravenous thrombolysis (IVT) and intra-arterial thrombectomy (IAT). The delay between alarming the Emergency Medical Services (EMS) dispatch office and IVT/IAT initiation, that is, the 'total system delay' (TSD), depends on logistics and team effort. A promising method to reduce TSD is real-time audio-visual feedback to caregivers involved. With 'A Reduction in Time with Electronic Monitoring in Stroke' (ARTEMIS), we aim to investigate the effect of real-time audio-visual feedback on actual TSD to IVT/IAT to caregivers. Methods and analysis ARTEMIS is a multiregional, multicentre, randomised open end-point trial including patients ≥18 years considered IVT/IAT-eligible by the EMS dispatch office or on-site EMS personnel. Patients are electronically tracked and randomised for real-time audio-visual feedback on TSD to caregivers via premounted handhelds and tablets throughout the TSD trajectory. Primary outcome is TSD to IVT/IAT. Secondary outcomes comprise proportion of IVT/IAT-treated patients, symptomatic intracerebral haemorrhage, IVT/IAT-treated stroke mimics, clinical outcome after three months and cost-effectiveness. Separate analyses for IAT-patients with or without prior IVT, within or out of office hours and EMS region will be performed. With 75 IAT-patients and 225 IVT-patients in each arm, we will be able to demonstrate a 20 min difference in TSD to IAT and a 10 min difference in TSD to IVT (p=0.05 and power=0.8). Ethics and dissemination Study findings will be disseminated through peer-reviewed journals and (inter)national conference presentations. Trial registration number NCT02808806; Pre-results. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
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