Jason P Appleton
Pre‐hospital transdermal glyceryl trinitrate for transient ischaemic attack: Data from the RIGHT‐2 trial
Appleton, Jason P; Dixon, Mark; Woodhouse, Lisa J; Anderson, Craig S; Ankolekar, Sandeep; Cala, Lesley; England, Timothy J; Godolphin, Peter J; Krishnan, Kailash; Mair, Grant; Muir, Keith W; Potter, John; Price, Chris I; Randall, Marc; Robinson, Thompson G; Roffe, Christine; Rothwell, Peter M; Sandset, Else Charlotte; Saver, Jeffrey L; Siriwardena, A Niroshan; Wardlaw, Joanna M; Sprigg, Nikola; Bath, Philip M
Authors
Mark Dixon
Dr LISA WOODHOUSE L.Woodhouse@nottingham.ac.uk
RESEARCH FELLOW
Craig S Anderson
Sandeep Ankolekar
Lesley Cala
Professor Tim England Timothy.England@nottingham.ac.uk
PROFESSOR OF STROKE MEDICINE
Peter J Godolphin
Kailash Krishnan
Grant Mair
Keith W Muir
John Potter
Chris I Price
Marc Randall
Thompson G Robinson
Christine Roffe
Peter M Rothwell
Else Charlotte Sandset
Jeffrey L Saver
A Niroshan Siriwardena
Joanna M Wardlaw
Professor NIKOLA SPRIGG nikola.sprigg@nottingham.ac.uk
PROFESSOR OF STROKE MEDICINE
Professor PHILIP BATH philip.bath@nottingham.ac.uk
STROKE ASSOCIATION PROFESSOR OF STROKE MEDICINE
Abstract
Background and purpose
Ambulance trials assessing interventions in suspected stroke patients will recruit patients with currently active symptoms that will resolve into transient ischaemic attack (TIA). The safety and efficacy of glyceryl trinitrate (GTN) in the pre-specified subgroup of patients with TIA in the Rapid Intervention with Glyceryl Trinitrate in Hypertensive Stroke Trial 2 (RIGHT-2) was assessed.
Methods
RIGHT-2 was a pre-hospital-initiated multicentre randomized sham-controlled blinded-endpoint trial that randomized patients with presumed ultra-acute stroke within 4 h of symptom onset to transdermal GTN or sham. Final diagnosis was determined by site investigators. The primary outcome was a shift in modified Rankin Scale (mRS) scores at 90 days analysed using ordinal logistic regression reported as adjusted common odds ratio with 95% confidence intervals (CIs). Secondary outcomes included death or dependence (mRS >2).
Results
In all, 109 of 1149 (9.5%) patients had a final diagnosis of TIA (GTN 57, sham 52) with mean age 73 (SD 13) years, 19 (17.4%) had pre-morbid mRS >2, and onset to randomization was 80 min (interquartile range 49, 105). GTN lowered blood pressure by 7.4/5.2 mmHg compared with sham by hospital arrival. At day 90, GTN had no effect on shift in mRS scores (common odds ratio for increased dependence 1.47, 95% CI 0.70–3.11) but was associated with increased death or dependence (mRS >2): GTN 29 (51.8%) versus sham 23 (46.9%), odds ratio 3.86 (95% CI 1.09–13.59).
Conclusions
Pre-hospital ultra-acute transdermal GTN did not improve overall functional outcome in patients with investigator-diagnosed TIA compared with sham treatment.
Citation
Appleton, J. P., Dixon, M., Woodhouse, L. J., Anderson, C. S., Ankolekar, S., Cala, L., England, T. J., Godolphin, P. J., Krishnan, K., Mair, G., Muir, K. W., Potter, J., Price, C. I., Randall, M., Robinson, T. G., Roffe, C., Rothwell, P. M., Sandset, E. C., Saver, J. L., Siriwardena, A. N., …Bath, P. M. (2024). Pre‐hospital transdermal glyceryl trinitrate for transient ischaemic attack: Data from the RIGHT‐2 trial. European Journal of Neurology, 31(12), Article e16502. https://doi.org/10.1111/ene.16502
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 17, 2024 |
Online Publication Date | Oct 11, 2024 |
Publication Date | 2024-12 |
Deposit Date | Sep 20, 2024 |
Publicly Available Date | Sep 20, 2024 |
Journal | European Journal of Neurology |
Print ISSN | 1351-5101 |
Electronic ISSN | 1468-1331 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 31 |
Issue | 12 |
Article Number | e16502 |
DOI | https://doi.org/10.1111/ene.16502 |
Keywords | stroke, blood pressure, transient ischaemic attack, clinical trial |
Public URL | https://nottingham-repository.worktribe.com/output/39728224 |
Publisher URL | https://onlinelibrary.wiley.com/doi/10.1111/ene.16502 |
Additional Information | Received: 2024-07-16; Accepted: 2024-09-17; Published: 2024-10-11 |
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Copyright Statement
© 2024 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.
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