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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

Pre‐hospital transdermal glyceryl trinitrate for transient ischaemic attack: Data from the RIGHT‐2 trial Thumbnail


Authors

Jason P Appleton

Mark Dixon

Craig S Anderson

Sandeep Ankolekar

Lesley Cala

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



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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Euro J of Neurology - 2024 - Appleton - Pre‐hospital transdermal glyceryl trinitrate for transient ischaemic attack Data (329 Kb)
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/

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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