Prehospital Transdermal Glyceryl Trinitrate for Ultra-Acute Intracerebral Hemorrhage: Data From the RIGHT-2 Trial.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
11 2019
Historique:
pubmed: 8 10 2019
medline: 31 3 2020
entrez: 8 10 2019
Statut: ppublish

Résumé

Background and Purpose- Pilot trials suggest that glyceryl trinitrate (GTN; nitroglycerin) may improve outcome when administered early after stroke onset. Methods- We undertook a multicentre, paramedic-delivered, ambulance-based, prospective randomized, sham-controlled, blinded-end point trial in adults with presumed stroke within 4 hours of ictus. Participants received transdermal GTN (5 mg) or a sham dressing (1:1) in the ambulance and then daily for three days in hospital. The primary outcome was the 7-level modified Rankin Scale at 90 days assessed by central telephone treatment-blinded follow-up. This prespecified subgroup analysis focuses on participants with an intracerebral hemorrhage as their index event. Analyses are intention-to-treat. Results- Of 1149 participants with presumed stroke, 145 (13%; GTN, 74; sham, 71) had an intracerebral hemorrhage: time from onset to randomization median, 74 minutes (interquartile range, 45-110). By admission to hospital, blood pressure tended to be lower with GTN as compared with sham: mean, 4.4/3.5 mm Hg. The modified Rankin Scale score at 90 days was nonsignificantly higher in the GTN group: adjusted common odds ratio for poor outcome, 1.87 (95% CI, 0.98-3.57). A prespecified global analysis of 5 clinical outcomes (dependency, disability, cognition, quality of life, and mood) was worse with GTN; Mann-Whitney difference, 0.18 (95% CI, 0.01-0.35; Wei-Lachin test). GTN was associated with larger hematoma and growth, and more mass effect and midline shift on neuroimaging, and altered use of hospital resources. Death in hospital but not at day 90 was increased with GTN. There were no significant between-group differences in serious adverse events. Conclusions- Prehospital treatment with GTN worsened outcomes in patients with intracerebral hemorrhage. Since these results could relate to the play of chance, confounding, or a true effect of GTN, further randomized evidence on the use of vasodilators in ultra-acute intracerebral hemorrhage is needed. Clinical Trial Registration- URL: http://www.controlled-trials.com. Unique identifier: ISRCTN26986053.

Identifiants

pubmed: 31587658
doi: 10.1161/STROKEAHA.119.026389
pmc: PMC6824503
doi:

Substances chimiques

Nitroglycerin G59M7S0WS3

Banques de données

ISRCTN
['ISRCTN26986053']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3064-3071

Subventions

Organisme : British Heart Foundation
ID : CS/14/4/30972
Pays : United Kingdom

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Auteurs

Philip M Bath (PM)

From the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
Stroke, Nottingham University Hospitals National Health Service (NHS) Trust, City Hospital Campus, United Kingdom (P.M.B., K.K., N.S.).

Lisa J Woodhouse (LJ)

From the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).

Kailash Krishnan (K)

Stroke, Nottingham University Hospitals National Health Service (NHS) Trust, City Hospital Campus, United Kingdom (P.M.B., K.K., N.S.).

Jason P Appleton (JP)

From the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).

Craig S Anderson (CS)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, Australia (C.S.A.).
The George Institute China at Peking University Health Science Center, Beijing, China (C.S.A.).
Neurology Department, Royal Prince Alfred Hospital, Sydney Health Partners, NSW, Australia (C.S.A.).

Eivind Berge (E)

Department of Internal Medicine (E.B., A.N.S), Oslo University Hospital, Norway.
Department of Neurology (E.C.S.), Oslo University Hospital, Norway.

Lesley Cala (L)

Faculty of Health and Medical Sciences, University of Western Australia (L.C.).

Mark Dixon (M)

From the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
East Midlands Ambulance Service NHS Trust, Nottingham, United Kingdom (M.D.).

Timothy J England (TJ)

Vascular Medicine, Division of Medical Sciences, GEM, Royal Derby Hospital Centre (T.J.E.), University of Nottingham, United Kingdom.

Peter J Godolphin (PJ)

Nottingham Clinical Trials Unit, Queen's Medical Centre (P.J.G., T.H., A.A.M.), University of Nottingham, United Kingdom.

Trish Hepburn (T)

Nottingham Clinical Trials Unit, Queen's Medical Centre (P.J.G., T.H., A.A.M.), University of Nottingham, United Kingdom.

Grant Mair (G)

Centre for Clinical Brain Sciences, Edinburgh Imaging and UK Dementia Research Institute at the University of Edinburgh, Chancellor's Building (G.M., J.M.W.).

Alan A Montgomery (AA)

Nottingham Clinical Trials Unit, Queen's Medical Centre (P.J.G., T.H., A.A.M.), University of Nottingham, United Kingdom.

Stephen J Phillips (SJ)

Department of Medicine, Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, Canada (S.J.P.).

John Potter (J)

Bob Champion Research and Education Building, University of East Anglia, Norwich, United Kingdom (J.P.).

Chris I Price (CI)

Institute of Neuroscience, Newcastle University, United Kingdom (C.I.P.).

Marc Randall (M)

Department of Neurology, Leeds Teaching Hospitals NHS Trust, United Kingdom (M.R.).

Thompson G Robinson (TG)

Department of Cardiovascular Sciences and NIHR Leicester Biomedical Research Centre, University of Leicester, United Kingdom (T.G.R.).

Christine Roffe (C)

Stroke Research in Stoke, Institute for Science and Technology in Medicine, Keele University, Stoke-on-Trent, United Kingdom (C.R.).

Peter M Rothwell (PM)

Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, United Kingdom (P.M.R.).

Else C Sandset (EC)

Research and Development, The Norwegian Air Ambulance Foundation, Oslo, Norway (E.C.S.).

Nerses Sanossian (N)

Department of Neurology, University of Southern California Keck School of Medicine, Los Angeles (N.S.).

Jeffrey L Saver (JL)

Department of Neurology and Comprehensive Stroke Center, David Geffen School of Medicine at UCLA (J.L.S.).

A Niroshan Siriwardena (AN)

Department of Internal Medicine (E.B., A.N.S), Oslo University Hospital, Norway.
Community and Health Research Unit, University of Lincoln, United Kingdom (A.N.S.).

Graham Venables (G)

Department of Neurology, Royal Hallamshire Hospital, Sheffield, United Kingdom (G.V.).

Joanna M Wardlaw (JM)

Centre for Clinical Brain Sciences, Edinburgh Imaging and UK Dementia Research Institute at the University of Edinburgh, Chancellor's Building (G.M., J.M.W.).

Nikola Sprigg (N)

From the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
Stroke, Nottingham University Hospitals National Health Service (NHS) Trust, City Hospital Campus, United Kingdom (P.M.B., K.K., N.S.).

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