Effect of Glyceryl Trinitrate on Hemodynamics in Acute Stroke.


Journal

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

Informations de publication

Date de publication:
02 2019
Historique:
pubmed: 11 1 2019
medline: 17 10 2019
entrez: 11 1 2019
Statut: ppublish

Résumé

Background and Purpose- Increased blood pressure (BP), heart rate, and their derivatives (variability, pulse pressure, rate-pressure product) are associated with poor clinical outcome in acute stroke. We assessed the effects of glyceryl trinitrate (GTN) on hemodynamic parameters and these on outcome in participants in the ENOS trial (Efficacy of Nitric Oxide in Stroke). Methods- Four thousand and eleven patients with acute stroke and raised BP were randomized within 48 hours of onset to transdermal GTN or no GTN for 7 days. Peripheral hemodynamics were measured at baseline (3 measures) and daily (2 measures) during treatment. Between-visit BP variability over days 1 to 7 (as SD) was assessed in quintiles. Functional outcome was assessed as modified Rankin Scale and cognition as telephone mini-mental state examination at day 90. Analyses were adjusted for baseline prognostic variables. Data are mean difference or odds ratios with 95% CI. Results- Increased baseline BP (diastolic, variability), heart rate, and rate-pressure product were each associated with unfavorable functional outcome at day 90. Increased between-visit systolic BP variability was associated with an unfavourable shift in modified Rankin Scale (highest quintile adjusted odds ratio, 1.65; 95% CI, 1.37-1.99), worse cognitive scores (telephone mini-mental state examination: highest quintile adjusted mean difference, -2.03; 95% CI, -2.84 to -1.22), and increased odds of death at day 90 (highest quintile adjusted odds ratio, 1.57; 95% CI, 1.12-2.19). GTN lowered BP and rate-pressure product and increased heart rate at day 1 and reduced between-visit systolic BP variability. Conclusions- Increased between-visit BP variability was associated with poor functional and cognitive outcomes and increased death 90 days after acute stroke. In addition to lowering BP and rate-pressure product, GTN reduced between-visit systolic BP variability. Agents that lower BP variability in acute stroke require further study.

Identifiants

pubmed: 30626285
doi: 10.1161/STROKEAHA.118.023190
pmc: PMC6358219
doi:

Substances chimiques

Nitroglycerin G59M7S0WS3

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

405-412

Subventions

Organisme : Medical Research Council
ID : G0501797
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CS/14/4/30972
Pays : United Kingdom

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Auteurs

Jason P Appleton (JP)

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

Lisa J Woodhouse (LJ)

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

Daniel Bereczki (D)

Department of Neurology, Semmelweis University, Budapest, Hungary (D.B.).

Eivind Berge (E)

Department of Internal Medicine and Cardiology, Oslo University Hospital, Norway (E.B.).

Hanne K Christensen (HK)

Department of Neurology, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark (H.K.C.).

Rónán Collins (R)

Stroke Services, Trinity College Dublin, Tallaght Hospital, Ireland (R.C.).

John Gommans (J)

Department of Medicine, Hawke's Bay District Health Board, Hastings, New Zealand (J.G.).

George Ntaios (G)

Department of Medicine, University of Thessaly, Larissa, Greece (G.N.).

Serefnur Ozturk (S)

Department of Neurology, Selcuk University Faculty of Medicine, Konya, Turkey (S.O.).

Szabolcs Szatmari (S)

Department of Neurology, Clinical County Emergency Hospital, Targu Mures, Romania (S.S.).

Joanna M Wardlaw (JM)

Division of Neuroimaging Sciences, Centre for Clinical Brain Sciences, UK Dementia Research Institute at the University of Edinburgh, (J.M.W.).

Nikola Sprigg (N)

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

Peter M Rothwell (PM)

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

Philip M Bath (PM)

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

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Classifications MeSH