Predictors of Atrial Fibrillation Development in Patients With Embolic Stroke of Undetermined Source: An Analysis of the RE-SPECT ESUS Trial.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
30 11 2021
Historique:
pubmed: 16 10 2021
medline: 8 1 2022
entrez: 15 10 2021
Statut: ppublish

Résumé

A proportion of patients with embolic stroke of undetermined source have silent atrial fibrillation (AF) or develop AF after the initial evaluation. Better understanding of the risk for development of AF is critical to implement optimal monitoring strategies with the goal of preventing recurrent stroke attributable to underlying AF. The RE-SPECT ESUS trial (Randomized, Double-Blind Evaluation in Secondary Stroke Prevention Comparing the Efficacy and Safety of the Oral Thrombin Inhibitor Dabigatran Etexilate Versus Acetylsalicylic Acid in Patients With Embolic Stroke of Undetermined Source) provides an opportunity to assess predictors for developing AF and associated recurrent stroke. RE-SPECT ESUS was a randomized, controlled trial (564 sites, 42 countries) assessing dabigatran versus aspirin for the prevention of recurrent stroke in patients with embolic stroke of undetermined source. Of 5390 patients enrolled and followed for a median of 19 months, 403 (7.5%) were found to develop AF reported as an adverse event or using cardiac monitoring per standard clinical care. Univariable and multivariable regression analyses were performed to define predictors of AF. In the multivariable model, older age (odds ratio for 10-year increase, 1.99 [95% CI, 1.78-2.23]; Besides age, the most important variable, several other factors, including hypertension, higher body mass index, and lack of diabetes, are independent predictors of AF after embolic stroke of undetermined source. When baseline NT-proBNP was available, only older age and elevation of this biomarker were predictive of subsequent AF. Understanding who is at higher risk of developing AF will assist in identifying patients who may benefit from more intense, long-term cardiac monitoring. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02239120.

Sections du résumé

BACKGROUND
A proportion of patients with embolic stroke of undetermined source have silent atrial fibrillation (AF) or develop AF after the initial evaluation. Better understanding of the risk for development of AF is critical to implement optimal monitoring strategies with the goal of preventing recurrent stroke attributable to underlying AF. The RE-SPECT ESUS trial (Randomized, Double-Blind Evaluation in Secondary Stroke Prevention Comparing the Efficacy and Safety of the Oral Thrombin Inhibitor Dabigatran Etexilate Versus Acetylsalicylic Acid in Patients With Embolic Stroke of Undetermined Source) provides an opportunity to assess predictors for developing AF and associated recurrent stroke.
METHODS
RE-SPECT ESUS was a randomized, controlled trial (564 sites, 42 countries) assessing dabigatran versus aspirin for the prevention of recurrent stroke in patients with embolic stroke of undetermined source. Of 5390 patients enrolled and followed for a median of 19 months, 403 (7.5%) were found to develop AF reported as an adverse event or using cardiac monitoring per standard clinical care. Univariable and multivariable regression analyses were performed to define predictors of AF.
RESULTS
In the multivariable model, older age (odds ratio for 10-year increase, 1.99 [95% CI, 1.78-2.23];
CONCLUSIONS
Besides age, the most important variable, several other factors, including hypertension, higher body mass index, and lack of diabetes, are independent predictors of AF after embolic stroke of undetermined source. When baseline NT-proBNP was available, only older age and elevation of this biomarker were predictive of subsequent AF. Understanding who is at higher risk of developing AF will assist in identifying patients who may benefit from more intense, long-term cardiac monitoring. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02239120.

Identifiants

pubmed: 34649459
doi: 10.1161/CIRCULATIONAHA.121.055176
doi:

Substances chimiques

Peptide Fragments 0
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0
Dabigatran I0VM4M70GC
Aspirin R16CO5Y76E

Banques de données

ClinicalTrials.gov
['NCT02239120']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1738-1746

Commentaires et corrections

Type : CommentIn

Auteurs

Maria Cecilia Bahit (MC)

INECO Neurociencias, Cardiology Department, Rosario, Argentina (M.C.B.).

Ralph L Sacco (RL)

Miller School of Medicine, University of Miami, Florida (R.L.S.).

J Donald Easton (JD)

University of California San Francisco (J.D.E.).

Juliane Meyerhoff (J)

TA Cardiometabolism & Respiratory Medicine (J.M.), Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.

Lisa Cronin (L)

Clinical Development Cardiometabolism, Boehringer Ingelheim Ltd/Ltée, Burlington, Canada (L.C.).

Eva Kleine (E)

Biostatistics and Data Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim am Rhein, Germany (E.K.).

Claudia Grauer (C)

Clinical Research, Boehringer Ingelheim Pharma GmbH & Co KG, Biberach, Germany (C.G.).

Martina Brueckmann (M)

Faculty of Medicine Mannheim, University of Heidelberg, Germany (M.B.).

Hans-Christoph Diener (HC)

Institute for Medical Informatics, Biometry and Epidemiology, Faculty of Medicine, University Duisburg-Essen, Essen, Germany (H.-C.D.).

Renato D Lopes (RD)

Duke Clinical Research Institute, Durham, North Carolina (R.D.L., C.B.G.).

Michael Brainin (M)

Clinical Development Cardiometabolism (M.B.), Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.

Phillippe Lyrer (P)

University Hospital Basel, Switzerland (P.L.).

Rolf Wachter (R)

Clinic and Policlinic for Cardiology, University Hospital Leipzig, Germany Clinic for Cardiology and Pneumology, University Medicine Göttingen, Germany DZHK (German Center for Cardiovascular Research), partner site Göttingen, Germany (R.W.).

Tomas Segura (T)

Department of Neurology, Hospital General Universitario de Albacete, Universidad de Castilla-La Mancha, Albacete, Spain (T.S.).

Christopher B Granger (CB)

Duke Clinical Research Institute, Durham, North Carolina (R.D.L., C.B.G.).

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