Characteristics of Recurrent Ischemic Stroke After Embolic Stroke of Undetermined Source: Secondary Analysis of a Randomized Clinical Trial.


Journal

JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536

Informations de publication

Date de publication:
01 10 2020
Historique:
pubmed: 7 7 2020
medline: 22 6 2021
entrez: 7 7 2020
Statut: ppublish

Résumé

The concept of embolic stroke of undetermined source (ESUS) unifies a subgroup of cryptogenic strokes based on neuroimaging, a defined minimum set of diagnostic tests, and exclusion of certain causes. Despite an annual stroke recurrence rate of 5%, little is known about the etiology underlying recurrent stroke after ESUS. To identify the stroke subtype of recurrent ischemic strokes after ESUS, to explore the interaction with treatment assignment in each category, and to examine the consistency of cerebral location of qualifying ESUS and recurrent ischemic stroke. The NAVIGATE-ESUS trial was a randomized clinical trial conducted from December 23, 2014, to October 5, 2017. The trial compared the efficacy and safety of rivaroxaban and aspirin in patients with recent ESUS (n = 7213). Ischemic stroke was validated in 309 of the 7213 patients by adjudicators blinded to treatment assignment and classified by local investigators into the categories ESUS or non-ESUS (ie, cardioembolic, atherosclerotic, lacunar, other determined cause, or insufficient testing). Five patients with recurrent strokes that could not be defined as ischemic or hemorrhagic in absence of neuroimaging or autopsy were excluded. Data for this secondary post hoc analysis were analyzed from March to June 2019. Patients were randomly assigned to receive rivaroxaban, 15 mg/d, or aspirin, 100 mg/d. Association of recurrent ESUS with stroke characteristics. A total of 309 patients (205 men [66%]; mean [SD] age, 68 [10] years) had ischemic stroke identified during the median follow-up of 11 (interquartile range [IQR], 12) months (annualized rate, 4.6%). Diagnostic testing was insufficient for etiological classification in 39 patients (13%). Of 270 classifiable ischemic strokes, 156 (58%) were ESUS and 114 (42%) were non-ESUS (37 [32%] cardioembolic, 26 [23%] atherosclerotic, 35 [31%] lacunar, and 16 [14%] other determined cause). Atrial fibrillation was found in 27 patients (9%) with recurrent ischemic stroke and was associated with higher morbidity (median change in modified Rankin scale score 2 [IQR, 3] vs 0 (IQR, 1]) and mortality (15% vs 1%) than other causes. Risk of recurrence did not differ significantly by subtype between treatment groups. For both the qualifying and recurrent strokes, location of infarct was more often in the left (46% and 54%, respectively) than right hemisphere (40% and 37%, respectively) or brainstem or cerebellum (14% and 9%, respectively). In this secondary analysis of randomized clinical trial data, most recurrent strokes after ESUS were embolic and of undetermined source. Recurrences associated with atrial fibrillation were a minority but were more often disabling and fatal. More extensive investigation to identify the embolic source is important toward an effective antithrombotic strategy. ClinicalTrials.gov Identifier: NCT02313909.

Identifiants

pubmed: 32628266
pii: 2767712
doi: 10.1001/jamaneurol.2020.1995
pmc: PMC7550970
doi:

Substances chimiques

Factor Xa Inhibitors 0
Platelet Aggregation Inhibitors 0
Rivaroxaban 9NDF7JZ4M3
Aspirin R16CO5Y76E

Banques de données

ClinicalTrials.gov
['NCT02313909']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1233-1240

Commentaires et corrections

Type : ErratumIn

Auteurs

Roland Veltkamp (R)

Division of Brain Sciences, Imperial College London, London, United Kingdom.
Department of Neurology, Alfried Krupp Krankenhaus, Essen, Germany.

Lesly A Pearce (LA)

currently a biostatistics consultant, St Catharines, Ontario, Canada.

Eleni Korompoki (E)

Division of Brain Sciences, Imperial College London, London, United Kingdom.
Department of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.

Mukul Sharma (M)

Population Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Scott E Kasner (SE)

Department of Neurology, University of Pennsylvania, Philadelphia.

Danilo Toni (D)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Sebastian F Ameriso (SF)

Departamento de Neurología, Fleni, Buenos Aires, Argentina.

Hardi Mundl (H)

Bayer AG, Wuppertal, Germany.

Turgut Tatlisumak (T)

Department of Clinical Neuroscience, Institute of Neurosciences and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Graeme J Hankey (GJ)

Faculty of Health and Medical Sciences, Medical School, University of Western Australia, Perth, Australia.

Arne Lindgren (A)

Department of Clinical Sciences and Neurology, Lund University, Lund, Sweden.
Department of Neurology, Skåne University Hospital, Lund, Sweden.

Scott D Berkowitz (SD)

Bayer, LLC, Whippany, New Jersey.

Antonio Arauz (A)

Instituto Nacional de Neurologia y Neurocirugia Manual Velasco Suarez, Mexico City, Mexico.

Serefnur Ozturk (S)

Department of Neurology, Faculty of Medicine, Selcuk University, Konya, Turkey.

Keith W Muir (KW)

Institute of Neuroscience and Psychology, University of Glasgow, Queen Elizabeth University Hospital, Glasgow, United Kingdom.

Ángel Chamorro (Á)

Department of Neuroscience, Hospital Clinic of Barcelona, Institute Reçerca Biomèdica August Pi i Sunyer, University of Barcelona, Barcelona, Spain.

Kanjana Perera (K)

Population Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Ashfaq Shuaib (A)

Department of Medicine, University of Alberta, Edmonton, Canada.

Salvatore Rudilosso (S)

Department of Neuroscience, Hospital Clinic of Barcelona, Institute Reçerca Biomèdica August Pi i Sunyer, University of Barcelona, Barcelona, Spain.

Ashkan Shoamanesh (A)

Population Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Stuart J Connolly (SJ)

Population Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Robert G Hart (RG)

Population Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

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Classifications MeSH