In-Hospital ECG Findings, Changes in Medical Management, and Cardiovascular Outcomes in Patients With Acute Stroke or Transient Ischemic Attack.
ECG
beta‐blocker
mortality
stroke
transient‐ischemic attack
Journal
Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524
Informations de publication
Date de publication:
17 01 2023
17 01 2023
Historique:
pubmed:
12
1
2023
medline:
19
1
2023
entrez:
11
1
2023
Statut:
ppublish
Résumé
Background In patients with acute ischemic stroke, little is known regarding the frequency of abnormal ECG findings other than atrial fibrillation and their association with cardiovascular outcomes. We aim to analyze the frequency and type of abnormal ECG findings, subsequent changes in medical treatment, and their association with cardiovascular outcomes in patients with acute ischemic stroke. Methods and Results In the investigator-initiated multicenter MonDAFIS (impact of standardized monitoring for detection of atrial fibrillation in ischemic stroke) study, 3465 patients with acute ischemic stroke or transient ischemic attack and without known atrial fibrillation were randomized 1:1 to receive Holter-ECG for up to 7 days in-hospital with systematic evaluation in a core cardiology laboratory (intervention group) or standard diagnostic care (control group). Outcomes included predefined abnormal ECG findings (eg, pauses, atrial fibrillation, brady-/tachycardias), medical management in the intervention group, and combined vascular end point (recurrent stroke, myocardial infarction, major bleeds, or all-cause death) and mortality at 24 months in both randomization groups. Predefined abnormal ECG findings were detected in 326 of 1693 (19.3%) patients in the intervention group. Twenty of these 326 patients (6.1%) received a pacemaker, and 62 of 326 (19.0%) patients had newly initiated or discontinued β-blocker medication. Discontinuation of β-blockers was associated with a higher death rate in the control group than in the intervention group during 24 months after enrollment (adjusted hazard ratio, 11.0 [95% CI, 2.4-50.4];
Identifiants
pubmed: 36628982
doi: 10.1161/JAHA.122.027149
pmc: PMC9939074
doi:
Banques de données
ClinicalTrials.gov
['NCT02204267']
Types de publication
Randomized Controlled Trial
Multicenter Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e027149Investigateurs
Michael Bauerle
(M)
T Büttner
(T)
Michael Besselmann
(M)
Elmar Busch
(E)
Petra Dem
(P)
Joanna Dietzel
(J)
Eva-Maria Kampschulte
(EM)
Gesa Nöhren
(G)
Larissa Pfeiler
(L)
Rainer Dziewas
(R)
Wolfgang Köhler
(W)
Sven Ehrlich
(S)
Annette Evens
(A)
Karen Louise Harvey
(KL)
Marie Prince
(M)
Debora Wilkes
(D)
Louise Tyler
(L)
Georg Gahn
(G)
Gerhard F Hamann
(GF)
Andreas Hartmann
(A)
Jens Diekmann
(J)
Fedor Heidenreich
(F)
T Helberg
(T)
F Hoffmann
(F)
Gerhard J Jungehulsing
(GJ)
Christos Krogias
(C)
Matthias Maschke
(M)
Stefan Merkelbach
(S)
Johannes Muehler
(J)
Ludwig Niehaus
(L)
Martin Nückel
(M)
P Oschmann
(P)
Frederick Palm
(F)
Christian Urbanek
(C)
Gabor C Petzold
(GC)
Waltraud Pfeilschifter
(W)
Peter Ringleb
(P)
Michael Rosenkranz
(M)
Georg Royl
(G)
Renate B Schnabel
(RB)
Andreas Steinbrecher
(A)
Elke Leinisch
(E)
Robert Stingele
(R)
Christian Tanislav
(C)
Andrea Rocco
(A)
Christoph Leithner
(C)
Wolfram Döhner
(W)
Patrick Nagel
(P)
Mattias Roser
(M)
Andreas Rillig
(A)
Nikolaus Marx
(N)
Otto Busse
(O)
André Scherag
(A)
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