Timing of revascularization in patients with transient ST-segment elevation myocardial infarction: a randomized clinical trial.


Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
14 01 2019
Historique:
received: 14 05 2018
accepted: 05 10 2018
pubmed: 30 10 2018
medline: 18 4 2020
entrez: 30 10 2018
Statut: ppublish

Résumé

Patients with acute coronary syndrome who present initially with ST-elevation on the electrocardiogram but, subsequently, show complete normalization of the ST-segment and relief of symptoms before reperfusion therapy are referred to as transient ST-segment elevation myocardial infarction (STEMI) and pose a therapeutic challenge. It is unclear what the optimal timing of revascularization is for these patients and whether they should be treated with a STEMI-like or a non-ST-segment elevation myocardial infarction (NSTEMI)-like invasive approach. The aim of the study is to determine the effect of an immediate vs. a delayed invasive strategy on infarct size measured by cardiac magnetic resonance imaging (CMR). In a randomized clinical trial, 142 patients with transient STEMI with symptoms of any duration were randomized to an immediate (STEMI-like) [0.3 h; interquartile range (IQR) 0.2-0.7 h] or a delayed (NSTEMI-like) invasive strategy (22.7 h; IQR 18.2-27.3 h). Infarct size as percentage of the left ventricular myocardial mass measured by CMR at day four was generally small and not different between the immediate and the delayed invasive group (1.3%; IQR 0.0-3.5% vs. 1.5% IQR 0.0-4.1%, P = 0.48). By intention to treat, there was no difference in major adverse cardiac events (MACE), defined as death, reinfarction, or target vessel revascularization at 30 days (2.9% vs. 2.8%, P = 1.00). However, four additional patients (5.6%) in the delayed invasive strategy required urgent intervention due to signs and symptoms of reinfarction while awaiting angiography. Overall, infarct size in transient STEMI is small and is not influenced by an immediate or delayed invasive strategy. In addition, short-term MACE was low and not different between the treatment groups.

Identifiants

pubmed: 30371767
pii: 5145843
doi: 10.1093/eurheartj/ehy651
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

283-291

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

Jorrit S Lemkes (JS)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Gladys N Janssens (GN)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Nina W van der Hoeven (NW)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Peter M van de Ven (PM)

Department of Epidemiology and Biostatistics, VU University, De Boelelaan 1089a, Amsterdam, the Netherlands.

Koen M J Marques (KMJ)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Alexander Nap (A)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Maarten A H van Leeuwen (MAH)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.
Department of Cardiology, Isala Heart Center, Dokter van Heesweg 2, Zwolle, the Netherlands.

Yolande E A Appelman (YEA)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Paul Knaapen (P)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Niels J W Verouden (NJW)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Cornelis P Allaart (CP)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Stijn L Brinckman (SL)

Department of Cardiology, Tergooi Hospital, Rijksstraatweg 1, Blaricum, the Netherlands.

Colette E Saraber (CE)

Department of Cardiology, Tergooi Hospital, Rijksstraatweg 1, Blaricum, the Netherlands.

Koos J Plomp (KJ)

Department of Cardiology, Tergooi Hospital, Rijksstraatweg 1, Blaricum, the Netherlands.

Jorik R Timmer (JR)

Department of Cardiology, Isala Heart Center, Dokter van Heesweg 2, Zwolle, the Netherlands.

Elvin Kedhi (E)

Department of Cardiology, Isala Heart Center, Dokter van Heesweg 2, Zwolle, the Netherlands.

Renicus S Hermanides (RS)

Department of Cardiology, Isala Heart Center, Dokter van Heesweg 2, Zwolle, the Netherlands.

Martijn Meuwissen (M)

Department of Cardiology, Amphia Hospital, Molengracht 21, Breda, the Netherlands.

Jeroen Schaap (J)

Department of Cardiology, Amphia Hospital, Molengracht 21, Breda, the Netherlands.

Arno P van der Weerdt (AP)

Department of Cardiology, Medical Center Leeuwarden, Henri Dunantweg 2, Leeuwarden, the Netherlands.

Albert C van Rossum (AC)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.

Robin Nijveldt (R)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.
Department of Cardiology, Radboud University Medical Center, Geert Grooteplein Zuid 10, Nijmegen, the Netherlands.

Niels van Royen (N)

Department of Cardiology, Amsterdam UMC, VU University Amsterdam, De Boelelaan 1117, Amsterdam, the Netherlands.
Department of Cardiology, Radboud University Medical Center, Geert Grooteplein Zuid 10, Nijmegen, the Netherlands.

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