Do Patients need Lifelong β-Blockers after an Uncomplicated Myocardial Infarction?


Journal

American journal of cardiovascular drugs : drugs, devices, and other interventions
ISSN: 1179-187X
Titre abrégé: Am J Cardiovasc Drugs
Pays: New Zealand
ID NLM: 100967755

Informations de publication

Date de publication:
Oct 2019
Historique:
pubmed: 5 3 2019
medline: 27 2 2020
entrez: 5 3 2019
Statut: ppublish

Résumé

The lifelong use of β-adrenoceptor antagonists (β-blockers) after a myocardial infarction (MI) has been the standard of care based on trials performed before the era of revascularization, when heart failure was common. Large randomized trials in the mid-1980s demonstrated that β-blockers played a major role in improving the in-hospital and long-term survival of patients admitted for MI. However, the implementation of rapid myocardial reperfusion led to a substantial survival benefit and a reduction of heart failure because of reduced infarct size. Modern large longitudinal registries did not provide sufficient evidence to support long-term β-blocker therapy in patients with uncomplicated acute MI. The long-term prescription of this therapy has become a matter of debate given the lack of contemporary evidence, frequent side effects, and treatment adherence issues. Furthermore, this shift into the reperfusion era led to a downgraded recommendation for the use of β-blockers in post-MI patients (class IIa B recommendation) in the 2017 European Society of Cardiology (ESC) recommendations for the treatment of ST-segment elevation MI (STEMI). Three large ongoing multicenter randomized trials (AβYSS, REDUCE-SWEDEHEART, and REBOOT-CNIC) are evaluating early discontinuation of β-blockers after an uncomplicated acute MI. The tested hypothesis is that β-blocker withdrawal is safe versus major adverse cardiovascular events and improves quality of life by reducing side effects. Thus, the present review summarizes the exhaustive evidence-based data for long-term β-blocker use after uncomplicated MI and the ongoing trials.

Identifiants

pubmed: 30828768
doi: 10.1007/s40256-019-00338-4
pii: 10.1007/s40256-019-00338-4
doi:

Substances chimiques

Adrenergic beta-Antagonists 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

431-438

Auteurs

Michel Zeitouni (M)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France.

Mathieu Kerneis (M)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France.

Benoit Lattuca (B)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France.
ACTION Study Group, Cardiology Department, Nîmes University Hospital, Montpellier University, Nîmes, France.

Paul Guedeney (P)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France.

Guillaume Cayla (G)

ACTION Study Group, Cardiology Department, Nîmes University Hospital, Montpellier University, Nîmes, France.

Jean-Philippe Collet (JP)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France.

Gilles Montalescot (G)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France.

Johanne Silvain (J)

Sorbonne Université, ACTION Study Group, APHP, INSERM, UMRS 1166, Hôpital Pitié-Salpêtrière, Institut de Cardiologie- Bureau 7-2ème étage, 47-83 bld de l'Hôpital, 75013, Paris, France. johanne.silvain@aphp.fr.

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