The IC-D score for predicting prophylactic cardioverter-defibrillator implantation following acute myocardial infarction.


Journal

Pacing and clinical electrophysiology : PACE
ISSN: 1540-8159
Titre abrégé: Pacing Clin Electrophysiol
Pays: United States
ID NLM: 7803944

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 29 03 2021
received: 24 02 2021
accepted: 04 04 2021
pubmed: 14 4 2021
medline: 27 1 2022
entrez: 13 4 2021
Statut: ppublish

Résumé

A reduced left ventricular ejection fraction (LVEF) ≤35% ≥6 weeks following an acute myocardial infarction (MI) may indicate prophylactic implantation of a cardioverter-defibrillator (ICD). We sought to find predictors of absence of significant left ventricular (LV) remodeling post-MI. All consecutive patients hospitalized for acute MI with an LVEF ≤35% at discharge in our institution from 2010 were retrospectively included. Patients were assigned to two groups according to the persistence of an LVEF ≤35% (ICD+) or a recovery >35% (ICD-). Logistic regression was performed to build a predictive score, which was then externally validated. Among a total of 1533 consecutive MI patients, 150 met inclusion criteria, 53 (35%) in the ICD+ group and 97 in the ICD group. After multivariable analyses, an LVEF ≤25% at discharge (adjusted OR 6.23 [2.47 to 17.0], p < .0001) and a CPK peak at the MI acute phase >4600 UI/L (adjusted OR 9.99 [4.27 to 25.3], p < .0001) both independently predicted non-recovery at 6 weeks. The IC-D (Increased Cpk-LV Dysfunction) score predicted persistent LVEF ≤35% with areas under curve of 0.83 and 0.73, in the study population and in a multicenter validation cohort of 150 patients, respectively (p < .0001). The association of a severely reduced LVEF and a major release of myocardial necrosis biomarkers at the acute phase of MI predict unfavorable remodeling, and prophylactic ICD implantation.

Sections du résumé

BACKGROUND BACKGROUND
A reduced left ventricular ejection fraction (LVEF) ≤35% ≥6 weeks following an acute myocardial infarction (MI) may indicate prophylactic implantation of a cardioverter-defibrillator (ICD). We sought to find predictors of absence of significant left ventricular (LV) remodeling post-MI.
METHODS METHODS
All consecutive patients hospitalized for acute MI with an LVEF ≤35% at discharge in our institution from 2010 were retrospectively included. Patients were assigned to two groups according to the persistence of an LVEF ≤35% (ICD+) or a recovery >35% (ICD-). Logistic regression was performed to build a predictive score, which was then externally validated.
RESULTS RESULTS
Among a total of 1533 consecutive MI patients, 150 met inclusion criteria, 53 (35%) in the ICD+ group and 97 in the ICD group. After multivariable analyses, an LVEF ≤25% at discharge (adjusted OR 6.23 [2.47 to 17.0], p < .0001) and a CPK peak at the MI acute phase >4600 UI/L (adjusted OR 9.99 [4.27 to 25.3], p < .0001) both independently predicted non-recovery at 6 weeks. The IC-D (Increased Cpk-LV Dysfunction) score predicted persistent LVEF ≤35% with areas under curve of 0.83 and 0.73, in the study population and in a multicenter validation cohort of 150 patients, respectively (p < .0001).
CONCLUSIONS CONCLUSIONS
The association of a severely reduced LVEF and a major release of myocardial necrosis biomarkers at the acute phase of MI predict unfavorable remodeling, and prophylactic ICD implantation.

Identifiants

pubmed: 33846979
doi: 10.1111/pace.14244
doi:

Substances chimiques

Anticoagulants 0
Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

973-979

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Nicolas Clementy (N)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

Reda Bensaid (R)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

Jérémie Bouteau (J)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

Joël Fedida (J)

Cardiology Department, Bicêtre Hospital, Kremlin-Bicêtre, France.

Yoann Kiavue (Y)

Cardiology Department, Georges Pompidou European Hospital, Paris, France.

Pierre Socie (P)

Cardiology Department, Chartres Louis Pasteur Hospital, Le Coudray, France.

Romain Ackermann (R)

Cardiology Department, Orleans La Source Hospital, Orleans, France.

Marc Goralski (M)

Cardiology Department, Orleans La Source Hospital, Orleans, France.

Laurent Fauchier (L)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

Anne Bernard (A)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

Denis Angoulvant (D)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

Dominique Babuty (D)

Cardiology Department, Trousseau Hospital, University of Tours, Tours, France.

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