Prevalence, clinical determinants and prognostic implications of coronary procedural complications of percutaneous coronary intervention in non-ST-segment elevation myocardial infarction: Insights from the contemporary multinational TAO trial.


Journal

Archives of cardiovascular diseases
ISSN: 1875-2128
Titre abrégé: Arch Cardiovasc Dis
Pays: Netherlands
ID NLM: 101465655

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 17 04 2020
revised: 11 07 2020
accepted: 07 09 2020
pubmed: 2 2 2021
medline: 30 4 2021
entrez: 1 2 2021
Statut: ppublish

Résumé

Few data are available on procedural complications of percutaneous coronary intervention (PCI) in the setting of acute coronary syndrome in the contemporary era. We sought to describe the prevalence of procedural complications of PCI in a non-ST-segment elevation acute coronary syndrome (NSTE ACS) cohort, and to identify their clinical characteristics and association with clinical outcomes. Patients randomized in TAO (Treatment of Acute coronary syndrome with Otamixaban), an international randomized controlled trial (ClinicalTrials.gov Identifier: NCT01076764) that compared otamixaban with unfractionated heparin plus eptifibatide in patients with NSTE ACS who underwent PCI, were included in the analysis. Procedural complications were collected prospectively, categorized and adjudicated by a blinded Clinical Events Committee, with review of angiograms. A multivariable model was constructed to identify independent clinical characteristics associated with procedural complications. A total of 8656 patients with NSTE ACS who were enrolled in the TAO trial underwent PCI, and 451 (5.2%) experienced at least one complication. The most frequent complications were no/slow reflow (1.5%) and dissection with decreased flow (1.2%). Procedural complications were associated with the 7-day ischaemic outcome of death, myocardial infarction or stroke (24.2% vs. 6.0%, odds ratio 5.01, 95% confidence interval 3.96-6.33; P<0.0001) and with Thrombolysis In Myocardial Infarction major and minor bleeding (6.2% vs. 2.3%, odds ratio 2.79, 95% confidence interval 1.86-4.2; P<0.0001). Except for previous coronary artery bypass grafting, multivariable analysis did not identify preprocedural clinical predictors of complications. In a contemporary NSTE ACS population, procedural complications with PCI remain frequent, are difficult to predict based on clinical characteristics, and are associated with worse ischaemic and haemorrhagic outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Few data are available on procedural complications of percutaneous coronary intervention (PCI) in the setting of acute coronary syndrome in the contemporary era.
AIM OBJECTIVE
We sought to describe the prevalence of procedural complications of PCI in a non-ST-segment elevation acute coronary syndrome (NSTE ACS) cohort, and to identify their clinical characteristics and association with clinical outcomes.
METHODS METHODS
Patients randomized in TAO (Treatment of Acute coronary syndrome with Otamixaban), an international randomized controlled trial (ClinicalTrials.gov Identifier: NCT01076764) that compared otamixaban with unfractionated heparin plus eptifibatide in patients with NSTE ACS who underwent PCI, were included in the analysis. Procedural complications were collected prospectively, categorized and adjudicated by a blinded Clinical Events Committee, with review of angiograms. A multivariable model was constructed to identify independent clinical characteristics associated with procedural complications.
RESULTS RESULTS
A total of 8656 patients with NSTE ACS who were enrolled in the TAO trial underwent PCI, and 451 (5.2%) experienced at least one complication. The most frequent complications were no/slow reflow (1.5%) and dissection with decreased flow (1.2%). Procedural complications were associated with the 7-day ischaemic outcome of death, myocardial infarction or stroke (24.2% vs. 6.0%, odds ratio 5.01, 95% confidence interval 3.96-6.33; P<0.0001) and with Thrombolysis In Myocardial Infarction major and minor bleeding (6.2% vs. 2.3%, odds ratio 2.79, 95% confidence interval 1.86-4.2; P<0.0001). Except for previous coronary artery bypass grafting, multivariable analysis did not identify preprocedural clinical predictors of complications.
CONCLUSIONS CONCLUSIONS
In a contemporary NSTE ACS population, procedural complications with PCI remain frequent, are difficult to predict based on clinical characteristics, and are associated with worse ischaemic and haemorrhagic outcomes.

Identifiants

pubmed: 33518473
pii: S1875-2136(21)00004-8
doi: 10.1016/j.acvd.2020.09.005
pii:
doi:

Substances chimiques

Anticoagulants 0
Cyclic N-Oxides 0
Factor Xa Inhibitors 0
Platelet Aggregation Inhibitors 0
Pyridines 0
Heparin 9005-49-6
Eptifibatide NA8320J834
otamixaban S173RED00L

Banques de données

ClinicalTrials.gov
['NCT01076764']

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

187-196

Informations de copyright

Copyright © 2021. Published by Elsevier Masson SAS.

Auteurs

Jeremie Abtan (J)

FACT (an F-CRIN network), DHU-FIRE, Hôpital Bichat, AP-HP, 75018 Paris, France; Université Paris-Diderot, Sorbonne Paris Cité, 75013 Paris, France; Inserm U1148, 75877 Paris, France. Electronic address: jeremie.abtan@aphp.fr.

Stephen D Wiviott (SD)

TIMI Study Group, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, 02115 Boston, MA, USA.

Emmanuel Sorbets (E)

Hôpital Avicenne, Université Paris 13, AP-HP, 93000 Bobigny, France.

Batric Popovic (B)

Cardiology Department, CHRU Nancy, 54000 Nancy, France.

Yedid Elbez (Y)

FACT (an F-CRIN network), DHU-FIRE, Hôpital Bichat, AP-HP, 75018 Paris, France; Université Paris-Diderot, Sorbonne Paris Cité, 75013 Paris, France; Inserm U1148, 75877 Paris, France.

Shamir R Mehta (SR)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, L8N 3Z5 Hamilton, ON, Canada.

Marc S Sabatine (MS)

TIMI Study Group, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, 02115 Boston, MA, USA.

Christoph Bode (C)

Medizinische Universitatsklinik, 79106 Freiburg, Germany.

Charles V Pollack (CV)

Department of Emergency Medicine, Thomas-Jefferson University Hospital and Sidney Kimmel Medical College, Thomas-Jefferson University, 19107 Philadelphia, PA, USA.

Marc Cohen (M)

Division of Cardiology, Newark Beth Israel Medical Center, Mount-Sinai School of Medicine, 07112 Newark, NJ, USA.

Tiziano Moccetti (T)

Division of Cardiology, Fondazione Cardiocentro Ticino, 6900 Lugano, Switzerland.

Peep Laanmets (P)

North Estonia Medical Centre, 13419 Tallinn, Estonia.

David Faxon (D)

TIMI Study Group, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, 02115 Boston, MA, USA.

Andrzej Okreglicki (A)

Faculty of Health Sciences, Hatter Institute for Cardiovascular Research in Africa & IIDMM, University of Cape Town, 7935 Cape Town, South Africa.

Gregory Ducrocq (G)

FACT (an F-CRIN network), DHU-FIRE, Hôpital Bichat, AP-HP, 75018 Paris, France; Université Paris-Diderot, Sorbonne Paris Cité, 75013 Paris, France; Inserm U1148, 75877 Paris, France.

Ph Gabriel Steg (PG)

FACT (an F-CRIN network), DHU-FIRE, Hôpital Bichat, AP-HP, 75018 Paris, France; Université Paris-Diderot, Sorbonne Paris Cité, 75013 Paris, France; Inserm U1148, 75877 Paris, France; NLHI, ICMS, Royal Brompton Hospital, Imperial College, SW3 6LY London, UK.

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Classifications MeSH