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Impact of presentation and transfer delays on complete ST-segment resolution before primary percutaneous coronary intervention: Insights from the ATLANTIC trial

  • Enrico Fabris
  • , Arnoud Van't Hof*
  • , Christian W. Hamm
  • , Frédéric Lapostolle
  • , Jens Flensted Lassen
  • , Shaun G. Goodman
  • , Jurriën M. Ten Berg
  • , Leonardo Bolognese
  • , Angel Cequier
  • , Mohamed Chettibi
  • , Christopher J. Hammett
  • , Kurt Huber
  • , Magnus Janzon
  • , Béla Merkely
  • , Robert F. Storey
  • , Uwe Zeymer
  • , Warren J. Cantor
  • , Hélène Rousseau
  • , Eric Vicaut
  • , Gilles Montalescot
  • *Kontaktforfatter
  • Isala Clinics
  • Trieste Hospital
  • Kerckhoff Heart and Thorax Center
  • Avicenne Hospital
  • St. Michael's Hospital
  • St. Antonius Hospital
  • Azienda Ospedaliera Arezzo
  • Hospital Clinic of Barcelona
  • Centre Hospitalo Universitaire Frantz Fanon
  • Royal Brisbane and Women’s Hospital
  • Wilhelminenspital
  • Linköping University
  • Semmelweis University
  • The University of Sheffield
  • University of Toronto
  • Lariboisière Hospital
  • Pierre and Marie Curie University
  • Rigshospitalet
  • IHF GmbH Institut für Herzinfarktforschung
  • Klinikum Ludwigshafen

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

Aims: The aim of this study was to identify predictors of complete ST-segment resolution (STR) pre-primary percutaneous coronary intervention (PCI) in patients enrolled in the ATLANTIC trial. Methods and results: ECGs recorded at the time of inclusion (pre-hospital [pre-H]-ECG) and in the catheterisation laboratory before angiography (pre-PCI-ECG) were analysed by an independent core laboratory. Complete STR was defined as ≥70%. Complete STR occurred pre-PCI in 12.8% (204/1, 598) of patients and predicted lower 30-day composite MACCE (OR=0.10, 95% CI: 0.002-0.57, p=0.001) and total mortality (OR=0.16, 95% CI: 0.004-0.95, p=0.035). Independent predictors of complete STR included the time from index event to pre-H-ECG (OR=0.94, 95% CI: 0.89-1.00, p=0.035), use of heparins before pre- PCI-ECG (OR=1.75, 95% CI: 1.25-2.45, p=0.001) and time from pre-H-ECG to pre-PCI-ECG (OR=1.09, 95% CI: 1.03-1.16, p=0.005). In the pre-H ticagrelor group, patients with complete STR had a significantly longer delay between pre-H-ECG and pre-PCI-ECG compared to patients without complete STR (median 53 [44-73] vs. 49 [38.5-61] mins, p=0.001); however, this was not observed in the control group (in-hospital ticagrelor) (50 [40-67] vs. 49 [39-61] mins, p=0.258). Conclusions: Short patient delay, early administration of anticoagulant and ticagrelor if a long transfer delay is expected may help to achieve reperfusion prior to PCI. Pre-H treatment may be beneficial in patients with longer transfer delays, allowing the drug to become biologically active. ClinicalTrials.gov Identifier: NCT01347580.

OriginalsprogEngelsk
TidsskriftEuroIntervention
Vol/bind13
Udgave nummer1
Sider (fra-til)69-77
ISSN1774-024X
DOI
StatusUdgivet - 15. maj 2017
Udgivet eksterntJa

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© Europa Digital & Publishing 2017. All rights reserved.

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