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Original research article
Two-year outcome after early or late Intervention in non-ST elevation acute coronary syndrome
  1. Erik A Badings1,
  2. Wouter S Remkes2,
  3. Salem H K The3,
  4. Jan-Henk E Dambrink2,
  5. Geert Tjeerdsma4,
  6. Saman Rasoul5,6,
  7. Jorik R Timmer2,
  8. Marloes L J van der Wielen3,
  9. Dirk J A Lok1,
  10. Renicus S Hermanides2,
  11. Jan Van Wijngaarden1,
  12. Harry Suryapranata2,7 and
  13. Arnoud W J van ’t Hof2
  1. 1 Department of Cardiology, Deventer Ziekenhuis, Deventer, Netherlands
  2. 2 Department of Cardiology, Isala klinieken, Zwolle, Netherlands
  3. 3 Department of Cardiology, Treant Zorggroep locatie ziekenhuis Bethesda, Hoogeveen, Netherlands
  4. 4 Department of Cardiology, Ziekenhuis De Tjongerschans, Heerenveen, Netherlands
  5. 5 Department of Cardiology, Maastricht UMC, Maastricht, Netherlands
  6. 6 Department of Cardiology, Atrium Medisch Centrum, Heerlen, Netherlands
  7. 7 Department of Cardiology, Radboudumc, Nijmegen, Netherlands
  1. Correspondence to Dr Arnoud W J van ’t Hof, Isala Klinieken, Department of Cardiology, Dokter van Heesweg 2 8025 AB Zwolle, The Netherlands; a.w.j.vant.hof{at}isala.nl

Abstract

Objective To compare long-term outcome of an early to a delayed invasive strategy in high-risk patients with non-ST elevation acute coronary syndrome (NSTE-ACS).

Methods This prospective, multicentre trial included patients with NSTE-ACS and at least two out of three of the following high-risk criteria: (1) evidence of extensive myocardial ischaemia on ECG, (2) elevated biomarkers for myocardial necrosis and (3) age above 65 years. Patients were randomised to either an early (angiography and revascularisation if appropriate <12 hours) or a delayed invasive strategy (>48 hours after randomisation). Endpoint for this prespecified long-term follow-up was the composite incidence of death or reinfarction after 2 years. Data collection was performed by telephone contact with the patients, their relatives or general practitioner and by review of hospital records.

Results Endpoint status after 2-year follow-up was collected in 521 of 542 initially enrolled patients. Incidence of death or reinfarction was 11.8% in the early and 13.1% in the delayed treatment group (relative risk (RR)=0.90, 95% CI 0.57 to 1.42). No significant differences were found in occurrence of the individual components of the primary endpoint: death 6.1% vs 8.9%, RR 0.69 (95% CI 0.37 to 1.27), reinfarction 6.5% vs 5.4%, RR 1.20 (95% CI 0.60 to 2.38). Post-hoc subgroup analysis showed statistical significant interaction between age and treatment strategy on outcome (p=0.02).

Conclusions After 2 years follow-up, no difference in incidence of death or reinfarction was seen between early to late invasive strategy. These findings are in line with results of other studies with longer follow-up. Older patients seem to benefit more from early invasive treatment.

  • Percutaneous coronary intervention
  • Acute coronary syndromes

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Footnotes

  • Contributors All authors have contributed to the conception, design, analysis and interpretation of the data, revising of the drafts and have approved the final version of the manuscript.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.