Article Text

Download PDFPDF
Randomised controlled trial
Early invasive strategy in patients with non-ST segment elevation acute coronary syndrome delays death or MI by 18 months
  1. Robert Henderson
  1. Trent Cardiac Centre, Nottingham University Hospitals, Nottingham, UK
  1. Correspondence to: Dr Robert Henderson, Trent Cardiac Centre, Nottingham University Hospitals, City Hospital Campus, Hucknall Road, Nottingham, NG51PB, UK; robert.henderson{at}nuh.nhs.uk

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Commentary on: Wallentin L, Lindhagen L, Ärnström E, et al. Early invasive versus non-invasive treatment in patients with non-ST-elevation acute coronary syndrome (FRISC-II): 15 year follow-up of a prospective, randomised, multicentre study. Lancet 2016;388:1903–11.

Context

The role of coronary arteriography in patients with non-ST segment elevation acute coronary syndrome is controversial. Many cardiologists advocate a ‘routine invasive strategy’, which comprises coronary arteriography within a few days of presentation and myocardial revascularisation determined by the angiographic findings, but this exposes patients to procedural risks and incurs significant costs. Other clinicians favour a ‘selective invasive strategy’, with coronary arteriography reserved for patients with recurrent myocardial ischaemia.

Randomised trials of these treatment strategies suggest that a routine invasive strategy reduces the risk of recurrent ischaemia and death or recurrent myocardial infarction over 5 years.1 In the RITA-3 trial, a routine invasive strategy was also associated with lower cardiovascular …

View Full Text

Footnotes

  • Competing interests The author is a Member of the Executive Committee of the The British Heart Foundation RITA-3 Randomised Trial, a Member of the NICE Guideline Development Group for Clinical Guideline 94 Unstable angina and NSTEMI: early management and a Member of an Advisory Board for Creavo Medical Technologies.

  • Provenance and peer review Commissioned; internally peer reviewed.