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Validity of inducible ischaemia as a surrogate for adverse outcomes in stable coronary artery disease
  1. Adam Timmis1,2,
  2. Antony Raharja1,
  3. R Andrew Archbold2,
  4. Anthony Mathur1,2
  1. 1 Barts and The London School of Medicine and Dentistry, Queen Mary University London, London, UK
  2. 2 Department of Interventional Cardiology, Barts Heart Centre, London, UK
  1. Correspondence to Professor Adam Timmis, Barts Heart Centre, London EC1A 7BE, UK; a.d.timmis{at}qmul.ac.uk

Abstract

Regional myocardial ischaemia is commonly expressed as exertional angina in patients with stable coronary artery disease (CAD). It also associates with prognosis, risk tending to increase with the severity of ischaemia. The validity of myocardial ischaemia as a surrogate for adverse clinical outcomes, however, has not been well established. Thus, in cohort studies, ischaemia testing has failed to influence rates of myocardial infarction and coronary death. Moreover, in clinical studies, pharmacological and interventional treatments that are effective in correcting ischaemia have rarely been shown to reduce cardiovascular (CV) risk. This contrasts with statins and other anti-inflammatory drugs that have no direct effect on ischaemia but improve CV outcomes by modifying the atherothrombotic disease process. Despite this, and with little evidence of patient benefit, stress testing is commonly used during the follow-up of patients with stable CAD when the demonstration of ischaemic change may be seen as a target for treatment, independently of symptomatic status. Substitution of a symptom-driven management strategy has the potential to reduce rates of non-invasive stress testing, unnecessary downstream revascularisation procedures and use of valuable resources in patients with stable CAD without adverse consequences for CV risk.

  • cardiac imaging and diagnostics
  • chronic coronary disease

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Footnotes

  • Contributors AR performed the initial literature review, wrote the first draft of the manuscript and critically reviewed all subsequent drafts. AT edited the first draft and wrote all subsequent drafts. RAA was responsible for some of the original thought behind this review and edited and critically reviewed the final drafts of the manuscript. AM edited and critically reviewed the final drafts of the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent Obtained.

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