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Rationale and design of the British Heart Foundation (BHF) Coronary Microvascular Angina (CorMicA) stratified medicine clinical trial - 18/06/18

Doi : 10.1016/j.ahj.2018.03.010 
Thomas J. Ford, MBChB (Hons), FRACP a, b, c, David Corcoran, BMedSci (Hons), MRCP b, Keith G. Oldroyd, MD(Hons), FRCP a, b, Margaret McEntegart, PhD, FRCP a, b, Paul Rocchiccioli, PhD, FRCP a, b, Stuart Watkins, MD, FRCP a, Katriona Brooksbank, PhD b, Sandosh Padmanabhan, PhD, FRCP b, Naveed Sattar, FMedSci b, Andrew Briggs, PhD d, Alex McConnachie, PhD e, Rhian Touyz, MBBCh, MSc(Med), PhD, FRCP, FRSE b, Colin Berry, PhD, FRCP a, b,
a West of Scotland Heart and Lung Centre, Golden Jubilee National Hospital, Glasgow, United Kingdom 
b British Heart Foundation Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom 
c University of New South Wales, Sydney, Australia 
d Centre for Population and Health Sciences, University of Glasgow, Glasgow, United Kingdom 
e Robertson Centre for Biostatistics, Institute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom 

Reprint requests: Colin Berry, PhD, FRCP, British Heart Foundation Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, 126 University Place, University of Glasgow, Glasgow, G12 8TA, Scotland, United Kingdom.British Heart Foundation Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, 126 University Place, University of Glasgow, Glasgow, G12 8TAScotlandUnited Kingdom

Abstract

Background

Coronary angiography is performed to assess for obstructive coronary artery disease (CAD), but “nonobstructive CAD” is a common finding. Microvascular or vasospastic angina may be relevant, but routine confirmatory testing is not evidence based and thus rarely performed.

Aim

The aim was to assess the effect of stratified medicine guided by coronary function testing on the diagnosis, treatment, and well-being of patients with angina and nonobstructive CAD.

Design

The BHF CorMicA trial is a prospective, multicenter, randomized, blinded, sham-controlled trial of stratified medicine (NCT03193294). All-comers referred for elective coronary angiography for investigation of suspected CAD will be screened. Following informed consent, eligible patients with angina and nonobstructive CAD will be randomized 1:1 immediately in the catheter laboratory to either coronary artery function–guided diagnosis and treatment (intervention group) or not (control group). Coronary function will be assessed using a pressure-temperature–sensitive guidewire and adenosine followed by pharmacological testing with intracoronary acetylcholine. Patients will be stratified into endotypes with linked therapy. The primary outcome is change in Seattle Angina Questionnaire score at 6 months. Secondary outcomes include safety, feasibility, diagnostic utility (impact on diagnosis and diagnostic certainty), and clinical utility (impact on treatment and investigations). Health status is a key secondary outcome assessed according to the following domains: quality of life, treatment satisfaction, illness perception, physical activity, and anxiety-depression score. Patients with obstructive disease who are not randomized will form a registry group who will be followed up as a comparator for secondary outcomes including health status. Health and economic outcomes will be evaluated in the longer term using electronic health record linkage.

Value

CorMicA is a proof-of-concept clinical trial of a disruptive stratified intervention with potential benefits to patients and health care providers.

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Graphical abstract




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Plan


 Statement of competing interests: C. B. is employed by the University of Glasgow, which holds consultancy and research agreements with companies that have commercial interests in the diagnosis and treatment of angina. The companies include Abbott Vascular, AstraZeneca, Boehringer Ingelheim, Menarini Pharmaceuticals, and Siemens Healthcare. K. G. O. has received consultant and speaker fees from Abbott Vascular and Volcano Corporation which manufacture pressure wires. S. W. has worked as a consultant for Abbott Vascular. None of these companies have had any involvement with this study. None of the other authors have any potential conflicts of interest.
☆☆ Contributors: C. B. designed the study. T. J. F. wrote the first draft and revised draft with C. B. D. C., K. G. O., M. M. E., P. R., S. W., K. B., S. P., B. S., A. B., A. M., and R. T. edited the manuscript and devised aspects of the study protocol.


© 2018  The Authors. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 201

P. 86-94 - juillet 2018 Retour au numéro
Article précédent Article précédent
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