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5 Effect of remote ischaemic preconditioning on coronary artery function in patients with stable coronary artery disease

Authors :
Alex McConnachie
Keith G. Oldroyd
Jonathan Watt
David Corcoran
Barry Hennigan
Robin Young
Paul Welsh
Peter McCartney
Pio Cialdella
Richard Good
Naveed Sattar
A Bajrangee
Aadil Shaukat
Damien Collison
Margaret McEntegart
Colin Berry
David Carrick
Stuart Watkins
Source :
Abstracts.
Publication Year :
2018
Publisher :
BMJ Publishing Group Ltd and British Cardiovascular Society, 2018.

Abstract

Background Remote ischaemic preconditioning (RIPC) is a cardioprotective intervention invoking intermittent ischaemia in a tissue remote from the heart. Its mechanisms are incompletely understood. We hypothesised that RIPC might enhance coronary vasodilatation by an endothelium-dependent mechanism. Methods We performed a prospective, randomised, sham-controlled, blinded clinical trial. Patients with stable coronary artery disease undergoing elective angiography were randomised 1:1 to RIPC or sham. Endothelial-dependent and –independent function was assessed with intracoronary (ic) acetylcholine (ACh) and ic nitrate, respectively. Coronary luminal diameter was assessed by QCA. Primary outcome: between-group difference in mean% change in coronary luminal diameter following ACh. Results Following angiography, 60/75 patients (mean ±SD age 57.5±8.5 years; 80% male) were eligible and completed the protocol (n=30 RIPC, n=30 sham). The mean% change in coronary luminal diameter was −13.3±22.3% and −2.0±17.2% in the sham and RIPC groups respectively (difference 11.32%, 95% CI: 1.2 to 21.4, p=0.032) (figure 1). This remained significant with age and sex as covariates (difference 11.01%, 1.01–21.0, p=0.035). Conclusions RIPC attenuates the extent of vasoconstriction induced by intracoronary acetylcholine infusion, and this endothelium-dependent mechanism may contribute to its cardioprotective effects.

Details

Database :
OpenAIRE
Journal :
Abstracts
Accession number :
edsair.doi...........1b353f7816c027459c00d2ba1ba5a311
Full Text :
https://doi.org/10.1136/heartjnl-2018-bcis.5