A multi-centre randomized controlled trial investigating the effect of remote ischaemic preconditioning (RIPC) on blood and myocardial biomarkers of stress and injury-related signalling in patients having isolated coronary artery bypass grafting (CABG) or aortic valve replacement (AVR) using cardiopulmonary bypass (CPB)
File(s)
Author(s)
Moscarelli, Marco
Type
Thesis
Abstract
Objective: To compare markers of cardiac injury, inflammatory and oxidative responses, and myocardial cellular changes in the left and right ventricles of patients undergoing isolated coronary artery bypass grafting (CABG) or aortic valve replacement (AVR) using cardiopulmonary bypass (CPB) and cardioplegic arrest with or without remote ischaemic preconditioning (RIPC).
Methods: Two conditions were studied for each surgical stratum (CABG or AVR): (a) no RIPC and (b) RIPC following anaesthesia and before sternotomy. The control group (no RIPC) represented standard clinical practice. Left and right ventricular biopsies were collected before CPB and at the end of ischaemic cardioplegic arrest. Blood samples were collected before, during, and after the operation.
Results: Between March 2012 and April 2014, 124 patients agreed to participate in the study; 64 and 60 patients formed the CABG and AVR populations, respectively, and were randomised to receive RIPC or sham treatment. There were no differences in troponin release between groups (geometric mean ratio 0.92 (0.75,1.10), p=0.9; and 0.9 (0.35,1.44), p=0.65 CABG and AVR respectively). The postoperative course in each group was similar with no mortality. There were no significant differences in phosphorylation potential or energy charge in left and right ventricle biopsies or in circulating inflammatory markers between groups. No serious adverse events were reported.
Conclusions: RIPC did not confer significant cardioprotection as measured by troponin I release. This result was possibly related to the inability of the study to stratify anaesthesia regimens. Both RIPC and Tru-Cut ventricle biopsy procedures were safe.
Methods: Two conditions were studied for each surgical stratum (CABG or AVR): (a) no RIPC and (b) RIPC following anaesthesia and before sternotomy. The control group (no RIPC) represented standard clinical practice. Left and right ventricular biopsies were collected before CPB and at the end of ischaemic cardioplegic arrest. Blood samples were collected before, during, and after the operation.
Results: Between March 2012 and April 2014, 124 patients agreed to participate in the study; 64 and 60 patients formed the CABG and AVR populations, respectively, and were randomised to receive RIPC or sham treatment. There were no differences in troponin release between groups (geometric mean ratio 0.92 (0.75,1.10), p=0.9; and 0.9 (0.35,1.44), p=0.65 CABG and AVR respectively). The postoperative course in each group was similar with no mortality. There were no significant differences in phosphorylation potential or energy charge in left and right ventricle biopsies or in circulating inflammatory markers between groups. No serious adverse events were reported.
Conclusions: RIPC did not confer significant cardioprotection as measured by troponin I release. This result was possibly related to the inability of the study to stratify anaesthesia regimens. Both RIPC and Tru-Cut ventricle biopsy procedures were safe.
Version
Open Access
Date Issued
2018-01
Date Awarded
2018-07
Copyright Statement
Attribution NoDerivatives 4.0 International Licence (CC BY-ND)
Advisor
Punjabi, Prakash
Angelini, Gianni
Sponsor
Imperial College London
British Heart Foundation
Publisher Department
National Heart & Lung Institute
Publisher Institution
Imperial College London
Qualification Level
Doctoral
Qualification Name
Doctor of Medicine (Research) MD (Res)