Key result
New trial protocol evaluates whether remote ischemic preconditioning reduces MINS after major abdominal surgery.
Why the study?
Myocardial injury after non-cardiac surgery (MINS) is common and associated with adverse outcomes, but few prospective studies have used MINS as a primary outcome or tested remote ischaemic preconditioning (RIPC) for its prevention.
Does remote ischaemic preconditioning reduce myocardial injury after non-cardiac surgery in high-risk patients undergoing major abdominal surgery?
RCT (n=766)
Observer-blinded
1:1 ratio
Yes
Does remote ischaemic preconditioning reduce myocardial injury after non-cardiac surgery in high-risk patients undergoing major abdominal surgery?
This trial protocol describes a study to evaluate whether remote ischemic preconditioning reduces postoperative myocardial injury in high-risk patients undergoing major abdominal surgery.
INTRODUCTION: Myocardial injury after non-cardiac surgery (MINS) caused by an ischaemic mechanism is common and is associated with adverse short-term and long-term prognoses. However, MINS is a recent concept, and few studies have prospectively used it as a primary outcome. Remote ischaemic preconditioning (RIPC) is a non-invasive procedure that induces innate cardioprotection and may reduce MINS. METHODS AND ANALYSIS: This is a multicentre, randomised, sham-controlled, observer-blinded trial. Patients with a high clinical risk of cardiovascular events who are scheduled to undergo major abdominal surgery will be enrolled. A total of 766 participants will be randomised (1:1 ratio) to receive RIPC or control treatment before anaesthesia. RIPC will comprise four cycles of cuff inflation for 5 min to 200 mm Hg and deflation for 5 min. In the controls, an identical-looking cuff will be placed around the arm but will not be actually inflated. The primary outcome will be MINS, defined as at least one postoperative cardiac troponin (cTn) concentration above the 99th percentile upper reference limit of the cTn assay as a result of a presumed ischaemic mechanism. This trial will test the concentration of high-sensitivity cardiac troponin T (hs-cTnT). The secondary outcomes will be hs-cTnT levels reaching/above the prognostically important thresholds, peak hs-cTnT and total hs-cTnT release during the initial 3 days after surgery, length of hospital stay after surgery, length of stay in the intensive care unit, myocardial infarction, major adverse cardiovascular events, cardiac-related death, all-cause death within 30 days, 6 months, 1 year and 2 years after surgery, and postoperative complications and adverse events within 30 days after surgery. ETHICS AND DISSEMINATION: This study protocol (version 5.0 on 7 April 2023) was approved by the Ethics Committee of Sixth Affiliated Hospital of Sun Yat-sen University. The findings will be published in peer-reviewed journals. TRIAL REGISTRATION NUMBER: NCT05733208.
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Wang et al. (2023) conducted an RCT in Myocardial injury after non-cardiac surgery (MINS) (n=766). Remote ischaemic preconditioning (RIPC) vs. Sham control was evaluated on Myocardial injury after non-cardiac surgery (MINS), defined as at least one postoperative cardiac troponin concentration above the 99th percentile upper reference limit. This is a study protocol for a randomized trial to evaluate whether remote ischemic preconditioning reduces myocardial injury after major abdominal surgery in high-risk patients.
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