Key result
Ivabradine and atorvastatin enter planned trial testing perioperative MI reduction following emergent orthopedic surgery.
Why the study?
Does treatment with ivabradine and/or atorvastatin reduce the incidence of perioperative myocardial infarction in patients >60 years undergoing surgery for neck of femur fracture?
RCT (n=200)
Open-label
Computerized block randomization
No
Does treatment with ivabradine and/or atorvastatin reduce the incidence of perioperative myocardial infarction in patients >60 years undergoing surgery for neck of femur fracture?
This study protocol outlines a randomized controlled trial to investigate whether ivabradine and atorvastatin can reduce perioperative myocardial infarction in elderly patients undergoing emergent orthopedic lower limb surgery.
Planned RCT will test ivabradine and atorvastatin for perioperative MI reduction; leaves open efficacy and practice change in elderly hip fracture patients.
BACKGROUND: The incidence of perioperative myocardial infarction (PMI) globally is known to be around 2 to 3% and can prolong hospitalization, increased morbidity and mortality. Little is known about the pathophysiology and risk factors for PMI. We investigate the presence of elevated novel cardiac markers and preoperative coronary artery plaque through contemporary laboratory techniques to determine the correlation with PMI, as well as studying ivabradine and atorvastatin as protective pharmacotherapies against PMI in the context of orthopedic surgery. METHODS/DESIGN: We aim to enroll 200 patients aged above 60 years who suffer from neck of femur fracture requiring surgery. Patients will be randomized to four arms (no study drugs, atorvastatin only, ivabradine only and ivabradine and atorvastatin). Our primary outcome is incidence of PMI. All patients will receive an electrocardiogram, cardiac echocardiography, measurement of novel cardiac biomarkers and computed tomography (CT) coronary angiography. A telephone interview post discharge will be conducted at 30 days, 60 days and 1 year. DISCUSSION: We postulate that ivabradine and atorvastatin will reduce the rate and magnitude of PMI following surgery by reducing heart rate and attenuating catecholamine-induced tachycardia postoperatively. Secondly, we postulate that postoperative reduction in heart rate and catecholamine-induced tachycardia with ivabradine will correlate with a reduction in cardiovascular novel biomarkers which will reduce atrial stretch and postoperative incidence of arrhythmia. We aim to demonstrate that treatment with ivabradine and atorvastatin will cause a reduction in the incidence and magnitude of PMI, the benefit of which is derived primarily in patients with greater atherosclerotic burden as measured by higher CT coronary calcium scores. TRIAL REGISTRATION: This study protocol has been listed in the Australia New Zealand Clinical Trial Registry (registration number: ACTRN12612000340831) on 23 March 2012.
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Rudd et al. (2014) conducted an RCT in Neck of femur fracture (n=200). Ivabradine and atorvastatin vs. No treatment was evaluated on Frequency and magnitude of new myocardial injury (perioperative myocardial infarction) based on peak troponin I level on postoperative days 1, 2, 3 and 4. Ivabradine and atorvastatin will be evaluated in a planned randomized controlled trial of 200 patients to determine if they reduce the incidence and magnitude of perioperative myocardial infarction following emergent orthopedic surgery.
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