This descriptive cross-sectional study was performed on 60 patients undergoing CABG in Golestan Hospital, Ahvaz, Iran, after obtaining the necessary permits from the Ethics Committee of Anesthesiology and Pain Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran (IR.AJUMS.HGOLESTAN.REC.1399.060). The inclusion criteria consisted of patients scheduled for elective CABG surgery, the American Society of Anesthesiologists (ASA) class I, II, or III, absence of significant renal and hepatic problems, absence of any arrhythmia on the last electrocardiogram (ECG), and BMI less than 35 kg/m2. Patients with known electrolyte disorders before the surgery, known arrhythmias, need for emergent interventions, and an EF of less than 35% were excluded from the study.
After obtaining the approval of the proposal, permission from the Ethics Committee of Ahvaz Jundishapur University of Medical Sciences, and informed consent from patients who were candidates for CABG surgery, all eligible patients entered the study. The procedure was explained to the patients, and then the patients were visited by a cardiac surgery anesthesia fellowship. After the establishment of a safe line for surgery, the patients were transferred to the operating room. All patients with ASA class I, II, or III were included in the study.
All patients received 7 cc/kg of normal saline before induction. In preoperative evaluations, age, gender, BMI, smoking status, medical history of cardiovascular diseases (including hypertension, atrial fibrillation, congestive heart failure, and previous ischemic heart disease or CABG intervention), antihypertensive medication (eg, angiotensin-converting enzyme inhibitors, beta blockers, and calcium channel blockers), and history of insulin-dependent gestational diabetes (in female patients) were reassessed. Vital signs were assessed by ECG monitoring, pulse oximetry, and invasive blood pressure measurement through the arterial catheter during surgery. Intraoperative events, including hypotension (30% reduction in baseline mean arterial pressure [MAP] for longer than 5 minutes), MAP < 60 mmHg, and tachycardia (increase in the heart rate more than 30 bpm from the baseline heart rate for longer than 5 minutes), were recorded by anesthesia charts. Intraoperative bleeding volume (mL) and fluid balance during the first 24 hours after surgery were assessed to ensure basal blood pressure.
All patients underwent general anesthesia by a similar method (midazolam 0.25 mg/kg, fentanyl 3 μg/kg, etomidate 0.4 mg/kg, and cisatracurium 0.25 mg/kg). Anesthesia was maintained with midazolam 0.15 mg/kg/h, fentanyl 6 μg/kg/h, and cisatracurium 0.25 mg/kg/h infusion. Ventilation control was achieved using a mechanical ventilator maintained at 35 - 45 mmHg carbon dioxide pressure. The blood samples were taken for blood gas analysis and laboratory tests for potassium, sodium, magnesium, calcium, blood urea nitrogen (BUN), creatinine, and blood sugar levels at different time points, including before induction of anesthesia, after induction of anesthesia, before cardiopulmonary bypass (CPB), on CPB, after separation from CPB, and on entering the intensive care unit (ICU).
The CPB circuit was primed with glucose-free crystalloid solutions (ie, lactated Ringer’s solution, mannitol, and Voluven). The pump flow rate (with the direct flow and without pulse) was set at 2 - 2.4 L/min/m
2 according to the patient’s temperature and recorded continuously. After starting CPB, the patient was cooled to 32 - 34°C depending on the type of surgery and operating conditions. Membrane oxygenators and arterial filters were used during surgery. Del Nido cold cardioplegia solutions were used antegradely or retrogradely to establish chemical arrest before the implantation of the aortic clamp. Alpha acetate strategy was used in all patients to regulate arterial partial pressure of carbon dioxide at normal levels. During CPB, anesthesia was continued with continuous injections of anesthetics. In all patients, an attempt was made to maintain the hematocrit of patients above 24 to 27%; for this purpose, blood was transfused if necessary (
17). For this study, surgeons who used del Nido cardioplegia and had similar routines were used.
The blood samples were taken for blood gas analysis and laboratory tests for potassium, sodium, magnesium, calcium, BUN, creatinine, and blood sugar levels at different time points, including before induction of anesthesia, after induction of anesthesia, before CPB, on CPB, after separation from CPB, and on entering the ICU.
3.1. Primary Outcomes
All cardiac arrhythmias were recorded at the above-mentioned time points (ie, before induction of anesthesia, after induction of anesthesia, before CPB, on CPB, after separation from CPB, and on entering the ICU).
3.2. Secondary Outcomes
The levels of potassium, MAP, serum level of potassium, blood sugar, BUN, creatinine, calcium, magnesium, hemoglobin (Hb), and sodium were recorded.
3.3. Sample Size Calculation
The sample size was calculated using the sample size formula consisting of 58 patients, according to the significance level of 0.05 and the power of 0.8. The sample size was increased to 60 to improve the measurement accuracy.
3.4. Statistical Analysis
For quantitative variables, mean (and/or median) was used to describe the data center, and standard deviation (and/or interquartile range) was used to describe data scatter. Frequency and percentage were used for the description of qualitative variables. The Chi-square test (or Fisher’s exact test) and t-test (or Mann-Whitney U test) were used as necessary to analyze the data. P-values less than 0.05 were considered statistically significant. All analyzes were performed using SPSS software (version 22).