In this randomized-controlled trial conducted at Shahid Modarres hospital, Tehran, Iran, 31 ESRD patients who were candidate for elective renal transplantation from live donors were randomly selected and divided into case (n = 16) and control groups (n = 15). This clinical trial was registered in the Iranian registry of clinical trial (IRCT2015092612203N3). Written informed consent was obtained from all the patients.
Inclusion criteria included ASA functional class III and age of 18 - 70 years. Exclusion criteria included advanced cardiovascular disease (ASA functional class ≥ IV), potassium concentration > 5.5 mEq/L at admission, metabolic acidosis (pH < 7.15), axillary body temperature < 35°C or > 38.5°C before or during the surgery, need for blood transfusion during the surgery, and cadaveric renal transplantation. Patients with ischemic time > 30 minutes or the duration of surgery above 150 minutes were excluded from our study.
All demographic and clinical information was recorded before the surgery. The patients were preoxygenated by 100% O2 for 3 minutes and received 0.02 mg/kg midazolam + l2 µg/kg fentanyl as premedication followed by 5 mg/kg thiopental sodium for induction of anesthesia. A dose of 0.5 mg/kg atracurium was administered as muscle relaxant. Additional dose of atracurium was administered if needed. Last dose of atracurium was administered at declamping time. Anesthesia was maintained using 0.6% - 1% isoflurane and 50% nitrous oxide. All patients received 3 mg/kg furosemide and 0.5 mg/kg mannitol.
Invasive radial artery catheter was administered after positive Allen test for the measurement of blood pressure. Central vein pressure (CVP) was calculated repeatedly and maintained at 10 - 12 cm H2O (by infusion of fluid if needed) and body temperature was preserved at 36°C (using nasopharyngeal thermometer). Arterial pressure of O2, and CO2 (PaO2, PaCO2), HCO3, base excess (BE), and pH were studied on arterial blood gas (ABG) sample prior to the surgery and at declamping time. Train-of-four (TOF) was measured prior to anesthesia and then every 15 minutes during the surgery (to assess the need for further atracurium, TOF = 3 was our threshold for administration of additional dose of atracurium), 15 minutes after declamping time, and every 2 minutes until acceptable recovery (TOF 3 of 4). The time of achieving TOF 3 was recorded and compared between the groups. In all patients, the controlled mode of ventilator was used. Ventilator setting during operation was as follows: RR = 12, TV = 5 - 6 cc / kg, and Pmax = 35. The rate of ventilation was raised in respiratory acidosis.
Patients in the case group received sodium bicarbonate based on base excess in the first ABG sample, during the interval between anesthesia and initiation of surgery. The dose of sodium bicarbonate was calculated as follows: (base excess × 0.3× body weight)/2. Patients in the control group received 50 mL of sterile water for injection.
All data were gathered in a report sheet and analyzed by SPSS 12 (SPSS Inc. Chicago, IL, USA). Descriptive statistics was expressed as mean ± SD. Inferential statistics of chi-square and independent-test were used to analyze the data. Sample size was calculated based on power of 80 %. P value less than 0.05 was considered statistically significant.