We conducted a randomized, controlled, open-clinical trial for 18 months at the Rasoul Akram Medical Center. 88 patients including both male and female patients’ (ASA physical status I and II), aged 16 to 45 years, weight 40 to 95 kg, undergoing rhinoplasty, septoplasty, and functional endoscopic sinus surgery were studied. Because it was an open trial, all the patients who underwent the above-mentioned operations during the 18 month period and who were able to take metoprolol were included in this study. The study did not include patients with cardiovascular system pathology, cardiac failure, chronic hypotension, as well as patients with blood system pathology, coagulation disorder, anemia (Hb < 10 g/dL) and those prescribed aspirin or other medications affecting their coagulation system. Patients with kidney or liver dysfunctions were not included. Before surgery the patients’ blood cell count, urea, serum creatinine, and prothrombine time (PT) were recorded. Because each surgeon only operated on one type of the above-mentioned surgeries, three different surgeons participated in this study. The study protocol was approved by institutional research committee and patients also gave their informed written consent.
Patients who received metoprolol entered the study, and some patients were picked as the control group. Patients entering the study were divided into four groups and randomly and blindly assigned to receive: 50 mg metoprolol at night before the operation, 50 mg metoprolol on the day of operation, 50 mg metoprolol at night and on the day of the operation, or a placebo. All patients received premedication of 10 mg oxazepam and 150 mg ranitidine on the night and on the day of operation. For all patients the bed-head of the surgical table was raised 30°. After preparation and pre-oxygenation, patients were first pre-medicated with an infusion of midazolam 0.05 mg/kg, fentanyl 1 µg/kg, lidocaine 1 mg/kg. Induction of anesthesia was achieved with an infusion of thiopental 5 mg/kg and atracurium 0.5 mg/kg and after 3 to 5 minutes patients were intubated with the appropriate tube size. Anesthesia was maintained with an infusion of propofol (100 µg/Kg/min), in the 50:50 percent mix of oxygen and nitrous oxide anaesthesia. Following induction of the anesthesia, for patients in all groups, an infusion of 10 mg of atracurium per 30 minutes and 50 µg of fentanyl per hour were continued. After the patient’s preparation on the surgical table and following intubation, their systolic and diastolic blood pressure were measured in a non-invasive oscillometric way. Frequency of heart contractions was also recorded simultaneously.
In addition to an infusion of adrenalized lidocaine for all the patients, before starting surgery, surgeon infiltrated 1-2 mL 1% lidocaine with adrenalin 1/100,000 submucosally into the lateral nasal wall. During surgery systolic and diastolic blood pressure were measured every 15 minutes and pulse rate was recorded. These average values were analyzed for statistical evaluation. Cardiac electrical activity and end-expiratory CO2 were measured as well. To evaluate the quality of the operative field during surgery, in addition to blood-gas analysis, volume of sucked and collected blood, and the surgeon’s assessment of operative field condition, the quality scale proposed by Fromm and Boezaart was also used (
1):
1) Grade 0: No bleeding
2) Grade 1: Slight bleeding - no blood suctioning required.
3) Grade 2: Slight bleeding - occasional suctioning required.
4) Grade 3: Slight bleeding - frequent suctioning required. Operative field is visible for some seconds after evacuation.
5) Grade 4: Moderate bleeding - frequent suctioning required. Operative field is only visible immediately after evacuation.
6) Grade 5: Severe bleeding - constant suctioning required. Bleeding appears faster than can be removed by suction. Surgery is hardly possible, and sometimes impossible.
Surgical time was recorded from the first injection of regional anesthetic to the end of surgery. If a patient had excessive bleeding or a patient required additional medication to control blood pressure, an infusion of remifentanil was used and recorded. 10 to 15 minutes before ending surgery and after recording the surgeons’ opinion regarding the surgical field, the anesthetic agent was decreased. Patients’ agitation in the recovery room was assessed based on the Richmond Agitation Sedation Scale (RASS). Grades from 0 to 4 were assigned to the four levels of patient’s agitation: alert and calm, anxious, apprehensive, very apprehensive, and aggressive. All the patients after receiving discharge criteria from recovery were transferred to the ward.