After obtaining written informed consent from each patient and approval of the institutional review board, 160 candidates for elective femoral fracture surgeries (80 with and 80 without addiction) aged 18 - 65 years, with the American society of anesthesiologists (ASA) physical status I - II were selected for the current randomized clinical trial study (
Figure 1). Each group of 80 patients was divided into two groups of 40. Therefore, there were four stratified randomized groups (40 patients control-placebo ,40 patients control-clonidine,40 patients addicted-placebo and 40 patients addicted-clonidine) and also four stratified randomization lists to each combination of gender-addiction (addict male, addict female, non-addict male and non-addict female). All four groups were selected with the same gender frequency distribution: in each group there were 32 males and eight females. Stratified Permuted-block Randomization (with the length of four) was used to assign subjects to the treatment groups. The power of analysis was 90% and type I error of α = 0.05.
The exclusion criteria were significant underlying diseases (hypertension, cardiac, hepatic or renal disease, coagulation defects, diabetes mellitus); multiple trauma and any other fractures, receiving beta receptor antagonists, autonomic nervous system active drugs, anticoagulant agents, long-acting corticosteroids, calcium channel blockers, digoxin, tricyclic antidepressants or clonidine two weeks before operation and the history of allergic reaction to any of the drugs used in the study. Operation time of more than 180 minutes was another exclusion criterion. If the patient consumed at least four grams of opium per day (natural or semi synthetic Alkaloids) orally or by inhalation for more than six months, in the subject was sent to the opium addict group. 80 addict and 80 non-addict subjects with femur fractures were selected according to the subjects statement during the preoperative visit performed by one of the authors; then both groups were divided into two subgroups: 40 subjects in the clonidine and 40 in the placebo (sugar pill) groups, (according to the computer table of random numbers). All subjects, investigators, anesthesiologists, surgeons and nurses involved in the study were unaware of the assigned groups.
Before operation, routine laboratory tests as well as hemoglobin level, bleeding time, PT, PTT, and platelet count were checked for all patients in the four groups. The PT and PTT of each subject were divided by the control value of the laboratory and the results were recorded. Fasting time and pre-operation fluid therapy were similar in all four groups. Subjects in the clonidine groups (addict and non-addict) received oral clonidine 5 μg/kg, 90 minutes before operation. This period ensures maximum plasma concentrations after oral ingestion of the drug. Control groups received placebo with similar color and shape to clonidine preparation.
The next steps in the operating room were the same for the four groups, performed by the same team (an anesthetist and a technician) who were unaware of the type of premedication or addiction. Subjects in the four groups received 7 mL/kg of Ringerās solution before induction of anesthesia and were monitored by the same system for heart rate (HR) and SBP, and DBP and Electrocardiography; pulse oxymetry, end-tidal CO2, and urine output were also assessed. All subjects received fentanyl 2 μg/kg intravenously (IV) and midazolam 0.02 mg/kg IV as premedication 5 minutes before induction of anesthesia and induction of anesthesia was performed by thiopental 5 mg/kg and Atracurium 0.5 mg/kg IV. For the maintenance of anesthesia O2/N2O was used as 1/1 liter and propofol by the infusion dosage of 100 μg/kg/minute to preserve the value of Cerebral State Index (CSI) between 40 and 60. Systolic and diastolic blood pressure, heart rate, saturation of oxygen and cardiac rhythm were monitored and recorded 2 hours before surgery and at the time of anesthesia induction and each 10 minutes during the operation.
Intraoperative fluids for all patients included ringer lactate as maintenance fluid and normal saline for deficits and blood loss to a transfusion threshold of hemoglobin = 10 g/dL. All operations were performed by the same surgery team and all surgeons and anesthesiologists were blinded to patientās groups during the operations. After the by acquiring the criteria for reversal of neuromuscular blockade, the patientsā endotracheal tubes were extracted and by precise monitoring of hemodynamic and ventilation, they were transferred to postanesthesia care unit.
Intraoperative blood loss was estimated based on the volume of blood in the suction bottle and the weight of the bloody gauze pads. each pack of surgical pads were weighed before and after blood soaking and each milliliter of blood was considered nearly 1.06 mg; therefore, by weighing the pads and considering the volume of blood in the suction bottle the final blood loss could be estimated. The same anesthesiologist was responsible for all patients and he was unaware of the study details. The following data were recorded for each patient: age, gender, weight, and operation time. When patients acquired post anesthesia recovery score (modified Aldrete score) > 9, the nurse of anesthesia let them leave the recovery room and be transferred to the orthopedic ward. The anesthesiologist who managed the subjects and recorded the volume of blood loss during surgery did not have any information about opium addiction and premedication of the subjects. All data were analyzed using SPSS (version 17.0; SPSS Inc. Chicago, IL). For statistical data analysis, student t test, Chi-square test and analysis of variance (ANOVA) with interaction were used. P values less than 0.05 were considered significant.