The present study was a single-blinded non-randomized clinical trial (RCT). After approving the study protocol by the Ethics Committee (code of ethics: IR. IUMS-FMD.REC1396.9511174001) and by the Iranian Clinical Trial Registration Center (no.: IRCT20121107011398N13), a total number of 108 patients including men and women over the age of 50 years, with the diagnosis of proximal femoral bone fracture who were scheduled for open fixation surgery, were enrolled in the study. Exclusion criteria were: Preoperative cognitive impairment, significant auditory impairment, alcoholism, and drug abuse, American society of anesthesiologists physical status (ASA-PS) > III, acid-base and electrolyte abnormalities, patient’s dissatisfaction, a history of similar surgery in the past month, history of a recent cerebrovascular accident as well as taking psychotropic drugs and benzodiazepines in the week before or inadvertently after surgery.
Mini-Mental State examination (MMSE) and Wechsler tests were used to evaluate postoperative delirium and POCD, both of which were used once before surgery to assess the baseline cognitive status of patients, and three times after surgery i.e., in three successive days. The MMSE test can measure patients’ orientation to time and place, as well as the patient’s attention, memory, and computing power (
16). Wechsler’s test is a set of intelligence tests used to assess the patient’s verbal and nonverbal cognition and the capacity and ability of the patient’s overall intelligence and cognitive ability (
17).
The primary outcome of this study was POCD, and the secondary outcome was postoperative delirium. Delirium was diagnosed using DSM-IV criteria, and POCD diagnosis was performed using patient-acquired scores from MMSE and Wechsler tests. A decrease of up to 2 points in these tests was considered as mild cognitive impairment, and a decrease of more than 2 points in the postoperative phase as compared to preoperative values was considered as severe cognitive impairment (delirium equivalent).
After obtaining informed consent, the patients were divided into two groups: general (GA) or spinal (SA) anesthesia. The type of anesthesia was selected by an anesthesiologist who was unaware of the study protocol. In the GA group after routine monitoring (ECG, NIBP, SPO2, ET-Co2, BT), for premedication, fentanyl 2 µg/kg and for induction of anesthesia, lidocaine 1 mg/kg, propofol 1.5 mg/kg, and cisatracurium 0.2 mg/kg body weight was used. The patients were then intubated, and for maintenance of anesthesia, propofol 50 - 150 µg/kg/min was infused. Cisatracurium 0.05 mg/kg every 30 min and fentanyl 50 µg every hour was repeated. At the end of the surgery, the neuromuscular block was reversed with 40 µg/kg of neostigmine and 20 µg/kg of atropine, and the patients were extubated according to the clinical criteria.
In the spinal anesthesia group, 12.5 - 15 mg hypertonic bupivacaine plus 25 µg fentanyl in the sitting position were used for spinal anesthesia. In some patients (6 cases), the epidural catheter had been fixed in the L2-L3 before doing spinal anesthesia. Benzodiazepine was not used in any of the study group members during the operation and postoperative phase. In order to control the postoperative pain, 1gr of paracetamol was infused at the end of the operation, and 3 g was perfused with a patient-controlled analgesia pump.
Patients’ level of education, drug history, and preoperative laboratory tests, including the plasma hematocrit, plasma glucose, and serum electrolytes, were recorded. The type of surgery, duration of operation and anesthesia, mean intraoperative blood pressure, the blood loss during operation, amount of fluid administered, and in case of transfusion, the type and amount of the blood products used were recorded as well.
3.1. Sample Size Determination and Data Analysis Method
A reduction of POCD incidence from 40% to 15% was considered clinically significant. Power analysis was performed using an online calculator available from the University of British Columbia (Vancouver, BC, Canada) considering α = 0.05 with a power (β) of 80 percent. The sample size was determined to be a minimum of 47 patients in each group. Data were analyzed using SPSS-V22 software. Qualitative variables were reported by relative frequency, percentage, and quantitative variables using mean and standard deviation. Independent t-test, chi-square, Fisher exact test, and Mann-Whitney test were used to examine the significance of the variables. The level of significance was set at 0.05.