This prospective, randomized, double-blind study was approved by the institutional review board of Haeundae Paik hospital, Busan, Republic of Korea (2012 - 064). Written informed consent was obtained from all of the patients and the neurocognitive function tests were explained to them before surgery. This study protocol conformed to the ethical guidelines of the 1975 Helsinki declaration.
Fifty six elderly patients (> 60-years-old) with the American society of anesthesiologist physical status 1 - 3, scheduled to undergo orthopedic surgery (duration of anesthesia > two hours) were recruited. Exclusion criteria were CNS-related diseases (including dementia), medication with tranquilizers or antidepressants, inability to perform neurocognitive function tests, severe visual or auditory dysfunction, alcohol abuse or drug dependence, and a history of a cerebrovascular accident within the previous three years.
Patients were randomly divided into two groups using a computer-generated randomization program (www.random.org): K group received intravenous (IV) bolus, a total of 3 mL mixed with 0.9% normal saline and 0.5 mg/kg ketamine (50 mg/mL, Huons, Seongnam, Korea), and N group received IV 0.9% normal saline (3 mL). The patients enrolled in the present study were not premedicated because preoperative medications including benzodiazepine and anticholinergics can cause POCD (
6).
Upon arrival in the operating room, the patients were monitored by electrocardiogram (ECG), non-invasive blood pressure, and pulse oximetry. After applying standard monitor to the patients, ketamine and 0.9% normal saline were administrated by a nurse who was blinded into the study before induction of anesthesia. General anesthesia was induced with IV propofol 2 mg/kg and rocuronium 0.6 mg/kg, maintained with desflurane 5 - 6 vol%, medical air (FiO2 0.5), and remifentanil 0.02 - 0.1 mcg/kg/hour. Remifentanil was titrated due to clinical needs (hemodynamic, autonomic, and somatic signs) depending on stimulus of surgery. Bispectral index (BIS, aspect medical system, Norwood, MA, USA) remained at 40 - 60 during surgery. End-tidal carbon dioxide concentration remained at 35 - 45 mmHg using continuous gas analysis equipment (Datex-Ohmeda S/5; Datex-Ohmeda Inc. Louisville, CO). The esophageal temperature (DeRoyal Inc. Powell, TN, USA) was measured through the surgery and maintained at 35.5 - 36.5°C. On completion of the operation, the administration of desflurane was discontinued and the fraction of inspired oxygen was increased to 100%. To reverse the neuromuscular block, IV pyridostigmine 10 mg and IV glycopyrrolate 0.2 mg were administered. Extubation was performed when the patient obeyed commands and recovered regular self-breathing.
Intravenous patient-controlled analgesia (IV-PCA) or intermittent bolus IV analgesics were used for postoperative pain targeting a visual analog scale of 2 - 3 depending on the type of surgery. The IV PCA solution contained fentanyl, ketorolac, and 3 mg of ramosetron mixed with 100 mL normal saline. The continuous infusion rate was set at 2 mL/hour, the bolus at 2 mL, and the lockout time at 15 minutes. The initial dose of fentanyl was 15 - 20 mcg/kg and that of ketorolac was 2 - 3 mg/kg, depending on the physical status and body weight of the patient as well as the surgical procedure the patient underwent. In patients not using IV PCA, meperidine, fentanyl, and ketorolac were used as rescue analgesics.
Neurocognitive function tests were conducted by a trained investigator who was blinded into the study before surgery (baseline test) and on postoperative day one (POD 1) and postoperative day six (POD 6) in a quiet environment. Serum CRP concentrations were measured.
Patients had cognitive dysfunction when the two Z-scores in more than two tests or the combined Z-score was 1.96 or more. In addition, the following factors were recorded and compared between the two groups. Duration of anesthesia and surgery, frequency of transfusion, and ketamine-related complications (psychosis or hemodynamic changes) were also recorded.
It was estimated that 28 patients in each group were needed to show a difference in POCD between 47% and 7% (
5), assuming a type I error of 0.05, a type II error of 0.2 and a 10% drop-out rate.
Statistical analyses were performed by SPSS version 21.0 (SPSS Inc. Chicago, IL, USA) and Medcalc 11.6.1.0 (Medcalc software bvba, Ostend, Belgium). The data were expressed as mean ± standard deviation (SD), median (interquartile range) or number of patients. The chi-square test was used to compare categorical variables, and the independent t test or Mann-Whitney U test was used to compare continuous variables between the K and N groups. An analysis of variance with repeated measures was performed to determine the difference between the groups and over time. P value < 0.05 was considered statistically significant.