In a randomized clinical trial, after considering the inclusion and exclusion criteria and after taking informed written consent, 120 patients were selected from all the patients entering the orthopedic operating room. The following conditions were considered as study inclusion criteria:
-Patients with 18 to 65 years of age
-Being operated by the same orthopedic surgeon
-Elective surgery
- Only lower limb operation
In addition, the following conditions were considered as exclusion criteria:
-History of underlying medical disorders
-History of drug or substance abuse
-Emergent or urgent surgery
-History of underlying low back pain
-Any decision by the patient to quit the study at any time during the perioperative period
-Any technical failure that led to change the plan of study was conducted to exclude the case from the survey
The patients were randomly allocated to three groups of 40 based on a random table of numbers.
Group A: patients were anesthetized using general anesthesia (GA) for the surgical operation; moreover, an epidural catheter was inserted to administer epidural analgesia during the postoperative period. Therefore, they were the GA plus lumbar epidural analgesia (LEA) (GA + LEA) group.
Group B: Patients were anesthetized using GA for the surgical operation; in addition, intravenous patient-controlled analgesia (IVPCA) was used for suppressing acute postoperative pain (GA + IVPCA group).
Group C: Patients were anesthetized using spinal anesthesia for the surgical operation; in addition, IVPCA was used for suppressing acute postoperative pain (Spinal + IVPCA group).
The patients were anesthetized by a constant anesthesiologist. Moreover, all the patients were visited the night before the operation by a constant colleague to obtain written informed consent and description of the study. During any stages of the study, if any patients decided to leave the project, it was enough to tell one of the study colleagues. After patient entry to the operating room, each patient was visited by a constant colleague who had not been in touch with the patients the last night; moreover, he did not have any affairs regarding patient care in the postoperative period. Instead, another colleague outside the operating room visited the patients for postoperative care (including postoperative acute pain management). Inside the operating room, each patient was randomly allocated to one of the study groups. Selection for entering each group was done using a table of random numbers. GA in group A and B were done using the same method. In group C, the patients received spinal anesthesia using a 25G spinal needle, through the L3 - L4 interspace and median approach. While monitoring the patients, they were sedated and then, changed to lateral decubitus position. Then the location was prepared and draped. A guardian nurse looked after the patient in this position. Then 3.5 mL of plain bupivacaine was administered after achieving positive result in barbottage test. At the end of the surgery, the patients were transferred to the post anesthesia care unit (PACU). The anesthesia block level was managed to be at about the level of T10. For induction of GA in groups A and B, after application of standard monitoring devices including electrocardiography, oxygen saturation, and noninvasive blood pressure monitoring, the patients received 10 mL/kg of lactated Ringer’s solution in 15 minutes. Then the patient received 0.02 mg/kg of IV midazolam accompanied with 2 µg/kg fentanyl, 5 mg/kg of sodium thiopental, and 0.5 mg/kg of atracurium. Then they were intubated and received0.6% to 1.2% isoflurane through inhalational route to keep Bispectral index (BIS) level in the range of 40 to 60 out of 100. In addition, neuromuscular monitoring was used to monitor administration of atracurium during operation and for reversing their effects at the end of surgery. For all the patients, tourniquet was applied. After termination of the operation, reversal of neuromuscular blockade and recovering full consciousness, the patients were extubated and transferred to the PACU. All surgeries lasted shorter than three hours. If duration of surgeries were longer than three hours, blood loss was more than 1 L, or patients were hydrated more than 4 L during the operation, the cases were excluded from the study. In addition, any technical failure that led to changing the plan of study would exclude the case from the study. Preoperative plasma BNP levels were measured using the venous blood samples the night before operation; in addition, postoperative samples were taken 24 hours after surgery. For measurement of pro-BNP, we used the following method:
For preoperative plasma BNP measurement, we took a venous blood sample in a lithium-heparin tube and transferred them to a constant laboratory, using a box with room temperature. We had our patients to lie supine and calm for 15 - 20 minutes, without stress or agitation; since we wanted to eliminate confounding agents of plasma pro-BNP levels. Bayer ADVIA Centaur™ immunoassay operation (Bayer Healthcare LLC, Diagnostic division, Leverkusen, Germany) was our measurement method for plasma pro-BNP levels (
13). Data entry and analysis was done using SPSS 16(SPSS Inc., Chicago, IL, USA). Data analysis was performed through ANOVA. P value < 0.05 was considered statistically significant.