None listed
Conditions
Brief summary
Background: Hypothermia is the most common thermoregulatory disorder encountered during anesthetic methods and it can cause complications. The aim of our study is to determine the effects of anesthetic technique and ambient temperature on thermoregulation in patients undergoing lower extremity surgery. Methods: Our study included 90 male patients aged 18-60 years within the American Society of Anesthesiologists (ASA) I-II risk group who were scheduled for lower extremity surgery. Patients were randomly divided into three groups according to the applied anesthetic technique: general anesthesia (GA), epidural anesthesia (EA), and femoral-sciatic block (FS). These groups were then divided into subgroups according to room temperature: the temperature for group I was 20-22 degrees C and the temperature for group II was 23-25 degrees C. Therefore, we labeled the groups as follows: Group GA I, GA II, EA I, EA II, FS I and FS II. Probes for measuring the tympanic membrane and peripheral temperature were placed in patients, and their mean skin temperature (MST) and mean body temperature (MBT) were assessed immediately before the induction of anesthesia and 5, 10, 15, 20, 30, 45, 60, 90 and 120 minutes after the induction of anesthesia. Once patients were in the post anesthesia care unit, the tympanic membrane, axillary temperature, shivering, visual analog scale (VAS) and nausea-vomiting scores were recorded. Results: With the method of anesthesia, tympanic and mean body temperature (MBT) decreased, while mean skin temperature (MSK) increased in all of the patients. There was no significant difference in tympanic temperatures between either of the room temperature or anesthetic method groups. MST was lower in the GA I group than in the GA II group at 5, 10, 15, 20, 60 and 90 minutes, while the MBT was significantly lower at the basal level (p<0.05). MST at 5 minutes was significantly lower in the GA I group as compared to the FS I group (p<0.05). The shivering score in the GA I group and the VAS scores in the GA I and GA II groups were significantly higher than those of the other groups (p<0.05). During the postoperative period, there was no significant difference in tympanic and axillary temperature or nausea and vomiting scores. Conclusions: There were no significant differences between applied anesthetic techniques, and room temperature only affected the patient group undergoing general anesthesia.
Interventions
patients were divided into three groups according to their applied anesthesia technique: Group EA (epidural anesthesia, n=30) and Group FS (femoral sciatic block, n=30). Then, these groups were divided into two each based on the ambient temperature of the operating room, which was either 20-22 degrees C or 23-25 degrees C. The final distribution of the patients into four subgroups is as follows: Group EA I = patients undergoing epidural anesthesia (EA) (n=15) with a surgical room temperature (RT) of 20-22 degrees C, Group EA II = patients undergoing EA (n=15) with a surgical RT of 23-25 degrees C, Group FS I = patients undergoing femoral sciatic block (FS) (n=15) with a surgical RT of 20-22 degreesC, and Group FS II = patients undergoing FS (n=15) with a surgical RT of 23-25 degrees C. After the skin was cleaned with antiseptic solution, the EA group patients were seated and locally anesthetized by 2 ml 2% lidocaine subcutaneous infiltration at the L4-5 level in the midline skin. Epidural anesthesia was performed by using a 16 G Touhy needle according to the loss of resistance technique. After reaching the epidural space, an 18 G epidural catheter was inserted through a Touhy needle and directed towards the head. After the absence of intravascular and intrathecal area was assessed by negative aspiration, the catheter tip was placed 3-4 cm within the epidural space. Three ml of 2% lidocaine was given as a test dose and waited for 5 minutes. After receiving a negative response to the test dose, 10-20 ml of 0.5% levobupivacaine and 50 micro g fentanyl was administered. Three L/min oxygen was given to patients with a facemask. The level of sensory block was checked in 5-minute intervals by the Pinprick test, and additional doses were administered as needed. Patients with the sensory block degree up to T10 were included in the study, but patients who developed higher levels of sensory block were excluded. Patients in Group FS were applied a sciatic block by using the classical Labat technique. After patients were placed at a lateral decubitus position, the posterior superior iliac spine and trochanter major were localized and marked. The vertical medial line was drawn in the middle of the line connecting those two points and the injection point was determined to be 4 cm along this line. After the area was cleaned with antiseptic solutions and covered, 1 ml of 2% lidocaine was injected subcutaneously to create local anesthesia at the injection point. The block, together with the nerve stimulator (Stimuplex HNS 11, Braun Freiburg, Germany), was made with a 150 mm block needle entering vertical to the skin. The initial current of the nerve stimulator was set to 1.5-2 mA, and after the plantar or dorsal flexion was obtained, the current was reduced to 0.3-0.5 mA. After a negative aspiration test was observed, 25 ml of 0.375% levobupivacaine solution was injected. The patient was laid in the supine position for the femoral block and the inguinal ligament was determined by drawing a line connecting the to the anterior superior spine iliac and lateral corner of simfisis pubis. An injection point was marked 2 cm lateral to the pulse of the femoral artery and 2 cm distal to the inguinal ligament line. The area was cleaned with an antiseptic solution and wraped with a sterile. An eighty-mm-long nerve block needle was connected to the nerve stimulator and was forwarded in the cranial direction parallel to the femoral artery at an angle 30-40° to the skin surface. The needle was forwarded until quadriceps femoris muscle contractions and patella movements were seen. Then, the stimulation current intensity was reduced to 0.3-0.5 mA and was followed by observance of negative aspiration, after which a 20 ml 0.375% levobupivacaine solution was injected.
Sponsors
Study design
Eligibility
Inclusion criteria
The study was included 90 male patients aged between 18-60 years whose physical status was in the American Society of Anesthesiologists (ASA) I-II risk group and were scheduled for lower extremity surgery. In all cases, to avoid errors in body temperature measurements arising from the diurnal rhythm, body temperature measurements were taken in the morning between 08:30 and 13:00 hours.
Exclusion criteria
Patients with inflammatory diseases, diabetes mellitus, muscle disease, hypo/hyperthyroidism, cardiac, hepatic and renal diseases, Parkinson disease, Reynold syndrome, a history of using drugs that are known to affect body temperature (Beta-blockers, calcium channel blockers, clonidine, steroids, anti-epileptic, non-steroidal anti-inflammatory drugs, benzodiazepine), vertebral column anatomical disorder, bleeding diathesis, anticoagulant use, infection at the region of procedure, neurological deficits, drug and alcohol addiction, obesity, and those with allergies to local anesthetics were excluded from the study. In addition, patients whose surgery was shorter than 60 minutes and longer than 180 minutes and those surgeries where a tourniquet was used were also excluded from the study. Patients having a greater than 30% change in hemodynamic parameters during the surgery, those who needed to use a vasopressor or vasodilator, and those who required a blood transfusion were excluded from the study as well.