Vol 3 No 4 (2017): Autumn

Published: 2017-10-28

Research Article(s)

  • XML | PDF | downloads: 158 | views: 6760 | pages: 365-372

    Background: The present study has evaluated the effect of intrathecal Sufentanil and Meperidine on patients’ shivering after caesarean section.
    Methods: The present study was a double-blind randomized clinical trial that was conducted on 120 patients. Spinal anesthesia was administered using 2 cc (10 mg) of bupivacaine along with 2.5 µg (0.5 cc) of Sufentanil for the first group, 25 mg (0.5 cc) of Meperidine for the second group and 0.5 cc normal saline for the control group.
    The severity of patients’ shivering was recorded during the surgery and in the recovery room. Heart rate, respiratory rate, systolic and diastolic blood pressures, oxygen saturation, and core and skin temperatures were measured before anesthesia, 5th minute, 10th minute and then every 15 minutes until the end of the surgery and then every 15 minutes into the recovery until discharge from recovery. The Apgar score of the neonates were also recorded at the 1st and 5th minutes after birth.
    Results: The mean score of shivering was significantly lower in the Meperidine group (0.1 ± 0.07) than the Sufentanil group (1.2 ± 0.3) and the control group (4.1 ± 0.5) (p< 0.05). The frequency of incidence of shivering was also decreased in Meperidine (5.3%) and Sufentanil (42.1%) groups compared to the control group (p< 0.001). Changes in blood pressure from the 25th minute to the 45th minute of the surgery and during the first 45 minutes into the recovery had more stability in the Meperidine and Sufentanil groups (p< 0.05). Changes in the heart rate respiratory rate, core and skin temperatures and infants’ Apgar score had no statistical difference between the three groups (p > 0.05).
    Conclusion: Using intrathecal Meperidine and Sufentanil, besides decreasing the incidence of shivering (with more effectiveness from Meperidine), would also increase the block density and quality of relaxation in the patients. It would also lead to improved hemodynamic stability without affecting the sensory block level and infant’s Apgar score.

  • XML | PDF | downloads: 172 | views: 378 | pages: 373-377

    Background: Maternal bradycardia and hypotension are the most common intraoperative complications after spinal anesthesia during cesarean delivery. Prophylactic administration of ondansetron has been reported to provide a protective effect. In this study we evaluated the effect of intravenous granisetron, another serotonin 5-HT3 receptor antagonist, on prevention of these complications.
    Methods: Thirty-four ASA class I-II patients undergoing elective cesarean section under spinal anesthesia were randomly allocated into two equal groups, control saline (n=17) or granisetron groups (n=17). After insertion of standard monitorings,5ml/kg lactated Ringer’s solution was infused over 15 minutes. In saline group 3ml of 0.9% saline and in granisetrone 3mg (3ml) granisetron was injected intravenously five minutes before spinal anesthesia. Systolic and diastolic blood pressure and heart rate were all recorded every two minutes during first twenty minutes and then every five minutes until the end of surgery and compared between the groups.
    Results: Demographic data and median of sensory block level were not statistically different between the groups. There was no statistical difference between the study groups regarding the systolic, diastolic and heart rate at measured points except at second minutes after spinal anesthesia that was lower in saline group (P=0.01).
    Conclusion: This study showed that intravenous granisetron has little protective effect on attenuation of hemodynamic responses of parturients undergoing elective cesarean section under spinal anesthesia.

  • XML | PDF | downloads: 157 | views: 333 | pages: 378-381

    Background: Pain relief is one of the most important goals in patients undergoing surgery without using high-dose opioid analgesics due to their complications.   The aim of this study was to evaluate the effect of using low-dose ketamine after spinal anesthesia on the severity of postoperative pain in the patients with orthopedic surgery.
    Methods: The present double-blind clinical trial after obtaining approval was performed on 60 patients with lower limb fracture. The patients were selected by convenience sampling method and then divided into two equal (n=30) intervention and control groups using random number table. The patients in the intervention group after spinal anesthesia received 0.2mg/kg intravenous ketamine diluted with 10cc normal saline. The same amount of normal saline was injected intravenously in the control group. Then, the intensity of pain using VAS and the level of need for analgesics were measured in both groups at different times up to 24 hours after surgery.
    Results: The intervention group included 21 males and 9 females with a mean age of 30 ± 1.2 years and control group consisted of 19 males and 11 females with a mean age of 29 ± 4 years. There was no significant difference between the age and sex of the patients in the intervention and control groups (P=0.677), (P=0.589). In the intervention group with the VAS, the lowest pain score was found at the first turn of the assessment (2.4 ± 0.6), and the highest pain at 24 h (4.3 ± 2.6). The control group had the lowest pain score at the first turn of the assessment (3.6 ± 0.8) and the maximum pain at the first turn of the assessment (5.2 ± 1.7). According to independent t-test, there was a significant difference between the two groups at all times, except for the first turn of the assessment. In the intervention group, 12 (40%) patients did not receive analgesics within 24 hours. In the control group, 2 (6.7%) had no analgesics. Chi-square showed a significant difference between the two groups (P=0.002).
    Conclusion: The present study showed that low-dose intravenous ketamine could relieve pain in patients and reduce postoperative analgesics.

  • XML | PDF | downloads: 150 | views: 295 | pages: 382-384

    Background: The pain induced by intravenous injection of propofol is controlled using a variety of methods, but there is no consensus in choosing the best effective method. Therefore, this study was conducted to compare premedication injections of magnesium sulfate, ketamine and lidocaine on pain induced by intravenous injection of propofol.
    Methods: The present double-blind clinical trial was conducted on 150 patients with elective orthopedic surgery under general anesthesia. The patients were randomly assigned into three groups of 50; Group I: 2 cc magnesium sulfate 20%, Group II: 2 cc Ketamine at a dose of 0.1mg/kg and Group III: 2 cc lidocaine 2% at a dose of 0.05mg/kg. One minute after injecting the drugs, 2mg/kg intravenous propofol was injected in all groups and then a trained unaware expert evaluated the severity of subsequent pain using a Numeric Pain Rating Scale.
    Results: The mean age of the patients was 39.3±12.3 years, and the mean weight was 67.4±11.5 kg. The patients consisted of 98 (65.4%) males and 52 (34.6%) females. Ten in the Group magnesium sulfate, eight in the Group ketamine and seven in the Group lidocaine complained of pain. The mean pain severity was 0.85±0.38 in the Group magnesium sulfate, 0.66±0.26 in the Group ketamine and 0.62±0.22 in the Group lidocaine (P=0.513).
    Conclusion: The Group lidocaine showed further pain relief compared to other two groups, but there was no statistically significant difference.

  • XML | PDF | downloads: 139 | views: 208 | pages: 385-388

    Background: This study aimed to determine the effects of two muscle relaxants, i.e. atracurium and cisatracurium, on airway pressure of pediatric patients during general anesthesia maintained by propofol.
    Methods: This double-blind clinical trial included 68 two-five-year-old candidates for elective lower abdominal surgeries under propofol anesthesia. The patients were randomized to two groups to receive either atracurium or cisatracurium as muscle relaxant. The changes in airway pressures were evaluated during the procedure.
    Results: Peak airway pressure from the 10th to the 45th minutes and plateau airway pressure from the fifth to the 45th minutes after the induction of anesthesia were significantly lower in the cisatracurium group (P = 0.005). Four patients (11.8%) from the atracurium group developed laryngospasm. However, the two groups had no significant difference in this regard (P = 0.11).
    Conclusion: Comparison of the two muscle relaxants showed that cisatracurium had lower peak and plateau airway pressure in pediatric patients under general anesthesia maintained by propofol.

Review Article(s)

Case Report(s)