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1.
Acta Anaesthesiol Scand ; 51(10): 1350-3, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17711564

ABSTRACT

BACKGROUND: There are few studies on stress responses to laparoscopic surgery in children. This study was conducted to assess the blood glucose levels in children undergoing laparoscopy. We also studied the effect of two different intravenous (i.v.) solutions on blood glucose in open and laparoscopic procedures. METHODS: One hundred and twenty healthy children, aged 2-12 years, undergoing either open or laparoscopic surgery, were randomized to receive either dextrose normal saline (DS) or Ringer's lactate peri-operatively (RL). All patients had blood glucose measurements performed immediately after induction but prior to the i.v. infusion of any fluid. Blood glucose was again measured 1 h after induction in the open cases and 1 h after insufflation in the laparoscopy cases. RESULTS: In the groups, baseline blood glucose values were comparable. In all groups, blood glucose concentrations increased from the immediate post-induction (baseline) values. When RL was infused, the 1-h blood glucose was higher in the laparoscopy group as compared with the open group. However, when DS was infused the difference between the 1-h blood glucose in the open and laparoscopic procedures was not statistically significant. In the laparoscopy group, the 1-h blood glucose value was significantly higher in the patients receiving dextrose solution. CONCLUSION: Laparoscopic procedures in children are associated with a rise in blood glucose levels similar to open surgery. The hyperglycaemic response was more pronounced when dextrose-containing solutions were infused peri-operatively.


Subject(s)
Blood Glucose/metabolism , Laparoscopy , Adolescent , Child , Child, Preschool , Female , Humans , Male , Pediatrics
3.
Eur J Anaesthesiol ; 20(11): 904-10, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14649343

ABSTRACT

BACKGROUND AND OBJECTIVE: Intrathecal injections of the benzodiazepine midazolam have been reported to cause antinociception in animals and pain relief in human beings, including the potentiation of opioid analgesia. This study compared the efficacy of the addition of midazolam to a mixture of buprenorphine and bupivacaine used for spinal anaesthesia. METHODS: The study was prospective, randomized, and observer blinded. It involved 60 patients (30 per group), ASA I and II, age 20-40 yr, undergoing minor and intermediate lower abdominal surgery under spinal anaesthesia. Patients were randomized into two groups: the control group received a spinal injection of hyperbaric bupivacaine (15 mg) plus buprenorphine (0.15 mg) and the experimental group received a spinal injection of the same two drugs and doses but supplemented with intrathecal midazolam (2 mg). RESULTS: The duration of postoperative analgesia in the control group was 9.24 +/- 2.57 h (mean +/- SEM), and 21.33 +/- 12.69 h in the midazolam treated group (P < 0.001). Patients treated with intrathecal midazolam had better pain relief judged by visual analogue score on coughing (P = 0.0013) and a nursing mobility score (P < 0.0001). Adverse effects were minor and their incidence was similar in both groups. CONCLUSIONS: We conclude that intrathecal midazolam 2 mg improves the quality and duration of postoperative pain relief afforded by intrathecal buprenorphine and bupivacaine.


Subject(s)
Bupivacaine/therapeutic use , Buprenorphine/therapeutic use , Midazolam/therapeutic use , Pain, Postoperative/prevention & control , Abdomen/surgery , Adult , Analgesics, Opioid/adverse effects , Analgesics, Opioid/therapeutic use , Anesthesia, Spinal , Anesthetics, Combined/adverse effects , Anesthetics, Combined/therapeutic use , Anesthetics, Intravenous/adverse effects , Anesthetics, Intravenous/therapeutic use , Anesthetics, Local/adverse effects , Anesthetics, Local/therapeutic use , Bupivacaine/adverse effects , Buprenorphine/adverse effects , Chi-Square Distribution , Drug Synergism , Humans , Injections, Spinal , Midazolam/adverse effects , Pain Measurement , Pain, Postoperative/drug therapy , Prospective Studies , Time Factors
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