The Prophylactic Effect of Propofol on the Side Effects of Intrathecal Morphine.
10.4097/kjae.1995.29.5.701
- Author:
Hae Soung LEE
1
;
In Cheol CHOI
;
Jeong Gill LEEM
;
Dong Myung LEE
Author Information
1. Department of Anesthesiology, College of Medicine, University of Ulsan, Seoul, Korea.
- Publication Type:Original Article ; Randomized Controlled Trial
- Keywords:
Propofol;
Intrathecal morphine;
Complication;
pruritus
- MeSH:
Anesthesia, Spinal;
Glucose;
Humans;
Hypnotics and Sedatives;
Incidence;
Morphine*;
Nausea;
Pain, Postoperative;
Propofol*;
Pruritus;
Respiratory Insufficiency;
Tetracaine;
Urinary Retention;
Vomiting;
Water
- From:Korean Journal of Anesthesiology
1995;29(5):701-708
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
While intrathecal morphine in small doses has been effective in controlling postoperative pain, many patients have been suffered from the side effects. In recent studies, it has been suggested that small dose of propofol can attenuate these side effects of intrathecal morphine. We have studied the effect of propofol and tried to find the optimum dose that can reduce side effects of intrathecal morphine. Sixty patients of ASA class 1 scheduled for anorectal surgery were allocated randomly to receive either a bolus dose of propofol 0.5 mg/kg followed by an infusion of 1 mg/kg/24hr(group Pl) or 2 mg/kg/24hr(group P2) and no bolus dose followed by 1,000 ml 5% dextrose water(control group). In this study, postoperartive sedation, nausea, vomiting, pruritus and urinary retention were evaluated immediate postoperatively, 12 hour, 24 hour and 48 hour after spinal anesthesia using 1% tetracaine 5 mg with 10% dextrose water 5 ml and morphine 0.3 mg. As time passed, all the complications subsided significantly. However, there was no significant difference among 3 groups except pruritus. The incidence of pruritus was lower in the group P1 and group P2(80%, 50% respectively) than the control group(90%). In the 12 hour-after evaluation, there was no patient of grade 3 pruritus in the group P2 but 5 patients in the control group(p<0.001) and 3 patients in the group Pl had itching(p<0.05). The higher doses of propofol, the greater sedative effect observed. However, there was no clinicaliy serious problem (e.g. respiratory depression, deep sedation). In conclusion, we recommend that an adequate infusion dose of propofol for reducing the incidence and severity of pruritus is 2 mg/kg/24hr.
