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KMID : 0356919940270010040
Korean Journal of Anesthesiology
1994 Volume.27 No. 1 p.40 ~ p.47
Effects of Oral Clonidine Premedication on the Spinal Anesthesia




Abstract
Oral clonidine premedication appears to inhibit the outflow of sympathoadrenal activity and adrenocortical hormone release, thereby decreasing the minimum alveolar anesthetic concentration clonidine premediacation for spinal anesthesia, similar
to
intrathecal administration of clonidine, has prolonging effect of sensory and motor blocks.
The purposes of this study are to assess the effects of oral clonidine premedication on the duration of tetracaine spinal anesthesia, and the hemodynamic changes during spinal anesthesia. Twenty patients undergoing hemorrhoidectomy, TURP, and
device
removal of lower extremity under spinal anesthesia (0.5% hyperbaric tetracaine), were given diazepam 10 mg orally (Group 1, n=10) or clonidine 150 §¶orally (Group 2, n=10) 1 hour before the anesthesia.
@ES The results were the following:
@EN (1) No significant differences was noted between two groups in either the maximum level of sensory extension or time to maximum level of sensory blockade between two groups. In Group 2, the time for two-segment regression was prolonged
compared
with
group 1 but not significant. The time for regression to L1 was significantly prolonged in Group 2 (238¡¾37.74min) compared with Group 1 (167.6¡¾24.85min)(P<0.05).
(2) The number of patient in Bromage's scale score 3 of motor blockade between 180min and 260min after spinal anesthesia was 10 times higher in Group 2 compaired with Group 1 (P<0.05).
(3) In Group 1, the lowest systolic blood pressure during spinal anesthesia was significantly low compared with that before premedication (P<0.05). In Group 2, systolic blood pressure before spinal anes5hesia, mean systolic blood pressure during
first
20mins of spinal anesthesia and the lowest systolic blood pressure were significantly reduced respectively comparing with those before premedication. Significant difference (P<0.05) was noted between Group 1 and 2 in mean systolic blood pressure
during
the first 20 mins of spinal ansthesia and in lowest systolic blood pressure during spinal anesthesia. In both groups, the lowest heart rate was significantly lower after than before premedication (P<0.01), but the difference in the amount of
heart
rate
change between two groups was not significant.
In conclusion, prolongation of sensory and motor blocks of spinal anesthesia with hyperbaric 0.5% tetracaine may be accomplished with oral premedication of 150 §¶clonidine without serious clinical complication.
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