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Anesth Analg 2002;94:609-614
© 2002 International Anesthesia Research Society


ANESTHETIC PHARMACOLOGY

Oral Clonidine Premedication Reduces the Awakening Concentration of Propofol

Hideyuki Higuchi, MD*, Yushi Adachi, MD{dagger}, Shinya Arimura, MD*, Mie Ogata, MD*, and Tetsuo Satoh, MD{dagger}

*Department of Anesthesia, Self Defense Force Central Hospital, Tokyo; and {dagger}Department of Anesthesiology, National Defense Medical College, Saitama, Japan

Address correspondence and reprint requests to Hideyuki Higuchi, MD, Department of Anesthesia, Self Defense Force Hanshin Hospital, 4-1-50 Kushiro, Kawanishi, Hyogo 666-0024, Japan. Address e-mail to higu-chi{at}ka2.so-net.ne.jp

To investigate the effects of oral clonidine premedication on emergence from propofol/fentanyl anesthesia, we studied 72 healthy male patients who were undergoing elective orthopedic surgery: the Control group, the 2.5 µg/kg Clonidine group, and the 5.0 µg/kg Clonidine group (n = 24 each). Nothing was administered to the Control group. Clonidine (2.5 or 5.0 µg/kg) was orally administered 90 min before the induction of anesthesia in the Clonidine groups. Patients were anesthetized with computer-assisted continuous infusion of propofol and fentanyl, with the three groups receiving the same concentrations of propofol (3 µg/mL) and fentanyl (1 ng/mL) starting 20 to 30 min before the end of surgery. Propofol infusion was then abruptly discontinued at the end of surgery in all patients. After propofol was discontinued, the response to verbal commands was evaluated every 30 s, and arterial blood samples for propofol and clonidine concentrations were taken when the patients opened their eyes. The time required to respond to a verbal command was 14.9 ± 8.3 min for the 5.0 µg/kg Clonidine group, and this was significantly longer than the Control (8.2 ± 5.0 min) and the 2.5 µg/kg Clonidine (9.0 ± 3.7 min) groups (P < 0.01). Serum propofol concentration at awakening in the 5.0 µg/kg Clonidine group was 1.0 ± 0.4 µg/mL, which was significantly smaller than the Control (1.6 ± 0.4 µg/mL) and the 2.5 µg/kg Clonidine (1.4 ± 0.3 µg/mL) groups (P < 0.01). The blood clonidine concentration was associated with a decrease in the awakening propofol concentration. In conclusion, 5 µg/kg oral clonidine premedication decreases the awakening propofol concentration and delays arousal from propofol/fentanyl anesthesia.

IMPLICATIONS: Preanesthetic medication with 5 µg/kg oral clonidine, but not 2.5 µg/kg clonidine, is associated with prolonged recovery from propofol/fentanyl anesthesia.




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M. T. Pawlik, E. Hansen, D. Waldhauser, C. Selig, and T. S. Kuehnel
Clonidine Premedication in Patients with Sleep Apnea Syndrome: A Randomized, Double-Blind, Placebo-Controlled Study
Anesth. Analg., November 1, 2005; 101(5): 1374 - 1380.
[Abstract] [Full Text] [PDF]




Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins and Stanford University Libraries' HighWire Press®. Copyright 2002 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 2002 by the International Anesthesia Research Society.