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BJA Advance Access originally published online on February 11, 2005
British Journal of Anaesthesia 2005 94(4):536-541; doi:10.1093/bja/aei086
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© The Board of Management and Trustees of the British Journal of Anaesthesia 2005. All rights reserved. For Permissions, please e-mail: journal.permissions{at}oupjournals.org

Clonidine produces a dose-dependent impairment of baroreflex-mediated thermoregulatory responses to positive end-expiratory pressure in anaesthetized humans

T. Mizobe1,*, Y. Nakajima1, M. Sunaguchi1, H. Ueno1 and D. I. Sessler2

1 Department of Anesthesiology, Kyoto Prefectural University of Medicine, Kyoto, Japan. 2 The Outcome ResearchTM Institute and Departments of Anesthesiology and Pharmacology, University of Louisville, Louisville, KY, USA

* Corresponding author: Department of Anesthesiology, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto 602-8566, Japan. E-mail: toshim{at}koto.kpu-m.ac.jp

Background. Perioperative hypothermia is common and results from anaesthesia-induced inhibition of thermoregulatory control. Hypothermia is blunted by baroreceptor unloading caused by positive end-expiratory pressure (PEEP), and is mediated by an increase in the vasoconstriction threshold. Premedication with clonidine impairs normal thermoregulatory control. We therefore determined the effect of clonidine on PEEP-induced hypothermia protection.

Methods. Core temperature was evaluated in patients undergoing combined general and epidural anaesthesia for lower abdominal surgery. They were assigned to an end-expiratory pressure of zero (ZEEP) or 10 cm H2O PEEP. The PEEP group was divided into three blinded subgroups that received placebo (Cl-0), clonidine 150 µg (Cl-150) and clonidine 300 µg (Cl-300) respectively. Placebo or clonidine was given orally 30 min before surgery. We evaluated core temperature and thermoregulatory vasoconstriction. We also determined plasma epinephrine, norepinephrine, angiotensin II concentrations and plasma renin activity.

Results. Core temperature after 180 min of anaesthesia was 35.1 (0.4)°C in the ZEEP group. PEEP significantly increased final core temperature to 35.8 (0.5)°C (Cl-0 group). Clonidine produced a linear, dose-dependent impairment of PEEP-induced hypothermia protection: final core temperatures were 35.4 (0.3)°C in the Cl-150 group and 35.0 (0.6)°C in the Cl-300 group. Similarly, clonidine produced a linear and dose-dependent reduction in vasoconstriction threshold: Cl-0, 36.4 (0.3)°C; Cl-150, 35.8 (0.3)°C; Cl-300, 35.4 (0.6)°C. Plasma norepinephrine, angiotensin II concentrations and renin activity were consistent with the thermoregulatory responses.

Conclusion. Baroreceptor unloading by PEEP normally moderates perioperative hypothermia. However, clonidine premedication produces a linear, dose-dependent reduction in this benefit.


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