Effect of clonidine pre-medication on propofol requirements during lower extremity vascular surgery: a randomized controlled trial

Authors: Morris, J.1; Acheson, M.2; Reeves, M.3; Myles, P. S.2

Source: BJA: British Journal of Anaesthesia, Volume 95, Number 2, August 2005 , pp. 183-188(6)

Publisher: Oxford University Press

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

Abstract:

Background. Pre-medication with clonidine reduces the requirement for volatile agents during general anaesthesia. This may also be true for anaesthesia with propofol, but the amount of dose reduction has not been measured. Because clonidine also affects cardiac output and thus regional blood flow it could alter the pharmacokinetics of propofol. This randomized, double-blind placebo-controlled trial aimed to study the effect of clonidine pre-medication on dose requirement for propofol during lower extremity vascular surgery using the bispectral index (BIS) as a measure of anaesthetic depth.

Methods. After oral pre-medication with either clonidine 3 mug kg-1 or placebo, 39 subjects had lower limb vascular surgery using propofol infusion for anaesthesia. Anaesthetic depth was adjusted to a BIS of 45. Predicted plasma propofol concentrations were noted every 30 min from a target-controlled propofol infusion pump and arterial samples were taken at the same time for propofol measurements.

Results. Patients in both groups were anaesthetized to similar depths of anaesthesia as indicated by BIS readings (P=0.44). The groups had comparable mean (95% CI) arterial concentrations of propofol, 4.8 (3.5–6.1) mug ml-1 in the patients given clonidine, and 4.6 (3.4–5.7) mug ml-1 in the patients given placebo (P=0.81). However, the average plasma concentration predicted by the target-controlled infusion was less in the clonidine group [3.2 (2.9–3.5)] than in the group given placebo [3.6 (3.3–3.9)] mug ml-1 (P<0.05).

Conclusions. Pre-medication with clonidine reduces the requirement for propofol, which is a pharmacokinetic effect and not a pharmacodynamic central sedative effect.

Keywords: anaesthetics i.v; propofol; pharmacokinetics; premedication; clonidine

Document Type: Research article

DOI: 10.1093/bja/aei172

Affiliations: 1: Department of Anaesthesia and Pain Management, Royal Melbourne Hospital, Parkville, Victoria, Australia. 2: Department of Anaesthesia and Pain Management, Alfred Hospital, Melbourne, Victoria, Australia. 3: North West Regional Hospital, Burnie, Tasmania, Australia.

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$40.03 plus tax      Refund Policy

 

OR

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages.
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A