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Randomized Controlled Trial
. 2009 Mar;56(3):213-21.
doi: 10.1007/s12630-008-9036-z. Epub 2009 Jan 28.

Sympathectomy-mediated vasodilatation: a randomized concentration ranging study of epidural bupivacaine

Affiliations
Randomized Controlled Trial

Sympathectomy-mediated vasodilatation: a randomized concentration ranging study of epidural bupivacaine

Yehuda Ginosar et al. Can J Anaesth. 2009 Mar.

Erratum in

  • Can J Anaesth. 2010 Jun;57(6):626

Abstract

Purpose: We tested the hypothesis that the development of sympathectomy-mediated vasodilatation is dependent on the concentration rather than the dose of epidural local anesthetic administered.

Methods: Sixty subjects receiving lumbar epidural bupivacaine were randomised to one of three groups: A: 10 ml 0.5% (50 mg); B: 10 ml 0.25% (25 mg); and C: 40 ml 0.0625% (25 mg). Groups A and B had equal volume but a twofold difference in drug dose, while groups B and C had equal drug dose, but a fourfold difference in drug volume. At baseline and 5, 10, and 20 min following epidural bupivacaine administration, we assessed the following indices of sympathectomy: pulse oximeter perfusion index in the toe and finger, skin temperature in the toe and finger, and mean arterial pressure. We also assessed sensory level (pinprick, cold, and light touch) and motor block.

Results: There was an increase in the pulse oximeter perfusion index by 20 min of 280%, 303%, and 59% in groups A, B, and, C, respectively. There was a significant sympathectomy-mediated vasodilatation in the toe for both groups A (P = 0.002) and B (P < 0.001) but not C (P = 0.22). Vasoconstriction in the finger was observed in group A only (P = 0.015) but not in group B (P = 0.09) or group C (P = 0.20). There were similar blood pressure changes and similar sensory changes in all groups. The intensity of motor block increased with increasing drug concentration.

Conclusions: Our observations suggest that drug concentration is more important than drug dose in determining the degree of sympathectomy following lumbar epidural local anesthesia.

Trial registration: ClinicalTrials.gov NCT00197353.

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