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A randomised controlled trial of perineural vs intravenous dexamethasone for foot surgery

A randomised controlled trial of perineural vs intravenous dexamethasone for foot surgery Summary We used 20 ml ropivacaine 0.75% for ankle blocks before foot surgery in 90 participants who we allocated in equal numbers to: perineural dexamethasone 8 mg and intravenous saline 0.9%; perineural saline 0.9% and intravenous dexamethasone 8 mg; or perineural and intravenous saline 0.9%. Dexamethasone increased the median (IQR (range)) time for the return of some sensation or movement, from 14.6 (10.8–18.8 (5.5–38.0)) h with saline to 24.1 (19.3–29.3 (5.0–44.0)) h when given perineurally, p = 0.00098, and to 20.9 (18.3–27.8 (8.8–31.3)) h when given intravenously, p = 0.0067. Dexamethasone increased the median (IQR (range)) time for the return of normal neurology, from 17.6 (14.0–21.0 (9.5–40.5)) h with saline to 27.5 (22.0–36.3 (7.0–53.0)) h when given perineurally, p = 0.00016, and to 24.0 (20.5–32.3 (13.0–42.5)) h when given intravenously, p = 0.0022. Dexamethasone did not affect the rates of block success, postoperative pain scores, analgesic use, or nausea and vomiting. The route of dexamethasone administration did not alter its effects. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Anaesthesia Wiley

A randomised controlled trial of perineural vs intravenous dexamethasone for foot surgery

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References (36)

Publisher
Wiley
Copyright
Copyright © 2016 © The Association of Anaesthetists of Great Britain and Ireland
ISSN
0003-2409
eISSN
1365-2044
DOI
10.1111/anae.13346
pmid
26682721
Publisher site
See Article on Publisher Site

Abstract

Summary We used 20 ml ropivacaine 0.75% for ankle blocks before foot surgery in 90 participants who we allocated in equal numbers to: perineural dexamethasone 8 mg and intravenous saline 0.9%; perineural saline 0.9% and intravenous dexamethasone 8 mg; or perineural and intravenous saline 0.9%. Dexamethasone increased the median (IQR (range)) time for the return of some sensation or movement, from 14.6 (10.8–18.8 (5.5–38.0)) h with saline to 24.1 (19.3–29.3 (5.0–44.0)) h when given perineurally, p = 0.00098, and to 20.9 (18.3–27.8 (8.8–31.3)) h when given intravenously, p = 0.0067. Dexamethasone increased the median (IQR (range)) time for the return of normal neurology, from 17.6 (14.0–21.0 (9.5–40.5)) h with saline to 27.5 (22.0–36.3 (7.0–53.0)) h when given perineurally, p = 0.00016, and to 24.0 (20.5–32.3 (13.0–42.5)) h when given intravenously, p = 0.0022. Dexamethasone did not affect the rates of block success, postoperative pain scores, analgesic use, or nausea and vomiting. The route of dexamethasone administration did not alter its effects.

Journal

AnaesthesiaWiley

Published: Mar 1, 2016

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