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Effects of medetomidine and medetomidine-butorphanol combination on Schirmer tear test 1 readings in dogs
R. F. Sanchez*, D. Mellor* and J. Mould*†
  *Small Animal Clinical Studies and   Comparative Epidemiology and Informatics, Institute of Comparative Medicine, Faculty of Veterinary Medicine, University of Glasgow, Bearsden Rd., Bearsden, Glasgow G61 1QH, UK
Correspondence to Address communications to: bvR. Sanchez bv Tel.: (00)-44-156861661 e-mail: r.sanchez@vet.gla.ac.uk; r.sanchez@eyevetclinic.co.uk

Dr Sanchez's and Mr Mould's Present address is Eye Veterinary Hospital, Marlbrook, Leominster, Herefordshire, HR6 0PH, U.K.

Copyright © 2006 American College of Veterinary Ophthalmologists
KEYWORDS
butorphanol • dog • medetomidine • Schirmer tear test • sedation • tear production

Abstract

AbstractINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES

Medetomidine is a commonly used sedative in veterinary medicine whether administered alone or in combination with an opioid such as butorphanol. There are no previous studies that look at the effects of this drug on sequential Schirmer tear test (STT) 1 readings in dogs, including effects on tear production after reversal of the drug. The present study looked at two groups of 10 dogs each that were sedated with intravenous medetomidine or a combination of medetomidine and butorphanol. All dogs had tear readings taken presedation, 15 min postsedation, and 15 min after reversal of medetomidine with atipamezole. Results revealed that intravenous sedation with medetomidine and medetomidine-butorphanol in dogs with no history of ophthalmic disease and presedation STT 1 readings above 15 mm/min, causes a significant decrease in tear production that is measurable at 15 min postsedation. Readings returned to near presedation values within 15 min postreversal in most cases. It is therefore recommended that all eyes be treated with a tear substitute from the time the sedative is given until at least 15 min after reversal.


DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1463-5224.2005.00432.x About DOI

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