
Effect of methadone and acepromazine premedication on tear production in dogs
Author(s) -
Volk Hayley A,
West Ellie,
LinnPearl Rose,
Fricker Georgina V,
Panti Ambra,
Gould David J
Publication year - 2018
Publication title -
veterinary record open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.504
H-Index - 12
ISSN - 2052-6113
DOI - 10.1136/vetreco-2018-000298
Subject(s) - premedication , acepromazine , anesthesia , medicine , general anaesthesia , methadone , surgery , heart rate , blood pressure
Objectives To evaluate the combined effect of intramuscular acepromazine and methadone on tear production in dogs undergoing general anaesthesia for elective, non‐ocular procedures. Design Prospective, non‐randomised, pre‐post treatment study. Setting Patients were recruited from a referral practice in the UK. Methods Thirty client‐owned dogs were enrolled in this study and received a combined intramuscular premedication of methadone (0.3 mg/kg) and acepromazine (0.02 mg/kg) before general anaesthesia for elective, non‐ocular procedures. Full ophthalmic examination was performed and tear production was quantified using the Schirmer tear test‐1 (STT‐1). On the day of general anaesthesia, an STT‐1 was performed before (STT‐1a) and after (STT‐1b) intramuscular premedication with methadone/acepromazine. Results Using a general linear model, a significant effect on STT‐1 results was found for premedication with methadone/acepromazine (P=0.013), but not eye laterality (P=0.527). Following premedication, there was a significant reduction observed in the mean STT‐1 readings of left and right eyes between STT‐1a (20.4±2.8 mm/min) and STT‐1b (16.9±4.1 mm/min; P<0.001). Significantly more dogs had an STT‐1 reading less than 15 mm/min in one or both eyes after premedication (30 per cent; 9/30 dogs) compared with before premedication (6.7 per cent; 2/30 dogs; P=0.042). Conclusions An intramuscular premedication of methadone and acepromazine results in a decrease in tear production in dogs before elective general anaesthesia. This may contribute to the risk of ocular morbidities, such as corneal ulceration, particularly in patients with lower baseline tear production.