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- Author or Editor: Lynelle F. Graham x
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Abstract
OBJECTIVE To compare the doses of propofol required to induce general anesthesia in dogs premedicated with acepromazine maleate or trazodone hydrochloride and compare the effects of these premedicants on cardiovascular variables in dogs anesthetized for orthopedic surgery.
DESIGN Prospective, randomized study.
ANIMALS 30 systemically healthy client-owned dogs.
PROCEDURES 15 dogs received acepromazine (0.01 to 0.03 mg/kg [0.005 to 0.014 mg/lb], IM) 30 minutes before anesthetic induction and 15 received trazodone (5 mg/kg [2.27 mg/lb] for patients > 10 kg or 7 mg/kg [3.18 mg/lb] for patients ≤ 10 kg, PO) 2 hours before induction. Both groups received morphine sulfate (1 mg/kg [0.45 mg/lb], IM) 30 minutes before induction. Anesthesia was induced with propofol (4 to 6 mg/kg [1.82 to 2.73 mg/lb], IV, to effect) and maintained with isoflurane or sevoflurane in oxygen. Bupivacaine (0.5 mg/kg [0.227 mg/lb]) and morphine (0.1 mg/kg [0.045 mg/lb]) were administered epidurally. Dogs underwent tibial plateau leveling osteotomy (n = 22) or tibial tuberosity advancement (8) and were monitored throughout anesthesia. Propofol induction doses and cardiovascular variables (heart rate and systemic, mean, and diastolic arterial blood pressures) were compared between groups.
RESULTS The mean dose of propofol required for anesthetic induction and all cardiovascular variables evaluated did not differ between groups. Intraoperative hypotension developed in 6 and 5 dogs of the acepromazine and trazodone groups, respectively; bradycardia requiring intervention developed in 3 dogs/group. One dog that received trazodone had priapism 24 hours later and was treated successfully. No other adverse effects were reported.
CONCLUSIONS AND CLINICAL RELEVANCE At the described dosages, cardiovascular effects of trazodone were similar to those of acepromazine in healthy dogs undergoing anesthesia for orthopedic surgery.
Abstract
OBJECTIVE: To determine the intracoelemic (ICe) dose of alfaxalone required to induce loss of righting reflex (LRR) in garter snakes (Thamnophis sirtalis) and to evaluate the tactile stimulus response in unanesthetized and alfaxalone-anesthetized snakes.
ANIMALS: 8 healthy mature garter snakes.
PROCEDURES: During the first of 3 phases, snakes received each of 3 doses (10, 20, and 30 mg/kg) of alfaxalone, ICe, with a 2-week washout period between treatments. Times to LRR and return of righting reflex were determined after each dose. During phase 2, unanesthetized snakes underwent tactile stimulation testing with Semmes-Weinstein monofilaments once daily for 3 consecutive days to determine the baseline tactile pressure required to elicit purposeful movement. During phase 3, snakes were anesthetized with alfaxalone (30 mg/kg, ICe), and the tactile pressure required to induce purposeful movement was assessed at predetermined times after LRR.
RESULTS: Intracoelomic administration of alfaxalone at doses of 10, 20, and 30 mg/kg induced LRR in 0, 5, and 8 snakes, respectively. For snakes with LRR, median time to LRR following the 30-mg/kg dose (3.8 minutes) was significantly shorter than that following the 20-mg/kg dose (8.3 minutes); median time to return of righting reflex did not differ between the 2 doses. Mean ± SD tactile pressure that resulted in purposeful movement in unanesthetized snakes was 16.9 ± 14.3 g. When snakes were anesthetized, the mean tactile pressure that resulted in purposeful movement was significantly increased from baseline at 10, 20, and 30 minutes after LRR.
CONCLUSIONS AND CLINICAL RELEVANCE: Results suggested ICe administration of alfaxalone might be effective for anesthetizing garter snakes.
