The aim of this study was to assess the effects of four different drugs used for anaesthesia premedication on intraocular pressure and pupil size in dogs. A prospective, randomised, double-blind clinical study was carried out. The subjects were forty client-owned healthy dogs (20 males and 20 females), aged 8.0 ± 2.9 years, with body weights of 11.8 ± 8.5 kg (mean ± SD) and without ocular abnormalities that were scheduled for periodontal treatment. Animals were randomly allocated into four groups and received intravenously either medetomidine 0.01 mg/kg, acepromazine 0.02 mg/kg, fentanyl 0.01 mg/kg or butorphanol 0.2 mg/kg. Intraocular pressure, pupil size, heart rate, respiratory frequency and systolic and diastolic arterial pressures were measured prior to (baseline) and at five and 10 minutes after premedication (T5, T10). Data were analysed by Anderson-Darling, Bartlett’s, ANOVA and Dunnett’s tests (P < 0.05). Significant increases of intraocular pressure were observed at T5 and T10 in the fentanyl group. Significant decreases of pupil size at T5 and T10 were detected in the fentanyl, butorphanol and medetomidine groups. In the fentanyl group, heart rate dropped significantly at T10, while respiratory frequency was elevated at T5 and T10. In the medetomidine group, heart rate and respiratory frequency were decreased at T5 and T10. In the butorphanol group, systolic arterial pressure was decreased at T5 and diastolic arterial pressure was decreased at T5 and T10. In the acepromazine group, systolic arterial pressure was decreased at T10. Within ten minutes after intravenous administration in healthy dogs, fentanyl significantly increased intraocular pressure and fentanyl, butorphanol and medetomidine decreased pupil size.
The goal of the presented research was to assess the influence of continuously administered fentanyl on the intraocular pressure, pupil size and aqueous tear production in dogs. A prospective, randomised, double “blind” clinical study was performed. Twenty-five non-painful dogs, 13 breeds, a body weight of 10.0 ± 5.4 kg (mean ± SD) and age of 6.5 ± 3.3 years, 12 males and 13 females with no ocular abnormalities were randomly allocated into two groups receiving an intravenous injection of saline (SAL) 0.3 ml/kg followed by an infusion 2 ml/kg/h or an intravenous injection of fentanyl (FEN) 0.005 mg/kg (diluted in 0.3 ml/kg) followed by an infusion 0.005 mg/kg/h (diluted in 2 ml/kg/h). The intraocular pressure (IOP), pupil size (PS), pulse rate (PR), respiratory frequency (f<sub>R</sub>) and systolic and diastolic arterial pressures (SAP, DAP) were measured before (baseline) and at 2, 5, 10, 20 and 30 minutes after the premedication. The Schirmer Tear Test I (STT-I) was measured prior to and at 30 min after the premedication. The data were analysed by Bartlett’s, Anderson-Darling and Dunnett’s tests, the t-test and an analysis of variance (ANOVA) (P < 0.05). Relative to the baseline, in the fentanyl group, the PS was significantly decreased at all time points, the PR was significantly decreased at T<sub>30</sub> and the f<sub>R</sub> was significantly decreased at T<sub>5</sub>, T<sub>10</sub>, T<sub>20</sub> and T<sub>30</sub>. There were no other significant changes in the IOP, STT-I, SAP and DAP relative to the baseline. Compared to the control group, in the fentanyl group, the PS was significantly smaller at T<sub>2</sub>, T<sub>5</sub>, T<sub>10</sub>, T<sub>20</sub> and T<sub>30</sub>, the PR was significantly lower at T<sub>2</sub>, T<sub>20</sub> and T<sub>30</sub> and the f<sub>R</sub> was significantly higher at T<sub>20</sub>. Within thirty minutes of a constant rate infusion of fentanyl in the healthy non-painful dogs, the intraocular pressure and aqueous tear production were not affected. However, the fentanyl significantly decreased pupil size. This fact should be considered, when planning analgesia where miosis is undesirable.
The objective of this prospective randomised clinical study was to determine the differences in the tracheal, oesophageal and rectal temperature in spontaneously breathing or mechanically ventilated dogs. A total of thirty dogs were allocated to the SPO-group breathing spontaneously (n = 15) or the MEC-group ventilated mechanically (n = 15). Anaesthesia was established using a medetomidine-butorphanol-propofol-isoflurane combination. The tracheal (T-Tra), oesophageal (T-Oes), rectal (T-Rec), inspired gas (T-Gas), room (T-Room) temperatures, respiratory frequency (f<sub>R</sub>), heart rate (HR), mean arterial pressure (MAP) and end-tidal carbon dioxide concentration (ETCO<sub>2</sub>) were measured after connecting to a re-breathing system (baseline) and subsequently in 10-minute intervals for 60 minutes. The data were analysed using ANOVA and Steel-Dwass tests (P < 0.05). In the SPO-group, the T-Tra, was significantly lower at T30, T40, T50, T60, the T-Oes and T-Rec at T40, T50, T60, compared to the baseline. In the MEC-group, the T-Tra and T-Oes was significantly lower at T30, T40<sub>,</sub> T50, T60, the T-Rec at T40, T50, T60, compared to the baseline. In the SPO-group, the f<sub>R</sub> was significantly lower for all the times and the ETCO<sub>2</sub> higher at T10, T20, T30, T40, T50 compared to the MEC-group. No other differences were detected. During anaesthesia, there is a comparable decrease in body temperatures, regardless of whether the dogs are breathing spontaneously or ventilated mechanically.
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