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1.
Vet Ophthalmol ; 13 Suppl: 35-40, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20840082

ABSTRACT

OBJECTIVE: To evaluate the achievement of a bilateral mydriasis in raptors induced by a concurrent topical application of rocuronium bromide and to assess any side effects that might result from its use. Animals studied Ten healthy adult common buzzards (Buteo buteo) and 10 healthy adult little owls (Athene noctua). PROCEDURES: Common buzzards (Group 1) received a single dose of 0.40 mg of rocuronium bromide in each eye (total dose 0.80 mg/bird), whereas the little owls (Group 2) received a single dose of 0.20 mg in each eye (total dose 0.40 mg/bird). The drug was topically instilled in all the birds of both groups. The pupil diameter was measured with a pupillary gauge and the assessment of the pupillary light reflexes was performed using a standard light source. RESULTS: Maximal pupillary diameter was 8.10 ± 0.56 mm in the right eye and 8.05 ± 0.59 mm in the left eye for Group 1 and 10.0 ± 0.75 mm in both eyes for Group 2. No statistical differences were evidenced between the achieved pupillary diameters of both eyes in each group. The maximal pupillary diameter was achieved at T110 min and T40 min for Groups 1 and 2, respectively. The drug did not cause noticeable adverse effects in the examined birds. CONCLUSIONS: A single concurrent topical administration of rocuronium bromide to the eyes of the examined birds induced a complete bilateral mydriasis in both eyes without causing any adverse effect.


Subject(s)
Androstanols/pharmacology , Falconiformes , Mydriasis/veterinary , Neuromuscular Nondepolarizing Agents/pharmacology , Strigiformes , Administration, Topical , Androstanols/administration & dosage , Animals , Neuromuscular Nondepolarizing Agents/administration & dosage , Rocuronium
2.
Vet Ophthalmol ; 13 Suppl: 9-13, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20840085

ABSTRACT

OBJECTIVE: To evaluate the mydriatic efficacy of a neuromuscular blocking agent (rocuronium bromide) applied topically to only one eye of nocturnal birds of prey and to assess for any general and/or local adverse effects due to its use. Animal studied Twelve healthy adult tawny owls (Strix aluco) were randomly divided in two groups. PROCEDURES: Six birds (Group 1) received a single dose of 0.35 mg of rocuronium bromide. The second group of subjects (Group 2) received two doses of 0.35 mg of rocuronium bromide (total 0.70 mg/eye). In both groups, the curariform agent was instilled topically. Pupil diameter was measured with a pupillary gauge in 10 min intervals for a total of 100 min and then every 20 min for a total of 240 min. The assessment of the pupillary light reflex was performed using a standard light source during pupillary size recording. RESULTS: Maximal pupillary diameter was 11.5 ± 0.3 mm for Group 1 and 11.0 ± 0.6 mm for Group 2 and no statistically significant differences were detected among the two groups. The maximal pupillary diameter was achieved at T80 for Group 1, and at T60 for Group 2. A complete fundus examination was possible on all treated eyes of subjects of both groups. The drug did not cause any noticeable adverse effects in any of the examined birds. CONCLUSION: Results of the present study suggest that a single topical administration of 0.35 mg of rocuronium bromide to the eyes of healthy tawny owls results in sufficient mydriasis to allow for a complete examination of the fundus.


Subject(s)
Androstanols/pharmacology , Mydriasis/veterinary , Neuromuscular Nondepolarizing Agents/pharmacology , Strigiformes , Administration, Topical , Androstanols/administration & dosage , Animals , Dose-Response Relationship, Drug , Female , Male , Mydriasis/chemically induced , Neuromuscular Nondepolarizing Agents/administration & dosage , Rocuronium
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