Baboons’ management requires chemical restraint. Three intramuscular sedative protocols in captive hamadryas baboons (
Papio hamadryas) undergoing health-check and male vasectomy were compared. Animals were assigned to TZD_G (
n = 17; tiletamine/zolazepam 3 mg/kg + dexmedetomidine 20 μg/kg), KDM_G (
n
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Baboons’ management requires chemical restraint. Three intramuscular sedative protocols in captive hamadryas baboons (
Papio hamadryas) undergoing health-check and male vasectomy were compared. Animals were assigned to TZD_G (
n = 17; tiletamine/zolazepam 3 mg/kg + dexmedetomidine 20 μg/kg), KDM_G (
n = 23; ketamine 6 mg/kg + dexmedetomidine 30 μg/kg + methadone 0.2 mg/kg), or MDM_G (
n = 9; midazolam 2 mg/kg + dexmedetomidine 60 μg/kg + methadone 0.2 mg/kg). Propofol was titrated intravenously for anaesthetic induction and maintenance. Sedation time and quality and cardiopulmonary parameters were recorded. Atipamezole (TZD_G 0.2 mg/kg, KDM_G 0.3 mg/kg, MDM_G 0.6 mg/kg) and flumazenil (MDM_G 0.02 mg/kg) were administered intramuscularly post-procedure. Recovery time and quality were recorded. Data were reported as median (interquartile range) or regression coefficient (B). Sedation was deepest in TZD_G (20, 20–20; KDM_G 20, 19–20; MDM_G 19, 15–20;
p = 0.017). MDM_G had a significantly higher heart rate (B = 10.27,
p = 0.001), respiratory rate (B = 9.09,
p < 0.001), and lower end-tidal carbon dioxide (B = −3.00,
p = 0.03) than TZD_G, while KDM_G had a lower respiratory rate than TZD_G (B = −3.67,
p = 0.02) and a higher temperature (B = 1.66
p = 0.001). TZD_G showed the longest recovery (minutes: 19, 11.5–30; KDM_G: 6, 4–12; MDM_G: 4, 2.5–5;
p < 0.001), while MDM_G the best recovery (0, 0–0; TZD_G: 9, 6–12; KDM_G: 0, 0–6;
p < 0.001). TZD produced deepest sedation but bad recovery; KDM offered optimal sedation and recovery, and cardiopulmonary stability; MDM provided lighter sedation and excellent recovery.
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