Efficacy and safety of three different opioid-based immobilisation combinations in blesbok (Damaliscus pygargus phillipsi)

Authors

Keywords:

Blesbok, opioids, azaperone, medetomidine, immobilisation

Abstract

African wildlife species are increasingly being immobilised with combinations of a low dose of potent opioids combined with medetomidine and azaperone. The physiological effects of these combinations in comparison to conventional potent opioidazaperone combinations have scarcely been evaluated. In this cross-over study conducted on eight captive blesbok, we compared the physiological variables of blesbok immobilised with 2 mg of thiafentanil + 10 mg of azaperone (TA); 0.5 mg thiafentanil + 1.5 mg medetomidine (TM), and 0.5 mg thiafentanil + 1.5. mg medetomidine + 10 mg azaperone (TMA). Thiafentanil’s effects were antagonised with naltrexone at 10 mg naltrexone per mg thiafentanil, and the medetomidine effects with atipamezole at 5 mg atipamezole per mg medetomidine. The physiological variables were compared between treatment groups using descriptive statistics and repeated measures ANOVA. The TA combination resulted in the shortest induction and recovery times, higher heart rates, respiratory rates, PaO2, SpO2, and lower MAP and A-a gradients, but with less muscle relaxation. The TM and TMA combinations caused marked bradycardia and hypoxaemia. The hypoxaemia was most severe in animals immobilised with TMA, and four of eight blesbok immobilised had a PaO2 < 35 mmHg at the 10- or 15-minute sampling point. These blesbok were provided supplementary oxygen, which corrected the hypoxaemia. The TA combinations caused the lowest degree of physiological compromise. All three combinations were effective for the immobilisation of blesbok, but as the low-dose thiafentanil and high-dose medetomidine combinations caused marked hypoxaemia, supplementary oxygen is recommended when using these combinations.

Author Biographies

  • A Roug, University of Pretoria

    Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria and Department of Production Animal Studies, Faculty of Veterinary Science, University of Pretoria, South Africa

  • C Smith, Wildlifevets.com

    Wildlifevets.com, Ngongoni Game Lodge, South Africa

  • JP Raath, Wildlifevets.com

    Wildlifevets.com, Ngongoni Game Lodge and Wildlife Pharmaceuticals South Africa (Pty) Ltd., South Africa

  • LCR Meyer, University of Pretoria

    Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria and Department of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria, South Africa

  • LL Laubscher, Wildlife Pharmaceuticals South Africa (Pty) Ltd

    Wildlife Pharmaceuticals South Africa (Pty) Ltd., South Africa

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Published

2023-09-26

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Section

Original Research