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Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation

Chemical immobilisation is essential for veterinarians to perform medical procedures in wild African ungulates. Potent opioids combined with neuroleptic drugs are most often used for this purpose. The present study aimed at comparing the quality of immobilisation and effects on physiological variabl...

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Autores principales: Gaudio, Eugenio, Laubscher, Liesel L., Meyer, Leith C.R., Hoffman, Louwrens C., Raath, Jacobus P., Pfitzer, Silke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424704/
https://www.ncbi.nlm.nih.gov/pubmed/34476958
http://dx.doi.org/10.4102/jsava.v92i0.2161
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author Gaudio, Eugenio
Laubscher, Liesel L.
Meyer, Leith C.R.
Hoffman, Louwrens C.
Raath, Jacobus P.
Pfitzer, Silke
author_facet Gaudio, Eugenio
Laubscher, Liesel L.
Meyer, Leith C.R.
Hoffman, Louwrens C.
Raath, Jacobus P.
Pfitzer, Silke
author_sort Gaudio, Eugenio
collection PubMed
description Chemical immobilisation is essential for veterinarians to perform medical procedures in wild African ungulates. Potent opioids combined with neuroleptic drugs are most often used for this purpose. The present study aimed at comparing the quality of immobilisation and effects on physiological variables between a high (high etorphine-azaperone [HE]: 0.09 mg kg(–1)) and low etorphine dose (low etorphine-azaperone [LE]: 0.05 mg kg(–1)), both combined with azaperone (0.35 mg kg(–1)), in 12 adult female boma-acclimatised blesbok. It was hypothesised that a reduction in etorphine’s dose in combination with azaperone would result in less cardiorespiratory impairment but likely worsen the quality of immobilisation. Both treatments resulted in rapid induction and recovery times. Overall inter-treatment differences occurred in pulse rate (HE and LE: 52 ± 15 and 44 ± 11 beats minute(–1), p < 0.0001), respiratory rate (HE and LE: 15 ± 4 and 17 ± 4 breaths minute(–1), p < 0.006), partial pressure of exhaled carbon dioxide (HE and LE: 62.0 ± 5.0 and 60.0 ± 5.6 millimetre of mercury [mmHg], p < 0.028) and arterial carbon dioxide (HE and LE: 58.0 ± 4.5 and 55.0 ± 3.9 mmHg, p < 0.002). Both HE and LE led to bradycardia, hypertension and marked hypoxia to a similar extent. Furthermore, quality of induction, immobilisation and recovery were similar in both treatments. The role of azaperone in the development of cardiorespiratory compromise and gas exchange impairment that occurred when these combinations were used is still unclear. Further studies are recommended to elucidate drug- and dose-specific physiological effects in immobilised antelope.
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spelling pubmed-84247042021-09-13 Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation Gaudio, Eugenio Laubscher, Liesel L. Meyer, Leith C.R. Hoffman, Louwrens C. Raath, Jacobus P. Pfitzer, Silke J S Afr Vet Assoc Original Research Chemical immobilisation is essential for veterinarians to perform medical procedures in wild African ungulates. Potent opioids combined with neuroleptic drugs are most often used for this purpose. The present study aimed at comparing the quality of immobilisation and effects on physiological variables between a high (high etorphine-azaperone [HE]: 0.09 mg kg(–1)) and low etorphine dose (low etorphine-azaperone [LE]: 0.05 mg kg(–1)), both combined with azaperone (0.35 mg kg(–1)), in 12 adult female boma-acclimatised blesbok. It was hypothesised that a reduction in etorphine’s dose in combination with azaperone would result in less cardiorespiratory impairment but likely worsen the quality of immobilisation. Both treatments resulted in rapid induction and recovery times. Overall inter-treatment differences occurred in pulse rate (HE and LE: 52 ± 15 and 44 ± 11 beats minute(–1), p < 0.0001), respiratory rate (HE and LE: 15 ± 4 and 17 ± 4 breaths minute(–1), p < 0.006), partial pressure of exhaled carbon dioxide (HE and LE: 62.0 ± 5.0 and 60.0 ± 5.6 millimetre of mercury [mmHg], p < 0.028) and arterial carbon dioxide (HE and LE: 58.0 ± 4.5 and 55.0 ± 3.9 mmHg, p < 0.002). Both HE and LE led to bradycardia, hypertension and marked hypoxia to a similar extent. Furthermore, quality of induction, immobilisation and recovery were similar in both treatments. The role of azaperone in the development of cardiorespiratory compromise and gas exchange impairment that occurred when these combinations were used is still unclear. Further studies are recommended to elucidate drug- and dose-specific physiological effects in immobilised antelope. AOSIS 2021-08-24 /pmc/articles/PMC8424704/ /pubmed/34476958 http://dx.doi.org/10.4102/jsava.v92i0.2161 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Gaudio, Eugenio
Laubscher, Liesel L.
Meyer, Leith C.R.
Hoffman, Louwrens C.
Raath, Jacobus P.
Pfitzer, Silke
Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation
title Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation
title_full Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation
title_fullStr Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation
title_full_unstemmed Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation
title_short Evaluation of two different etorphine doses combined with azaperone in blesbok (Damaliscus pygargus phillipsi) immobilisation
title_sort evaluation of two different etorphine doses combined with azaperone in blesbok (damaliscus pygargus phillipsi) immobilisation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424704/
https://www.ncbi.nlm.nih.gov/pubmed/34476958
http://dx.doi.org/10.4102/jsava.v92i0.2161
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