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dc.contributor.authorGardoni, Nino
dc.contributor.authorBjörck, Sven
dc.contributor.authorMorelli, Jacopo
dc.contributor.authorEvans, Alina
dc.contributor.authorBarros, Daniela Sá Braz
dc.contributor.authorWiklund, Rikard
dc.contributor.authorGræsli, Anne Randi
dc.contributor.authorThiel, Alexandra
dc.contributor.authorArnemo, Jon Martin
dc.contributor.authorLian, Marianne
dc.date.accessioned2024-02-22T16:26:38Z
dc.date.available2024-02-22T16:26:38Z
dc.date.created2023-08-28T10:00:25Z
dc.date.issued2023
dc.identifier.citationFrontiers in Veterinary Science. 2023, 10 .en_US
dc.identifier.issn2297-1769
dc.identifier.urihttps://hdl.handle.net/11250/3119449
dc.description.abstractChemical immobilization of captive European bison (Bison bonasus) is often required for veterinary care, transportation, or husbandry practices playing an important role in conservation breeding and reintroduction of the species. We evaluated the efficiency and physiological effects of an etorphine-acepromazine-xylazine combination with supplemental oxygen in 39 captive European bison. Animals were darted with a combination of 1.4 mg of etorphine, 4.5 mg of acepromazine, and 20 mg of xylazine per 100 kg based on estimated body mass. Arterial blood was sampled on average 20 min after recumbency and again 19 min later and analyzed immediately with a portable i-STAT analyzer. Simultaneously, heart rate, respiratory rate, and rectal temperature were recorded. Intranasal oxygen was started after the first sampling at a flow rate of 10 mL.kg−1.min−1 of estimated body mass until the end of the procedure. The initial mean partial pressure of oxygen (PaO2) was 49.7 mmHg with 32 out of 35 sampled bison presenting with hypoxemia. We observed decreased respiratory rates and pH and mild hypercapnia consistent with a mild respiratory acidosis. After oxygen supplementation hypoxemia was resolved in 21 out of 32 bison, but respiratory acidosis was accentuated. Bison immobilized with a lower initial drug dose required supplementary injections during the procedure. We observed that lower mean rectal temperatures during the immobilization event were significantly associated with longer recovery times. For three bison, minor regurgitation was documented. No mortality or morbidity related to the immobilizations were reported for at least 2 months following the procedure. Based on our findings, we recommend a dose of 0.015 mg.kg−1 etorphine, 0.049 mg.kg−1 acepromazine, and 0.22 mg.kg−1 xylazine. This dose reduced the need for supplemental injections to obtain a sufficient level of immobilization for routine management and husbandry procedures in captive European bison. Nevertheless, this drug combination is associated with development of marked hypoxemia, mild respiratory acidosis, and a small risk of regurgitation. Oxygen supplementation is strongly recommended when using this protocol.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectarterial blood gasen_US
dc.subjectchemical immobilizationen_US
dc.subjectetorphine hydrochlorideen_US
dc.subjecthypoxemiaen_US
dc.subjectrespiratory acidosisen_US
dc.subjectungulateen_US
dc.subjectwisenten_US
dc.subjectxylazine hydrochlorideen_US
dc.titleArterial oxygenation and acid–base status before and during oxygen supplementation in captive European bison (Bison bonasus) immobilized with etorphine-acepromazine-xylazineen_US
dc.title.alternativeArterial oxygenation and acid–base status before and during oxygen supplementation in captive European bison (Bison bonasus) immobilized with etorphine-acepromazine-xylazineen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2023 Gardoni, Björck, Morelli, Evans, Barros, Wiklund, Græsli, Thiel, Arnemo and Lian.en_US
dc.subject.nsiVDP::Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480en_US
dc.source.pagenumber0en_US
dc.source.volume10en_US
dc.source.journalFrontiers in Veterinary Scienceen_US
dc.identifier.doi10.3389/fvets.2023.1125919
dc.identifier.cristin2170089
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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