Williams Maggie, Caulkett Nigel, Neuhaus Peter, Ruckstuhl Kathreen, Boysen Soren, Fahlman Åsa
J Zoo Wildl Med. 2018 Sep;49(3):662-670. doi: 10.1638/2017-0161.1.
Chemical immobilization is a key aspect of wildlife management. To minimize dose-dependent adverse effects, immobilization protocols often include two or more synergistic agents, which allows for reductions in individual drug dosages. Free-ranging bighorn sheep ( Ovis canadensis) in Canada ( n = 74) were remotely injected with a combination of medetomidine (0.16 ± 0.04 mg/kg) and ketamine (4.0 ± 1.4 mg/kg) (MK), or combination of medetomidine (0.14 ± 0.06 mg/kg), azaperone (0.21 ± 0.11 mg/kg), and alfaxalone (0.45 ± 0.21 mg/kg) (MAA). Once recumbency was achieved, arterial blood samples were collected and immediately analyzed for blood gas and acid-base status. Rectal temperature, heart rate, and respiratory rate were recorded upon recumbency and throughout anesthesia at 5-15 min intervals. At conclusion of the procedures, medetomidine was reversed by intramuscular atipamezole at five times the medetomidine dose. Induction times (mean ± standard deviation) of animals that became immobilized with one dart (8.7 ± 3.2 min, 7.3 ± 3.9 min) and recovery times of all animals (3.4 ± 1.5 min, 3.9 ± 1.6 min) were not significantly different between MK and MAA groups, respectively. Both MK and MAA groups experienced severe hypoxemia (PaO 42 ± 9 mmHg, 40 ± 10 mmHg, respectively). PaCO was significantly higher ( P = 0.0248) in the MK group (median 54 mmHg) than the MAA group (median 48 mmHg) with a trend towards lower pH (7.40 vs 7.42, respectively, P = 0.07). Initially, MK animals had higher heart rates than MAA animals (median 49 vs 40 beats/min), which decreased over time. In bighorn sheep, both MK and MAA produced reliable, reversible immobilization with smooth inductions and recoveries. However, less respiratory depression was seen with MAA than MK.
化学保定是野生动物管理的一个关键方面。为了将剂量依赖性不良反应降至最低,保定方案通常包括两种或更多种协同剂,这使得可以降低每种药物的剂量。对加拿大74只自由放养的大角羊(加拿大盘羊)进行远程注射美托咪定(0.16±0.04毫克/千克)和氯胺酮(4.0±1.4毫克/千克)的组合(MK),或美托咪定(0.14±0.06毫克/千克)、阿扎哌隆(0.21±0.11毫克/千克)和阿法沙龙(0.45±0.21毫克/千克)的组合(MAA)。一旦动物卧倒,采集动脉血样并立即分析血气和酸碱状态。卧倒时以及整个麻醉过程中每隔5 - 15分钟记录直肠温度、心率和呼吸频率。在操作结束时,通过肌肉注射五倍于美托咪定剂量的阿替美唑来逆转美托咪定的作用。用一支 dart 实现保定的动物的诱导时间(平均值±标准差)(8.7±3.2分钟,7.3±3.9分钟)以及所有动物的恢复时间(3.4±1.5分钟,3.9±1.6分钟)在MK组和MAA组之间分别没有显著差异。MK组和MAA组均出现严重低氧血症(分别为PaO₂ 42±9毫米汞柱,40±10毫米汞柱)。MK组的PaCO₂显著高于MAA组(P = 0.0248)(中位数54毫米汞柱对48毫米汞柱),pH值有降低趋势(分别为7.40对7.42,P = 0.07)。最初,MK组动物的心率高于MAA组动物(中位数49对40次/分钟),且随时间下降。在大角羊中,MK和MAA均产生可靠、可逆的保定效果,诱导和恢复过程平稳。然而,与MK相比,MAA引起的呼吸抑制较轻。