戊巴比妥钠在新西兰大白兔(Oryctolagus cuuniculus)肾内和静脉注射安乐死的比较。

Jessica L LeGrand, Sarah M Ozawa, Marnie G Silverstein-Metzler, Jenny M Estes, Nina A Moiseiwitsch, Jazz Q Stephens, Hannah M Atkins, Olivia A Petritz
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引用次数: 0

摘要

兔的外周静脉通路很难获得。当发生故障时,迫切需要有可供选择的血管通路。AVMA将戊巴比妥的肾内注射归类为安乐死的可接受条件。动物必须处于无意识状态,只有很少的研究报告使用静脉内给药。采用53只新西兰大白兔进行3项独立分析,通过评估心肺骤停时间(TCPA)来评估和衡量新西兰大白兔肾内安乐死方式的疗效、效率和有效性。用氯胺酮40 mg/kg和右美托咪定50 μg/kg肌内注射给药,时间从注射开始到观察到心脏和呼吸停止时结束。静脉注射戊巴比妥后心脏和呼吸骤停明显加快(心脏,6 ~ 24 s,中位9 s;呼吸,6 - 19秒,中位数9秒;P < 0.001)比肾内途径(心脏途径,40 ~ 900秒,中位411秒;呼吸,23 - 900秒,中位数120秒;P < 0.001),在安乐死注射过程中未观察到动物的不良反应。4只动物在给药后15 min内未达到TCPA。尽管与静脉安乐死相比,肾内安乐死的TCPA时间更长(P < 0.001),但本研究表明,麻醉下的肾内入路是静脉入路的可行选择,因为它可以可靠地进行,而不会观察到动物的痛苦或器官病理改变。从这项研究的总体信息可以帮助指导实验室和执业临床医生考虑这种技术。然而,诸如心肺骤停的可变时间和技术技能等因素也应考虑在内。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Intrarenal and Intravenous Injections of Sodium Pentobarbital for Euthanasia in New Zealand White Rabbits (Oryctolagus cuniculus).

Peripheral venous access in rabbits can be difficult to obtain. When failure occurs, there is a dire need for alternative vascular access routes to be available. The AVMA categorizes intrarenal injection of pentobarbital as acceptable with conditions for euthanasia. Animals must be in an unconscious state, and only minimal studies using intrarenal administration have been reported. A total of 53 rabbits were used to conduct 3 separate analyses to assess and measure the efficacy, efficiency, and validity of the intrarenal route for euthanasia in New Zealand White rabbits by assessing the time to cardiopulmonary arrest (TCPA). Animals were sedated with 40 mg/kg ketamine and 50 μg/kg dexmedetomidine intramuscularly into the lumbar muscles, and timing started at the beginning of the injection and ended when cardiac and respiratory arrest were observed. Cardiac and respiratory arrest following intravenous injection of pentobarbital was significantly quicker (cardiac, 6 to 24 s, median 9 s; respiratory, 6 to 19 s, median 9 s; P < 0.001) than for the intrarenal route (cardiac, 40 to 900 s, median 411 s; respiratory, 23 to 900 s, median 120 s; P < 0.001), with no negative animal reactions observed during euthanasia injection performance. Four animals did not achieve TCPA within 15 min after administration. Although TCPA was longer with intrarenal compared with intravenous euthanasia (P < 0.001), this study demonstrates that the intrarenal approach under anesthesia is a feasible alternative to the intravenous approach, as it can be reliably performed without observed animal distress or alterations in organ pathology. The overall information from this study can help guide both laboratory and practicing clinicians considering this technique. Still, factors such as variable times to cardiopulmonary arrest and technical skill should be considered.

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