Use of 2 sedation protocols to successfully validate a sedation assessment scale in bearded dragons (Pogona vitticeps).

IF 1.4 3区 农林科学 Q2 VETERINARY SCIENCES
Renata H Pinho, Maya Reed, Kelsey Chapman, Daniel S J Pang
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引用次数: 0

Abstract

Objective: To validate a sedation assessment scale by evaluating 2 sedation protocols in bearded dragons.

Methods: In a randomized, blinded, crossover study, 10 bearded dragons were sedated IM with dexmedetomidine (0.1 mg/kg) and methadone (2 mg/kg; DM), and dexmedetomidine (0.1 mg/kg), methadone (2 mg/kg), and ketamine (10 mg/kg; DMK). Sedation assessment was performed with video recording at baseline (T0) and every 5 minutes from 10 to 60 minutes after injection (T10 to T60). After T60, atipamezole (1 mg/kg) was given IM. Behaviors used to assess sedation in several species were tested. Construct validity (ie, does a scale measure what is intended) was evaluated by comparing sedation scores over time using the Friedman and Dunn post hoc tests and between treatments, using a Mann-Whitney test. Scores of 25 videos randomly selected from a total of 216 recorded videos were used to calculate intra- and inter-rater reliability using the intraclass correlation coefficient. Internal consistency was calculated using the Cronbach α coefficient.

Results: Data from a pilot animal (DM) and a misinjection (DMK) were excluded. No adverse events were observed. Six out of 10 evaluated items were selected for the sedation scale. Sedation scores were higher with DMK than DM (T10 to T60). The intraclass correlation coefficient > 0.81 for all raters indicates "very good" intra-rater (95% CI, 0.66 to 1) and inter-rater (95% CI, 0.71 to 1) reliability. Internal consistency was "excellent" (α = 0.904).

Conclusions: Deep sedation occurred with DMK but not DM. The sedation scale demonstrated validity, responsiveness, and reliability.

Clinical relevance: The validated sedation scale aids consistency in evaluating sedation in bearded dragons.

使用两种镇静方案成功验证胡须龙(Pogona vitticeps)的镇静评估量表。
目的:通过对两种镇静方案的评价,验证一种镇静评定量表的有效性。方法:采用随机、盲法、交叉试验,将10只大胡子龙分别用右美托咪定(0.1 mg/kg)和美沙酮(2 mg/kg; DM)以及右美托咪定(0.1 mg/kg)、美沙酮(2 mg/kg)和氯胺酮(10 mg/kg; DMK)进行IM镇静。在基线(T0)和注射后10 ~ 60分钟(T10 ~ T60)每5分钟录像一次镇静评估。T60后给予阿替帕唑(1mg /kg) IM。测试了几种物种用于评估镇静的行为。结构效度(即,量表是否衡量了预期效果)是通过弗里德曼和邓恩事后测试和曼-惠特尼测试来比较镇静评分随时间的变化来评估的。从216个录制视频中随机选择25个视频的分数,使用类内相关系数计算评分内和评分间的信度。内部一致性采用Cronbach α系数计算。结果:排除了中试动物(DM)和误注射(DMK)的数据。未观察到不良事件。从10个评估项目中选择6个作为镇静量表。DMK组镇静评分高于DM组(T10 ~ T60)。所有评分者的类内相关系数> 0.81表明评分者内部(95% CI, 0.66至1)和评分者之间(95% CI, 0.71至1)的信度“非常好”。内部一致性为“优”(α = 0.904)。结论:DMK组有深度镇静,DM组无深度镇静。镇静量表具有良好的效度、反应性和可靠性。临床相关性:经验证的镇静量表有助于一致性评估大胡子龙的镇静作用。
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来源期刊
CiteScore
1.70
自引率
10.00%
发文量
186
审稿时长
3 months
期刊介绍: The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.
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