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Preliminary evaluation of probiotic effects on gastrointestinal signs in dogs with multicentric lymphoma undergoing multi-agent chemotherapy: A randomised, placebo-controlled study. 初步评估益生菌对接受多种药物化疗的多中心淋巴瘤患犬胃肠道症状的影响:随机安慰剂对照研究。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2021-03-29 eCollection Date: 2021-12-01 DOI: 10.1002/vro2.2
Maria C Jugan, Raelene M Wouda, Mary Lynn Higginbotham

Background: Gastrointestinal (GI) toxicity is a major dose-limiting factor in dogs undergoing chemotherapy. A proposed mechanism of GI toxicity includes chemotherapy-driven GI dysbiosis. This study was designed to determine the effects of probiotic administration on GI side-effects in dogs receiving multi-agent chemotherapy.

Methods: Ten client-owned dogs with multicentric lymphoma were enrolled in a prospective, randomised, placebo-controlled single-blinded study. On the first day of the cyclophosphamide doxorubicin vincristine prednisone (CHOP)-based chemotherapy protocol, dogs were randomised to receive either daily oral probiotic at a dose of 200 × 109 cfu/10 kg (n = 5) or daily oral placebo (n = 5). Complete blood count, faecal score (FS), faecal microbiome analysis (qPCR) and adverse events scores were performed at baseline and on the day of each subsequent chemotherapy dose, as well as 3 days after doxorubicin (days 0, 7, 14, 21, 24 and 28).

Results: Overall, 40% of dogs had an abnormal GI microbiome at baseline, specifically decreased faecal C. hiranonis and Fusobacterium abundances. Dogs receiving probiotics had increased faecal Streptococcus (p = 0.02) and E. coli. (p = 0.01). No dogs receiving probiotics experienced diarrhoea (FS ≥ 3.5) compared to four of five receiving placebo. (F 2.895; p = 0.13).

Conclusion: GI microbiome dysbiosis was common in this group of dogs with multicentric lymphoma. Probiotics were well-tolerated, with no negative side effects. Further studies are needed to explore broader microbiome and metabolome changes, as well as clinical benefit.

背景:胃肠道 (GI) 毒性是限制犬化疗剂量的一个主要因素。消化道毒性的一个拟议机制包括化疗导致的消化道菌群失调。本研究旨在确定服用益生菌对接受多种药物化疗的犬消化道副作用的影响:十只患有多中心淋巴瘤的客户自养犬被纳入一项前瞻性、随机、安慰剂对照单盲研究。在以环磷酰胺-多柔比星-长春新碱-泼尼松(CHOP)为基础的化疗方案开始的第一天,狗被随机分配到每天口服益生菌(剂量为 200 × 109 cfu/10 kg,n = 5)或每天口服安慰剂(n = 5)。在基线期、随后每次化疗当天以及多柔比星治疗后 3 天(第 0、7、14、21、24 和 28 天)进行全血细胞计数、粪便评分 (FS)、粪便微生物组分析 (qPCR) 和不良事件评分:总的来说,40%的狗在基线时胃肠道微生物组异常,特别是粪便中的平滑肌酵母菌和镰刀菌丰度下降。接受益生菌治疗的狗粪便中链球菌(p = 0.02)和大肠杆菌(p = 0.01)增加。(p = 0.01).服用益生菌的狗没有出现腹泻(FS ≥ 3.5),而服用安慰剂的五只狗中有四只出现腹泻。(F 2.895; p = 0.13):结论:在这组患有多中心淋巴瘤的狗中,消化道微生物群失调很常见。益生菌的耐受性良好,没有不良副作用。还需要进一步的研究来探讨更广泛的微生物组和代谢组变化以及临床益处。
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引用次数: 0
Evaluation of a smartphone-based electrocardiogram device accuracy in field and in hospital conditions in horses. 评估基于智能手机的马匹心电图设备在野外和医院条件下的准确性。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-12-21 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000441
Elena Alberti, Luca Stucchi, Valeria Pesce, Giovanni Stancari, Elisabetta Ferro, Francesco Ferrucci, Enrica Zucca

Background: Due to compactness and cheapness, smartphone ECG (sECG) could be very useful to equine practitioners. However, previous studies have evaluated the accuracy of sECG in hospitalised horses only. Different conditions in the field could influence the accuracy of the device. The aim of this study is to compare the accuracy of sECG in field and in hospital conditions.

Methods: This is a prospective study. Paired standard base-apex ECG (stECG) and sECG were recorded in hospitalised horses and in subjects examined in field conditions. ECGs were analysed for heart rate and rhythm, presence/type of arrhythmias, presence/duration of artefacts, electrocardiographic waves and interval parameters by a blinded clinician. Statistical analysis evaluated the agreement between stECG and sECG and the differences in the prevalence of artefact in field and hospital conditions.

Results: Nineteen (hospital) and 40 (field) paired ECGs were analysed. Agreement between stECG and sECG was found for heart rate and rhythm, evaluation of atrioventricular block and premature complexes, P wave and PQ interval duration, and QRS complex duration and polarity. No differences were found between artefacts recorded in hospital and in field conditions.

Conclusion: sECG is a feasible tool for evaluation of rhythm in horses and is as accurate in field as in ambulatory conditions.

背景:智能手机心电图(sECG)小巧、便宜,对马术从业人员非常有用。然而,以往的研究仅评估了住院马匹的智能手机心电图仪的准确性。野外的不同条件可能会影响设备的准确性。本研究的目的是比较 sECG 在野外和医院条件下的准确性:这是一项前瞻性研究。方法:这是一项前瞻性研究,对住院马匹和在野外条件下接受检查的受试者记录了配对的标准基础心电图(stECG)和 sECG。由盲人临床医师对心电图进行分析,包括心率和心律、心律失常的存在/类型、伪像的存在/持续时间、心电图波和间期参数。统计分析评估了 stECG 和 sECG 之间的一致性,以及现场和医院条件下伪影发生率的差异:对 19 张(医院)和 40 张(现场)配对心电图进行了分析。结果:分析了 19 张(医院)和 40 张(现场)配对心电图,发现 stECG 和 sECG 在心率和心律、房室传导阻滞和早搏复合体评估、P 波和 PQ 间期持续时间、QRS 复合体持续时间和极性方面具有一致性。结论:sECG 是评估马匹心律的可行工具,在野外和流动条件下同样准确。
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引用次数: 0
Plants and mushrooms associated with animal poisoning incidents in South Africa. 与南非动物中毒事件有关的植物和蘑菇。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-19 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000402
Moleseng Claude Moshobane, Alessia Bertero, Carine Marks, Cindy Stephen, Natasha Palesa Mothapo, Lorraine Middleton, Francesca Caloni

Background: There is extensive literature on animal poisoning from plants and mushrooms worldwide; however, there is limited account of poisoning from South Africa.

Methods: This study sought to describe and provide an overview of animal poison exposures in South Africa. Poisoning episodes reported to the Poisons Information Helpline of the Western Cape, jointly run by the Poisons Information Centres at the Red Cross War Memorial Children's Hospital and Tygerberg Hospital over a period of approximately 2.5 years, from June 2015 to November 2017, were analysed to identify exposure patterns, severity and clinical outcomes.

Results: Alien plant species accounted for most cases (n=10) of reported poison exposures. Among the 26 recorded animal poisoning episodes, the dog was the most commonly implicated species (n=24), whereas just two enquiries were related to other animals (one rabbit and one cow). There were 20 plant cases and 6 mushroom cases (all dogs). There was only one fatal case involving cycad in a dog.

Conclusion: Features of animal poisoning in South Africa were similar to those in other countries. The reported cases of animals exposed to poisonous plants and mushrooms could represent only a fraction of the actual exposures. Since most reported cases involved taxa that could not be identified to species level, more attention should be paid in case reporting and in animal poisoning prevention, engaging the public to enable people to recognise potentially hazardous plants and reduce the risk of poisoning in animals.

背景:在世界范围内,有大量关于植物和蘑菇引起动物中毒的文献;然而,有关南非中毒的报道有限。方法:本研究试图描述并提供南非动物中毒暴露的概述。由红十字战争纪念儿童医院和Tygerberg医院的毒物信息中心在2015年6月至2017年11月约2.5年的时间里联合运营的西开普省毒物信息帮助热线报告的中毒事件进行了分析,以确定暴露模式、严重程度和临床结果。结果:外来植物占报告中毒病例的大多数(n=10)。在记录的26起动物中毒事件中,狗是最常见的涉及物种(n=24),而只有两起调查与其他动物有关(一只兔子和一只牛)。植物病例20例,蘑菇病例6例(均为犬)。只有一例与苏铁有关的致命病例。结论:南非动物中毒的特点与其他国家相似。报道的动物接触有毒植物和蘑菇的案例只能代表实际接触的一小部分。由于大多数报告的病例涉及的分类群无法识别到物种水平,因此应更加重视病例报告和动物中毒预防,让公众参与,使人们认识到潜在的危险植物,减少动物中毒的风险。
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引用次数: 0
Detection of Chlamydiaceae in Swiss wild birds sampled at a bird rehabilitation centre. 在鸟类康复中心采样的瑞士野生鸟类中检测衣原体科。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-12 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000437
Sandro Stalder, Hanna Marti, Nicole Borel, Prisca Mattmann, Barbara Vogler, Nina Wolfrum, Sarah Albini

Background: Annually, 800-1500 wild birds are admitted to the rehabilitation centre of the Swiss Ornithological Institute, Sempach, Lucerne, Switzerland. The workers of the centre come in close contact with the avian patients and might therefore be exposed to zoonotic agents shed by these birds, such as Chlamydia psittaci.

Methods: In the present study, 91 choanal, 91 cloacal and 267 faecal swabs from 339 wild birds of 42 species were investigated using a stepwise diagnostic approach.

Results: Chlamydiaceae were detected in 0.9 per cent (0.3-2.6 per cent) of birds (n=3), all of them members of the Columbidae family. The Chlamydiaceae species of two of these birds (one Eurasian collared dove, one fancy pigeon) were identified as C psittaci types B and E by PCR and outer membrane protein A genotyping.

Conclusion: The findings of the current study suggest that zoonotic transmission of Chlamydiaceae is very unlikely for songbird and waterfowl species tested herein, while pigeons might pose a risk to workers at rehabilitation centres.

背景:每年有800-1500只野生鸟类进入瑞士鸟类研究所的康复中心,位于瑞士卢塞恩的Sempach。中心的工作人员与禽流感病人有密切接触,因此可能会接触由这些禽鸟传播的人畜共患病原体,例如鹦鹉热衣原体。方法:采用分步诊断法对42种339只野生鸟类的粪拭子、鼻拭子和粪拭子分别进行了91份、91份和267份的调查。结果:有0.9%(0.3 ~ 2.6%)的鸟类(n=3)检出衣原体科,均为耧菜科。经PCR和外膜蛋白A基因分型鉴定,其中2只衣原体科鸟类(1只欧亚颈鸽和1只花鸽)分别为鹦鹉C型B和E型。结论:目前的研究结果表明,衣原体科的人畜共患传播在本文测试的鸣禽和水禽物种中是非常不可能的,而鸽子可能对康复中心的工作人员构成风险。
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引用次数: 4
Reproductive parameters in some captive-bred cockatoo species (genus Cacatua and Eolophus). 一些人工饲养凤头鹦鹉(caatua属和Eolophus属)的生殖参数。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-12 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000405
Stefano Paolo Marelli, Ahmad Abdel Sayed, Michele Magni, Lorenzo Crosta, Petra Schnitzer, Maria Strillacci, Fabio Luzi, Silvia Cerolini, Luisa Zaniboni

Background: Cockatoo reproduction in captivity supplies a powerful tool to limit the economic motivation to capture endangered species from the wild; nevertheless, scientific data about reproductive parameters in cockatoos are very rare. The aim of the present work was to investigate the reproductive performance of different species of the Cacatua genus reared in the same facility to evaluate adaptability to captive breeding and to identify the main problems in ex situ conservation of some cockatoo species.

Methods: Data of 28 eggs from 19 reproductive pairs from 9 cockatoo species were analysed. Statistical analysis was carried out by SAS NPAR1WAY procedure: species was considered source of variation.

Results: Species effect does not significantly influence reproductive variables; differences were recorded in eggs fertility and embryo liveability. Bird adaptive ability to captive breeding has been described through reproductive parameters.

Conclusion: Our results show the importance and the maintenance of natural species-specific behaviours and habits, and they underline the relevance of data collection about reproductive performance in endangered species kept in captivity to improve breeding management in conservation programmes.

背景:凤头鹦鹉的圈养繁殖为限制从野外捕获濒危物种的经济动机提供了有力的工具;然而,关于凤头鹦鹉生殖参数的科学数据非常罕见。本研究的目的是研究在同一设施中饲养的不同种类的caatua属的繁殖性能,以评估圈养繁殖的适应性,并确定一些种类的凤头鹦鹉迁地保护的主要问题。方法:对9种凤头鹦鹉19对生殖对28枚卵的资料进行分析。采用SAS NPAR1WAY程序进行统计分析,认为物种是变异源。结果:物种效应对生殖变量影响不显著;记录了卵子育性和胚胎存活率的差异。通过繁殖参数描述了鸟类对圈养繁殖的适应能力。结论:我们的研究结果显示了自然物种特有行为和习性的重要性和维护,并强调了收集濒危圈养物种繁殖性能的数据对改善保护计划中的繁殖管理的重要性。
{"title":"Reproductive parameters in some captive-bred cockatoo species (genus <i>Cacatua</i> and <i>Eolophus</i>).","authors":"Stefano Paolo Marelli,&nbsp;Ahmad Abdel Sayed,&nbsp;Michele Magni,&nbsp;Lorenzo Crosta,&nbsp;Petra Schnitzer,&nbsp;Maria Strillacci,&nbsp;Fabio Luzi,&nbsp;Silvia Cerolini,&nbsp;Luisa Zaniboni","doi":"10.1136/vetreco-2020-000405","DOIUrl":"https://doi.org/10.1136/vetreco-2020-000405","url":null,"abstract":"<p><strong>Background: </strong>Cockatoo reproduction in captivity supplies a powerful tool to limit the economic motivation to capture endangered species from the wild; nevertheless, scientific data about reproductive parameters in cockatoos are very rare. The aim of the present work was to investigate the reproductive performance of different species of the <i>Cacatua</i> genus reared in the same facility to evaluate adaptability to captive breeding and to identify the main problems in ex situ conservation of some cockatoo species.</p><p><strong>Methods: </strong>Data of 28 eggs from 19 reproductive pairs from 9 cockatoo species were analysed. Statistical analysis was carried out by SAS NPAR1WAY procedure: species was considered source of variation.</p><p><strong>Results: </strong>Species effect does not significantly influence reproductive variables; differences were recorded in eggs fertility and embryo liveability. Bird adaptive ability to captive breeding has been described through reproductive parameters.</p><p><strong>Conclusion: </strong>Our results show the importance and the maintenance of natural species-specific behaviours and habits, and they underline the relevance of data collection about reproductive performance in endangered species kept in captivity to improve breeding management in conservation programmes.</p>","PeriodicalId":23565,"journal":{"name":"Veterinary Record Open","volume":"7 1","pages":"e000405"},"PeriodicalIF":1.4,"publicationDate":"2020-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/vetreco-2020-000405","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38631205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Efficacy of a live intranasal vaccine against parainfluenza type 3 and bovine respiratory syncytial virus in young calves with maternally derived antibodies. 一种抗3型副流感和牛呼吸道合胞病毒的鼻内活疫苗对具有母源性抗体的小牛的有效性。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-06 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000429
Lucy Metcalfe, Mathieu Chevalier, Marie-Pascale Tiberghien, Edmond Jolivet, Milan Huňady, Sioned Timothy, Corinne Philippe-Reversat

Trial design: Two randomised controlled vaccination trials with artificial challenges were carried out in addition to a serological survey of levels of maternally derived antibodies (MDA) to parainfluenza type 3 virus (PI3V) and bovine respiratory syncytial virus (BRSV) in European calves.

Participants: Ten-day-old calves with and without MDA were included in the two vaccine trials.

Interventions: Intranasal administration of a bivalent modified live (PI3V/BRSV) vaccine followed by artificial challenge approximately three months post vaccination.

Objective: The study aimed to assess the efficacy of a modified live respiratory vaccine, Bovalto Respi Intranasal (Boehringer Ingelheim). In order to assess the interference of MDA, both seropositive and seronegative calves were used.

Randomisation: PI3V and BRSV serological status was determined seven days before vaccination; calves without maternal antibodies became the MDA- vaccinates. Calves with MDA were ranked according to individual titres and allocated alternately to MDA+ vaccinate and MDA+ control groups.

Blinding: Treatment was carried out by the unblinded study director. Animal care and veterinary examinations were conducted by personnel unaware of the treatments received. The serological survey used blood samples obtained from calves on commercial farms in five European countries, Germany, Spain, Italy, Ireland and the UK, to determine the levels of MDA to PI3V and BRSV in calves approximately two weeks of age.

Results: A total of 36 calves were included in the two challenge studies and 32 of these completed the challenge studies. Twenty-one calves were included in the PI3V challenge study, with six of six MDA- and six of seven MDA+ vaccinated calves and five of five MDA+ unvaccinated control calves being challenged with PI3V. Fifteen calves were included in the BRSV challenge study, with five of five MDA- and five of five MDA+ vaccinated calves and five of five MDA+ unvaccinated control calves being challenged with BRSV.

Outcome: For both challenges, clinical scores and nasal shedding were significantly higher in control animals compared with vaccinates (PI3V challenge: clinical scores P=0.001, nasal shedding P=0.001; BRSV challenge: clinical scores P=0.016, nasal shedding P=0.002) and not significantly different between MDA+ and MDA- vaccinated animals for both challenges (P>0.05). A total of 254 samples from six countries were tested in the serological survey of MDA.

Conclusion: The results of the challenge studies demonstrated the efficacy of the vaccine in the presence of BRSV and PI3V MDA under laboratory conditions. The field assessment confirmed that the MDA titres in the MDA+ calves corresponded to those typically found on farms.

试验设计:除了对欧洲犊牛的3型副流感病毒(PI3V)和牛呼吸道合胞病毒(BRSV)母源抗体(MDA)水平进行血清学调查外,还进行了两项随机对照疫苗接种试验。参与者:在两项疫苗试验中均包括有和没有MDA的10天大小牛。干预措施:鼻内注射二价改性活疫苗(PI3V/BRSV),然后在接种后大约三个月进行人工攻毒。目的:本研究旨在评估改良呼吸活疫苗Bovalto Respi鼻内疫苗(勃林格殷格翰公司)的疗效。为了评估丙二醛的干扰作用,同时使用血清阳性和血清阴性的小牛。随机化:接种前7天确定PI3V和BRSV血清学状态;没有母体抗体的小牛成为丙二醛疫苗。将感染MDA的犊牛按个体滴度排序,交替分配到MDA+接种组和MDA+对照组。盲法:由非盲法研究主任进行治疗。动物护理和兽医检查是由不知道所接受治疗的人员进行的。血清学调查使用了从五个欧洲国家(德国、西班牙、意大利、爱尔兰和英国)的商业农场获得的小牛血液样本,以确定大约两周龄的小牛中丙二醛到PI3V和BRSV的水平。结果:共36头犊牛参与了两项挑战研究,其中32头犊牛完成了挑战研究。21头小牛被纳入PI3V攻击研究,6头MDA-疫苗和7头MDA+疫苗中的6头以及5头MDA+未接种疫苗的对照小牛中的5头受到PI3V攻击。15头小牛被纳入BRSV攻击研究,5头MDA-疫苗和5头MDA+疫苗的小牛中有5头和5头MDA+疫苗的小牛中有5头受到BRSV攻击,5头MDA+疫苗未接种的对照小牛中有5头受到BRSV攻击。结果:对于这两种挑战,对照动物的临床评分和鼻脱落均显著高于接种疫苗的动物(PI3V挑战:临床评分P=0.001,鼻脱落P=0.001;BRSV攻毒:临床评分P=0.016,鼻脱落P=0.002), MDA+和MDA-接种动物在两种攻毒情况下均无显著差异(P>0.05)。在MDA血清学调查中,对来自6个国家的254个样本进行了检测。结论:在实验室条件下,攻毒研究的结果证明了该疫苗在BRSV和PI3V MDA存在下的有效性。实地评估证实,MDA阳性犊牛的MDA滴度与农场中典型的MDA滴度相符。
{"title":"Efficacy of a live intranasal vaccine against parainfluenza type 3 and bovine respiratory syncytial virus in young calves with maternally derived antibodies.","authors":"Lucy Metcalfe,&nbsp;Mathieu Chevalier,&nbsp;Marie-Pascale Tiberghien,&nbsp;Edmond Jolivet,&nbsp;Milan Huňady,&nbsp;Sioned Timothy,&nbsp;Corinne Philippe-Reversat","doi":"10.1136/vetreco-2020-000429","DOIUrl":"https://doi.org/10.1136/vetreco-2020-000429","url":null,"abstract":"<p><strong>Trial design: </strong>Two randomised controlled vaccination trials with artificial challenges were carried out in addition to a serological survey of levels of maternally derived antibodies (MDA) to parainfluenza type 3 virus (PI3V) and bovine respiratory syncytial virus (BRSV) in European calves.</p><p><strong>Participants: </strong>Ten-day-old calves with and without MDA were included in the two vaccine trials.</p><p><strong>Interventions: </strong>Intranasal administration of a bivalent modified live (PI3V/BRSV) vaccine followed by artificial challenge approximately three months post vaccination.</p><p><strong>Objective: </strong>The study aimed to assess the efficacy of a modified live respiratory vaccine, Bovalto Respi Intranasal (Boehringer Ingelheim). In order to assess the interference of MDA, both seropositive and seronegative calves were used.</p><p><strong>Randomisation: </strong>PI3V and BRSV serological status was determined seven days before vaccination; calves without maternal antibodies became the MDA- vaccinates. Calves with MDA were ranked according to individual titres and allocated alternately to MDA+ vaccinate and MDA+ control groups.</p><p><strong>Blinding: </strong>Treatment was carried out by the unblinded study director. Animal care and veterinary examinations were conducted by personnel unaware of the treatments received. The serological survey used blood samples obtained from calves on commercial farms in five European countries, Germany, Spain, Italy, Ireland and the UK, to determine the levels of MDA to PI3V and BRSV in calves approximately two weeks of age.</p><p><strong>Results: </strong>A total of 36 calves were included in the two challenge studies and 32 of these completed the challenge studies. Twenty-one calves were included in the PI3V challenge study, with six of six MDA- and six of seven MDA+ vaccinated calves and five of five MDA+ unvaccinated control calves being challenged with PI3V. Fifteen calves were included in the BRSV challenge study, with five of five MDA- and five of five MDA+ vaccinated calves and five of five MDA+ unvaccinated control calves being challenged with BRSV.</p><p><strong>Outcome: </strong>For both challenges, clinical scores and nasal shedding were significantly higher in control animals compared with vaccinates (PI3V challenge: clinical scores P=0.001, nasal shedding P=0.001; BRSV challenge: clinical scores P=0.016, nasal shedding P=0.002) and not significantly different between MDA+ and MDA- vaccinated animals for both challenges (P>0.05). A total of 254 samples from six countries were tested in the serological survey of MDA.</p><p><strong>Conclusion: </strong>The results of the challenge studies demonstrated the efficacy of the vaccine in the presence of BRSV and PI3V MDA under laboratory conditions. The field assessment confirmed that the MDA titres in the MDA+ calves corresponded to those typically found on farms.</p>","PeriodicalId":23565,"journal":{"name":"Veterinary Record Open","volume":"7 1","pages":"e000429"},"PeriodicalIF":1.4,"publicationDate":"2020-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/89/74/vetreco-2020-000429.PMC7651721.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38713416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Efficacy of oral Cynara scolymus and Silybum marianum on toxicity of imidocarb dipropionate in horses. 马口服蛇尾草和水飞蓟对二丙酸咪虫威毒性的影响。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-05 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000416
Fernando Mosquera Jaramillo, Diego Darley Velasquez Piñeros, Rodrigo Romero Corrêa, Fabio Celidonio Pogliani, Bruno Cogliati, Raquel Yvonne Arantes Baccarin

Background: Despite hepatotoxic effects, imidocarb dipropionate is the drug of choice for treatment of equine piroplasmosis. It is important, therefore, to identify adjuvant therapies that may improve the safety of imidocarb dipropionate by reducing the risk of liver damage during its use. The aim of the present study was to evaluate the hepatoprotective and hepatoregulatory effects of treatment with Cynara scolymus and Silybum marianum during administration of imidocarb dipropionate.

Methods: Ten healthy horses, seroconverted to Theileria equi by C-ELISA, were treated with 5 mg/kg/day of imidocarb dipropionate for three consecutive days. The study population was divided into two groups. The control group did not receive any complementary treatments. The treated group received a daily oral supplement containing C scolymus and S marianum for 30 days. Physical, haematological and histological examinations of hepatic fragments were performed.

Results: All haematological values remained within normal range for the study population. Histological analysis revealed that treated group animals had 62 per cent less lobular inflammation, 55 per cent less pigment accumulation, 65 per cent less steatosis and 57 per cent less portal inflammation than control group animals, with an equivalent percentage of hydropic degeneration.

Conclusion: C scolymus and S marianum supplements resulted in beneficial hepatoprotective effects in horses treated with imidocarb dipropionate.

背景:尽管有肝毒性作用,吡虫威二丙酸是治疗马螺形体病的首选药物。因此,重要的是确定辅助疗法,通过降低使用期间肝损害的风险来提高吡虫威二丙酸的安全性。本研究的目的是评价在吡虫威二丙酸给药期间,用棘草和水飞蓟治疗肝保护和肝调节的作用。方法:10匹经C-ELISA法血清转化为马伊勒菌的健康马,连续3天给予5 mg/kg/d的吡虫威二丙酸。研究人群被分为两组。对照组不接受任何辅助治疗。治疗组每日口服含有猪头菌和马粪菌的补品,连用30 d。对肝碎片进行物理、血液学和组织学检查。结果:研究人群的所有血液学值保持在正常范围内。组织学分析显示,与对照组动物相比,治疗组动物小叶炎症减少62%,色素积累减少55%,脂肪变性减少65%,门脉炎症减少57%,水变性的比例相同。结论:二丙酸咪唑威对马有良好的保肝作用。
{"title":"Efficacy of oral <i>Cynara scolymus</i> and <i>Silybum marianum</i> on toxicity of imidocarb dipropionate in horses.","authors":"Fernando Mosquera Jaramillo,&nbsp;Diego Darley Velasquez Piñeros,&nbsp;Rodrigo Romero Corrêa,&nbsp;Fabio Celidonio Pogliani,&nbsp;Bruno Cogliati,&nbsp;Raquel Yvonne Arantes Baccarin","doi":"10.1136/vetreco-2020-000416","DOIUrl":"https://doi.org/10.1136/vetreco-2020-000416","url":null,"abstract":"<p><strong>Background: </strong>Despite hepatotoxic effects, imidocarb dipropionate is the drug of choice for treatment of equine piroplasmosis. It is important, therefore, to identify adjuvant therapies that may improve the safety of imidocarb dipropionate by reducing the risk of liver damage during its use. The aim of the present study was to evaluate the hepatoprotective and hepatoregulatory effects of treatment with <i>Cynara scolymus</i> and <i>Silybum marianum</i> during administration of imidocarb dipropionate.</p><p><strong>Methods: </strong>Ten healthy horses, seroconverted to <i>Theileria equi</i> by C-ELISA, were treated with 5 mg/kg/day of imidocarb dipropionate for three consecutive days. The study population was divided into two groups. The control group did not receive any complementary treatments. The treated group received a daily oral supplement containing <i>C scolymus</i> and <i>S marianum</i> for 30 days. Physical, haematological and histological examinations of hepatic fragments were performed.</p><p><strong>Results: </strong>All haematological values remained within normal range for the study population. Histological analysis revealed that treated group animals had 62 per cent less lobular inflammation, 55 per cent less pigment accumulation, 65 per cent less steatosis and 57 per cent less portal inflammation than control group animals, with an equivalent percentage of hydropic degeneration.</p><p><strong>Conclusion: </strong><i>C scolymus</i> and <i>S marianum</i> supplements resulted in beneficial hepatoprotective effects in horses treated with imidocarb dipropionate.</p>","PeriodicalId":23565,"journal":{"name":"Veterinary Record Open","volume":"7 1","pages":"e000416"},"PeriodicalIF":1.4,"publicationDate":"2020-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/31/d4/vetreco-2020-000416.PMC7646365.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38595465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Use of fever detection in combination with thoracic ultrasonography to identify respiratory disease, and compare treatments of antimicrobials and NSAID: a randomised study in dairy calves. 使用发热检测结合胸部超声检查来识别呼吸道疾病,并比较抗菌剂和非甾体抗炎药的治疗:一项针对奶牛的随机研究。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-04 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000415
Sophie A Mahendran

Background: This study explored the combined use of fever detection and thoracic ultrasonography to identify calves with early onset bovine respiratory disease (BRD). Thoracic ultrasonography was then used to assess the efficacy of antimicrobial and non-steroidal anti-inflammatory drug (NSAID) treatment for early onset BRD through a randomised study design.

Methods: Calves were recruited from a single dairy farm in the UK, and fitted with a TempVerified FeverTag, which was activated when a calf developed fever (a temperature of 39.7°C for six hours). On identification of fever, a Wisconsin calf score was used to provide a diagnosis of BRD by exclusion of other causes. Calves were randomly assigned to experimental groups; group 1 (NSAID) received flunixin meglumine, group 2 (antimicrobial) received florfenicol, group 3 (both) received both drugs. A thoracic ultrasound was conducted within 48 hours of fever detection, and again 14 days later to assess lung pathology.

Results: A total of 152 calves were recruited, with a relative BRD prevalence of 49 per cent (74/152). Thirty-two calves required a secondary treatment (due to continued fever), causing exclusion from statistical analysis of the change in ultrasound score and resulting in the study being underpowered for detecting statistical significance. Initial thoracic ultrasound scores were very low, with 70/74 calves scoring either 0 or 1, indicating few comet tails and no lung consolidation was seen and potential overdiagnosis of BRD. For assessment of therapy efficacy, no effect of experimental group was detected on average daily growth rates (mean 0.85 kg/day, P=0.89). Calves also displayed very few clinical signs at the time of fever detection. These factors combined suggest a high rate of false positive identification (low specificity) for BRD through fever detection alone. Calves given the NSAID only were more likely to require repeat treatments due to fever recurrence (OR=3.10 (95 per cent CI 0.86 to 11.15), P=0.083). Also calves affected by their first case of fever at an older age (21 v 28 days old) were less likely to go on to have further fever episodes (OR=0.95 (95 per cent CI 0.90 to 0.99), P=0.026).

Conclusion: This study demonstrated calves given only an NSAID at occurrence of fever due to BRD may be more likely to require repeat treatments throughout the preweaning period. The use of fever detection alone for BRD indicated a low specificity for definitive diagnosis as shown by the low thoracic ultrasound scores and lack of clinical signs. The study was underpowered to assess the ultrasonic effects of the different treatment protocols on lung pathology.

背景:本研究探讨了结合发热检测和胸部超声检查来识别犊牛早发性牛呼吸道疾病(BRD)。然后通过随机研究设计,使用胸部超声检查评估抗菌和非甾体抗炎药(NSAID)治疗早发性BRD的疗效。方法:从英国的一个奶牛场招募小牛,并安装了温度验证发烧标签,当小牛发烧时(温度为39.7°C,持续6小时),该标签就会被激活。在确定发烧,威斯康星小牛评分被用来提供诊断BRD排除其他原因。将犊牛随机分为试验组;组1(非甾体抗炎药组)给予氟尼新大聚胺,组2(抗菌药物组)给予氟苯尼考,组3(两组)同时给予两种药物。48小时内进行胸部超声检查,14天后再次进行肺部病理检查。结果:总共招募了152头小牛,相对BRD患病率为49%(74/152)。32头小牛需要二次治疗(由于持续发烧),导致超声评分变化的统计分析被排除在外,导致研究在检测统计意义方面的能力不足。最初的胸部超声评分很低,70/74的小牛得分为0或1,表明很少有彗星尾,未见肺实变,可能过度诊断BRD。在评估治疗效果时,实验组对平均日生长率无影响(平均0.85 kg/day, P=0.89)。小牛在发热检测时也表现出很少的临床症状。这些因素综合起来表明,仅通过发热检测,BRD的假阳性鉴定率很高(特异性低)。仅给予非甾体抗炎药的小牛更有可能因发烧复发而需要重复治疗(OR=3.10 (95% CI 0.86至11.15),P=0.083)。此外,犊牛在较大年龄(21日龄或28日龄)出现首次发热的可能性较小(OR=0.95 (95% CI 0.90至0.99),P=0.026)。结论:本研究表明,在BRD引起发烧时仅给予非甾体抗炎药的犊牛更有可能在整个断奶前需要重复治疗。单独使用发热检测BRD表明明确诊断的特异性较低,这体现在胸部超声评分较低和缺乏临床体征。该研究不足以评估不同治疗方案对肺部病理的超声影响。
{"title":"Use of fever detection in combination with thoracic ultrasonography to identify respiratory disease, and compare treatments of antimicrobials and NSAID: a randomised study in dairy calves.","authors":"Sophie A Mahendran","doi":"10.1136/vetreco-2020-000415","DOIUrl":"https://doi.org/10.1136/vetreco-2020-000415","url":null,"abstract":"<p><strong>Background: </strong>This study explored the combined use of fever detection and thoracic ultrasonography to identify calves with early onset bovine respiratory disease (BRD). Thoracic ultrasonography was then used to assess the efficacy of antimicrobial and non-steroidal anti-inflammatory drug (NSAID) treatment for early onset BRD through a randomised study design.</p><p><strong>Methods: </strong>Calves were recruited from a single dairy farm in the UK, and fitted with a TempVerified FeverTag, which was activated when a calf developed fever (a temperature of 39.7°C for six hours). On identification of fever, a Wisconsin calf score was used to provide a diagnosis of BRD by exclusion of other causes. Calves were randomly assigned to experimental groups; group 1 (NSAID) received flunixin meglumine, group 2 (antimicrobial) received florfenicol, group 3 (both) received both drugs. A thoracic ultrasound was conducted within 48 hours of fever detection, and again 14 days later to assess lung pathology.</p><p><strong>Results: </strong>A total of 152 calves were recruited, with a relative BRD prevalence of 49 per cent (74/152). Thirty-two calves required a secondary treatment (due to continued fever), causing exclusion from statistical analysis of the change in ultrasound score and resulting in the study being underpowered for detecting statistical significance. Initial thoracic ultrasound scores were very low, with 70/74 calves scoring either 0 or 1, indicating few comet tails and no lung consolidation was seen and potential overdiagnosis of BRD. For assessment of therapy efficacy, no effect of experimental group was detected on average daily growth rates (mean 0.85 kg/day, P=0.89). Calves also displayed very few clinical signs at the time of fever detection. These factors combined suggest a high rate of false positive identification (low specificity) for BRD through fever detection alone. Calves given the NSAID only were more likely to require repeat treatments due to fever recurrence (OR=3.10 (95 per cent CI 0.86 to 11.15), P=0.083). Also calves affected by their first case of fever at an older age (21 v 28 days old) were less likely to go on to have further fever episodes (OR=0.95 (95 per cent CI 0.90 to 0.99), P=0.026).</p><p><strong>Conclusion: </strong>This study demonstrated calves given only an NSAID at occurrence of fever due to BRD may be more likely to require repeat treatments throughout the preweaning period. The use of fever detection alone for BRD indicated a low specificity for definitive diagnosis as shown by the low thoracic ultrasound scores and lack of clinical signs. The study was underpowered to assess the ultrasonic effects of the different treatment protocols on lung pathology.</p>","PeriodicalId":23565,"journal":{"name":"Veterinary Record Open","volume":"7 1","pages":"e000415"},"PeriodicalIF":1.4,"publicationDate":"2020-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7d/1b/vetreco-2020-000415.PMC7643518.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38614412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Dexmedetomidine and ketamine simultaneous administration in tigers (Panthera tigris): pharmacokinetics and clinical effects. 右美托咪定与氯胺酮同时给药虎的药代动力学及临床效果。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-11-03 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000412
Federica Di Cesare, Petra Cagnardi, Roberto Villa, Vanessa Rabbogliatti, Lorena Lucatello, Francesca Capolongo, Daniela Gioeni, Michele Capasso, William Magnone, Giuliano Ravasio

Background: The study determines the pharmacokinetic profiles of dexmedetomidine (DEX), ketamine (KET) and its active metabolite, norketamine (NORKET), after simultaneous administration. Moreover, the study evaluates the sedative effects of this protocol, its influence on the main physiological variables and the occurrence of adverse effects.

Methods: Eighteen captive tigers were initially administered with a mixture of DEX (10 µg/kg) and KET (2 mg/kg) by remote intramuscular injection. In case of individual and specific needs, the protocol was modified and tigers could receive general anaesthesia, propofol or additional doses of DEX and KET.

Results: Based on the immobilisation protocol, nine animals were assigned to the standard protocol group and the other nine to the non-standard protocol group. Higher area under the first moment curve (AUMC0-last) and longer mean residence time (MRT0-last) (P<0.05) were observed in the non-standard protocol group for DEX, KET and NORKET, and higher area under the concentration-time curve from administration to the last measurable concentration (AUC0-last) only for KET. The KET metabolisation rate was similar (P=0.296) between groups. No differences between groups were detected in terms of stages of sedation and recoveries. All physiological variables remained within normality ranges during the whole observation period. During the hospitalisation period, no severe adverse reactions and signs of resedation were observed.

Conclusion: The simultaneous administration of 10 µg/kg of DEX and 2 mg/kg of KET can be considered an effective protocol for chemical immobilisation of captive tigers, along with dosage adjusments or when other drugs are needed.

背景:本研究确定了右美托咪定(DEX)、氯胺酮(KET)及其活性代谢物诺氯胺酮(NORKET)在同时给药后的药动学特征。此外,本研究还评估了该方案的镇静作用、对主要生理变量的影响以及不良反应的发生情况。方法:对18只圈养老虎进行远程肌内注射,初始注射DEX(10µg/kg)和KET (2 mg/kg)的混合物。在个别和特殊需要的情况下,修改了方案,老虎可以接受全身麻醉、异丙酚或额外剂量的DEX和KET。结果:根据固定方案,9只动物被分配到标准方案组,另外9只动物被分配到非标准方案组。只有KET的第一弯矩曲线下面积(AUMC0-last)更高,平均停留时间(MRT0-last) (P0-last)更长。两组间KET代谢率相似(P=0.296)。在镇静和恢复的阶段方面,两组之间没有发现差异。在整个观察期内,所有生理指标均处于正常范围内。在住院期间,未观察到严重的不良反应和镇静迹象。结论:同时给药10µg/kg的DEX和2 mg/kg的KET可作为圈养老虎化学固定的有效方案,并可在需要时调整剂量或使用其他药物。
{"title":"Dexmedetomidine and ketamine simultaneous administration in tigers (<i>Panthera tigris</i>): pharmacokinetics and clinical effects.","authors":"Federica Di Cesare,&nbsp;Petra Cagnardi,&nbsp;Roberto Villa,&nbsp;Vanessa Rabbogliatti,&nbsp;Lorena Lucatello,&nbsp;Francesca Capolongo,&nbsp;Daniela Gioeni,&nbsp;Michele Capasso,&nbsp;William Magnone,&nbsp;Giuliano Ravasio","doi":"10.1136/vetreco-2020-000412","DOIUrl":"https://doi.org/10.1136/vetreco-2020-000412","url":null,"abstract":"<p><strong>Background: </strong>The study determines the pharmacokinetic profiles of dexmedetomidine (DEX), ketamine (KET) and its active metabolite, norketamine (NORKET), after simultaneous administration. Moreover, the study evaluates the sedative effects of this protocol, its influence on the main physiological variables and the occurrence of adverse effects.</p><p><strong>Methods: </strong>Eighteen captive tigers were initially administered with a mixture of DEX (10 µg/kg) and KET (2 mg/kg) by remote intramuscular injection. In case of individual and specific needs, the protocol was modified and tigers could receive general anaesthesia, propofol or additional doses of DEX and KET.</p><p><strong>Results: </strong>Based on the immobilisation protocol, nine animals were assigned to the standard protocol group and the other nine to the non-standard protocol group. Higher area under the first moment curve (AUMC<sub>0-last</sub>) and longer mean residence time (MRT<sub>0-last</sub>) (P<0.05) were observed in the non-standard protocol group for DEX, KET and NORKET, and higher area under the concentration-time curve from administration to the last measurable concentration (AUC<sub>0-last</sub>) only for KET. The KET metabolisation rate was similar (P=0.296) between groups. No differences between groups were detected in terms of stages of sedation and recoveries. All physiological variables remained within normality ranges during the whole observation period. During the hospitalisation period, no severe adverse reactions and signs of resedation were observed.</p><p><strong>Conclusion: </strong>The simultaneous administration of 10 µg/kg of DEX and 2 mg/kg of KET can be considered an effective protocol for chemical immobilisation of captive tigers, along with dosage adjusments or when other drugs are needed.</p>","PeriodicalId":23565,"journal":{"name":"Veterinary Record Open","volume":"7 1","pages":"e000412"},"PeriodicalIF":1.4,"publicationDate":"2020-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/vetreco-2020-000412","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38595464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Thirteen-month duration of immunity of an oral canine vaccine against challenge with Bordetella bronchiseptica. 犬口服疫苗对支气管脓毒杆菌攻击的13个月免疫期。
IF 1.4 Q2 VETERINARY SCIENCES Pub Date : 2020-10-16 eCollection Date: 2020-01-01 DOI: 10.1136/vetreco-2020-000423
Maya Scott-Garrard, Xinshuo Wang, Yu-Wei Chiang, Frederic David

Background: Very few studies have evaluated the duration of immunity of Bordetella bronchiseptica vaccines in dogs, and to date, no studies have been published on the duration of immunity of oral canine Bordetella bronchiseptica vaccines. This study was designed to determine the effectiveness of a single dose of an oral B bronchiseptica vaccine in dogs when challenged 13 months after vaccination.

Methods: Two groups of approximately eight-week-old beagles were vaccinated once with 1 ml of placebo vaccine (oral, n=17) or 1 ml of Recombitek Oral Bordetella (oral, n=17). Thirteen months after vaccination, both groups were challenged with virulent B bronchiseptica via aerosolisation.

Results: Thirteen of 17 dogs in the placebo group (76.5 per cent) and no dogs in the Recombitek Oral Bordetella vaccine group (0.0 per cent) developed spontaneous cough of two or more consecutive days (disease case definition). Dogs in the Recombitek Oral Bordetella group had a significantly lower prevalence of disease with prevented fraction of 1 (100 per cent prevention). In addition, the number of days coughing, duration of cough and prevalence of tracheal and nasal shedding were significantly lower for dogs vaccinated with Recombitek Oral Bordetella.

Conclusions: The study demonstrated that vaccination with Recombitek Oral Bordetella is effective in preventing disease and reducing shedding 13 months after vaccination when compared with dogs vaccinated with a placebo.

背景:很少有研究评估狗对支气管脓毒杆菌疫苗的免疫持续时间,到目前为止,还没有关于口服犬支气管脓毒杆菌疫苗免疫持续时间的研究发表。本研究旨在确定在接种疫苗13个月后,单剂量口服B支菌病疫苗对犬的有效性。方法:两组约8周龄的小猎犬分别接种1 ml安慰剂疫苗(口服,n=17)或1 ml Recombitek oral Bordetella疫苗(口服,n=17)。接种疫苗13个月后,两组均通过雾化方式感染毒力强的结核分枝杆菌。结果:安慰剂组17只狗中有13只(76.5%),而Recombitek口服博德泰拉疫苗组没有狗(0.0%)出现连续两天或更长时间的自发性咳嗽(疾病病例定义)。Recombitek口腔博德泰拉组的狗的患病率显著降低,预防比例为1(100%预防)。此外,接种Recombitek Oral Bordetella疫苗的狗的咳嗽天数、咳嗽持续时间以及气管和鼻腔脱落的发生率均显著降低。结论:该研究表明,与接种安慰剂的狗相比,接种Recombitek Oral Bordetella疫苗在接种后13个月有效预防疾病并减少脱落。
{"title":"Thirteen-month duration of immunity of an oral canine vaccine against challenge with <i>Bordetella bronchiseptica</i>.","authors":"Maya Scott-Garrard,&nbsp;Xinshuo Wang,&nbsp;Yu-Wei Chiang,&nbsp;Frederic David","doi":"10.1136/vetreco-2020-000423","DOIUrl":"https://doi.org/10.1136/vetreco-2020-000423","url":null,"abstract":"<p><strong>Background: </strong>Very few studies have evaluated the duration of immunity of <i>Bordetella bronchiseptica</i> vaccines in dogs, and to date, no studies have been published on the duration of immunity of oral canine <i>Bordetella bronchiseptica</i> vaccines. This study was designed to determine the effectiveness of a single dose of an oral <i>B bronchiseptica</i> vaccine in dogs when challenged 13 months after vaccination.</p><p><strong>Methods: </strong>Two groups of approximately eight-week-old beagles were vaccinated once with 1 ml of placebo vaccine (oral, n=17) or 1 ml of Recombitek Oral Bordetella (oral, n=17). Thirteen months after vaccination, both groups were challenged with virulent <i>B bronchiseptica</i> via aerosolisation.</p><p><strong>Results: </strong>Thirteen of 17 dogs in the placebo group (76.5 per cent) and no dogs in the Recombitek Oral Bordetella vaccine group (0.0 per cent) developed spontaneous cough of two or more consecutive days (disease case definition). Dogs in the Recombitek Oral Bordetella group had a significantly lower prevalence of disease with prevented fraction of 1 (100 per cent prevention). In addition, the number of days coughing, duration of cough and prevalence of tracheal and nasal shedding were significantly lower for dogs vaccinated with Recombitek Oral Bordetella.</p><p><strong>Conclusions: </strong>The study demonstrated that vaccination with Recombitek Oral Bordetella is effective in preventing disease and reducing shedding 13 months after vaccination when compared with dogs vaccinated with a placebo.</p>","PeriodicalId":23565,"journal":{"name":"Veterinary Record Open","volume":"7 1","pages":"e000423"},"PeriodicalIF":1.4,"publicationDate":"2020-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/vetreco-2020-000423","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38623522","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
期刊
Veterinary Record Open
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