标题 坦桑尼亚北部野生动物保护区附近牛群非洲动物锥虫病病例中锥虫灭活失败原因的纵向观察(单一队列)研究

Shauna Richards, Davide Pagnossin, Paul Samson Buyugu, Oliver Manangwa, Furaha Mramba, Emmanuel Sindoya, Edith Paxton, Steve J. Torr, Ryan Ritchie, Giovanni E. Rossi, Lawrence Nnadozie Anyanwu, Michael Barrett, Liam J. Morrison, Harriet Auty
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Purposive sampling targeted herds with high utilization of the prophylactic trypanocide isometamidium chloride (ISM). When a farmer administered a trypanocide (ISM, diminazine aceturate, homidium), the project veterinarian assessed administration and treatment outcomes were determined based on PCR results from blood samples. A multivariable mixed model was utilized to evaluate risk factors for prophylaxis failure. Quality analysis was performed on trypanocide samples using High Performance Liquid Chromatography. A total of 630 cattle from 21 farms were monitored for a year-long period. A total of 295 trypanocide administrations were reported, predominantly being ISM (56%) used for prophylaxis (87%). One-third of trypanocide administrations were not given adequately, and many trypanocides were given to animals that tested negative for trypanosome infections by PCR. Failures occurred in 7% (95% CI 3.0-14%) of curative treatments, and 44% (95% CI 35-42%) of prophylactic administrations. 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引用次数: 0

摘要

牛的非洲动物锥虫病(AAT)主要通过使用杀锥虫剂和杀虫剂来控制。杀锥虫剂可用于治疗和预防,但经常有失败的报道;失败的原因可能是抗药性、药物不达标或用药不当。这项在坦桑尼亚开展的研究旨在量化杀锥虫失败的原因。从 2019 年 12 月到 2022 年 10 月,在塞伦盖蒂区的高风险 AAT 地区开展了为期一年的纵向观察研究。有目的的取样以预防性杀锥虫药异甲脒氯化物(ISM)使用率高的牧群为目标。当牧场主施用杀锥虫剂(ISM、乙酸二甲脒、高脒)时,项目兽医会对施用情况进行评估,并根据血样的 PCR 结果确定治疗效果。采用多变量混合模型评估预防失败的风险因素。使用高效液相色谱法对杀灭锥虫剂样本进行了质量分析。对 21 个农场的 630 头牛进行了为期一年的监测。报告共使用了 295 次杀灭锥虫药物,主要是用于预防的 ISM(56%)(87%)。三分之一的锥虫灭活剂使用不充分,许多锥虫灭活剂是给经 PCR 检测锥虫感染呈阴性的动物使用的。7%(95% CI 3.0-14%)的治疗性用药和44%(95% CI 35-42%)的预防性用药出现失败。ISM的品牌与预防失败的几率明显相关(p = 0.011)。在质量分析中,有两个 ISM 样品未检测到 ISM 异构体,但其余的 ISM 和 DA 样品(n=46)均在可接受水平范围内。药物造假、杀灭锥虫剂使用不当以及抗药性都是导致杀灭锥虫剂失效的原因,从而限制了对急性疟原虫的有效控制,并对人类疾病风险产生了影响。为了遏制杀灭锥虫失败,需要采取多模式方法来管理杀灭锥虫剂的使用,以解决所有诱因。
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Title Longitudinal Observational (single cohort) Study on the Causes of Trypanocide Failure in cases of African Animal Trypanosomosis in Cattle Near Wildlife Protected Areas of Northern Tanzania
African animal trypanosomosis (AAT) in cattle is primarily managed through trypanocide administration and insecticide application. Trypanocides can be used for both treatment and prophylaxis, but failure is often reported; this may occur due to resistance, substandard drugs, or inappropriate administration. This study in Tanzania aims to quantify reasons for trypanocide failure. An observational year-long longitudinal study was conducted in high-risk AAT areas in Serengeti District from December 2019-October 2022. Purposive sampling targeted herds with high utilization of the prophylactic trypanocide isometamidium chloride (ISM). When a farmer administered a trypanocide (ISM, diminazine aceturate, homidium), the project veterinarian assessed administration and treatment outcomes were determined based on PCR results from blood samples. A multivariable mixed model was utilized to evaluate risk factors for prophylaxis failure. Quality analysis was performed on trypanocide samples using High Performance Liquid Chromatography. A total of 630 cattle from 21 farms were monitored for a year-long period. A total of 295 trypanocide administrations were reported, predominantly being ISM (56%) used for prophylaxis (87%). One-third of trypanocide administrations were not given adequately, and many trypanocides were given to animals that tested negative for trypanosome infections by PCR. Failures occurred in 7% (95% CI 3.0-14%) of curative treatments, and 44% (95% CI 35-42%) of prophylactic administrations. The brand of ISM was significantly associated with odds of prophylaxis failure (p = 0.011). On quality analysis, two ISM samples had no detectable ISM isomers, but the remainder of ISM and DA samples (n=46) fell within the range of acceptable levels. Drug counterfeiting, inadequate use of trypanocides, and resistance are all contributing to trypanocide failure, limiting effective AAT control and with implications for human disease risk. In order to curb trypanocide failure a multi-modal approach to managing the use of trypanocides is required to address all contributing factors.
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