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首页> 外文期刊>Foodborne pathogens and disease >Quantitative risk from fluoroquinolone-resistant Salmonella and Campylobacter due to treatment of dairy heifers with enrofloxacin for bovine respiratory disease.
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Quantitative risk from fluoroquinolone-resistant Salmonella and Campylobacter due to treatment of dairy heifers with enrofloxacin for bovine respiratory disease.

机译:用恩诺沙星治疗牛小母牛引起的氟喹诺酮耐药沙门氏菌和弯曲杆菌的定量风险。

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The objective of this study was to evaluate the human health impact of using fluoroquinolones to treat bovine respiratory disease (BRD) in dairy heifers less than 20 months of age. Specifically, this study quantified the probability of persistent symptoms in humans treated with a fluoroquinolone, for a fluoroquinolone-resistant Campylobacter, Salmonella, or multidrug-resistant (MDR) Salmonella infection acquired following the consumption of ground beef. To comply with a Food and Drug Administration requirement for approval of enrofloxacin use in dairy heifers, a binomial event tree was constructed following Food and Drug Administration guidance 152. Release was estimated from the slaughter of dairy cattle carrying fluoroquinolone-resistant bacteria attributed to the proposed use in dairy heifers. For exposure, human foodborne exposure to Campylobacter, Salmonella, and MDR Salmonella after consumption of ground beef was estimated. The consequence assessment included illness, fluoroquinolone treatment, and persistent symptoms in patients treated with a fluoroquinolone. Using best available data to estimate the parameters and probabilities of each event, stochastic simulation was used to represent uncertainty and variability in many of the parameters. A scenario analysis was performed to evaluate the uncertainty of the following parameters: (1) probability of resistance development in treated animals, (2) portion of illnesses attributable to ground beef, and (3) probability of persistent symptoms in patients 18 years of age and over treated with a fluoroquinolone. The population at risk was restricted to people 18 years of age and over, as fluoroquinolones are not labeled for treatment of gastroenteritis in children. The mean annual increased risk of cases in the U.S. population (18 years of age and over) where compromised fluoroquinolone treatment resulted in persistent symptoms was estimated to be 1 in 61 billion (one case every 293 years) for Salmonella, 1 in 33 billion (one case every 158 years) for MDR Salmonella, and 1 in 2.8 billion (one case every 13 years) for Campylobacter.
机译:这项研究的目的是评估使用氟喹诺酮类药物治疗小于20个月大的奶牛的牛呼吸道疾病(BRD)对人类健康的影响。具体来说,这项研究量化了食用碎牛肉后,对氟喹诺酮类耐药的弯曲杆菌,沙门氏菌或耐多药(MDR)沙门氏菌感染的人,用氟喹诺酮治疗后持续出现症状的可能性。为了符合食品药品监督管理局批准在奶牛小母牛中使用恩诺沙星的要求,根据食品药品监督管理局的指导152建造了一个二项式事件树。据估计,携带拟耐受氟喹诺酮的细菌的奶牛屠宰量释放量用于奶牛小母牛。对于暴露,估计食用碎牛肉后人类食源性弯曲杆菌,沙门氏菌和MDR沙门氏菌的暴露。结果评估包括疾病,氟喹诺酮治疗和氟喹诺酮治疗的患者的持续症状。利用最佳可用数据估计每个事件的参数和概率,使用随机模拟来表示许多参数的不确定性和可变性。进行了情景分析,以评估以下参数的不确定性:(1)被治疗动物产生抗药性的可能性,(2)碎牛肉引起的部分疾病,以及(3)18岁患者持续症状的可能性并且用氟喹诺酮处理过。高危人群仅限于18岁及以上的人群,因为氟喹诺酮类药物未标明可治疗儿童胃肠炎。在美国人群(18岁及以上)中,氟喹诺酮治疗不良导致持续症状的病例的年平均增加风险估计为沙门氏菌占610亿分之一(每293年1例),330亿分之1(耐多药沙门氏菌为每158年1例,弯曲杆菌属为28亿分之一(每13年1例)。

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