Kate S KuKanich, Elayna E Anderson, Astrid D Carcamo Tzic, Butch KuKanich
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引用次数: 0
摘要
为了优化治疗尿路感染的剂量方案,我们对犬尿液中氯霉素的排泄情况进行了评估。七只健康的雄性纯种比格犬和六只健康的客户饲养的不同品种的狗分别口服一次 50 毫克/千克剂量的氯霉素。分别在基线时间、服用氯霉素后 6、8、12 和 24 小时收集尿液。测量氯霉素尿液浓度,并与大肠杆菌的流行病学临界值(16 微克/毫升)进行比较。8 小时后,所有狗的平均氯霉素浓度为 266.9 微克/毫升(90% CI 136.2-397.7 微克/毫升),但比格犬的氯霉素浓度低于客户饲养的狗。12 小时后,所有犬只的平均氯霉素浓度为 111.0 微克/毫升(90% CI 36.9-185.0 微克/毫升),比格犬(10.6 微克/毫升,90% CI 1.4-19.8 微克/毫升)低于客户饲养的犬(228.0 微克/毫升,90% CI 103.0-353.1 微克/毫升)。所有狗的尿液半衰期相似(1.8-3.8 小时)。此外,所有客户饲养的狗在 12 小时内的尿液浓度都远高于 16 微克/毫升,这表明 12 小时一次的用药可能适用于患有易感下尿路感染的非比格犬。需要对患有尿路感染的狗进行临床试验,并进一步研究潜在的品种差异。
Potential for extending the chloramphenicol dosing interval for canine urinary tract infections.
Canine urinary excretion of chloramphenicol was evaluated to optimize a dosing protocol for treating urinary tract infections. Seven healthy male intact purpose-bred Beagles and six healthy client-owned dogs of various breeds each received a single oral 50 mg/kg dose of chloramphenicol. Urine was collected at baseline, and 6, 8, 12, and 24 h after chloramphenicol. Chloramphenicol urine concentrations were measured and compared to the epidemiological cutoff value for E. coli (16 mcg/mL). At 8 h, mean chloramphenicol concentration from all dogs was 266.9 mcg/mL (90% CI 136.2-397.7 mcg/mL) but was lower in Beagles than client-owned dogs. At 12 h, mean chloramphenicol concentration from all dogs was 111.0 mcg/mL (90% CI 36.9-185.0 mcg/mL) and was lower in Beagles (10.6 mcg/mL, 90% CI 1.4-19.8 mcg/mL) than client-owned dogs (228.0 mcg/mL, 90% CI 103.0-353.1 mcg/mL). Urine half-life was similar for all dogs (1.8-3.8 h). This justifies dosing chloramphenicol 50 mg/kg PO q 8 h. All client-owned dogs additionally maintained concentrations well above 16 mcg/mL, for 12 h, suggesting that q 12-h dosing might be appropriate for non-Beagle dogs with susceptible lower urinary tract infections. A clinical trial in dogs with urinary tract infections is needed as well as further investigation into potential breed differences.
期刊介绍:
The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.