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Relationship Status between Vancomycin Loading Dose and Treatment Failure in Patients with MRSA Bacteremia: It’s Complicated

机译:患有MRSA菌血症患者的万古霉素载剂量和治疗失败的关系状态:这很复杂

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IntroductionA one-time vancomycin loading dose of 25–30?mg/kg is recommended in the current iteration of the vancomycin consensus guidelines in order to more rapidly achieve target serum concentrations and hasten clinical improvement. However, there are few clinical data to support this practice, and the extents of its benefits are largely unknown. MethodsA multicenter, retrospective, cohort study was performed to assess the impact of a vancomycin loading dose (≥?20?mg/kg) on clinical outcomes and rates of nephrotoxicity in patients with methicillin-resistant Staphylococcus aureus (MRSA) bacteremia. The study matched patients in a 1:1 fashion based on age, Pitt bacteremia score, and bacteremia source. The primary outcome was composite treatment failure (30-day mortality, bacteremia duration?≥?7?days after vancomycin initiation, persistent signs and symptoms of infection?≥?7?days after vancomycin initiation, or switch to an alternative antimicrobial agent). Secondary outcomes included duration of bacteremia, length of stay post-bacteremia onset, and nephrotoxicity. ResultsA total of 316 patients with MRSA bacteremia were included. Median first doses in the loading dose and non-loading dose groups were 23.0?mg/kg and 14.3?mg/kg, respectively ( P ConclusionThese findings suggest that initial vancomycin doses above a certain threshold may decrease clinical failures without increasing toxicity and that weight-based dosing might not be the optimal strategy.
机译:出台一次性万古霉素装载剂量为25-30〜30?Mg / kg,推荐在当前迭代的万古霉素共识准则中,以更快地达到目标血清浓度和急剧临床改善。但是,很少有临床数据来支持这种做法,并且其益处的范围主要是未知的。方法采用多中心,回顾性,队列队列研究,以评估万古霉素负载剂量(≥12mg/ kg)对甲氧西林金黄色葡萄球菌(MRSA)菌血症患者的临床结果和肾毒性急性的影响。基于年龄,皮特菌血症评分和菌血症来源,研究患者1:1时尚患者。主要结果是复合治疗衰竭(30天死亡率,菌血症持续时间?≥?7?≥Mancomycin发育后的持续症状和感染症状?≥?7?2-8-8-天气霉素发起后,或切换到另一种抗微生物剂后)。二次结果包括菌血症的持续时间,植物后患者的持续时间发作,以及肾毒性。结果总共316例MRSA菌血症患者。中位数在装载剂量和非负载剂量基团中的​​第一剂量分别为23.0×mg / kg和14.3×mg / kg(p结束的结果表明,在某个阈值上方的初始万古霉素剂量可能降低临床失败而不增加毒性,重量被淘汰的给药可能不是最佳策略。

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