Administration of a β-Lactam Prior to Vancomycin as the First Dose of Antibiotic Therapy Improves Survival in Patients With Bloodstream Infections.

Joe Amoah, Eili Y Klein, Kathleen Chiotos, Sara E Cosgrove, Pranita D Tamma
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引用次数: 8

Abstract

Background: Prompt initiation of antibiotic therapy improves the survival of patients with bloodstream infections (BSIs). We sought to determine if the sequence of administration of the first dose of antibiotic therapy (ie, β-lactam or vancomycin, if both are deemed necessary and cannot be administered simultaneously) impacts early mortality for patients with BSI.

Methods: We conducted a multicenter, observational study of patients ≥13 years with BSIs to evaluate the association of the sequence of antibiotic administration with 7-day mortality using inverse probability of treatment weighting (IPTW) incorporating propensity scores. Propensity scores were generated based on demographics, Pitt bacteremia score, intensive care unit status, highest lactate, highest white blood cell count, Charlson comorbidity index, severe immunocompromise, administration of active empiric therapy, combination therapy, and time from emergency department arrival to first antibiotic dose.

Results: Of 3376 eligible patients, 2685 (79.5%) received a β-lactam and 691 (20.5%) received vancomycin as their initial antibiotic. In the IPTW cohort, exposed and unexposed patients were similar on all baseline variables. Administration of a β-lactam agent prior to vancomycin protected against 7-day mortality (adjusted odds ratio [aOR], 0.48 [95% confidence interval {CI}, .33-.69]). Similar results were observed when evaluating 48-hour mortality (aOR, 0.45 [95% CI, .24-.83]). Administration of vancomycin prior to a β-lactam was not associated with improved survival in the subgroup of 524 patients with methicillin-resistant Staphylococcus aureus BSI (aOR, 0.93 [95% CI, .33-2.63]).

Conclusions: For ill-appearing patients likely to be experiencing a BSI, prioritizing administration of a β-lactam over vancomycin may reduce early mortality, underscoring the significant impact of a relatively simple practice change on improving patient survival.

在万古霉素之前给予β-内酰胺作为第一剂量抗生素治疗可提高血液感染患者的生存率。
背景:及时开始抗生素治疗可提高血液感染(bsi)患者的生存率。我们试图确定第一剂抗生素治疗的给药顺序(即β-内酰胺或万古霉素,如果两者被认为是必要的,不能同时给药)是否影响BSI患者的早期死亡率。方法:我们对≥13年bsi患者进行了一项多中心观察性研究,使用结合倾向评分的治疗加权逆概率(IPTW)来评估抗生素给药顺序与7天死亡率的关系。倾向评分是根据人口统计学、皮特菌血症评分、重症监护病房状态、最高乳酸、最高白细胞计数、Charlson合病指数、严重免疫功能低下、给予积极经验性治疗、联合治疗以及从急诊室到达第一次抗生素剂量的时间产生的。结果:在3376例符合条件的患者中,2685例(79.5%)使用β-内酰胺,691例(20.5%)使用万古霉素作为初始抗生素。在IPTW队列中,暴露和未暴露的患者在所有基线变量上相似。在使用万古霉素之前使用β-内酰胺类药物可预防7天死亡率(校正优势比[aOR], 0.48[95%可信区间{CI}, 0.33 - 0.69])。在评估48小时死亡率时观察到类似的结果(aOR, 0.45 [95% CI, 0.24 - 0.83])。在524例耐甲氧西林金黄色葡萄球菌BSI患者亚组中,在服用β-内酰胺之前服用万古霉素与生存率的提高无关(aOR, 0.93 [95% CI, 0.33 -2.63])。结论:对于可能正在经历BSI的症状不佳的患者,优先使用β-内酰胺而不是万古霉素可能会降低早期死亡率,强调了相对简单的实践改变对提高患者生存率的重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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