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Evaluating antibiotic stewardship programs in patients with bacteremia using administrative data: a cohort study

机译:使用行政数据评估菌血症患者的抗生素管理计划:一项队列研究

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When introducing new antibiotic guidelines for empirical treatment of bacteremia, it is imperative to evaluate the performance of the new guideline. We examined the utility of administrative data to evaluate the effect of new antibiotic guidelines and the prognostic impact of appropriate empirical treatment. We categorized 2,008 adult patients diagnosed with bacteremia between 2010 and 2012 according to whether they received cephalosporins or fluoroquinolones (old regimen) or not (new regimen). We used administrative data to extract individual level data on mortality, readmission, and appropriateness of treatment, and computed adjusted hazard ratios (HRs) and 95 % confidence intervals (CIs) for 30-day mortality and post-discharge readmission by regimen and appropriateness of treatment. In total, 945 (47.1 %) were treated by the old regimen and 1,063 (52.9 %) by the new. The median length of stay (8 days) did not differ by regimen and neither did the proportion of those receiving appropriate empirical treatment (84.1 % vs. 85.5 %). However, fewer patients with the new regimen were admitted to the intensive care unit (ICU; 3.8 % vs. 12.0 %) and they had lower 30-day mortality (16.4 % vs. 23.4 %). The adjusted 30-day mortality HR for appropriate versus inappropriate treatment was 0.79 (95 % CI 0.62-1.01) and 0.83 (95 % CI 0.66-1.05) for the new versus the old regimen. The HR for 30-day readmission for appropriate versus inappropriate treatment was 0.91 (95 % CI 0.73-1.13) and 1.05 (95 % CI 0.87-1.25) for the new versus the old regimen. This study demonstrates that administrative data can be useful for evaluating the effect and quality of new bacteremia treatment guidelines.
机译:当引入新的抗生素准则进行经验性菌血症治疗时,必须评估新准则的性能。我们检查了行政数据的实用性,以评估新抗生素指南的效果以及适当经验治疗的预后影响。我们根据在2010年至2012年之间是否接受头孢菌素或氟喹诺酮类药物(旧方案)(新方案)或未接受头孢菌素或氟喹诺酮类药物的成年患者,对2,008名成年患者进行了分类。我们使用行政数据提取有关死亡率,再入院率和治疗适宜性的个人水平数据,并根据治疗方案和适当性计算出30天死亡率和出院后再入院的调整后的危险比(HRs)和95%置信区间(CIs)。治疗。总体而言,旧方案治疗了945(47.1%),新方案治疗了1,063(52.9%)。中位住院时间(8天)在治疗方案上没有差异,接受适当经验治疗的患者比例也没有差异(84.1%对85.5%)。但是,接受新方案治疗的重症监护病房的患者较少(ICU; 3.8%比12.0%),他们的30天死亡率更低(16.4%比23.4%)。新方案与旧方案相比,适当和不适当治疗的调整后30天死亡率HR为0.79(95%CI 0.62-1.01)和0.83(95%CI 0.66-1.05)。新旧方案相比,适当和不适当治疗的30天再入院HR为0.91(95%CI 0.73-1.13)和1.05(95%CI 0.87-1.25)。这项研究表明,行政数据可用于评估新菌血症治疗指南的效果和质量。

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