Boel J, Søgaard M, Andreasen V, Jarløv J O, Arpi M
Department of Clinical Microbiology, Herlev Hospital, University of Copenhagen, Herlev Ringvej 75, 2730, Herlev, Denmark,
Eur J Clin Microbiol Infect Dis. 2015 Jul;34(7):1475-84. doi: 10.1007/s10096-015-2378-x. Epub 2015 Apr 17.
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.
在引入用于菌血症经验性治疗的新抗生素指南时,评估新指南的执行情况至关重要。我们研究了行政数据在评估新抗生素指南效果及适当经验性治疗的预后影响方面的效用。我们根据2010年至2012年间2008例诊断为菌血症的成年患者是否接受头孢菌素或氟喹诺酮类药物(旧方案)将其分类(新方案)。我们使用行政数据提取关于死亡率、再入院率和治疗适当性的个体水平数据,并计算按治疗方案和治疗适当性划分的30天死亡率及出院后再入院率的调整风险比(HRs)和95%置信区间(CIs)。总体而言,945例(47.1%)接受旧方案治疗,1063例(52.9%)接受新方案治疗。住院时间中位数(8天)在不同治疗方案间无差异,接受适当经验性治疗的患者比例也无差异(84.1%对85.5%)。然而,新方案组入住重症监护病房(ICU)的患者较少(3.8%对12.0%),且30天死亡率较低(16.4%对23.4%)。新方案与旧方案相比,适当治疗与不适当治疗的调整30天死亡率HR分别为0.79(95%CI 0.62 - 1.01)和0.83(95%CI 0.66 - 1.05)。新方案与旧方案相比,适当治疗与不适当治疗的30天再入院率HR分别为0.91(95%CI 0.73 - 1.13)和1.05(95%CI 0.87 - 1.25)。本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。