Becton, Dickinson & Company, Franklin Lakes, NJ, USA.
Merck & Co., Inc., Kenilworth, NJ, USA.
J Hosp Infect. 2019 Oct;103(2):134-141. doi: 10.1016/j.jhin.2019.06.005. Epub 2019 Jun 19.
Multi-drug resistant (MDR) Pseudomonas aeruginosa can negatively affect patients and hospitals.
To evaluate excess mortality and cost burden among patients hospitalized with suspected respiratory infections due to MDR P. aeruginosa vs patients with non-MDR P. aeruginosa in 78 United States (US) hospitals.
This study analyzed electronically captured microbiological and outcomes data of patients hospitalized with non-duplicate P. aeruginosa isolates from respiratory sources collected ≥3 days after admission to identify hospital-onset MDR or non-MDR P. aeruginosa per the Centers for Disease Control and Prevention definition. The risk of multi-drug resistance was estimated on mortality, length of stay (LOS), cost, operation gain/loss, and 30-day readmission. A sensitivity analysis was conducted utilizing a cohort with pharmacy data available.
Of 523 MDR and 1381 non-MDR P. aeruginosa cases, unadjusted mortality was 23.7% vs 18.0% and multi-variable-adjusted mortality was 20.0% (95% confidence interval (CI): 14.3-27.2%) vs 15.5% (95% CI: 11.2-20.9%; P=0.026), the average adjusted excess LOS was 6.7 days (P<0.001); excess cost per case was US$22,370 higher (P=0.002) and operational loss per case was US$10,661 (P=0.024) greater, and the multi-variable adjusted readmission rate was 16.2% (95% CI: 11.2-22.9%) vs 11.1% (95% CI: 7.8-15.6%; P=0.006). The sensitivity analysis yielded similar results.
Compared with suspected infections due to non-MDR P. aeruginosa, patients with MDR P. aeruginosa had higher risk of mortality, readmission, and longer LOS, as well as US$20,000 incremental cost and >US$10,000 incremental net loss per case after controlling for patient and hospital characteristics.
多重耐药(MDR)铜绿假单胞菌会对患者和医院产生负面影响。
评估 78 家美国医院中,因多重耐药铜绿假单胞菌引起疑似呼吸道感染而住院的患者与非多重耐药铜绿假单胞菌引起疑似呼吸道感染而住院的患者相比,其超额死亡率和费用负担。
本研究分析了电子捕获的微生物学和结局数据,这些数据来自于呼吸道来源的非重复铜绿假单胞菌分离株,这些分离株在入院后至少 3 天采集,以根据疾病控制和预防中心的定义确定医院获得性多重耐药或非多重耐药铜绿假单胞菌。通过死亡率、住院时间(LOS)、成本、运营收益/损失和 30 天再入院来估计多药耐药的风险。进行了敏感性分析,利用可用药房数据的队列进行分析。
在 523 例 MDR 和 1381 例非 MDR 铜绿假单胞菌病例中,未经调整的死亡率为 23.7%比 18.0%,多变量调整后的死亡率为 20.0%(95%置信区间(CI):14.3-27.2%)比 15.5%(95% CI:11.2-20.9%;P=0.026),平均调整后的超额 LOS 为 6.7 天(P<0.001);每例病例的超额费用高出 22370 美元(P=0.002),每例病例的运营损失高出 10661 美元(P=0.024),多变量调整后的再入院率为 16.2%(95% CI:11.2-22.9%)比 11.1%(95% CI:7.8-15.6%;P=0.006)。敏感性分析得出了类似的结果。
与非多重耐药铜绿假单胞菌引起的疑似感染相比,多重耐药铜绿假单胞菌感染患者的死亡率、再入院率和 LOS 更高,且每例患者的增量成本超过 2 万美元,净损失超过 1 万美元。