Barnes-Jewish Hospital, St Louis, MO, USA.
Washington University in St Louis, MO, USA.
Ann Pharmacother. 2019 Dec;53(12):1207-1213. doi: 10.1177/1060028019867114. Epub 2019 Jul 26.
Little evidence exists for de-escalation of nosocomial pneumonia therapy without positive cultures. The purpose of this study was to identify potential predictors of treatment failure following de-escalation to a fluoroquinolone in culture-negative nosocomial pneumonia. The study involved a single-center, retrospective cohort of patients admitted with diagnosis of nosocomial pneumonia and positive chest radiography who received at least 24 hours of fluoroquinolone monotherapy following at least 24 hours of appropriate empirical antibiotics. Treatment failure was defined using a composite of all-cause death within 30 days of discharge, treatment re-escalation, or readmission for pneumonia within 30 days of discharge. The Cox proportional hazards model was used to analyze predictors of treatment failure. Duration of empirical antibiotics and significant univariable exploratory predictors were included in multivariable analysis. Of 164 patients, 23 (14%) failed de-escalation. Duration of empirical antibiotics (68.5 ± 32.1 vs 65.8 ± 35 hours) was not associated with treatment failure in univariable (Hazard Ratio [HR] = 1.002 [95% CI = 0.991-1.013]) or multivariable analyses (HR = 1.003 [95% CI = 0.991-1.015]). Significant exploratory predictors on univariable analysis included active cancer, intensive care unit (ICU) admission at empirical initiation, APACHE II score, and steroid use ≥20-mg prednisone equivalent. ICU admission at empirical initiation (HR = 2.439 [95% CI = 1.048-5.676]) and steroid use ≥20-mg prednisone equivalent (HR = 2.946 [95% CI = 1.281-6.772]) were associated with treatment failure on multivariable analysis. Duration of empirical antibiotics does not appear to influence failure of de-escalation to fluoroquinolone monotherapy in culture-negative nosocomial pneumonia.
在没有阳性培养物的情况下,降低医院获得性肺炎治疗的证据有限。本研究的目的是确定在培养阴性的医院获得性肺炎中,降级为氟喹诺酮类药物后治疗失败的潜在预测因素。这项研究涉及一个单中心、回顾性队列,纳入了因诊断为医院获得性肺炎和胸部放射学阳性而入院的患者,他们在接受至少 24 小时的适当经验性抗生素治疗后,至少接受了 24 小时的氟喹诺酮单药治疗。治疗失败的定义是出院后 30 天内全因死亡、治疗升级或因肺炎再入院。使用 Cox 比例风险模型分析治疗失败的预测因素。经验性抗生素的持续时间和有显著意义的单变量探索性预测因素被纳入多变量分析。在 164 名患者中,有 23 名(14%)降级治疗失败。在单变量分析中,经验性抗生素的持续时间(68.5 ± 32.1 与 65.8 ± 35 小时)与治疗失败无关(风险比[HR] = 1.002[95%置信区间 0.991-1.013])或多变量分析(HR = 1.003[95%置信区间 0.991-1.015])。单变量分析中有显著意义的探索性预测因素包括活动性癌症、经验性治疗开始时入住重症监护病房(ICU)、急性生理与慢性健康状况评分 II(APACHE II)评分和类固醇使用≥20-mg 泼尼松等效物。经验性治疗开始时入住 ICU(HR = 2.439[95%置信区间 1.048-5.676])和类固醇使用≥20-mg 泼尼松等效物(HR = 2.946[95%置信区间 1.281-6.772])与多变量分析中的治疗失败相关。经验性抗生素的持续时间似乎不会影响培养阴性的医院获得性肺炎降级为氟喹诺酮单药治疗的失败。