a Service Universitaire des Maladies Infectieuses et du Voyageur, Centre Hospitalier de Tourcoing , Tourcoing , France.
b Laboratoire de microbiologie, Centre Hospitalier de Tourcoing , Tourcoing , France.
Infect Dis (Lond). 2017 May;49(5):396-404. doi: 10.1080/23744235.2016.1277035. Epub 2017 Jan 16.
Pseudomonas aeruginosa is a common cause of ventilator-associated pneumonia (VAP). Guidelines recommend dual coverage of P. aeruginosa, but the beneficial effect of combination therapy is controversial. We described antibiotic prescriptions and evaluated the clinical impact of initial combination antibiotic therapy and de-escalation strategy in patients with VAP caused by P. aeruginosa.
Between 1994 and 2014, all 100 patients with VAP caused by P. aeruginosa in our intensive care unit (ICU) were included in a retrospective cohort study to evaluate the prognostic impact of initial combination antibiotic therapy.
Eighty-five patients received initial combination antibiotic therapy and 15 monotherapy. Nine patients received inadequate initial antibiotic therapy. De-escalation was performed in 42 patients. Thirty-nine patients died in the ICU. Factors independently associated with death were SAPS II score [SAPS II ≥40 versus <40: hazard ratio (HR) 2.49, 95% confidence interval (CI) 1.08-5.70, p = 0.03] and septic shock (HR = 4.80, 95% CI = 1.90-12.16, p < 0.01) at onset of VAP. Initial combination antibiotic therapy (HR = 1.97, 95% CI = 0.56-6.93, p = 0.29) and early de-escalation (HR = 0.59, 95% CI = 0.27-1.31, p = 0.19) had no impact on mortality. In multivariate analysis, the risk for inappropriate initial antibiotic therapy was higher in cases with multi-drug resistant P. aeruginosa [odd ratio (OR) = 7.11, 95% CI = 1.42-35.51, p = 0.02], but lower in cases with initial combination antibiotic therapy (OR = 0.12, 95% CI = 0.02-0.63, p = 0.01).
In our cohort, combination therapy increased the likelihood of appropriate therapy but did not seem to impact on mortality.
铜绿假单胞菌是呼吸机相关性肺炎(VAP)的常见病原体。指南推荐对铜绿假单胞菌进行双重覆盖,但联合治疗的有益效果存在争议。我们描述了抗生素的使用情况,并评估了铜绿假单胞菌引起的 VAP 患者初始联合抗生素治疗和降阶梯策略的临床影响。
在 1994 年至 2014 年间,我们重症监护病房(ICU)中所有 100 例由铜绿假单胞菌引起的 VAP 患者均纳入回顾性队列研究,以评估初始联合抗生素治疗的预后影响。
85 例患者接受初始联合抗生素治疗,15 例患者接受单药治疗。9 例患者接受了不充分的初始抗生素治疗。42 例患者进行了降阶梯治疗。39 例患者在 ICU 死亡。与死亡独立相关的因素是 SAPS II 评分[SAPS II≥40 与<40:危险比(HR)2.49,95%置信区间(CI)1.08-5.70,p=0.03]和 VAP 起始时的败血症性休克(HR=4.80,95%CI=1.90-12.16,p<0.01)。初始联合抗生素治疗(HR=1.97,95%CI=0.56-6.93,p=0.29)和早期降阶梯治疗(HR=0.59,95%CI=0.27-1.31,p=0.19)对死亡率没有影响。在多变量分析中,多重耐药铜绿假单胞菌感染的初始抗生素治疗不当的风险更高[比值比(OR)=7.11,95%CI=1.42-35.51,p=0.02],但初始联合抗生素治疗的风险更低(OR=0.12,95%CI=0.02-0.63,p=0.01)。
在我们的队列中,联合治疗增加了获得适当治疗的可能性,但似乎对死亡率没有影响。