Surgical ICU, Hôpital Edouard Herriot, 5 place d'Arsonval, Lyon 69437, France.
Crit Care. 2011;15(2):R112. doi: 10.1186/cc10136. Epub 2011 Apr 11.
Although Pseudomonas aeruginosa is a leading pathogen responsible for ventilator-associated pneumonia (VAP), the excess in mortality associated with multi-resistance in patients with P. aeruginosa VAP (PA-VAP), taking into account confounders such as treatment adequacy and prior length of stay in the ICU, has not yet been adequately estimated.
A total of 223 episodes of PA-VAP recorded into the Outcomerea database were evaluated. Patients with ureido/carboxy-resistant P. aeruginosa (PRPA) were compared with those with ureido/carboxy-sensitive P. aeruginosa (PSPA) after matching on duration of ICU stay at VAP onset and adjustment for confounders.
Factors associated with onset of PRPA-VAP were as follows: admission to the ICU with septic shock, broad-spectrum antimicrobials at admission, prior use of ureido/carboxypenicillin, and colonization with PRPA before infection. Adequate antimicrobial therapy was more often delayed in the PRPA group. The crude ICU mortality rate and the hospital mortality rate were not different between the PRPA and the PSPA groups. In multivariate analysis, after controlling for time in the ICU before VAP diagnosis, neither ICU death (odds ratio (OR) = 0.73; 95% confidence interval (CI): 0.32 to 1.69; P = 0.46) nor hospital death (OR = 0.87; 95% CI: 0.38 to 1.99; P = 0.74) were increased in the presence of PRPA infection. This result remained unchanged in the subgroup of 87 patients who received adequate antimicrobial treatment on the day of VAP diagnosis.
After adjustment, and despite the more frequent delay in the initiation of an adequate antimicrobial therapy in these patients, resistance to ureido/carboxypenicillin was not associated with ICU or hospital death in patients with PA-VAP.
铜绿假单胞菌是导致呼吸机相关性肺炎(VAP)的主要病原体,但铜绿假单胞菌 VAP(PA-VAP)患者的多药耐药性导致的死亡率增加,考虑到治疗充分性和 ICU 住院时间等混杂因素,尚未得到充分估计。
评估了 Outcomesrea 数据库中记录的 223 例 PA-VAP 病例。在调整了 ICU 入住 VAP 时的时间长短和混杂因素后,将对脲基/羧基耐药铜绿假单胞菌(PRPA)的患者与对脲基/羧基敏感铜绿假单胞菌(PSPA)的患者进行比较。
与 PRPA-VAP 发病相关的因素如下:入住 ICU 时发生感染性休克、入院时使用广谱抗生素、入院前使用脲基/羧基青霉素和感染前定植 PRPA。PRPA 组的抗菌治疗通常更延迟。PRPA 组和 PSPA 组的 ICU 死亡率和医院死亡率无差异。在多变量分析中,在控制了 VAP 诊断前 ICU 入住时间后,PRPA 感染既不增加 ICU 死亡的风险(比值比(OR)=0.73;95%置信区间(CI):0.32 至 1.69;P=0.46),也不增加医院死亡的风险(OR=0.87;95%CI:0.38 至 1.99;P=0.74)。在接受 VAP 诊断当天接受充分抗菌治疗的 87 例患者亚组中,这一结果保持不变。
调整后,尽管这些患者开始充分抗菌治疗的时间更频繁延迟,但在 PA-VAP 患者中,对脲基/羧基青霉素的耐药性与 ICU 或医院死亡率无关。