Infectious Diseases Service, IDIBELL, Hospital Universitari de Bellvitge, C/ Feixa Llarga S/n., L'Hospitalet de Llobregat, 08907 Barcelona, Spain.
Eur J Clin Microbiol Infect Dis. 2013 Mar;32(3):413-20. doi: 10.1007/s10096-012-1758-8. Epub 2013 Jan 24.
The prevalence of multidrug-resistant (MDR) Pseudomonas aeruginosa has increased over the past decade and a significant rise in these isolates in ventilator-associated pneumonia (VAP) has been observed. However, the impact of MDR on VAP outcome has not been analysed in depth. We investigated the risk factors for early and crude mortality in a retrospective study of microbiologically and clinically documented VAP. Ninety-one VAP episodes in 83 patients were included, 31 caused by susceptible P. aeruginosa and 60 by MDR strains, of which 42 (70 %) were extensively drug-resistant (XDR) P. aeruginosa. Thirteen episodes concomitantly presented P. aeruginosa bacteraemia, in seven of which the origin was the respiratory tract. Whereas susceptible P. aeruginosa episodes were more likely than MDR episodes to receive adequate empirical (68 % vs. 30 %; p < 0.001) and definitive antimicrobial therapy (96 % vs. 50 %; p < 0.001), susceptible P. aeruginosa VAP presented a trend towards early mortality (29 % vs. 15 %; p = 0.06). A logistic regression model with early mortality as the dependent variable identified multiorgan dysfunction syndrome (MODS) [odds ratio (OR) 10.4; 95 % confidence interval (CI) 1.7-63.5; p = 0.01] and inadequate antibiotic therapy (OR 4.27; 95 % CI 0.98-18.4; p = 0.052) as independent risk factors for early mortality. A similar analysis identified MODS (OR 4.31; 95 % CI 1.14-16.2; p = 0.03) as the only independent predictor of crude mortality. The severity of acute illness clinical presentation was the main predictor of mortality. Despite adequate antibiotic therapy, susceptible P. aeruginosa seems to cause major early mortality. Although adequate therapy is essential to treat VAP, the severity of acute illness is a more important factor than drug resistance.
过去十年,耐多药(MDR)铜绿假单胞菌的流行率有所上升,呼吸机相关性肺炎(VAP)中此类分离株的显著增加。然而,MDR 对 VAP 结果的影响尚未得到深入分析。我们对微生物学和临床确诊的 VAP 进行回顾性研究,以评估其早期和总死亡率的危险因素。共纳入 83 例患者的 91 例 VAP 发作,其中 31 例由敏感铜绿假单胞菌引起,60 例由 MDR 菌株引起,其中 42 例(70%)为广泛耐药(XDR)铜绿假单胞菌。13 例同时出现铜绿假单胞菌菌血症,其中 7 例起源于呼吸道。敏感铜绿假单胞菌组比 MDR 组更可能接受适当的经验性(68% vs. 30%;p<0.001)和明确的抗菌治疗(96% vs. 50%;p<0.001),但敏感铜绿假单胞菌 VAP 呈现出早期死亡率的趋势(29% vs. 15%;p=0.06)。以早期死亡率为因变量的逻辑回归模型确定多器官功能障碍综合征(MODS)[比值比(OR)10.4;95%置信区间(CI)1.7-63.5;p=0.01]和不适当的抗生素治疗(OR 4.27;95%CI 0.98-18.4;p=0.052)是早期死亡率的独立危险因素。类似的分析确定 MODS(OR 4.31;95%CI 1.14-16.2;p=0.03)是总死亡率的唯一独立预测因子。急性疾病临床表现的严重程度是死亡的主要预测因素。尽管进行了适当的抗生素治疗,但敏感铜绿假单胞菌似乎导致了严重的早期死亡。尽管适当的治疗对于治疗 VAP 是必要的,但急性疾病的严重程度是比耐药性更重要的因素。