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Impact of multidrug resistance on Pseudomonas aeruginosa ventilator-associated pneumonia outcome: Predictors of early and crude mortality

机译:多药耐药性对铜绿假单胞菌呼吸机相关性肺炎结局的影响:早期和粗略死亡率的预测因子

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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.
机译:在过去十年中,多药耐药性(MDR)铜绿假单胞菌的流行有所增加,并且在呼吸机相关性肺炎(VAP)中发现了这些分离株的显着上升。但是,尚未深入分析耐多药对VAP结果的影响。在一项微生物学和临床记录的VAP回顾性研究中,我们调查了早期和粗略死亡的危险因素。包括83例患者中的91例VAP发作,其中31例是由易感性铜绿假单胞菌引起的,而60例是由MDR菌株引起的,其中42例(70%)是广泛耐药(XDR)铜绿假单胞菌。十三例伴随出现铜绿假单胞菌菌血症,其中七例起源于呼吸道。相对于MDR发作,易感性铜绿假单胞菌发作更有可能接受适当的经验治疗(68%vs. 30%; p <0.001)和确定的抗菌治疗(96%vs. 50%; p <0.001),易感性铜绿假单胞菌VAP呈现出早期死亡率的趋势(29%比15%; p = 0.06)。以早期死亡率为因变量的逻辑回归模型确定了多器官功能障碍综合症(MODS)[比值比(OR)为10.4; 95%置信区间(CI)1.7-63.5; p = 0.01]和抗生素治疗不足(OR 4.27; 95%CI 0.98-18.4; p = 0.052)作为早期死亡的独立危险因素。类似的分析将MODS(OR 4.31; 95%CI 1.14-16.2; p = 0.03)确定为粗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率的主要预测指标。尽管进行了充分的抗生素治疗,但易感的铜绿假单胞菌似乎会导致严重的早期死亡。尽管适当的治疗对于治疗VAP是必不可少的,但急性疾病的严重程度是比耐药性更重要的因素。

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