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Validation of predictors of adverse outcomes in hospital-acquired pneumonia in the ICU

机译:验证ICU中医院获得性肺炎不良预后的预测因子

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Objective:: To validate a set of predictors of adverse outcomes in patients with ICU-acquired pneumonia in relation to clinically relevant assessment at 28 days. Design:: Prospective, observational study. Setting:: Six medical and surgical ICUs of a university hospital. Patients:: Three hundred thirty-five patients with ICU-acquired pneumonia. Interventions:: None. Measurements and Main Results:: Development of predictors of adverse outcomes was defined when at least one of the following criteria was present at an evaluation made 72-96 hours after starting treatment: no improvement of PaO2/FIO2, need for intubation due to pneumonia, persistence of fever or hypothermia with purulent respiratory secretions, greater than or equal to 50% increase in radiographic infiltrates, or occurrence of septic shock or multiple organ dysfunction syndrome. We also assessed the inflammatory response by different serum biomarkers. The presence of predictors of adverse outcomes was related to mortality and ventilator-free days at day 28. Sequential Organ Failure Assessment score was evaluated and related to mortality at day 28.One hundred eighty-four (55%) patients had at least one predictor of adverse outcomes. The 28-day mortality was higher for those with versus those without predictors of adverse outcomes (45% vs 19%, p < 0.001), and ventilator-free days were lower (median [interquartile range], 0 [0-17] vs 22 [0-28]) for patients with versus patients without predictors of adverse outcomes (p < 0.001). The lack of improvement of PaO2/FIO2 and lack of improvement in Sequential Organ Failure Assessment score from day 1 to day 5 were independently associated with 28-day mortality and fewer ventilator-free days. The marginal structural analysis showed an odds ratio of death 2.042 (95% CI, 1.01-4.13; p = 0.047) in patients with predictors of adverse outcomes. Patients with predictors of adverse outcomes had higher serum inflammatory response accordingly to biomarkers evaluated. Conclusions:: The presence of any predictors of adverse outcomes was associated with mortality and decreased ventilator-free days at day 28. The lack of improvement in the PaO2/FIO2 and Sequential Organ Failure Assessment score was independently associated with mortality in the multivariate analysis.
机译:目的::通过28天的临床相关评估,验证一组ICU获得性肺炎患者不良结局的预测指标。设计::前瞻性观察研究。地点:一家大学医院的六个医疗和外科ICU。患者:335例ICU获得性肺炎患者。干预措施:无。测量和主要结果:在开始治疗后72-96小时进行的评估中,至少有以下一项标准时,定义了不良结果的预测因素的发展:PaO2 / FIO2没有改善,由于肺炎需要插管,发烧或体温过低伴呼吸性脓性分泌物持续存在,放射线浸润增加或大于50%,或发生败血性休克或多器官功能障碍综合征。我们还通过不同的血清生物标志物评估了炎症反应。不良后果的预测因素的存在与第28天的死亡率和无呼吸机的天数有关。评估了器官功能衰竭评估评分,并与第28天的死亡率有关。184例(55%)患者中至少有一种预测因素不良后果。有无不良结果预测者的28天死亡率较高(45%比19%,p <0.001),无呼吸器天数较低(中位[四分位间距],0 [0-17] vs 22 [0-28])相对于没有不良预后指标的患者(p <0.001)。从第1天到第5天,PaO2 / FIO2缺乏改善和序贯器官衰竭评估得分的改善均与28天死亡率和无呼吸机天数减少独立相关。边缘结构分析显示,在具有不良结局预测指标的患者中,死亡的赔率比为2.042(95%CI,1.01-4.13; p = 0.047)。与评估的生物标志物相应,具有不良后果预测因素的患者血清炎症反应更高。结论:不良结果的任何预测因素的存在与死亡率和第28天无呼吸机天的减少有关。在多变量分析中,PaO2 / FIO2和序贯器官衰竭评估评分缺乏改善与死亡率独立相关。

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