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重症监护病房肺炎患者的疾病风险与死亡率预测。澳大利亚和新西兰重症监护实践(ANZPIC II)。

Disease risk and mortality prediction in intensive care patients with pneumonia. Australian and New Zealand practice in intensive care (ANZPIC II).

作者信息

Boots R J, Lipman J, Bellomo R, Stephens D, Heller R F

机构信息

Department of Intensive Care Medicine, Royal Brisbane and Women's Hospital, Burns, Trauma and Critical Care Research Centre, University of Queensland, Brisbane, Australia.

出版信息

Anaesth Intensive Care. 2005 Feb;33(1):101-11. doi: 10.1177/0310057X0503300116.

Abstract

This study of ventilated patients investigated pneumonia risk factors and outcome predictors in 476 episodes of pneumonia (48% community-acquired pneumonia, 24% hospital-acquired pneumonia, 28% ventilator-associated pneumonia) using a prospective survey in 14 intensive care units within Australia and New Zealand. For community acquired pneumonia, mortality increased with immunosuppression (OR 5.32, CI 95% 1.58-1799, P<0.01), clinical signs of consolidation (OR 2.43, CI 95% 1.09-5.44, P=0.03) and Sepsis-Related Organ Failure Assessment (SOFA) scores (OR 1.19, CI 95% 1.08-1.30, P<0.001) but improved if appropriate antibiotic changes were made within three days of intensive care unit admission (OR 0.42, CI 95% 0.20-0.86, P=0.02). For hospital-acquired pneumonia, immunosuppression (OR 6.98, CI 95% 1.16-42.2, P=0.03) and non-metastatic cancer (OR 3.78, CI 95% 1.20-11.93, P=0.02) were the principal mortality predictors. Alcoholism (OR 7.80, CI 95% 1.20-17.50, P<0.001), high SOFA scores (OR 1.44, CI 95% 1.20-1.75, P=0.001) and the isolation of "high risk" organisms including Pseudomonas aeruginosa, Acinetobacter spp, Stenotrophomonas spp and methicillin resistant Staphylococcus aureus (OR 4.79, CI 95% 1.43-16.03, P=0.01), were associated with increased mortality in ventilator-associated pneumonia. The use of non-invasive ventilation was independently protective against mortality for patients with community-acquired and hospital-acquired pneumonia (OR 0.35, CI 95% 0.18-0.68, P=0.002). Mortality was similar for patients requiring both invasive and non-invasive ventilation and non-invasive ventilation alone (21% compared with 20% respectively, P=0.56). Pneumonia risks and mortality predictors in Australian and New Zealand ICUs vary with pneumonia type. A history of alcoholism is a major risk factor for mortality in ventilator-associated pneumonia, greater in magnitude than the mortality effect of immunosuppression in hospital-acquired pneumonia or community-acquired pneumonia. Non-invasive ventilation is associated with reduced ICU mortality. Clinical signs of consolidation worsen, while rationalising antibiotic therapy within three days of ICU admission improves mortality for community-acquired pneumonia patients.

摘要

这项针对通气患者的研究,在澳大利亚和新西兰的14个重症监护病房中采用前瞻性调查,对476例肺炎病例(48%为社区获得性肺炎、24%为医院获得性肺炎、28%为呼吸机相关性肺炎)的肺炎危险因素和预后预测因素进行了调查。对于社区获得性肺炎,死亡率随着免疫抑制(比值比5.32,95%置信区间1.58 - 1799,P<0.01)、实变的临床体征(比值比2.43,95%置信区间1.09 - 5.44,P = 0.03)和脓毒症相关器官功能衰竭评估(SOFA)评分(比值比1.19,95%置信区间1.08 - 1.30,P<0.001)而增加,但如果在重症监护病房入院后三天内进行适当的抗生素更换,则死亡率会改善(比值比0.42,95%置信区间0.20 - 0.86,P = 0.02)。对于医院获得性肺炎,免疫抑制(比值比6.98,95%置信区间1.16 - 42.2,P = 0.03)和非转移性癌症(比值比3.78,95%置信区间1.20 - 11.93,P = 0.02)是主要的死亡预测因素。酗酒(比值比7.80,95%置信区间1.20 - 17.50,P<0.001)、高SOFA评分(比值比1.44,95%置信区间1.20 - 1.75,P = 0.001)以及分离出“高风险”微生物,包括铜绿假单胞菌、不动杆菌属、嗜麦芽窄食单胞菌和耐甲氧西林金黄色葡萄球菌(比值比4.79,95%置信区间1.43 - 16.03,P = 0.01),与呼吸机相关性肺炎患者死亡率增加相关。对于社区获得性和医院获得性肺炎患者,使用无创通气可独立降低死亡率(比值比0.35,95%置信区间0.18 - 0.68,P = 0.002)。需要有创通气和无创通气两者的患者与仅需要无创通气的患者死亡率相似(分别为21%和20%,P = 0.56)。澳大利亚和新西兰重症监护病房中的肺炎风险和死亡预测因素因肺炎类型而异。酗酒史是呼吸机相关性肺炎死亡的主要危险因素,其影响程度大于医院获得性肺炎或社区获得性肺炎中免疫抑制对死亡率的影响。无创通气与降低重症监护病房死亡率相关。实变的临床体征会恶化,而在重症监护病房入院后三天内合理调整抗生素治疗可改善社区获得性肺炎患者的死亡率。

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