Prognostic and Pathogenetic Value of Combining Clinical and Biochemical Indices in Patients With Acute Lung Injury

被引:327
作者
Ware, Lorraine B. [1 ]
Koyama, Tatsuki [2 ]
Billheimer, Dean [3 ,4 ]
Wu, William [2 ]
Bernard, Gordon R. [1 ]
Thompson, B. Taylor [5 ]
Brower, Roy G. [6 ]
Standiford, Theodore J. [7 ]
Martin, Thomas R. [8 ]
Matthay, Michael A. [9 ,10 ,11 ]
机构
[1] Vanderbilt Univ, Div Allergy Pulm & Crit Care Med, Dept Med, Sch Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Biostat, Nashville, TN 37232 USA
[3] Univ Arizona, Dept Agr & Biosyst Engn, Tucson, AZ USA
[4] Univ Arizona, Arizona Stat Consulting Lab, Tucson, AZ USA
[5] Massachusetts Gen Hosp, Boston, MA 02114 USA
[6] Johns Hopkins Univ Hosp, Baltimore, MD 21287 USA
[7] Univ Michigan, Ann Arbor, MI 48109 USA
[8] Univ Washington & Med Serv, VA Puget Sound Healthcare Syst, Seattle, WA USA
[9] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[10] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[11] Univ Calif San Francisco, Dept Anesthesia, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
RESPIRATORY-DISTRESS-SYNDROME; MYOCARDIAL-INFARCTION; HOSPITAL MORTALITY; OUTCOME PREDICTION; ACUTE PHYSIOLOGY; RABBITS; INTERLEUKIN-8; PROTEIN; INFLAMMATION; VENTILATION;
D O I
10.1378/chest.09-1484
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Background: No single clinical or biologic marker reliably predicts clinical outcomes in acute lung injury (ALI)/ARDS. We hypothesized that a combination of biologic and clinical markers would be superior to either biomarkers or clinical factors alone in predicting ALI/ARDS mortality and would provide insight into the pathogenesis of clinical ALI/ARDS. Methods: Eight biologic markers that reflect endothelial and epithelial injury, inflammation, and coagulation (von Willebrand factor antigen, surfactant protein D [SP-D]) tumor necrosis factor receptor-1, interleukin [IL]-6, IL-8, intercellular adhesion molecule-1, protein C, plasminogen activator inhibitor-1) were measured in baseline plasma from 549 patients in the ARDSNet trial of low vs high positive end-expiratory pressure. Mortality was modeled with multivariable logistic regression. Predictors were selected using backward elimination. Comparisons between candidate models were based on the receiver operating characteristics (ROC) and tests of integrated discrimination improvement. Results: Clinical predictors (Acute Physiology And Chronic Health Evaluation III [APACHE III], organ failures, age, underlying cause, alveolar-arterial oxygen gradient, plateau pressure) predicted mortality with an area under the ROC curve (AUC) of 0.82; a combination of eight biomarkers and the clinical predictors had an AUC of 0.85. The best performing hiomarkers were the neutrophil chemotactic factor, IL-8, and SP-D, a product of alveolar type 2 cells, supporting the concept that acute inflammation and alveolar epithelial injury are important pathogenetic pathways in human ALI/ARDS. Conclusions: A combination of biomarkers and clinical predictors is superior to clinical predictors or biomarkers alone for predicting mortality in ALI/ARDS and may be useful for stratifying patients in clinical trials. From a pathogenesis perspective, the degree of acute inflammation and alveolar epithelial injury are highly associated with the outcome of human ALI/ARDS. CHEST 2010; 137(2):288-296
引用
收藏
页码:288 / 296
页数:9
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