Midregional pro-atrial natriuretic peptide and procalcitonin improve survival prediction in VAP

被引:25
作者
Boeck, L. [1 ]
Eggimann, P. [4 ]
Smyrnios, N. [5 ]
Pargger, H. [2 ]
Thakkar, N. [5 ]
Siegemund, M. [2 ]
Marsch, S. [3 ]
Rakic, J. [1 ]
Tamm, M. [1 ]
Stolz, D. [1 ,6 ]
机构
[1] Univ Basel Hosp, Clin Pulm Med & Resp Cell Res, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Div Anesthesiol & Surg Intens Care Med, CH-4031 Basel, Switzerland
[3] Univ Basel Hosp, Div Med Intens Care Med, CH-4031 Basel, Switzerland
[4] Univ Lausanne Hosp, Dept Adult Crit Care Med, Lausanne, Switzerland
[5] UMass Mem Med Ctr, Div Pulm Allergy & Crit Care Med, Worcester, MA USA
[6] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
基金
瑞士国家科学基金会;
关键词
Biomarker; midregional pro-atrial natriuretic peptide; procalcitonin; prognosis; risk stratification; ventilator-associated pneumonia; VENTILATOR-ASSOCIATED PNEUMONIA; C-REACTIVE PROTEIN; INTENSIVE-CARE UNITS; PROGNOSTIC VALUE; SERUM PROCALCITONIN; CONTROLLED-TRIAL; TERMINAL-PROBNP; HEART-FAILURE; SOFA SCORE; APACHE-II;
D O I
10.1183/09031936.00023810
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Ventilator-associated pneumonia (VAP) affects mortality, morbidity and cost of critical care. Reliable risk estimation might improve end-of-life decisions, resource allocation and outcome. Several scoring systems for survival prediction have been established and optimised over the last decades. Recently, new biomarkers have gained interest in the prognostic field. We assessed whether midregional pro-atrial natriuretic peptide (MR-proANP) and procalcitonin (PCT) improve the predictive value of the Simplified Acute Physiologic Score (SAPS) II and Sequential Related Organ Failure Assessment (SOFA) in VAP. Specified end-points of a prospective multinational trial including 101 patients with VAP were analysed. Death < 28 days after VAP onset was the primary end-point. MR-proANP and PCT were elevated at the onset of VAP in nonsurvivors compared with survivors (p=0.003 and p=0.017, respectively) and their slope of decline differed significantly (p=0.018 and p=0.039, respectively). Patients with the highest MR-proANP quartile at VAP onset were at increased risk for death (log rank p=0.013). In a logistic regression model, MR-proANP was identified as the best predictor of survival. Adding MR-proANP and PCT to SAPS II and SOFA improved their predictive properties (area under the curve 0.895 and 0.880). We conclude that the combination of two biomarkers, MR-proANP and PCT, improve survival prediction of clinical severity scores in VAP.
引用
收藏
页码:595 / 603
页数:9
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