Early prognostic factors in septic shock cancer patients: a prospective study with a proteomic approach

被引:7
作者
Mokart, D. [1 ,2 ]
Saillard, C. [3 ]
Zemmour, C. [4 ]
Bisbal, M. [1 ,2 ]
Sannini, A. [1 ]
Chow-Chine, L. [1 ]
Brun, J. -P. [1 ]
Faucher, M. [1 ]
Boher, J. -M. [4 ]
Toiron, Y. [5 ,6 ]
Chabannon, C. [6 ,7 ,8 ,9 ]
Borg, J. -P. [5 ,6 ,7 ,10 ]
Goncalves, A. [5 ,6 ,7 ,8 ,11 ]
Camoin, L. [5 ,6 ]
机构
[1] Inst Paoli Calmettes, Dept Anesthesiol & Crit Care, Polyvalent Intens Care Unit, 232 Blvd Sainte Marguerite, F-13009 Marseille 09, France
[2] GRRROH, Paris, France
[3] Inst Paoli Calmettes, Dept Hematol, Marseille, France
[4] Inst Paoli Calmettes, Dept Clin Res & Innovat, Marseille, France
[5] CRCM, U1068, INSERM, Marseille, France
[6] CRCM, Marseille, France
[7] CRCM, UMR7258, CNRS, Marseille, France
[8] Aix Marseille Med Univ, Marseille, France
[9] Inst Paoli Calmettes, Cell Therapy Dept, Marseille, France
[10] Aix Marseille Univ, UM105, Marseille, France
[11] Inst Paoli Calmettes, Dept Med Oncol, Marseille, France
关键词
VON-WILLEBRAND-FACTOR; SEVERE SEPSIS; SYSTEMIC INFLAMMATION; DIASTOLIC DYSFUNCTION; NEUTROPENIC PATIENTS; CLEAVING PROTEASE; FLUID BALANCE; BIOMARKERS; MORTALITY; SURVIVAL;
D O I
10.1111/aas.13060
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundOrgan failures are the main prognostic factors in septic shock. The aim was to assess classical clinico-biological parameters evaluating organ dysfunctions at intensive care unit admission, combined with proteomics, on day-30 mortality in critically ill onco-hematology patients admitted to the intensive care unit for septic shock. MethodsThis was a prospective monocenter cohort study. Clinico-biological parameters were collected at admission. Plasma proteomics analyses were performed, including protein profiling using isobaric Tag for Relative and Absolute Quantification (iTRAQ) and subsequent validation by ELISA. ResultsSixty consecutive patients were included. Day-30 mortality was 47%. All required vasopressors, 32% mechanical ventilation, 33% non-invasive ventilation and 13% renal-replacement therapy. iTRAQ-based proteomics identified von Willebrand factor as a protein of interest. Multivariate analysis identified four factors independently associated with day-30 mortality: positive fluid balance in the first 24 h (odds ratio = 1.06, 95% CI = 1.01-1.12, P = 0.02), severe acute respiratory failure (odds ratio = 6.14(,) 95% CI = 1.04-36.15, P = 0.04), von Willebrand factor plasma level > 439 ng/ml (odds ratio = 9.7, 95% CI = 1.52-61.98, P = 0.02), and bacteremia (odds ratio = 6.98, 95% CI = 1.17-41.6, P = 0.03). ConclusionEndothelial dysfunction, revealed by proteomics, appears as an independent prognostic factor on day-30 mortality, as well as hydric balance, acute respiratory failure and bacteremia, in critically ill cancer patients admitted to the intensive care unit. Endothelial failure is underestimated in clinical practice and represents an innovative therapeutic target.
引用
收藏
页码:493 / 503
页数:11
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