sTREM-1 predicts intensive care unit and 28-day mortality in cancer patients with severe sepsis and septic shock

被引:46
作者
Ravetti, Cecilia Gomez [1 ,2 ]
Moura, Anselmo Dornas [2 ]
Vieira, Erica Leandro [1 ,3 ]
Pietra Pedroso, Enio Roberto [1 ]
Teixeira, Antonio Lucio [1 ,3 ]
机构
[1] Univ Fed Minas Gerais, Sch Med, Dept Internal Med, Postgrad Program Hlth Sci Infectol & Trop Med, Belo Horizonte, MG, Brazil
[2] ICU Mater Dei Hosp, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Sch Med, Interdisciplinary Lab Med Invest, Belo Horizonte, MG, Brazil
关键词
Septic shock; Severe sepsis; Cancer; Intensive care unit; Cytokines sTREM-1; HMGB-1; CRITICALLY-ILL PATIENTS; MYELOID CELLS-1; OUTCOMES; PROTEIN; EPIDEMIOLOGY; NEUTROPENIA; MANAGEMENT; ADMISSION;
D O I
10.1016/j.jcrc.2014.12.002
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Introduction: The innate immune response molecules and their use as a predictor of mortality in cancer patients with severe sepsis and septic shock are poorly investigated. Objective: To analyze the value of interleukin (IL)-1 beta, IL-6, IL-8, IL-10, IL-12, tumor necrosis factor alpha (TNF-alpha), soluble triggering receptor expressed on myeloid cells 1 (sTREM-1), and high-mobility group box 1 (HMGB-1) as predictors of mortality in cancer patients with severe sepsis and septic shock compared with septic patients without malignancies. Design: Prospective, observational cohort study. Setting: Tertiary level adult intensive care unit (ICU). Subjects: Seventy-five patients with severe sepsis or septic shock, 40 with cancer and 35 without. Interventions and Measurements: Laboratory data were collected at ICU admission, 24 and 48 hours after. Plasma concentrations of HMGB-1 and sTREM-1 were measured by enzyme-linked immunosorbent assay, whereas cytokines were measured by cytometric bead array. Results: Intensive care unit mortality in cancer and noncancer patients was 40% and 28.6% (P = .29), and 28-day mortality was 45% and 34.3% (P = .34). Proinflammatory cytokines IL-1 beta, IL-6, IL-8, IL-12, and TNF-alpha showed significantly higher values in the cancer group. Interleukin-10 at 48 hours (P = .01), sTREM-1 in all measurements (P < .01) and HMGB-1 at 24 hours (P = .01) showed significantly lower values in the cancer group. In addition, for the cancer group, sTREM-1 at 24 hours (P = .02) and 48 hours (P = .01) showed higher levels in nonsurvivors patients. The area under the receiver operating characteristic curve for predicting ICU mortality for sTREM-1 was 0.73 (95% confidence interval, 0.57-0.89; P = .01). Multivariate logistic analysis showed that the days spent in mechanical ventilation and levels of sTREM-1 and IL-1 beta at 48 hours were independent predictors of ICU mortality; corticosteroids requirement and levels of sTREM-1 and TNF-alpha at 24 hours were independent predictors of 28-day mortality. Conclusions: Patients with cancer have different immune profile in sepsis when compared with patients without cancer, as demonstrated for levels of cytokines, sTREM-1 and HMGB-1. sTREM-1 and days spent in mechanical ventilation proved to be good predictors of ICU and 28-day mortality in cancer patients. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:440.e7 / 440.e13
页数:7
相关论文
共 40 条
[1]
Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[2]
[Anonymous], 1991, CHEST, V101, P1644
[3]
Predictors of short-term mortality in critically ill patients with solid malignancies [J].
Azoulay, E ;
Moreau, D ;
Alberti, C ;
Leleu, G ;
Adrie, C ;
Barboteu, M ;
Cottu, P ;
Levy, V ;
Le Gall, JR ;
Schlemmer, B .
INTENSIVE CARE MEDICINE, 2000, 26 (12) :1817-1823
[4]
Soluble TREM-1 is not suitable for distinguishing between systemic inflammatory response syndrome and sepsis survivors and nonsurvivors in the early stage of acute inflammation [J].
Bopp, Christian ;
Hofer, Stefan ;
Bouchon, Axel ;
Zimmermann, Johannes B. ;
Martin, Eike ;
Weigand, Markus A. .
EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 2009, 26 (06) :504-507
[5]
Toward resolving the challenges of sepsis diagnosis [J].
Carrigan, SD ;
Scott, G ;
Tabrizian, M .
CLINICAL CHEMISTRY, 2004, 50 (08) :1301-1314
[6]
The epidemiology of sepsis in patients with malignancy [J].
Danai, Pajman A. ;
Moss, Marc ;
Mannino, David M. ;
Martin, Greg S. .
CHEST, 2006, 129 (06) :1432-1440
[7]
Underlying disorders and their impact on the host response to infection [J].
Dhainaut, JF ;
Claessens, YE ;
Janes, J ;
Nelson, DR .
CLINICAL INFECTIOUS DISEASES, 2005, 41 :S481-S489
[8]
Soluble triggering receptor expressed on myeloid cells 1 as an anti-inflammatory mediator in sepsis [J].
Giamarellos-Bourboulis, EJ ;
Zakynthinos, S ;
Baziaka, F ;
Papadomichelakis, E ;
Virtzili, S ;
Koutoukas, P ;
Armaganidis, A ;
Giamarellou, H ;
Roussos, C .
INTENSIVE CARE MEDICINE, 2006, 32 (02) :237-243
[9]
Surface triggering receptor expressed on myeloid cells 1 expression patterns in septic shock [J].
Gibot, S ;
Le Renard, PE ;
Bollaert, PE ;
Kolopp-Sarda, MN ;
Béné, MC ;
Faure, GC ;
Lévy, B .
INTENSIVE CARE MEDICINE, 2005, 31 (04) :594-597
[10]
Plasma level of a triggering receptor expressed on myeloid cells-1:: Its diagnostic accuracy in patients with suspected sepsis [J].
Gibot, S ;
Kolopp-Sarda, MN ;
Béné, MC ;
Cravoisy, A ;
Levy, B ;
Faure, GC ;
Bollaert, PE .
ANNALS OF INTERNAL MEDICINE, 2004, 141 (01) :9-15