Ravetti Cecilia Gómez, Moura Anselmo Dornas, Vieira Érica Leandro, Pedroso Ênio Roberto Pietra, Teixeira Antônio Lúcio
Postgraduate Program in Health Sciences: Infectology and Tropical Medicine, Department of Internal Medicine, School of Medicine, UFMG, Belo Horizonte, Minas Gerais, Brazil; ICU of Mater Dei Hospital, Belo Horizonte, Minas Gerais, Brazil.
ICU of Mater Dei Hospital, Belo Horizonte, Minas Gerais, Brazil.
J Crit Care. 2015 Apr;30(2):440.e7-13. doi: 10.1016/j.jcrc.2014.12.002. Epub 2014 Dec 4.
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.
To analyze the value of interleukin (IL)-1ß, IL-6, IL-8, IL-10, IL-12, tumor necrosis factor α (TNF-α), 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.
Prospective, observational cohort study.
Tertiary level adult intensive care unit (ICU).
Seventy-five patients with severe sepsis or septic shock, 40 with cancer and 35 without.
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.
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-1ß, IL-6, IL-8, IL-12, and TNF-α 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-1ß at 48 hours were independent predictors of ICU mortality; corticosteroids requirement and levels of sTREM-1 and TNF-α at 24 hours were independent predictors of 28-day mortality.
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.
对于癌症合并严重脓毒症和感染性休克患者,先天免疫反应分子及其作为死亡率预测指标的研究较少。
分析白细胞介素(IL)-1β、IL-6、IL-8、IL-10、IL-12、肿瘤坏死因子α(TNF-α)、髓系细胞表面表达的可溶性触发受体1(sTREM-1)和高迁移率族蛋白B1(HMGB-1)作为癌症合并严重脓毒症和感染性休克患者死亡率预测指标的价值,并与无恶性肿瘤的脓毒症患者进行比较。
前瞻性观察性队列研究。
三级成人重症监护病房(ICU)。
75例严重脓毒症或感染性休克患者,其中40例患有癌症,35例未患癌症。
在ICU入院时、入院后24小时和48小时收集实验室数据。采用酶联免疫吸附测定法测量血浆中HMGB-1和sTREM-1的浓度,采用细胞计数珠阵列法测量细胞因子。
癌症患者和非癌症患者的ICU死亡率分别为40%和28.6%(P = 0.29),28天死亡率分别为45%和34.3%(P = 0.34)。促炎细胞因子IL-1β、IL-6、IL-8、IL-12和TNF-α在癌症组中的值显著更高。癌症组中48小时时的白细胞介素-10(P = 0.01)、所有测量时间点的sTREM-1(P < 0.01)和24小时时的HMGB-1(P < 0.01)的值显著更低。此外,对于癌症组,24小时(P = 0.02)和48小时(P = 0.01)时非存活患者的sTREM-1水平更高。sTREM-1预测ICU死亡率的受试者工作特征曲线下面积为0.73(95%置信区间,0.57 - 0.89;P = 0.01)。多因素逻辑分析表明,机械通气天数、48小时时的sTREM-1和IL-1β水平是ICU死亡率的独立预测因素;24小时时的皮质类固醇需求、sTREM-1和TNF-α水平是28天死亡率的独立预测因素。
与无癌症患者相比,癌症患者在脓毒症中的免疫谱不同,细胞因子、sTREM-1和HMGB-1水平的差异即证明了这一点。sTREM-1和机械通气天数被证明是癌症患者ICU死亡率和28天死亡率的良好预测指标。