Division of Medicine, Akershus University Hospital, Sykehusveien 27, 1478, Lørenskog, Norway.
Intensive Care Med. 2012 May;38(5):820-9. doi: 10.1007/s00134-012-2546-8. Epub 2012 Apr 11.
To assess the prognostic information of chromogranin A (CgA), a marker associated with adrenergic tone and myocardial function, in patients with severe sepsis.
CgA levels were measured at the time of study inclusion and 72 h later in 232 patients with severe sepsis recruited from 24 ICUs in Finland (FINNSEPSIS study).
Sixty-five patients (28%) died during the index hospitalization. CgA levels at inclusion and after 72 h correlated with several established indices of risk in sepsis. Patients who died during the hospitalization had higher baseline CgA levels than hospital survivors: 14.0 (Q1-3, 7.4-27.4) versus 9.1 (5.9-15.8) nmol/l, P = 0.002, and after 72 h: 16.2 (9.0-31.1) versus 9.8 (6.0-18.0) nmol/l, P = 0.001. Prior cardiovascular disease (P = 0.04) and cardiovascular SOFA levels on day 3 (P = 0.03) were associated with higher CgA levels after 72 h by linear regression. CgA levels on study inclusion and after 72 h were independently associated with hospital mortality by logistic regression: OR (logarithmically transformed CgA levels) 1.95 (95% CI 1.01-3.77), P = 0.046 and OR 2.03 (95% CI 1.18-3.49), P = 0.01, respectively. The prognostic accuracy was comparable for CgA measurements and SAPS II score, and the addition of CgA measurements to the SAPS II score improved risk stratification of the patients as assessed by the category-free net reclassification index. A CgA level >6.6 nmol/l on study inclusion was associated with septic shock during the hospitalization.
CgA levels measured during hospitalization for severe sepsis are associated with cardiovascular dysfunction and may provide additional prognostic information in patients with severe sepsis.
评估嗜铬粒蛋白 A(CgA)作为一种与肾上腺素能张力和心肌功能相关的标志物在严重脓毒症患者中的预后信息。
在芬兰 24 个 ICU 招募的 232 例严重脓毒症患者中,在研究纳入时和 72 小时后测量 CgA 水平(FINNSEPSIS 研究)。
65 例患者(28%)在住院期间死亡。纳入时和 72 小时后的 CgA 水平与脓毒症的几个既定风险指标相关。住院期间死亡的患者基线 CgA 水平高于住院幸存者:14.0(Q1-3,7.4-27.4)比 9.1(5.9-15.8)nmol/L,P=0.002,72 小时后:16.2(9.0-31.1)比 9.8(6.0-18.0)nmol/L,P=0.001。通过线性回归,心血管疾病病史(P=0.04)和第 3 天心血管 SOFA 评分(P=0.03)与 72 小时后的 CgA 水平升高相关。通过逻辑回归,CgA 在纳入研究时和 72 小时后的水平与住院死亡率独立相关:OR(对数转换的 CgA 水平)1.95(95%CI 1.01-3.77),P=0.046 和 OR 2.03(95%CI 1.18-3.49),P=0.01。CgA 测量值和 SAPS II 评分的预后准确性相当,将 CgA 测量值添加到 SAPS II 评分中可通过无类别净重新分类指数评估患者的风险分层。纳入研究时 CgA 水平>6.6 nmol/L 与住院期间脓毒性休克相关。
严重脓毒症患者住院期间测量的 CgA 水平与心血管功能障碍相关,可能为严重脓毒症患者提供额外的预后信息。