Schupp Tobias, Weidner Kathrin, Rusnak Jonas, Jawhar Schanas, Forner Jan, Dulatahu Floriana, Brück Lea Marie, Lübke Johannes, Hoffmann Ursula, Bertsch Thomas, Behnes Michael, Akin Ibrahim
Department of Cardiology, Angiology, Haemostaseology and Medical Intensive Care, University Medical Centre Mannheim, Medical Faculty Mannheim, Heidelberg University, Heidelberg.
European Center for AngioScience (ECAS) and German Center for Cardiovascular Research (DZHK) partner site Heidelberg/Mannheim.
Blood Coagul Fibrinolysis. 2023 Apr 1;34(3):161-170. doi: 10.1097/MBC.0000000000001197. Epub 2023 Jan 31.
The study investigates the diagnostic and prognostic value of fibrinogen and the albumin-to-fibrinogen-ratio (AFR) in patients with sepsis and septic shock. Limited data regarding the prognostic value of fibrinogen and AFR during the course of sepsis or septic shock are available. Consecutive patients with sepsis and septic shock from 2019 to 2021 were included monocentrically. Blood samples were retrieved from the day of disease onset (day 1), as well as on day 2 and 3. Firstly, the diagnostic value of fibrinogen and the AFR for the diagnosis of a septic shock was tested. Secondly, the prognostic value of fibrinogen and AFR was tested with regard to the 30-day all-cause mortality. Statistical analyses included univariable t-tests, Spearman's correlations, C-statistics, Kaplan-Meier and multivariable Cox regression analyses. Ninety-one patients with sepsis and septic shock were included. With an area under the curve (AUC) of 0.653-0.801, fibrinogen discriminated patients with septic shock from those with sepsis. In the septic shock group, fibrinogen levels were shown to decrease from day 1 to 3 (median decrease 41%). In line, fibrinogen was a reliable predictor for 30-day all-cause mortality (AUC 0.661-0.744), whereas fibrinogen levels less than 3.6 g/l were associated with an increased risk of 30-day all-cause mortality (78 vs. 53%; log rank P = 0.004; hazard ratio = 2.073; 95% confidence interval 1.233-3.486; P = 0.006), which was still observed after multivariable adjustment. In contrast, the AFR was no longer associated with the risk of mortality after multivariable adjustment. Fibrinogen was a reliable diagnostic and prognostic tool for the diagnosis of septic shock as well as for 30-day all-cause mortality and superior compared with the AFR in patients admitted with sepsis or septic shock.
该研究调查了纤维蛋白原和白蛋白与纤维蛋白原比值(AFR)在脓毒症和脓毒性休克患者中的诊断和预后价值。关于脓毒症或脓毒性休克病程中纤维蛋白原和AFR预后价值的数据有限。纳入了2019年至2021年单中心连续的脓毒症和脓毒性休克患者。在疾病发作当天(第1天)以及第2天和第3天采集血样。首先,测试纤维蛋白原和AFR对脓毒性休克诊断的价值。其次,测试纤维蛋白原和AFR关于30天全因死亡率的预后价值。统计分析包括单变量t检验、Spearman相关性分析、C统计量、Kaplan-Meier分析和多变量Cox回归分析。纳入了91例脓毒症和脓毒性休克患者。纤维蛋白原曲线下面积(AUC)为0.653 - 0.801,可区分脓毒性休克患者和脓毒症患者。在脓毒性休克组中,纤维蛋白原水平从第1天到第3天呈下降趋势(中位数下降41%)。同样,纤维蛋白原是30天全因死亡率的可靠预测指标(AUC为0.661 - 0.744),而纤维蛋白原水平低于3.6 g/L与30天全因死亡率风险增加相关(78%对53%;对数秩检验P = 0.004;风险比 = 2.073;95%置信区间1.233 - 3.486;P = 0.006),多变量调整后仍可观察到。相比之下,多变量调整后AFR与死亡风险不再相关。纤维蛋白原是诊断脓毒性休克以及30天全因死亡率的可靠诊断和预后工具,在脓毒症或脓毒性休克患者中优于AFR。