Zhao Yongzhen, Jia Yumei, Li Chunsheng, Fang Yingying, Shao Rui
Department of Emergency Medicine, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China; Beijing Key Laboratory of Cardiopulmonary-Cerebral Resuscitation, Beijing Chaoyang Hospital, Capital Medical University, Beijing,China.
Department of Endocrinology, Beijing Chaoyang Hospital Affiliated to Capital Medical University, Beijing, China.
Am J Emerg Med. 2018 Jan;36(1):43-48. doi: 10.1016/j.ajem.2017.07.002. Epub 2017 Jul 4.
To evaluate the efficacy of soluble programmed death-1 (sPD-1) for risk stratification and prediction of 28-day mortality in patients with sepsis, we compared serum sPD-1 with procalcitonin (PCT), C-reactive protein (CRP), and the Mortality in Emergency Department Sepsis (MEDS) score.
A total of 60 healthy volunteers and 595 emergency department (ED) patients were recruited for this prospective cohort study. According to the severity of their condition on ED arrival, the patients were allocated to the systemic inflammatory response syndrome group (130 cases), sepsis group (276 cases), severe sepsis group (121 cases), and septic shock group (68 cases). In addition, all patients with sepsis were also divided into the survivor group (349 cases) and nonsurvivor group (116 cases) according to the 28-day outcomes.
When the severity of sepsis increased, the levels of sPD-1 gradually increased. The levels of sPD-1, PCT, CRP and the MEDS score were also higher in the nonsurvivor group compared to the survivor group. Logistic regression suggested that sPD-1, PCT, and the MEDS score were independent risk factors for 28-day mortality of patients with sepsis. Area under the curve (AUC) of sPD-1, PCT and the MEDS score for 28-day mortality was 0.725, 0.693, and 0.767, respectively, and the AUC was improved when all 3 factors were combined (0.843).
Serum sPD-1 is positively correlated with the severity of sepsis, and it is valuable for risk stratification of patients and prediction of 28-day mortality. Combining sPD-1 with PCT and the MEDS score improves the prognostic evaluation.
为评估可溶性程序性死亡因子1(sPD-1)在脓毒症患者28天死亡率风险分层及预测中的效能,我们将血清sPD-1与降钙素原(PCT)、C反应蛋白(CRP)及急诊科脓毒症死亡率(MEDS)评分进行了比较。
本前瞻性队列研究共纳入60名健康志愿者及595名急诊科患者。根据患者抵达急诊科时病情的严重程度,将患者分为全身炎症反应综合征组(130例)、脓毒症组(276例)、严重脓毒症组(121例)及脓毒性休克组(68例)。此外,所有脓毒症患者还根据28天预后分为存活组(349例)和非存活组(116例)。
随着脓毒症严重程度增加,sPD-1水平逐渐升高。非存活组的sPD-1、PCT、CRP水平及MEDS评分也高于存活组。Logistic回归分析表明,sPD-1、PCT及MEDS评分是脓毒症患者28天死亡率的独立危险因素。sPD-1、PCT及MEDS评分对28天死亡率的曲线下面积(AUC)分别为0.725、0.693及0.767,当将这3个因素联合时AUC有所提高(0.843)。
血清sPD-1与脓毒症严重程度呈正相关,对患者风险分层及28天死亡率预测具有重要价值。将sPD-1与PCT及MEDS评分联合可改善预后评估。