Association of ischemia modified albumin with mortality in qSOFA positive sepsis patients by sepsis-3 in the emergency department

被引:6
|
作者
Park, Jonghak [1 ]
Ahn, Sejoong [1 ]
Lee, Seonggeun [1 ]
Song, Juhyun [1 ]
Moon, Sungwoo [1 ,2 ]
Kim, Jooyeong [1 ]
Cho, Hanjin [1 ]
机构
[1] Korea Univ, Ansan Hosp, Dept Emergency Med, Ansan, South Korea
[2] Natl Med Ctr, Natl Emergency Med Ctr, Seoul, South Korea
来源
关键词
Sepsis; Septic shock; Mortality; Ischemia modified albumin; Emergency department; CRITICALLY-ILL PATIENTS; MYOCARDIAL-ISCHEMIA; MARKER; PROCALCITONIN; LACTATE;
D O I
10.1016/j.ajem.2021.01.059
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: The early detection and treatment of sepsis and septic shock patients in emergency departments are critical. Ischemia modified albumin (IMA) is a biomarker produced by ischemia and oxygen free radicals which are related to the pathogenesis of sepsis-induced organ dysfunction. This study aimed to investigate whether IMA was associated with short-term mortality in quick sequential organ failure assessment (qSOFA)-positive sepsis or septic shock patients screened by the sepsis management program. Method: From September 2019 to April 2020, patients who arrived at the emergency departments with qSOFApositive sepsis or septic shock were included in this retrospective observational study. Results: Among 124 patients analyzed, IMA was higher in the non-surviving group than in the surviving group (92.6 +/- 8.1 vs. 86.8 +/- 6.2 U/mL, p < 0.001). The area under the receiver operating characteristics curve was 0.703 (95% CI: 0.572-0.833, p < 0.001). The optimal IMA cutoff was 90.45 (sensitivity 60.9%, specificity 79.2%). IMA values were independently associated with 28-day mortality in the multivariate Cox proportional hazard model (adjusted hazard ratio (aHR) = 1.16, 95% CI: 1.06-1.27, p < 0.01). Conclusions: In this study, we showed that IMA in the emergency departments was associated with 28-day mortality in qSOFA-positive sepsis and septic shock patients. Further studies are needed to evaluate the clinical value of IMA as a useful biomarker in large populations and multicenter institutions. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:72 / 77
页数:6
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