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可溶性尿激酶型纤溶酶原激活物受体与坏死性软组织感染患者的死亡率和临床严重程度相关:一项前瞻性、观察性队列研究的结果。

SuPAR correlates with mortality and clinical severity in patients with necrotizing soft-tissue infections: results from a prospective, observational cohort study.

机构信息

Department of Anesthesiology, Center of Head and Orthopedics, Copenhagen University Hospital (Rigshospitalet), Copenhagen Ø, Denmark.

Clinical Research Center, Copenhagen University Hospital (Hvidovre), Hvidovre, Denmark.

出版信息

Sci Rep. 2019 Mar 25;9(1):5098. doi: 10.1038/s41598-019-41688-y.

DOI:10.1038/s41598-019-41688-y
PMID:30911053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6434142/
Abstract

Necrotizing soft tissue infections (NSTI) have a 90-day mortality rate of 18-22%. Tools are needed for estimating the prognosis and severity of NSTI upon admission. We evaluated soluble urokinase-type plasminogen activator receptor (suPAR) levels at admission as a prognostic marker of NSTI severity and mortality. In a prospective, observational cohort study, suPAR was measured in 200 NSTI patients. We compared admission suPAR levels in survivors and non-survivors, patients with septic shock and non-shock, amputation and non-amputation, correlations with Simplified Acute Physiology Score II (SAPS II) and the Sequential Organ Failure Assessment (SOFA) score. Admission suPAR levels were higher in septic shock vs. non-septic shock patients (9.2 vs. 5.8 ng/mL, p-value < 0.001) and non-survivors vs. survivors (11 vs. 6.1 ng/mL, p-value < 0.001) and correlated with SAPS II (r = 0.52, p < 0.001) and SOFA score (r = 0.64, p < 0.001). Elevated suPAR upon admission was associated with 90-day mortality (log-rank test p < 0.001), however not after adjustment for age, sex, and SOFA score. The AUC for suPAR and 90-day mortality was 0.77. We found that suPAR is a promising candidate for prognosis and severity in patients with NSTI.

摘要

坏死性软组织感染 (NSTI) 的 90 天死亡率为 18-22%。需要有工具来评估入院时 NSTI 的预后和严重程度。我们评估了入院时可溶性尿激酶型纤溶酶原激活物受体 (suPAR) 水平作为 NSTI 严重程度和死亡率的预后标志物。在一项前瞻性观察队列研究中,我们测量了 200 例 NSTI 患者的 suPAR。我们比较了存活者和非存活者、感染性休克和非感染性休克患者、截肢和非截肢患者的入院 suPAR 水平,以及与简化急性生理学评分 II (SAPS II) 和序贯器官衰竭评估 (SOFA) 评分的相关性。感染性休克患者的入院 suPAR 水平高于非感染性休克患者 (9.2 vs. 5.8 ng/mL,p 值 < 0.001),非存活者高于存活者 (11 vs. 6.1 ng/mL,p 值 < 0.001),与 SAPS II (r = 0.52,p < 0.001) 和 SOFA 评分 (r = 0.64,p < 0.001) 相关。入院时 suPAR 升高与 90 天死亡率相关 (对数秩检验 p < 0.001),但在校正年龄、性别和 SOFA 评分后无相关性。suPAR 和 90 天死亡率的 AUC 为 0.77。我们发现 suPAR 是预测 NSTI 患者预后和严重程度的有前途的候选标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/8691400e4fa4/41598_2019_41688_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/e82d82ccc7c8/41598_2019_41688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/a2125f26fe9b/41598_2019_41688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/6573d8388b43/41598_2019_41688_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/8691400e4fa4/41598_2019_41688_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/e82d82ccc7c8/41598_2019_41688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/a2125f26fe9b/41598_2019_41688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/6573d8388b43/41598_2019_41688_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e57/6434142/8691400e4fa4/41598_2019_41688_Fig4_HTML.jpg

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