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可溶性髓系细胞触发受体-1(sTREM-1)为基础的算法对坦桑尼亚门诊发热成人的预后准确性。

Prognostic Accuracy of Soluble Triggering Receptor Expressed on Myeloid Cells (sTREM-1)-based Algorithms in Febrile Adults Presenting to Tanzanian Outpatient Clinics.

机构信息

Sandra Rotman Centre for Global Health, University Health Network-Toronto General Hospital, Canada.

Infectious Diseases Service, University Hospital of Lausanne, Switzerland.

出版信息

Clin Infect Dis. 2020 Mar 17;70(7):1304-1312. doi: 10.1093/cid/ciz419.

Abstract

BACKGROUND

The inability to identify individuals with acute fever at risk of death is a barrier to effective triage and management of severe infections, especially in low-resource settings. Since endothelial and immune activation contribute to the pathogenesis of various distinct life-threatening infections, we hypothesized that measuring mediators of these pathways at clinical presentation would identify febrile adults at risk of death.

METHODS

Plasma concentrations of markers of endothelial (angiopoetin-1/2, soluble fms-like tyrosine kinase-1, soluble vascular cell adhesion molecule-1, soluble intercellular adhesion molecule-1) and immune (soluble triggering receptor expressed on myeloid cells [sTREM-1], interleukin-6, interleukin-8, chitinase-3-like protein-1, soluble tumor necrosis factor receptor-1, procalcitonin [PCT], C-reactive protein [CRP]) activation pathways were determined in consecutive adults with acute fever (≥38°C) at presentation to outpatient clinics in Dar es Salaam, Tanzania. We evaluated the accuracy of these mediators in predicting all-cause mortality and examined whether markers could improve the prognostic accuracy of clinical scoring systems, including the quick sequential organ failure assessment (qSOFA) and Glasgow coma scale (GCS).

RESULTS

Of 507 febrile adults, 32 died (6.3%) within 28 days of presentation. We found that sTREM-1 was the best prognostic marker for 28-day mortality (area under the receiver operating characteristic [AUROC] 0.87, 95% confidence interval [CI] 0.81-0.92) and was significantly better than CRP (P < .0001) and PCT (P = .0001). The prognostic accuracy of qSOFA and the GCS were significantly enhanced when sTREM-1 was added (0.80 [95% CI 0.76-0.83] to 0.91 [95% CI 0.88-0.94; P < .05] and 0.72 [95% CI 0.63-0.80] to 0.94 [95% CI 0.91-0.97; P < .05], respectively).

CONCLUSIONS

Measuring sTREM-1 at clinical presentation can identify febrile individuals at risk of all-cause febrile mortality. Adding severity markers such as sTREM-1 to simple clinical scores could improve the recognition and triage of patients with life-threatening infections in resource-limited settings.

摘要

背景

无法识别有急性发热风险的个体,这是有效分诊和严重感染管理的障碍,尤其是在资源匮乏的环境中。由于内皮细胞和免疫激活有助于各种不同危及生命的感染的发病机制,我们假设在临床出现时测量这些途径的介质会识别出有死亡风险的发热成年人。

方法

连续测量来自坦桑尼亚达累斯萨拉姆门诊就诊的急性发热(≥38°C)成人的内皮(血管生成素 1/2、可溶性 fms 样酪氨酸激酶 1、可溶性血管细胞黏附分子 1、可溶性细胞间黏附分子 1)和免疫(可溶性髓系细胞触发受体 1[sTREM-1]、白细胞介素 6、白细胞介素 8、壳聚糖酶 3 样蛋白 1、可溶性肿瘤坏死因子受体 1、降钙素[PCT]、C 反应蛋白[CRP])激活途径的标志物的血浆浓度。我们评估了这些介质预测全因死亡率的准确性,并研究了标志物是否可以提高临床评分系统(包括快速序贯器官衰竭评估[qSOFA]和格拉斯哥昏迷评分[GCS])的预后准确性。

结果

在 507 名发热成人中,有 32 人(6.3%)在就诊后 28 天内死亡。我们发现 sTREM-1 是预测 28 天死亡率的最佳预后标志物(接受者操作特征曲线 [AUROC] 0.87,95%置信区间 [CI] 0.81-0.92),并且明显优于 CRP(P <.0001)和 PCT(P =.0001)。当添加 sTREM-1 时,qSOFA 和 GCS 的预后准确性显著提高(0.80 [95% CI 0.76-0.83]至 0.91 [95% CI 0.88-0.94;P <.05]和 0.72 [95% CI 0.63-0.80]至 0.94 [95% CI 0.91-0.97;P <.05])。

结论

在临床出现时测量 sTREM-1 可以识别有全因发热死亡率风险的发热个体。在简单的临床评分中添加严重程度标志物(如 sTREM-1)可以提高资源有限环境中危及生命的感染患者的识别和分诊。

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