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急诊疑似感染患者单核细胞轴向光损失作为一种易于获得的预后生物标志物。

Axial light loss of monocytes as a readily available prognostic biomarker in patients with suspected infection at the emergency department.

机构信息

Department of Internal Medicine and Acute Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.

Central Diagnostic Laboratory, Division Laboratory, Pharmacy and Biomedical Genetics, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.

出版信息

PLoS One. 2022 Jul 11;17(7):e0270858. doi: 10.1371/journal.pone.0270858. eCollection 2022.

Abstract

OBJECTIVES

To evaluate the prognostic value of the coefficient of variance of axial light loss of monocytes (cv-ALL of monocytes) for adverse clinical outcomes in patients suspected of infection in the emergency department (ED).

METHODS

We performed an observational, retrospective monocenter study including all medical patients ≥18 years admitted to the ED between September 2016 and June 2019 with suspected infection. Adverse clinical outcomes included 30-day mortality and ICU/MCU admission <3 days after presentation. We determined the additional value of monocyte cv-ALL and compared to frequently used clinical prediction scores (SIRS, qSOFA, MEWS). Next, we developed a clinical model with routinely available parameters at the ED, including cv-ALL of monocytes.

RESULTS

A total of 3526 of patients were included. The OR for cv-ALL of monocytes alone was 2.21 (1.98-2.47) for 30-day mortality and 2.07 (1.86-2.29) for ICU/MCU admission <3 days after ED presentation. When cv-ALL of monocytes was combined with a clinical score, the prognostic accuracy increased significantly for all tested scores (SIRS, qSOFA, MEWS). The maximum AUC for a model with routinely available parameters at the ED was 0.81 to predict 30-day mortality and 0.81 for ICU/MCU admission.

CONCLUSIONS

Cv-ALL of monocytes is a readily available biomarker that is useful as prognostic marker to predict 30-day mortality. Furthermore, it can be used to improve routine prediction of adverse clinical outcomes at the ED.

CLINICAL TRIAL REGISTRATION

Registered in the Dutch Trial Register (NTR) und number 6916.

摘要

目的

评估单核细胞轴向光损失变异系数(单核细胞 cv-ALL)对急诊科(ED)疑似感染患者不良临床结局的预测价值。

方法

我们进行了一项观察性、回顾性单中心研究,纳入了 2016 年 9 月至 2019 年 6 月期间因疑似感染而入住 ED 的所有≥18 岁的成年住院患者。不良临床结局包括 30 天死亡率和就诊后 3 天内入住 ICU/MCU。我们确定了单核细胞 cv-ALL 的额外价值,并与常用的临床预测评分(SIRS、qSOFA、MEWS)进行了比较。接下来,我们在 ED 常规可用参数的基础上建立了一个临床模型,包括单核细胞 cv-ALL。

结果

共纳入 3526 例患者。单核细胞 cv-ALL 单独的 OR 为 30 天死亡率的 2.21(1.98-2.47),就诊后 3 天内入住 ICU/MCU 的 OR 为 2.07(1.86-2.29)。当单核细胞 cv-ALL 与临床评分相结合时,所有测试评分(SIRS、qSOFA、MEWS)的预后准确性均显著提高。ED 常规参数模型预测 30 天死亡率的最大 AUC 为 0.81,预测 ICU/MCU 入住的 AUC 为 0.81。

结论

单核细胞 cv-ALL 是一种易于获得的生物标志物,可作为预测 30 天死亡率的预后标志物。此外,它可用于改善 ED 不良临床结局的常规预测。

临床试验注册

在荷兰临床试验注册中心(NTR)注册,编号为 6916。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb73/9273078/9005479ae933/pone.0270858.g001.jpg

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