Development and validation of a novel mortality risk stratification simplified scoring scale for severe fever with thrombocytopenia syndrome

IF 8.5 1区 医学 Q1 INFECTIOUS DISEASES Clinical Microbiology and Infection Pub Date : 2025-02-06 DOI:10.1016/j.cmi.2025.02.004
Tao Chen , Meng Zhang , Qian Liu , Wensi Li , Zhilin Zeng , Chuanwen Chen , Yi Zhou , Tiantong Zhou , Yaping Li , Wei Wang , Quan Ming , Jun Zhu , Zhaohai Zeng , Feng Zhu , Weiming Yan , Peng Wang , Yuxin Niu , Yunhui Liu , Lanyue Huang , Wei Liu , Qin Ning
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Abstract

Objectives

The global incidence of severe fever with thrombocytopenia syndrome (SFTS) has markedly increased over the past decade. There is an urgent need to establish a reliable scoring system for predicting the mortality of patients with SFTS.

Methods

In this ambispective study, 714 patients with SFTS were recruited from 11 sites in China. Among these, 544 patients hospitalized for SFTS from May 2012 to June 2022 were included retrospectively in the training cohort, and 170 were prospectively enrolled between April 2021 and November 2023 in the validation cohort. Logistic regression analysis was performed to identify risk factors for 30-day mortality. A nomogram model (SFTS-logistic model) and a simplified scoring system (SFTS-Wuhan model) were established for predicting mortality. The performance of these models in terms of calibration, discrimination, and clinical utility was evaluated and validated.

Results

The 30-day mortality rate was 12.89% (92/714). The mean age was 65 years old (interquartile range, 57–71), and 322 (45.10%) patients were male. The SFTS-logistic model and SFTS-Wuhan model were developed based on seven independent risk factors, including age (adjusted OR [AOR], 1.062; 95% CI, 1.019–1.106), temperature at admission (AOR, 1.599; 95% CI, 1.095–2.336), white blood cell count (AOR, 0.799; 95% CI, 0.653–0.978), platelet count (AOR, 0.977, 95% CI, 0.959–0.996), aspartate aminotransferase (AOR, 1.001, 95% CI, 1.000–1.003), creatinine (AOR, 1.006; 95% CI, 1.001–1.011), and vasopressors use (AOR, 6.270; 95% CI, 1.397–28.146). Both models demonstrated good discrimination with areas under the receiver operating characteristic curve above 0.84, satisfactory calibration, and comparable clinical net benefit in the training and validation cohorts.

Discussion

The prognostic scoring model and its simplified surrogate can serve as robust tools for mortality risk stratification in SFTS, allowing the early identification of high-risk patients.
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开发和验证一种新的死亡率风险分层简化评分量表的重症发热伴血小板减少综合征。
目的:在过去十年中,全球发热伴血小板减少综合征(SFTS)的发病率显著增加。迫切需要建立一个可靠的评分系统来预测SFTS患者的死亡率。方法:在这项双视角研究中,从中国11个地点招募714例SFTS患者。其中,544例2012年5月至2022年6月期间因SFTS住院的患者被回顾性纳入培训队列,170例2021年4月至2023年11月期间被前瞻性纳入验证队列。采用Logistic回归分析确定30天死亡率的危险因素。建立了死亡率预测的nomogram model (SFTS-logistic model)和简化的scoring system (SFTS-Wuhan model)。评估和验证了这些模型在校准、鉴别和临床应用方面的性能。结果:30天死亡率为12.89%(92/714)。平均年龄65岁(IQR 57 ~ 71),男性322例(45.10%)。基于年龄(AOR=1.062, 95%CI(1.019 ~ 1.106))、入院时体温(AOR=1.599, 95%CI(1.095 ~ 2.336))、白细胞计数(AOR=0.799, 95%CI(0.653 ~ 0.978))、血小板计数(AOR=0.977, 95%CI(0.959 ~ 0.996))、天冬氨酸转氨酶(AOR=1.001, 95%CI(1.001 ~ 1.003))、肌酐(AOR=1.006, 95%CI(1.001 ~ 1.011))、血管升压药使用(AOR=6.270, 95%CI(1.397 ~ 28.146)) 7个独立危险因素建立SFTS-logistic模型和sfts -武汉模型。两种模型均表现出良好的辨别能力,ROC曲线下面积均在0.84以上,校准令人满意,在训练组和验证组中临床净效益相当。结论:预后评分模型及其简化的替代方法可以作为SFTS死亡风险分层的有力工具,允许早期识别高危患者。
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来源期刊
CiteScore
25.30
自引率
2.10%
发文量
441
审稿时长
2-4 weeks
期刊介绍: Clinical Microbiology and Infection (CMI) is a monthly journal published by the European Society of Clinical Microbiology and Infectious Diseases. It focuses on peer-reviewed papers covering basic and applied research in microbiology, infectious diseases, virology, parasitology, immunology, and epidemiology as they relate to therapy and diagnostics.
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