Admission D-Dimer-to-Albumin Ratio as a Predictor of Poor Prognosis in Patients with Severe Fever with Thrombocytopenia Syndrome: A Retrospective Cohort Study.

IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES
Infection and Drug Resistance Pub Date : 2026-07-18 eCollection Date: 2026-01-01 DOI:10.2147/IDR.S620018
Jiankang Zhang, Yu Yu, Nannan Feng, Jianguo Rao, Xiangjun Deng, Hongjuan Yin, Liangchen Wei, Xiaobo Ding, Lifen Hu, Ying Ye
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引用次数: 0

Abstract

Purpose: Severe fever with thrombocytopenia syndrome (SFTS) is a severe viral infection associated with rapid clinical deterioration and high mortality. This study evaluated the prognostic value of the D-dimer-to-albumin ratio (DAR) in hospitalized patients with SFTS.

Patients and methods: A total of 387 patients with SFTS were retrospectively included. Correlations between biomarkers and SFTSV RNA levels were evaluated by Spearman analysis. The prognostic performance of DAR and other candidate biomarkers was assessed using ROC analysis and DeLong's test. Multivariable Cox regression and Kaplan-Meier survival analyses were performed to determine the independent prognostic value of DAR.

Results: Of the 387 included patients, 314 (81.1%) survived and 73 (18.9%) died within 28 days after admission. Among the evaluated biomarkers, DAR showed the strongest correlation with SFTSV RNA level (r = 0.438, P < 0.001). DAR also demonstrated the best discriminative ability for predicting 28-day mortality (AUC=0.810, 95% CI, 0.745-0.874). Its prognostic performance was significantly better than that of PLR, CRP, ALB/PLT, LDH/ALB, FAR, and SII, and was comparable to that of NLR and PCT. The optimal cutoff value for DAR was 0.087, with a sensitivity of 73.8% and a specificity of 79.4%, and the highest Youden index. In univariate Cox regression analysis, patients with DAR >0.087 had a significantly increased risk of 28-day mortality (HR = 7.026, 95% CI: 4.228-11.677; P < 0.001). In multivariable Cox regression analysis adjusted for age, sex, cardiovascular comorbidity, neurologic symptoms, bleeding manifestations, SFTSV RNA viral load, onset-to-admission interval, and year of disease onset, DAR remained independently associated with poor outcome (adjusted HR, 4.475; 95% CI, 2.635-7.600; P < 0.001). This association remained significant when DAR was analyzed as a continuous variable. Kaplan-Meier analysis further showed significantly lower survival probability in patients with DAR >0.087.

Conclusion: DAR was significantly associated with poor prognosis in hospitalized patients with SFTS. As a simple and readily available admission-based biomarker, DAR may be useful for early risk stratification and clinical monitoring.

入院d -二聚体与白蛋白比率作为重症发热伴血小板减少综合征患者预后不良的预测因子:一项回顾性队列研究
目的:发热伴血小板减少综合征(SFTS)是一种伴有快速临床恶化和高死亡率的严重病毒感染。本研究评估了d -二聚体-白蛋白比(DAR)在住院SFTS患者中的预后价值。患者和方法:回顾性分析387例SFTS患者。采用Spearman分析评估生物标志物与SFTSV RNA水平的相关性。采用ROC分析和DeLong检验评估DAR和其他候选生物标志物的预后表现。采用多变量Cox回归和Kaplan-Meier生存分析来确定DAR的独立预后价值。结果:387例患者中,314例(81.1%)存活,73例(18.9%)在入院后28天内死亡。在评估的生物标志物中,DAR与SFTSV RNA水平相关性最强(r = 0.438, P < 0.001)。DAR在预测28天死亡率方面也表现出最好的判别能力(AUC=0.810, 95% CI, 0.745-0.874)。其预后表现明显优于PLR、CRP、ALB/PLT、LDH/ALB、FAR、SII,与NLR、PCT相当,DAR的最佳临界值为0.087,敏感性为73.8%,特异性为79.4%,约登指数最高。在单因素Cox回归分析中,DAR >0.087患者28天死亡风险显著增加(HR = 7.026, 95% CI: 4.228-11.677; P < 0.001)。在校正了年龄、性别、心血管合并症、神经系统症状、出血表现、SFTSV RNA病毒载量、发病至入院时间间隔和发病年份的多变量Cox回归分析中,DAR仍然与不良预后独立相关(校正HR为4.475;95% CI为2.635-7.600;P < 0.001)。当DAR作为一个连续变量进行分析时,这种关联仍然显著。Kaplan-Meier分析进一步显示,DAR患者的生存率显著降低。结论:住院SFTS患者DAR与预后不良有显著相关性。DAR是一种简单易行的基于入院的生物标志物,可用于早期风险分层和临床监测。
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来源期刊
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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