Evaluation of Sepsis Severity Using Combined High-Density Lipoprotein and Red Cell Distribution Width Indicators.

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
British journal of hospital medicine Pub Date : 2024-12-30 Epub Date: 2024-12-27 DOI:10.12968/hmed.2024.0473
Yan Gao, Yao Chen, Li Gao
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引用次数: 0

Abstract

Aims/Background Sepsis is a life-threatening condition resulting from dysregulated immune responses to infection, leading to organ dysfunction. High-density lipoprotein (HDL) and red cell distribution width (RDW) have shown significant correlations with sepsis severity, yet the combined prognostic value of HDL and RDW in evaluating sepsis severity and outcomes remains unclear. This study examines the relationship between HDL and RDW levels and sepsis severity, as well as evaluates the combined utility of these markers in predicting disease severity and patient outcomes. Methods This retrospective study included 103 patients diagnosed with sepsis. Clinical data, including HDL and RDW levels, were collected for analysis. Patients were divided into shock and non-shock groups based on the presence of septic shock and into survival and death groups based on 30-day in-hospital mortality. Multivariate logistic regression was used to identify factors influencing sepsis severity and prognosis, while the predictive value of HDL in combination with RDW was evaluated using receiver operating characteristic (ROC) curve analysis. Results Multivariate analysis identified sequential organ failure assessment (SOFA) score (OR = 6.566), interleukin-6 (IL-6) (OR = 2.568), HDL (OR = 0.864), and RDW (OR = 4.052) as independent predictors of sepsis severity (p < 0.05 for all). ROC analysis demonstrated that HDL combined with RDW yielded the highest diagnostic accuracy for sepsis severity, with an area under curve (AUC) of 0.962, sensitivity of 97.56%, and specificity of 91.94%. Additionally, SOFA score (OR = 2.354), interleukin-6 (IL-6) (OR = 1.446), HDL (OR = 0.870), and RDW (OR = 3.502) were independent prognostic indicators (p < 0.05 for all). ROC analysis for prognosis showed that HDL combined with RDW had the highest predictive efficacy for the prognosis of sepsis, with an AUC of 0.922, sensitivity of 79.31%, and specificity of 93.24%. Conclusion The combination of HDL and RDW is a robust indicator for the evaluation of sepsis severity and is a valuable prognostic tool for assessing 30-day mortality risk in sepsis patients.

高密度脂蛋白与红细胞分布宽度联合评价脓毒症严重程度。
目的/背景脓毒症是一种危及生命的疾病,由感染免疫反应失调引起,导致器官功能障碍。高密度脂蛋白(HDL)和红细胞分布宽度(RDW)与脓毒症严重程度有显著相关性,但HDL和RDW在评估脓毒症严重程度和结局方面的联合预后价值尚不清楚。本研究探讨了HDL和RDW水平与脓毒症严重程度之间的关系,并评估了这些标志物在预测疾病严重程度和患者预后方面的综合效用。方法对103例败血症患者进行回顾性研究。收集临床数据,包括HDL和RDW水平进行分析。根据是否存在感染性休克将患者分为休克组和非休克组,根据30天住院死亡率将患者分为生存组和死亡组。采用多因素logistic回归分析脓毒症严重程度及预后的影响因素,采用受试者工作特征(ROC)曲线分析评价HDL联合RDW的预测价值。结果多因素分析发现,顺序器官衰竭评分(SOFA) (OR = 6.566)、白细胞介素-6 (IL-6) (OR = 2.568)、HDL (OR = 0.864)和RDW (OR = 4.052)是脓毒症严重程度的独立预测因子(均p < 0.05)。ROC分析显示,HDL联合RDW对脓毒症严重程度的诊断准确率最高,曲线下面积(AUC)为0.962,敏感性为97.56%,特异性为91.94%。此外,SOFA评分(OR = 2.354)、白细胞介素-6 (IL-6) (OR = 1.446)、HDL (OR = 0.870)、RDW (OR = 3.502)为独立预后指标(均p < 0.05)。预后ROC分析显示,HDL联合RDW对脓毒症预后的预测效果最高,AUC为0.922,敏感性为79.31%,特异性为93.24%。结论HDL和RDW联合检测是评估脓毒症严重程度的可靠指标,是评估脓毒症患者30天死亡风险的有价值的预后工具。
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来源期刊
British journal of hospital medicine
British journal of hospital medicine 医学-医学:内科
CiteScore
1.50
自引率
0.00%
发文量
176
审稿时长
4-8 weeks
期刊介绍: British Journal of Hospital Medicine was established in 1966, and is still true to its origins: a monthly, peer-reviewed, multidisciplinary review journal for hospital doctors and doctors in training. The journal publishes an authoritative mix of clinical reviews, education and training updates, quality improvement projects and case reports, and book reviews from recognized leaders in the profession. The Core Training for Doctors section provides clinical information in an easily accessible format for doctors in training. British Journal of Hospital Medicine is an invaluable resource for hospital doctors at all stages of their career. The journal is indexed on Medline, CINAHL, the Sociedad Iberoamericana de Información Científica and Scopus.
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