The independent predictive value of admission serum ferritin concentration for prognosis in elderly patients with community-acquired pneumonia in the emergency department.

IF 4.8 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2025-01-10 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1505207
Xiangqun Zhang, Na Shang, Da Zhang, Junyuan Wu, Shubin Guo
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Abstract

Background: Community-acquired pneumonia (CAP) poses a significant health threat to the elderly population, leading to high morbidity and mortality rates. Serum ferritin, a critical indicator of iron metabolism, plays a pivotal role in inflammation and immune regulation. Nevertheless, its specific prognostic relevance in elderly patients with CAP remains unclear. This study aimed to evaluate the predictive capacity of serum ferritin in determining the prognosis of elderly patients with CAP and to investigate its effectiveness when combined with the sequential organ failure assessment (SOFA) or CURB-65 (confusion, uremia, respiratory rate, blood pressure, aged ≥65 years) scores.

Methods: This retrospective cohort study included 451 elderly patients (aged ≥65 years) diagnosed with CAP according to established criteria. Serum ferritin concentrations were measured upon admission and various prognostic indicators such as 28-day mortality, mechanical ventilation requirement, and vasopressor administration were analyzed in conjunction with white blood count (WBC), C-reactive protein (CRP), procalcitonin (PCT), lactate (Lac), SOFA scores, and CURB-65 scores. The independent predictive value of ferritin was assessed through receiver operating characteristic (ROC) curve analysis and multivariate logistic regression.

Results: Among the 451 patients, 99 (22%) died within 28 days. The area under the curve (AUC) of serum ferritin for predicting 28-day mortality was 0.75 (95%CI: 0.695-0.805). Ferritin outperformed WBC, CRP, and PCT in predictive performance, and its performance was comparable to Lac. When combined with SOFA or CURB-65 scores, the AUC of ferritin for predicting 28-day mortality increased to 0.84 and 0.847, respectively (P<0.001). Moreover, the AUC of ferritin for predicting vasopressor administration was 0.707, which increased to 0.864 and 0.822 when combined with SOFA or CURB-65 scores, respectively (P<0.001). Ferritin could predict mechanical ventilation requirement with an AUC of 0.618, but it was not an independent risk factor, and its predictive ability was not significantly different from other indicators.

Conclusion: Admission serum ferritin is an independent predictor for the prognosis of elderly patients with CAP, and it exhibits a strong ability to predict the 28-day mortality and vasopressor administration. The combination of ferritin with SOFA and CURB-65 scores significantly improves the prognostic predictive potency.

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急诊老年社区获得性肺炎患者入院时血清铁蛋白浓度对预后的独立预测价值
背景:社区获得性肺炎(CAP)对老年人群的健康构成重大威胁,导致高发病率和死亡率。血清铁蛋白是铁代谢的重要指标,在炎症和免疫调节中起关键作用。然而,其与老年CAP患者预后的具体相关性尚不清楚。本研究旨在评估血清铁蛋白对老年CAP患者预后的预测能力,并探讨其与序贯器官衰竭评估(SOFA)或CURB-65(精神错乱、尿毒症、呼吸频率、血压、年龄≥65岁)评分联合的有效性。方法:本回顾性队列研究纳入451例根据既定标准诊断为CAP的老年患者(年龄≥65岁)。入院时测定血清铁蛋白浓度,并结合白细胞计数(WBC)、c反应蛋白(CRP)、降钙素原(PCT)、乳酸(Lac)、SOFA评分和CURB-65评分分析各种预后指标,如28天死亡率、机械通气需求和血管升压剂给药。通过受试者工作特征(ROC)曲线分析和多因素logistic回归评估铁蛋白的独立预测值。结果:451例患者中,有99例(22%)在28天内死亡。血清铁蛋白曲线下面积(AUC)预测28天死亡率为0.75 (95%CI: 0.695-0.805)。铁蛋白在预测性能上优于WBC、CRP和PCT,其性能与Lac相当。当与SOFA或CURB-65评分联合使用时,铁蛋白预测老年CAP患者28天死亡率的AUC分别上升至0.84和0.847。(结论:入院血清铁蛋白是老年CAP患者预后的独立预测因子,对老年CAP患者28天死亡率和血管升压药物给药具有较强的预测能力。)铁蛋白联合SOFA和CURB-65评分可显著提高预后预测效力。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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