Novel model to predict risk of invasive fungal infection and fungal prophylaxis timing.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Xinyu Zuo, Xinyuan Ma, Miao Zhang, Richeng Mao, Jiexian Ma
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引用次数: 0

Abstract

Patients on immunosuppressive drugs or those who are critically ill are at high risk for invasive fungal infections (IFIs). The assessment of IFI risk and the initiation of prophylaxis in these patients remain unclear. A nomogram model was developed to evaluate clinical and immune indicators in relation to IFI risk and validated by immunocompromised patients. High-risk patients, as identified by the model, were selected for a prospective randomized study to assess the efficacy of the model and timing of fungal prophylaxis initiation. Patients deemed high risk received either fluconazole or a placebo until IFI occurrence or risk downgrade for 90 days. We compared the incidence of IFI and mortality between the two groups. The nomogram, created from a training cohort (n = 384), included age, IgG level, and CD4+ cell count as predictive indicators of IFI and was validated in a separate cohort (n = 281) with an area under the curve of 0.723. A total of 265 patients were recruited into the prospective study, with 163 high-risk patients randomly assigned to receive either fluconazole (n = 83) or a placebo (n = 80). The model had a positive predictive value of 48.8% and a negative predictive value of 90.2%. High-risk IFI defined by this model could be reduced to the low-risk cohort level with fluconazole prophylaxis (P < 0.01). This nomogram model reliably predicts the risk of IFI and timing of mycoprophylaxis in immunocompromised patients. Targeted mycoprophylaxis significantly reduces the incidence of IFI, particularly yeast infections, and may help to prevent fungal colonization.

Importance: We still lack enough evidence to decide when and how to begin fungal prophylaxis in immunocompromised patients. A model based on immune function indicator is an effective tool for predicting risk of invasive fungal infection (IFI) in immunocompromised patients. Patients were collected to evaluate the performance of the model retrospectively and prospectively.

Clinical trials: This study is registered with the Chinese Clinical Trial Registry as ChiCTR2400079810.

预测侵袭性真菌感染风险和真菌预防时机的新模型。
使用免疫抑制药物的患者或危重患者是侵袭性真菌感染(IFIs)的高危人群。这些患者的IFI风险评估和预防措施的开始仍不清楚。建立了一个nomogram模型来评估与IFI风险相关的临床和免疫指标,并由免疫功能低下的患者验证。高风险患者,通过模型识别,被选中进行前瞻性随机研究,以评估模型的有效性和真菌预防开始的时间。高风险患者接受氟康唑或安慰剂治疗,直至IFI发生或风险降低90天。我们比较了两组间IFI的发生率和死亡率。从训练队列(n = 384)创建的nomogram包括年龄、IgG水平和CD4+细胞计数作为IFI的预测指标,并在另一个单独的队列(n = 281)中进行验证,曲线下面积为0.723。这项前瞻性研究共招募了265名患者,其中163名高危患者随机分配接受氟康唑治疗(n = 83)或安慰剂治疗(n = 80)。模型的阳性预测值为48.8%,阴性预测值为90.2%。该模型定义的高风险IFI可以通过氟康唑预防降低到低风险队列水平(P < 0.01)。该nomogram模型可靠地预测了免疫功能低下患者IFI的风险和进行真菌预防的时机。有针对性的真菌预防显著降低IFI的发病率,特别是酵母菌感染,并可能有助于防止真菌定植。重要性:我们仍然缺乏足够的证据来决定免疫功能低下患者何时以及如何开始真菌预防。基于免疫功能指标的模型是预测免疫功能低下患者侵袭性真菌感染风险的有效工具。收集患者进行回顾性和前瞻性评估模型的性能。临床试验:本研究已在中国临床试验注册中心注册,注册号为ChiCTR2400079810。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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