当前血液学时代侵袭性真菌感染的流行病学变化。

IF 2.3 3区 医学 Q3 INFECTIOUS DISEASES
Patricia Monzó-Gallo, Christian Teijon-Lumbreras, Tommaso Francesco Aiello, Antonio Gallardo-Pizarro, Ana Martinez-Urrea, Mariana Chumbita, Emmanuelle Gras, Olivier Peyrony, Marta Bodro, Laura Magnano, Sabina Herrera, Maria Suarez-Lledó, Mateu Espasa, Francesc Marco, Alex Soriano, Carolina Garcia-Vidal
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引用次数: 0

摘要

我们的目的是描述当前血液治疗背景下住院血液病患者侵袭性真菌感染(IFI)和侵袭性霉菌感染(IMI)的流行病学和危险因素。对某三级医院连续住院血液病患者(2020-2023)进行回顾性观察队列研究。分析了两个人群:住院患者(FC)的整个队列和明确要求进行真菌学检测以排除IFI (SC)的患者亚群。使用EORTC-MSG标准对已证实或可能的IFI进行分类。确定IFI和IMI的危险因素。共有1975例患者被纳入FC,而1154例患者被纳入SC。IFI被诊断为64例(65次发作),IMI被诊断为43例(44次发作)。曲霉病是最常见的IFI(58.4%),其次是念珠菌病(18.5%)、耶氏肺孢子虫肺炎(15.4%)、毛霉病(6.2%)和镰孢病(4.6%)。FC患者IFI的独立危险因素包括急性白血病(aOR 2.40, 95% CI 1.37-4.10, p = 0.002)、皮质类固醇使用(aOR 2.36, 95% CI 1.40-4.03, p = 0.001)和移植物抗宿主病(aOR 2.13, 95% CI 0.93-4.46, p = 0.05)。IMI的危险因素为急性白血病(aOR 2.71, 95% CI 1.33-5.52, p = 0.006)、皮质类固醇使用(aOR 1.96, 95% CI 0.98-4-03, p = 0.05)和慢性肺部疾病(aOR 2.25, 95% CI 1.06-4.5, p = 0.02)。在SC中,皮质类固醇使用(aOR 2.45, 95% CI 1.44-4.25, p = 0.001)是IFI的独立危险因素,皮质类固醇使用(aOR 2.40, 95% CI 1.21-4.91, p = 0.01)和GVHD (aOR 2.95, 95% CI 1.23-6.52, p = 0.009)是与IMI相关的独立因素。IFI患者的死亡率明显高于非IFI患者(51.6% vs. 20.3%, p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiological shifts of Invasive Fungal Infections in the current era of haematology.

We aim to describe the epidemiology and risk factors for invasive fungal infections (IFI) and invasive mold infections (IMI) in hospitalized hematologic patients within the context of current hematologic therapies. Retrospective observational cohort study conducted on consecutive hematologic patients admitted to a tertiary hospital (2020-2023). Two populations were analysed: the full cohort of hospitalized patients (FC) and the subset of patients for whom mycological testing was specifically requested to rule out an IFI (SC). Proven or probable IFI was classified using EORTC-MSG criteria. Risk factors for IFI and IMI were identified. A total of 1975 patients where included in the FC whereas 1154 were included in the SC. IFI was diagnosed in 64 patients (65 episodes), and IMI in 43 patients (44 episodes). Aspergillosis was the most common IFI (58.4%), followed by candidemia (18.5%), Pneumocystis jirovecii pneumonia (PJP) (15.4%), mucormycosis (6.2%), and fusariosis (4.6%). Independent risk factors for IFI in the FC included acute leukemia (aOR 2.40, 95% CI 1.37-4.10, p = 0.002), corticosteroid use (aOR 2.36, 95% CI 1.40-4.03, p = 0.001) and graft versus host disease (GVHD) (aOR 2.13, 95% CI, 0.93-4.46, p = 0.05). For IMI, risk factors were acute leukemia (aOR 2.71, 95% CI 1.33-5.52, p = 0.006), corticosteroid use (aOR 1.96, 95% CI 0.98-4-03, p = 0.05) and chronic lung disease (aOR 2.25, 95% CI 1.06-4.5, p = 0.02). In the SC, corticosteroid use (aOR 2.45, 95% CI 1.44-4.25, p = 0.001) was the independent risk factor for IFI and corticosteroid use (aOR 2.40, 95% CI 1.21-4.91, p = 0.01) and GVHD (aOR 2.95, 95% CI 1.23-6.52, p = 0.009) were independent factors associated with IMI. Mortality was significantly higher in IFI patients compared to non-IFI patients (51.6% vs. 20.3%, p < 0.001). In this new era of haematology, the epidemiology of IFI is shifting, with Pneumocystis, Mucorales, and Fusarium becoming more prevalent. While corticosteroids and GVHD remain key risk factors, factors such as chronic lung disease are increasing its importance. Prolonged neutropenia may have decreased in relevance, likely due to prophylaxis. Preventing PJP has become a new challenge in IFI management.

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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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