Empirical Antifungal Treatment of Critically Ⅲ Patients With Influenza-Associated Acute Respiratory Distress Syndrome: A Propensity Score Weighted Observational Study

医学 经验性治疗 抗真菌 入射(几何) 倾向得分匹配 内科学 随机对照试验 观察研究 急性呼吸窘迫 梅德林 临床试验 急诊医学 疾病严重程度 重症监护医学 呼吸窘迫 侵袭性念珠菌病 抗真菌药 治疗组和对照组 重症监护室 机械通风 苦恼 隐球菌性脑膜炎
作者
Stefan Hatzl,Lisa Kriegl,Christina Geiger,Caroline Wilhelmer,Alexander C. Reisinger,Markus Keldorfer,Julia Auinger,Gernot Schilcher,Florian Krammer,Philipp Eller,Robert Krause
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:82 (3): e485-e493 被引量:4
标识
DOI:10.1093/cid/ciaf507
摘要

BACKGROUND: Influenza-associated pulmonary aspergillosis (IAPA) is a significant fungal complication in patients with influenza-induced acute-respiratory-distress-syndrome (ARDS). The impact of empirical antifungal treatment on IAPA incidence and outcomes remains unclear. METHODS: In this observational multicenter study (9 treatment centers), we included all consecutive patients admitted to intensive care units (ICUs) with influenza-associated ARDS between 1 September 2016 and 1 March 2025. We compared patients receiving empirical antifungal treatment with those who did not, focusing on 30-day IAPA incidence (primary outcome) and survival (secondary outcome). Propensity score weighting was used to account for baseline characteristic imbalances. IAPA cases were classified based on the Fungal-Infections-in-Adult-Patients-in-ICU (FUNDICU) consensus criteria. RESULTS: We included 172 patients, 61 (35%) of whom received empirical antifungal therapy (94% posaconazole). IAPA was diagnosed in 24 cases, with a median onset of 2 days after ICU admission. Of these, 20 occurred in the non-treatment group and 4 in the empirical treatment group. The 30-day IAPA incidence was 7.7% in the treatment group and 20.4% in the non-treatment group (P = .002). The sub-distributional hazard ratio (sHR) for IAPA incidence in the empirical treatment group compared with the non-treatment group was 0.21 (95% CI: 0.10-0.92, P = .045). However, there was no significant difference in 30-day ICU survival. CONCLUSIONS: In ICU patients with influenza ARDS, empirical antifungal treatment was associated with significantly reduced IAPA incidence, but this did not translate into improved survival. Randomized controlled trials are warranted to evaluate the efficacy and safety of patients' specific empirical antifungal treatment with regard to IAPA incidence and outcomes.
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