# Diagnosis, clinical features and survival analysis of invasive pulmonary aspergillosis among critically ill patients: a retrospective cohort study based on updated criteria

**Authors:** Liufang Gao, Shuiwen Li, Xiaolong Huang, Weizhe Huang, Zhu Chen, Yaogui Ning

PMC · DOI: 10.3389/fcimb.2026.1732182 · Frontiers in Cellular and Infection Microbiology · 2026-02-23

## TL;DR

This study finds that invasive pulmonary aspergillosis is a common and deadly condition in ICU patients, with specific diagnostic and treatment strategies improving survival.

## Contribution

The study evaluates updated diagnostic criteria and identifies effective mycological tests and clinical interventions for invasive pulmonary aspergillosis in critically ill patients.

## Key findings

- Invasive pulmonary aspergillosis (IPA) incidence was 7.1% among ICU pneumonia patients.
- BALF GM combined with molecular testing showed the highest diagnostic effectiveness for IPA.
- Anti-Aspergillus therapy and tracheostomy were associated with improved survival in IPA patients.

## Abstract

To evaluate the incidence, diagnostic performance, clinical characteristics, and prognostic determinants of invasive pulmonary aspergillosis (IPA) in critically ill patients, using updated EORTC/MSG and FUNDICU criteria.

We retrospectively analyzed a heterogenous ICU pneumonia cohort between Jan 2022 and Jun 2025. All included patients underwent at least one mycological assessment. IPA was diagnosed based on integrated EORTC/MSG and FUNDICU criteria. Diagnostic accuracy of mycological assays was evaluated, and clinical profiles were compared between IPA and non-IPA patients. Independent risk factors for mortality were identified via multivariate Cox regression.

Among 1835 patients, the IPA incidence was 7.1% (n=131). Of all mycological assays, bronchoalveolar lavage fluid galactomannan (BALF GM) demonstrated the highest sensitivity (85.5%) with robust specificity (82.9%). Molecular testing combined with BALF GM yielded a sensitivity of 64.4% and a specificity of 80.0%. Serum GM exhibited the lowest sensitivity (41.7%) but the highest specificity (89.2%); its combination with culture or molecular methods further enhanced specificity to >95%. Although patchy infiltrates were the most frequent radiological findings in both groups, consolidation (63.4% vs. 40.3%, P < 0.001), nodules (22.9% vs. 9.1%, P = 0.014), cavities (17.6% vs 3.9%, P = 0.004), and tree-in-bud signs (9.9% vs. 1.3%, P = 0.019) were significantly more prevalent in IPA patients. IPA patients experienced longer ICU stays (median 20 vs. 16 days) and significantly higher ICU mortality (55.0% vs 26.0%). Multivariable analysis identified IPA (HR: 2.064, 95% CI = 1.211-3.518, P = 0.008) and a prolonged interval from admission to the first positive mycological test (HR: 1.017, 95% CI = 1.004-1.031, P = 0.011) as independent risk factors for death. Conversely, anti-Aspergillus therapy (HR: 0.489, 95% CI = 0.275-0.871, P = 0.015) and tracheostomy (HR: 0.351, 95% CI = 0.222-0.557, P < 0.001) were associated with improved survival.

IPA is a common and lethal complication in ICU pneumonia patients, serving as an independent predictor of mortality. BALF GM, particularly when integrated with molecular testing, is the most effective mycological diagnostic method. Reducing the diagnostic window, initiating timely antifungal therapy, and proactive airway management (e.g., tracheostomy) may significantly improve clinical outcome for these critically ill patients.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** chronic kidney disease (MESH:D051436), neutropenic (MESH:D044504), ICU (MESH:C000657744), Cancer (MESH:D009369), opportunistic infection (MESH:D009894), diabetes (MESH:D003920), dyspnea (MESH:D004417), Failure (MESH:D051437), pulmonary aspergillosis (MESH:D055732), immune impairment (MESH:D020274), influenza (MESH:D007251), critically ill (MESH:D016638), liver disease (MESH:D008107), neutrophil defects (MESH:C563515), fever (MESH:D005334), ICU pneumonia (MESH:D011014), COPD (MESH:D029424), pulmonary infiltrates (MESH:D017254), Organ Failure (MESH:D009102), pleural effusions (MESH:D010996), cough (MESH:D003371), COVID 19 (MESH:D000086382), infection (MESH:D007239), CKD (MESH:D012080), Aspergillus bronchitis (MESH:D001991), leukemia (MESH:D007938), bronchiectasis (MESH:D001987), death (MESH:D003643), inherited neutrophil deficiency (MESH:C564275), immunodeficiency (MESH:D007153), neutropenia (MESH:D009503), Chronic pulmonary disease (MESH:D002908), aspergillus (MESH:D001228), Fungal Diseases (MESH:D009181), pulmonary fibrosis (MESH:D011658), Chronic respiratory airway abnormality (MESH:D015619), Mycosis (MESH:D015821), Decompensated cirrhosis (MESH:D006333), IA (MESH:D055744), CT (MESH:C000719218)
- **Chemicals:** GM (MESH:C012990), polysaccharide (MESH:D011134), prednisone (MESH:D011241)
- **Species:** Aspergillus fumigatus (species) [taxon 746128], A. flavus [taxon 315677], Homo sapiens (human, species) [taxon 9606], Aspergillus (genus) [taxon 5052]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968249/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968249/full.md

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Source: https://tomesphere.com/paper/PMC12968249