Evidence map›Paper›PMID 41181320›Full record

ArticleFrontiers in cellular and infection microbiology2025

Clinical features of influenza-associated pulmonary aspergillosis: a retrospective multicenter cohort study.

Jia-Xin Shi, Xiang-Rong Shao, Peng Wu, Xiang Wang, Kui Sheng, Qi-Chao Chen, Feng Jin

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jia-Xin ShiDepartment of Respiratory and Critical Care Medicine, Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China.
Xiang-Rong ShaoDepartment of Respiratory and Critical Care Medicine, Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China.
Peng WuDepartment of Respiratory and Critical Care Medicine, Jiangdu People's Hospital, Yangzhou, Jiangsu, China.
Xiang WangDepartment of Respiratory and Critical Care Medicine, Nanjing Drum Tower Hospital Group Yizheng Hospital, Yangzhou, Jiangsu, China.
Kui ShengDepartment of Respiratory and Critical Care Medicine, Gaoyou People's Hospital, Yangzhou, Jiangsu, China.
Qi-Chao ChenDepartment of Respiratory and Critical Care Medicine, Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China.
Feng JinDepartment of Respiratory and Critical Care Medicine, Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rationale: Influenza-associated pulmonary aspergillosis (IAPA) is a great clinical challenge, which has high morbidity and mortality in severe influenza infections. Unlike invasive pulmonary aspergillosis (IPA), IAPA often occurs in immunocompetent hosts. That IAPA lacks of specific manifestations makes it difficult to diagnose and causes a high mortality rate, which is becoming challenges toclinicians. Exploring the clinical characteristics of IAPA in depth is of great significance for guiding clinical practice. Objectives: To determine the clinical features of IAPA in order to support appropriate clinical management of this public health threat. Methods: A retrospective multicenter cohort study was conducted. The clinical characteristics, risk factors, diagnostic methods, treatment, and prognosis data of the participants were analyzed. Results: Diabetes and lymphopenia were important risk factors for IAPA. Pulmonary imaging showed that IAPA patients had more nodular lesions in the lungs, and a higher proportion of them were accompanied by cavitary lesions. The galactomannan (GM) test in bronchoalveolar lavage fluid (BALF) showed high sensitivity and specificity for diagnosing IPA. The positive rate of Conclusions: Diabetes and lymphopenia were important risk factors for IAPA. The comprehensive application of serum and BALF GM, M-ROSE and tNGS could significantly improve the detection rate of

Indexed as

Influenza, HumanPulmonary AspergillosisAdultAgedAspergillusBronchoalveolar Lavage FluidFemaleGalactoseHumansInvasive Pulmonary AspergillosisLungMaleMannansMiddle AgedPrognosisRetrospective StudiesgalactomannanGalactoseMannansGalactomannan (GM) testinfluenzainfluenza-associated pulmonary aspergillosis (IAPA)microbiology rapid on-site evaluation (M-ROSE)targeted next generation sequencing (tNGS)

Identifiers

PMID41181320
PMCPMC12572719

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