Evidence map›Paper›PMID 41932816›Full record

ArticleBMJ open respiratory research2026

Mortality and diagnostic practice variation in interstitial lung disease admissions: insights from a multicentre UK cohort study.

Laura Jane White, Jonathon Shaw, Bethan Powell, Nyan M Kyi, Alicia Sou, Gareth Edward Hughes, Dilanka Tilakaratne, Conal Hayton, Trishala Raj, Vi Truong and 16 more

Abstract readMulticenter Study
In one paragraph

Article in BMJ open respiratory research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

26 authors.

Laura Jane WhiteLancaster Medical School, Lancaster University, Lancaster, UK l.j.white@lancaster.ac.uk.ORCID http://orcid.org/0009-0003-1991-3897
Jonathon ShawDepartment of Respiratory Medicine, Stockport NHS Foundation Trust, Stockport, UK.
Bethan PowellDepartment of Respiratory Medicine, Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, UK.
Nyan M KyiDepartment of Respiratory Medicine, Northern Care Alliance NHS Foundation Trust, Salford, UK.
Alicia SouDepartment of Respiratory Medicine, Northern Care Alliance NHS Foundation Trust, Salford, UK.
Gareth Edward HughesDepartment of Respiratory Medicine, Bolton NHS Foundation Trust, Bolton, UK.ORCID http://orcid.org/0000-0003-2942-6489
Dilanka TilakaratneDepartment of Respiratory Medicine, Bolton NHS Foundation Trust, Bolton, UK.
Conal HaytonDepartment of Respiratory Medicine, Manchester University NHS Foundation Trust, Wythenshawe Hospital, Manchester, UK.
Trishala RajDepartment of Respiratory Medicine, Manchester University NHS Foundation Trust, Wythenshawe Hospital, Manchester, UK.
Vi TruongManchester Royal Infirmary, Department of Respiratory Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
Nashwah IsmailManchester Royal Infirmary, Department of Respiratory Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
Nawat KhanijounManchester Royal Infirmary, Department of Respiratory Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
Rebecca HuangDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Emma HardyDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Zainab AslamDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Mahum SohailDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Mahzaib BabarDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Amsal AmjadDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Naayaab KhanDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Martin ReganDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Oby OkpalaDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Ragavilasini SureshDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Jerome McintoshDepartment of Respiratory Medicine, Tameside and Glossop Integrated Care NHS Foundation Trust, Ashton-under-Lyne, UK.
Amy GadoudLancaster Medical School, Lancaster University, Lancaster, UK.
Timothy GatheralRespiratory Medicine, University Hospitals of Morecambe Bay NHS Foundation Trust, Kendal, UK.
Georges Ng Man KwongDepartment of Respiratory Medicine, Northern Care Alliance NHS Foundation Trust, Salford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterstitial lung diseases (ILDs) are a heterogeneous group of often progressive, unpredictable diseases. They frequently result in hospitalisations secondary to respiratory decompensation, termed ILD-related admissions. A proportion are due to an acute exacerbation of ILD (AEILD). All are associated with high mortality but are poorly characterised in real-world populations.

aimTo evaluate mortality outcomes and associated risk factors following ILD-related hospital admissions, including AEILD.

methodsWe conducted a multicentre retrospective cohort study of primary International Classification of Diseases Version 10 coded admissions for ILD between 1 January 2017 and 31 December 2019 across 11 NHS hospitals in the North West of England. AEILD events were classified using clinical criteria: <30-day respiratory deterioration not secondary to cardiac failure, pulmonary embolism or pneumothorax. The AEILD subgroup was divided into those with CT confirmation (definite AEILD) and without CT confirmation (suspected AEILD). Primary outcome was time from admission to death. Statistical analyses included Kaplan-Meier and multivariate proportional hazards modelling.

resultsOf 938 ILD-related admissions, 54.5% met study AEILD criteria. Overall, cumulative all-cause mortality to 90-days post-discharge was 40.2%. For the AEILD cohort, cumulative all-cause mortality to 90-days post-discharge was 47.6%. Median survival of the AEILD cohort was 107 days (95% CI 87.0 to 141.0 days) and the other ILD-related admission cohort 241.0 days (95% CI 208.0 to 308.0 days), with a statistically significant difference in survival (p<0.0001). 37.6% (192/511) of AEILD events had CT confirmation. Within the AEILD subgroup, median survival was higher in the CT group (144 days vs 100 days, p=0.027). AEILD was independently associated with mortality in a multivariate model. Preadmission oxygen, age and neutrophilia were associated with mortality in both ILD-admission and AEILD 90-day all-cause mortality models. 13.9% of admissions had documented palliative care input.

conclusionsMortality associated with ILD-related admissions is high, with AEILD events independently associated with mortality. Findings highlight the need for improved education, access to palliative care and targeted AEILD research.

Indexed as

HospitalizationLung Diseases, InterstitialAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsTomography, X-Ray ComputedUnited KingdomClinical EpidemiologyIdiopathic Pulmonary FibrosisImaging/CT MRI etcInterstitial FibrosisPalliative Care

Identifiers

PMID41932816
PMCPMC13052612

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.