Evidence map›Paper›PMID 42772883›Full record

ArticleBMJ open2026

Temporal trends in single and multiple organ fibrosis prevalence and primary care consultations: a population-based cohort study of 5.8 million individuals in England.

Georgie May Massen, Gisli Jenkins, Richard J Allen, Iain Stewart, Chris J Scotton, Rachel Chambers, Hilary Longhurst, Louise V Wain, Vidya Navaratnam, Jennifer K Quint and 1 more

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

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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

11 authors.

Georgie May MassenSchool of Public Health, Imperial College London, London, UK g.massen21@imperial.ac.uk.ORCID http://orcid.org/0000-0003-4355-6546
Gisli JenkinsNational Heart and Lung Institute, Imperial College London, London, UK.
Richard J AllenDivision of Public Health and Epidemiology, University of Leicester, Leicester, England, UK.
Iain StewartNational Heart and Lung Institute, Imperial College London, London, England, UK.ORCID http://orcid.org/0000-0002-1340-2688
Chris J ScottonFaculty of Health Sciences, University of Exeter, Exeter, England, UK.ORCID http://orcid.org/0000-0002-9671-9057
Rachel ChambersDepartment of Respiratory Medicine (UCL Respiratory), University College London, London, England, UK.
Hilary LonghurstDyskeratosis Congenita (DC) Action, London, UK.
Louise V WainDivision of Public Health and Epidemiology, University of Leicester, Leicester, Leicestershire, UK.
Vidya NavaratnamInstitute for Respiratory Health, The University of Western Australia, Perth, Western Australia, Australia.
Jennifer K QuintSchool of Public Health, Imperial College London, London, UK.ORCID http://orcid.org/0000-0003-0149-4869
DEMISTIFI Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo understand how prevalence estimates of single and multiple organ fibrosis have changed from 2012 to 2022.

designRetrospective population-based cohort study.

settingData from primary (Clinical Practice Research Datalink Aurum) and secondary care (Hospital Episode Statistics Admitted Patient Care) electronic health records were used to conduct this study.

participantsAdults aged 18 years and older whose primary and secondary care records were available for research.

main outcome measureFibrotic conditions previously determined from a Delphi survey of clinicians; diagnoses were found in either primary or secondary care records. The primary analysis estimated the prevalence of both single and multiple organ fibrosis. A secondary analysis used Cox proportional hazards models to investigate the association between the time-updated number of fibrotic conditions and risk of death, adjusting for age and sex.

resultsThe cohort consisted of 5 839 459 people with at least one fibrotic condition and a denominator of 18 784 962 people. Over the study period, prevalence of fibrotic conditions increased by 6.72%, and as of 2022, 19.95% (95% CI 19.92% to 19.98%) of adults had at least one fibrotic condition. The prevalence of multiple organ fibrosis increased from 4.78% (95% CI 4.76% to 4.79%) in 2012 to 8.51% (95% CI 8.50% to 8.53%) in 2022. In the year preceding diagnosis of single organ fibrosis, the median number of primary care consultations was 14 compared with 21 consultations for people with multiple organ fibrosis. Compared with people with single organ fibrosis, people with two fibrotic conditions had a mortality HR of 2.90 (95% CI 2.87 to 2.93), while people with three fibrotic conditions had a mortality HR of 5.22 (95% CI 5.14 to 5.30).

conclusionsThe prevalence of single and multiple organ fibrosis has substantially increased over a decade. People with multiple organ fibrosis access healthcare more than people with single organ fibrosis and are at a greater risk of mortality. Multiple organ fibrosis is estimated to affect more than 3 million people in the UK and is increasing. Better understanding of patterns of fibrotic multimorbidity may help to aid earlier diagnosis and opportunities for reducing mortality.

Indexed as

FibrosisPrimary Health CareAdolescentAdultAgedAged, 80 and overEnglandFemaleHumansMaleMiddle AgedPrevalenceProportional Hazards ModelsReferral and ConsultationRetrospective StudiesYoung AdultElectronic Health RecordsEPIDEMIOLOGYFibrosisPrevalence

Identifiers

PMID42772883
PMCPMC13599825

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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.