Evidence map›Paper›PMID 41878283›Full record

ArticleERJ open research2026

ENHANCE: a community partnership charting the evolution of early-life cystic fibrosis disease manifestations in a new era of management.

Don S Urquhart, Barry Linnane, Clare J Saunders, Mary Abkir, Anna M Georgiopoulos, Rebecca Dobra, Sarah Carroll, Maddie Still, Desmond W Cox, Emer Fitzpatrick and 10 more

Abstract read
In one paragraph

Article in ERJ open research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

20 authors.

Don S UrquhartDepartment of Paediatric Respiratory and Sleep Medicine, Royal Hospital for Children and Young People, Edinburgh, UK.ORCID https://orcid.org/0000-0002-9048-9692
Barry LinnaneSchool of Medicine and Centre for Interventions in Infection, Inflammation and Immunity (4i), University of Limerick, Limerick, Ireland.ORCID https://orcid.org/0000-0001-9243-2887
Clare J SaundersRoyal Brompton and Harefield Hospitals, part of Guys and St Thomas' NHS Foundation Trust, London, UK.
Mary AbkirRoyal Brompton and Harefield Hospitals, part of Guys and St Thomas' NHS Foundation Trust, London, UK.
Anna M GeorgiopoulosDepartment of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.ORCID https://orcid.org/0000-0002-0924-4031
Rebecca DobraRoyal Brompton and Harefield Hospitals, part of Guys and St Thomas' NHS Foundation Trust, London, UK.
Sarah CarrollPsychology Department, Children's Health Ireland, Dublin, Ireland.
Maddie StillCommunity Engagement Team Cystic Fibrosis Trust, London, UK.
Desmond W CoxCystic Fibrosis Centre, Children's Health Ireland, Dublin, Ireland.ORCID https://orcid.org/0000-0002-2127-7178
Emer FitzpatrickSchool of Medicine, University College Dublin, Dublin, Ireland.
Aidan BeeganData Management Core, Paediatric Academic Health Science Centre, Children's Health Ireland, Dublin, Ireland.ORCID https://orcid.org/0000-0001-7123-1605
Rebecca ThursfieldCystic Fibrosis Centre, Alder Hey Childrens NHS Foundation Trust, Liverpool, UK.
Jen BalfeCommunity Engagement Team, Cystic Fibrosis Ireland, Dublin, Ireland.
Alison TarrCommunity Engagement Team Cystic Fibrosis Trust, London, UK.
Karen LesterRCSI University of Medicine and Health Sciences, Dublin, Ireland.
Aoife CunninghamRCSI University of Medicine and Health Sciences, Dublin, Ireland.
Lucy PerremCystic Fibrosis Centre, Children's Health Ireland, Dublin, Ireland.ORCID https://orcid.org/0000-0003-4970-8889
Jane C DaviesRoyal Brompton and Harefield Hospitals, part of Guys and St Thomas' NHS Foundation Trust, London, UK.
Paul McNallyRCSI University of Medicine and Health Sciences, Dublin, Ireland.ORCID https://orcid.org/0000-0001-7102-1712
ENHANCE-CF study group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ENHANCE is a multicentre, longitudinal study examining the natural history of early cystic fibrosis (CF) disease manifestations in children. We hypothesise that the prevalence, presentation and natural history of disease manifestations of CF in young children will change significantly in the next decade with advances in the understanding and treatment of CF, including the use of therapies aimed at improving CFTR function. The study has been co-developed with the CF community, in order to try to answer questions of key importance to people with CF and their caregivers. The study will longitudinally monitor lung health using nitrogen multiple breath washout testing and spirometry, lung structure using spirometry-controlled computed tomography scanning, gastrointestinal health using gut microbiome, gut inflammation and abdominal symptom scores, pancreatic function using faecal elastase, liver function using liver blood tests and liver ultrasound, and sweat chloride. Mental health will be longitudinally assessed using questionnaires for mood (PROMIS, GAD-7), quality of life (CFQ-R) and psychosocial functioning (Pediatric Symptom Checklist). There are three cohorts in the study: infants with CF diagnosed by newborn screening (n=250), children aged 0-6 years and currently attending CF centres (n=200) and healthy newborn infant controls (100). The study will be conducted over 5 years in the first phase with a plan to extend through further phases in the future. We envisage that the study will provide important evidence to enable healthcare staff and families to guide the care of children with CF in the future.

Identifiers

PMID41878283
PMCPMC13006910

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Registered trials

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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.