Evidence map›Paper›PMID 42807824›Full record

ArticleERJ open research2026

Adjudication of exacerbations in bronchiectasis using modified EMBARC criteria in the CLEAR Trial.

Brenda O'Neill, Rohan Anand, Jeremy S Brown, Frances Butler, Lorcan McGarvey, Cecilia M O'Kane, Mike Clarke, Danny F McAuley, Adam T Hill, Anthony De Soyza and 7 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. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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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

17 authors.

Brenda O'NeillInstitute of Nursing and Health Research, Ulster University, Belfast, UK.
Rohan AnandWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.ORCID https://orcid.org/0000-0002-1957-5336
Jeremy S BrownUCL Respiratory, University College London, London, UK.
Frances ButlerYork Teaching Hospital NHS Foundation Trust, York, UK.
Lorcan McGarveyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.ORCID https://orcid.org/0000-0002-2860-0302
Cecilia M O'KaneWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Mike ClarkeCentre for Public Health, Queen's University Belfast, Belfast, UK.
Danny F McAuleyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.ORCID https://orcid.org/0000-0002-3283-1947
Adam T HillCentre for Inflammation Research, University of Edinburgh, Edinburgh, UK.
Anthony De SoyzaFreeman Hospital Newcastle, Newcastle, UK.ORCID https://orcid.org/0000-0002-8566-0344
James D ChalmersRadcliffe Department of Medicine, University of Oxford, Oxford, UK.
Andrew JacksonNorthern Ireland Clinical Trials Unit, Belfast, UK.
Ben McCulloughWellcome Trust-Wolfson Northern Ireland Clinical Research Facility, Queen's University Belfast, Belfast, UK.ORCID https://orcid.org/0009-0004-8871-4805
Fiona CopelandPCD Family Support Group, Ciliopathy Alliance, London, UK.
J Stuart ElbornWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Judy M BradleyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
CLEAR Investigator team

Funding

Wellcome Trust
6 · The paper itself

Abstract

Introduction: The EMBARC consensus criteria can be used to identify and categorise pulmonary exacerbations (PEs) in clinical trials. This paper describes methods used to independently adjudicate PEs using modified EMBARC criteria in a large multicentre bronchiectasis trial (CLEAR ISRCTN89040295). Methods: The Respiratory and Systemic Symptoms Questionnaire was used to objectively collect signs and symptoms at the onset of a PE. A mEMBARC PE was defined as ≥3 symptoms, with symptoms present for ≥48 h and prescription of an antibiotic. Individual sites recorded antibiotic use for PEs. An adjudication panel independently adjudicated and then agreed on PEs according to mEMBARC criteria. Data required to determine PEs using modified Fuchs criteria was also collected. Results: Sites reported 462 PEs from 203 patients reported in the CLEAR trial. The adjudication panel categorised these exacerbations as: 239 out of 462 (52%) fully qualifying mEMBARC PEs (meeting all mEMBARC criteria), 32 out of 462 (7%) partially qualifying mEMBARC PEs (≤3 symptoms present for ≥48 h or ≥3 symptoms present for <48 h and antibiotics prescribed) and 191 out of 462 (41%) non-mEMBARC PEs (antibiotics prescribed but symptoms and duration not met). When data were classified using modified Fuchs criteria a sensitivity analysis produced results that were consistent with the main trial results. Conclusion: PEs are increasingly used as the primary outcome in bronchiectasis trials, making accuracy in their identification essential. More rigorous capture of exacerbation symptoms and implementation of a standardised and reproducible decision-making process, supported by an independent adjudication panel, is important for capturing PEs and ensuring the integrity of trial outcomes.

Identifiers

PMID42807824
PMCPMC13617598

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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.