Evidence map›Paper›PMID 42276801›Full record

ArticleBMJ open2026

How do acute worsening events influence daily life and healthcare-seeking behaviour in patients with COPD: an international multicountry qualitative study.

Lars Dijk, Merijn M G Driessen, Yoran H Gerritsma, Clare Bolton, Carla Da Silva, Janwillem W H Kocks

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05492877 (A Phase IIa Randomised, Double Blind, Placebo Controlled, Parallel Arm, Multi-Centre Study to Evaluate the Efficacy and Safety of Mitiperstat), which is not on this 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.

NCT05492877 phase2completednot on this map

A Phase IIa Randomised, Double Blind, Placebo Controlled, Parallel Arm, Multi-Centre Study to Evaluate the Efficacy and Safety of Mitiperstat (AZD4831), for 12-24 Weeks, in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

TypeinterventionalSponsorAstraZenecaRan2022 to 2024Enrolled381ConditionsChronic Obstructive Pulmonary Disease (COPD)ArmsMitiperstat (AZD4831), Placebo
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

6 authors.

Lars DijkGeneral Practitioners Research Institute, Groningen, Netherlands larsdijk1998@gmail.com.ORCID http://orcid.org/0000-0002-9544-1487
Merijn M G DriessenGeneral Practitioners Research Institute, Groningen, Netherlands.
Yoran H GerritsmaGeneral Practitioners Research Institute, Groningen, Netherlands.
Clare BoltonGlobal Medical Affairs, Respiratory and Immunology, AstraZeneca, Cambridge, UK.
Carla Da SilvaEarly Respiratory and Immunology Clinical Development, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-6993-0546
Janwillem W H KocksGeneral Practitioners Research Institute, Groningen, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the impact of acute worsening events (AWEs), defined as clinically relevant deteriorations in peak expiratory flow, reliever use and/or symptoms, on patients' daily lives and identify behaviours linked to their recognition and management.

designA qualitative international substudy was conducted in the Netherlands, Spain, the USA, Canada and the UK (2023-2024).

participants19 patients with moderate-to-severe chronic obstructive pulmonary disease (COPD) from a randomised clinical trial participated. Interviews, triggered by AWEs and repeated 6 weeks later, were audio-recorded, transcribed and analysed.

resultsPatients varied in identifying bad days, reporting inability to perform physical activities, symptom worsening or the need for add-on treatment. Recognition of AWEs depended on their duration: shorter events (<2 days) often went unnoticed, while longer events were typically recognised. Most patients indicated they would seek healthcare if needed. Barriers included difficulty obtaining timely appointments (external) and a reactive attitude to worsenings (internal).

conclusionsAWEs significantly impact daily life but vary widely in recognition and thresholds for seeking care. Limited awareness of daily disease variations may contribute to both under-reporting of worsening events to healthcare providers and suboptimal self-management in COPD. TRIAL REGISTRATION NUMBER: NCT05492877.

Indexed as

Activities of Daily LivingPatient Acceptance of Health CarePulmonary Disease, Chronic ObstructiveAgedCanadaDisease ProgressionFemaleHumansMaleMiddle AgedQualitative ResearchPulmonary Disease, Chronic ObstructiveQUALITATIVE RESEARCHRESPIRATORY MEDICINE (see Thoracic Medicine)

Identifiers

PMID42276801
PMCPMC13264924

What OpenQuestion holds

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Registered trials

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.