Evidence map›Paper›PMID 40382637›Full record

ReviewBMC pulmonary medicine2025

The effect of a systematic multi-dimensional assessment in severe uncontrolled asthma: a literature review and protocol for an investigator-initiated, open-label, randomized-controlled trial (EXACT@home study).

L Bult, G J Braunstahl, J G J V Aerts, D Bänffer, J S J A van Campen, M S van Daalen, Y van Dooren, U Flanders, E S Geurts, P P Hekking and 12 more

Registry-linked trialAbstract readClinical Trial ProtocolReview
In one paragraph

Review in BMC pulmonary medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05831566 (Expertise Asthma COPD Program with Digital Support), 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.

NCT05831566 phase3recruitingnot on this map

Expertise Asthma COPD Program with Digital Support

TypeinterventionalSponsorFranciscus GasthuisRan2023 to 2026Enrolled138ConditionsAsthmaArmsBudesonide/Formoterol fumarate dihydrate
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

22 authors.

L BultDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands. l.bult@franciscus.nl.
G J BraunstahlDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
J G J V AertsDepartment of Pulmonary Medicine, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.
D BänfferPulmonary Rehabilitation Center Revant, Breda, the Netherlands.
J S J A van CampenDepartment of Pulmonary Medicine, Haaglanden Medical Center, The Hague, The Netherlands.
M S van DaalenDepartment of Hospital Pharmacy, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.
Y van DoorenDepartment of Pulmonary Medicine, Groene Hart Hospital, Gouda, The Netherlands.
U FlandersDepartment of Pulmonary Medicine, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
E S GeurtsDepartment of Physiotherapy, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
P P HekkingDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
R Heller-BaanDepartment of Pulmonary Medicine, Ikazia Hospital, Rotterdam, The Netherlands.
M J A JansDepartment of Pulmonary Medicine, Beatrix Hospital, Gorinchem, The Netherlands.
J H KappenDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
R C A MiesDepartment of Pulmonary Medicine, Maasstad Hospital, Rotterdam, The Netherlands.
B OppedijkDepartment of Pulmonary Medicine, Bravis Hospital, Bergen Op Zoom & Roosendaal, The Netherlands.
M de la Roij-HartmansDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
S Van der Sar-Van der BruggeDepartment of Pulmonary Medicine, Amphia Hospital, Breda, The Netherlands.
Y TürkDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
E VisDepartment of Pulmonary Medicine, Admiraal de Ruyter Hospital, Goes, The Netherlands.
R WoltersDepartment of Pulmonary Medicine, Haaglanden Medical Center, The Hague, The Netherlands.
E C VasbinderDepartment of Hospital Pharmacy, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.
J C C M In 't VeenDepartment of Pulmonary Medicine, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSevere asthma affects 3.6% of the asthma population, in which patients are uncontrolled despite optimal drug therapy and management of treatable traits. These patients are eligible for treatment with biologicals, which provide significant benefits but are costly and need precise indication. However, identifying all individual treatable traits before diagnosing severe asthma is challenging. A systematic multi-dimensional assessment may help identify and address these hidden traits, resulting in tailored treatment and reducing the number of unnecessary biological prescriptions.

methodsA literature review was conducted to address the knowledge gap on the effectiveness and added value of a systematic assessment and treatment in difficult-to-treat or severe asthma, followed by an outline of a study protocol to implement this in patients diagnosed with severe asthma.

resultsThe literature review revealed limited evidence on the effectiveness of systematic assessments in difficult-to-treat or severe asthma, largely due to the use of different study methods and outcome measures. Notably, only one of the selected articles employed a randomized controlled design. To address this gap, the EXpert Asthma Copd Trajectory with digital support (EXACT@home) study was proposed, which aims to improve the assessment and treatment of treatable traits in severe asthma before (re)considering treatment with biologicals. This study uses a prospective, open label, randomized controlled trial design with the primary aim of reducing biological prescriptions. Patients are eligible for inclusion if they have previously been diagnosed with severe uncontrolled asthma with an indication for treatment with biologicals. The intervention arm undergoes a 6-week systematic assessment program targeting treatable traits followed by tailored treatment, while the control arm directly receives treatment with biologicals. Both arms are followed for 12 months with secondary outcomes including asthma control, quality of life and exacerbation frequency. DISCUSSION: Difficult-to-treat or severe asthma requires tailored treatments based on individual treatable traits, but challenges remain in accurately identifying these traits. Existing literature highlights the beneficial effects of systematic assessments, but conclusive evidence is lacking. The EXACT@home study aims to provide high quality evidence on the effectiveness of such an assessment in the management of severe uncontrolled asthma, addressing a gap in the current literature.

trial registrationNCT05831566 (Clinicaltrials.gov), registered at 14-04-2023. PROTOCOL VERSION: version 6, date 27-03-2024.

Indexed as

Anti-Asthmatic AgentsAsthmaHumansRandomized Controlled Trials as TopicSeverity of Illness IndexAnti-Asthmatic AgentsDifficult-to-treat asthmaEHealthSevere asthmaSystematic assessmentTreatable traits

Identifiers

PMID40382637
PMCPMC12085824

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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.