Evidence map›Paper›PMID 37438554›Full record

ReviewAdvances in therapy2023

Assessing the Effects of Changing Patterns of Inhaled Corticosteroid Dosing and Adherence with Fluticasone Furoate and Budesonide on Asthma Management.

Peter Daley-Yates, Dave Singh, Juan M Igea, Luigi Macchia, Manish Verma, Norbert Berend, Maximilian Plank

Erratum issuedOpen access · hybridAbstract readReview
In one paragraph

Review in Advances in therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Inhaled Corticosteroid/Long-Acting βAdvances in therapy · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 5 countries.

Peter Daley-YatesGSK, Uxbridge, UK.
Dave SinghManchester University NHS Foundation Trust, Manchester, UK.
Juan M IgeaAllergoasma, Salamanca, Spain.
Luigi MacchiaUniversity of Bari, Bari, Italy.
Manish VermaGSK, Mumbai, India.
Norbert BerendWoolcock Institute for Medical Research, Glebe, NSW, Australia.
Maximilian PlankGSK, Prinzregentenpl. 9, 81675, Munich, Germany. maximilian.x.plank@gsk.com.
GlaxoSmithKline (Germany) · DEGlaxoSmithKline (India) · INManchester University NHS Foundation Trust · GBUniversity of Bari Aldo Moro · ITWoolcock Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPharmacological asthma management focuses on the use of inhaled corticosteroid (ICS)-containing therapies, which reduce airway inflammation and provide bronchoprotection, improving symptom control and reducing exacerbation risk. ICS underuse due to poor adherence is common, leading to poor clinical outcomes including increased risk of mortality. This article reviews efficacy versus systemic activity profiles for various adherence patterns and dosing regimens of fluticasone furoate (FF)-containing and budesonide (BUD)-containing asthma therapies in clinical trials and real-world studies.

methodsWe performed a structured literature review (1 January 2000-3 March 2022) and mathematical modelling analysis of FF-containing and BUD-containing regular daily dosing in patients with mild-to-severe asthma, as-needed BUD/formoterol (FOR) in mild asthma, and BUD/FOR maintenance and reliever therapy (MART) dosing in moderate-to-severe asthma, to assess efficacy (bronchoprotection) and systemic activity (cortisol suppression) profiles of dosing patterns of ICS use in multiple adherence scenarios.

resultsA total of 22 manuscripts were included in full-text review and 18 in the model simulations. Focusing on FF-containing or BUD-containing treatments at comparable adherence rates, regular daily FF or FF/vilanterol (VI) dosing provided more prolonged bronchoprotection and fewer systemic effects than daily BUD, daily BUD/FOR, or BUD/FOR MART dosing, especially in low adherence scenarios. In model simulations and the real-world setting, FF/VI generally provided longer bronchoprotection, lower systemic activity, and greater clinical benefits over BUD/FOR as well as consistently higher adherence.

conclusionIn this literature review and modelling analysis, FF/VI was found to show clinical advantages on asthma control over BUD/FOR. These findings have implications for helping clinicians select the most suitable inhaled therapy for their patients with asthma.

Indexed as

AsthmaBudesonideAdministration, InhalationAdrenal Cortex HormonesAndrostadienesBudesonide, Formoterol Fumarate Drug CombinationDrug CombinationsFluticasoneHumansAdrenal Cortex HormonesAndrostadienesBudesonideBudesonide, Formoterol Fumarate Drug CombinationDrug CombinationsFluticasonefluticasone furoateAdherenceAsthmaBronchoprotectionBudesonideDosing regimenFluticasone furoateSystemic effects

Identifiers

PMID37438554
PMCPMC10427546
OpenAlexW4384071816

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.