Evidence map›Paper›PMID 27184175›Full record

ArticleBMC pulmonary medicine2016

Effectiveness of initiating extrafine-particle versus fine-particle inhaled corticosteroids as asthma therapy in the Netherlands.

Thys van der Molen, Dirkje S Postma, Richard J Martin, Ron M C Herings, Jetty A Overbeek, Victoria Thomas, Cristiana Miglio, Richard Dekhuijzen, Nicolas Roche, Theresa Guilbert and 5 more

Erratum issuedOpen access · goldAbstract readComparative Study
In one paragraph

Article in BMC pulmonary medicine, 2016. 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Lung clearance index: assessment and utility in children with asthma.European respiratory review : an official journal of the European Respiratory Society · 2019
    Review
  6. Article
  7. Article
  8. Review
  9. Small Airways Disease, Biomarkers and COPD: Where are We?International journal of chronic obstructive pulmonary disease
    Review
  10. Review
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 10 institutions in 5 countries.

Thys van der MolenDepartment of General Practice, University of Groningen, University Medical Center, Groningen, The Netherlands.
Dirkje S PostmaDepartment of Pulmonary Medicine, University of Groningen, University Medical Center, Groningen, The Netherlands.
Richard J MartinNational Jewish Medical and Research Centre, Denver, USA.
Ron M C HeringsPharmo Institute for Drugs Outcome Research, Utrecht, The Netherlands.
Jetty A OverbeekPharmo Institute for Drugs Outcome Research, Utrecht, The Netherlands.
Victoria ThomasResearch in Real Life, Ltd, Cambridge, UK.
Cristiana MiglioResearch in Real Life, Ltd, Cambridge, UK.
Richard DekhuijzenRadboud University Medical Centre, Nijmegen, The Netherlands.
Nicolas RocheGroupe Hospitalier Cochin, AP-HP and University Paris Descartes, Paris, France.
Theresa GuilbertCincinnati Children's Hospital and Medical Center, Cincinnati, USA.
Elliot IsraelBrigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Wim van AalderenEmma's Children Hospital, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
Elizabeth V HillyerResearch in Real Life, Ltd, Cambridge, UK.
Simon van RysewykObservational & Pragmatic Research Institute Pte, Ltd, Singapore, Singapore.
David B PriceObservational & Pragmatic Research Institute Pte, Ltd, Singapore, Singapore. dprice@rirl.org.
Observational & Pragmatic Research Institute · SGPharmo Institute · NLBrigham and Women's Hospital · USCincinnati Children's Hospital Medical Center · USRadboud University Nijmegen · NLUniversité Paris Cité · FRUniversity Medical Center Groningen · NLUniversity of Amsterdam · NLUniversity of Colorado Denver · USUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost randomised clinical trials typically exclude a significant proportion of asthma patients, including those at higher risk of adverse events, with comorbidities, obesity, poor inhaler technique and adherence, or smokers. However, these patients might differentially benefit from extrafine-particle inhaled corticosteroids (ICS). This matched cohort, database study, compared the effectiveness of extrafine-particle with fine-particle ICS in a real-life population initiating ICS therapy in the Netherlands.

methodsData were from the Pharmo Database Network, comprising pharmacy and hospital discharge records, representative of 20 % of the Dutch population. The study population included patients aged 12 - 60, with a General Practice-recorded diagnosis for asthma (International Classification of Primary Care code R96), when available, ≥2 prescriptions for asthma therapy at any time in their recorded history, and receiving first prescription of ICS therapy as either extrafine-particle (ciclesonide or hydrofluoroalkane beclomethasone dipropionate [BDP]) or fine-particle ICS (fluticasone propionate or non-extrafine-particle-BDP). Patients were matched (1:1) on relevant demographic and clinical characteristics over 1-year baseline. Primary outcomes were severe exacerbation rates, risk domain asthma control and overall asthma control during the year following first ICS prescription. Secondary outcomes, treatment stability and being prescribed higher versus lower category of short-acting β2 agonists (SABA) dose, were compared over a 1-year outcome period using conditional logistic regression models.

resultsFollowing matching, 1399 patients were selected in each treatment cohort (median age: 43 years; males: 34 %). Median (interquartile range) initial ICS doses (fluticasone-equivalents in μg) were 160 (160 - 320) for extrafine-particle versus 500 (250 - 500) for fine-particle ICS (p < 0.001). Following adjustment for residual confounders, matched patients prescribed extrafine-particle ICS had significantly lower rates of exacerbations (adjusted rate ratio [95 % CI], 0.59 [0.47-0.73]), and significantly higher odds of achieving asthma control and treatment stability in the year following initiation than those prescribed fine-particle ICS, and this occurred at lower prescribed doses. Patients prescribed extrafine-particle ICS had lower odds of being prescribed higher doses of SABA (0.50 [0.44-0.57]).

conclusionIn this historical, matched study, extrafine-particle ICS was associated with better odds of asthma control than fine-particle ICS in patients prescribed their first ICS therapy in the Netherlands. Of importance, this was reached at significantly lower prescribed dose.

Indexed as

Particle SizeAdministration, InhalationAdrenal Cortex HormonesAdultAnti-Asthmatic AgentsAsthmaBeclomethasoneCohort StudiesDatabases, FactualFemaleFluticasoneHumansLogistic ModelsMaleMiddle AgedNetherlandsAdrenal Cortex HormonesAnti-Asthmatic AgentsBeclomethasoneciclesonideFluticasonePregnenedionesAsthmaEffectivenessExtrafine-particleFine-particleInhaled corticosteroids

Identifiers

PMID27184175
PMCPMC4869182
OpenAlexW2394947096

What OpenQuestion holds

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LicenceCC BY
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.