Evidence map›Paper›PMID 16168062›Full record

Trial reportRespiratory research2005

Tolerance to bronchodilation during treatment with long-acting beta-agonists, a randomised controlled trial.

Sarah Haney, Robert J Hancox

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Respiratory research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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.

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

16 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Advances in the Association Between theCurrent issues in molecular biology · 2026
    Review
  5. Article
  6. Article
  7. Dexamethasone rescues TGF-β1-mediated βRespiratory research · 2020
    Article
  8. Mechanopharmacology and Synergistic Relaxation of Airway Smooth Muscle.Journal of engineering and science in medical diagnostics and therapy · 2019
    Article
  9. Review
  10. Loss of bronchoprotection to Salbutamol during sputum induction with hypertonic saline: implications for asthma therapy.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
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

2 authors.

Sarah HaneyFreeman Hospital, Newcastle-upon-Tyne, UK. sas_haney@yahoo.co.uk
Robert J Hancox

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegular use of beta-agonists leads to tolerance to their bronchodilator effects. This can be demonstrated by measuring the response to beta-agonist following bronchoconstriction using methacholine. However most studies have demonstrated tolerance after a period of beta-agonist withdrawal, which is not typical of their use in clinical practice. This study assessed tolerance to the bronchodilator action of salbutamol during ongoing treatment with long-acting beta-agonist.

methodsRandom-order, double-blind, placebo-controlled, crossover trial. After 1 week without beta-agonists, 13 asthmatic subjects inhaled formoterol 12 microg twice daily or matching placebo for 1 week. Eight hours after the first and last doses subjects inhaled methacholine to produce a 20% fall in FEV1. Salbutamol 100, 200 and 400 microg (cumulative dose) was then given at 5-minute intervals and FEV1 was measured 5 minutes after each dose. After a 1 week washout subjects crossed over to the other treatment. Unscheduled use of beta-agonists was not allowed during the study. The main outcome variable was the area under the salbutamol response curve.

resultsThe analysis showed a significant time by treatment interaction indicating that the response to salbutamol fell during formoterol therapy compared to placebo. After 1 week of formoterol the area under the salbutamol response curve was 48% (95% confidence interval 28 to 68%) lower than placebo. This reduction in response remained significant when the analyses were adjusted for changes in the pre-challenge FEV1 and dose of methacholine given (p = 0.001).

conclusionThe bronchodilator response to salbutamol is significantly reduced in patients taking formoterol. Clinically relevant tolerance to rescue beta-agonist treatment is likely to occur in patients treated with long-acting beta-agonists.

Indexed as

Bronchial Provocation TestsAdministration, InhalationAdrenergic beta-AgonistsAdultAlbuterolAsthmaBronchoconstrictionBronchodilator AgentsCross-Over StudiesDose-Response Relationship, DrugDouble-Blind MethodDrug ToleranceEthanolaminesFemaleFormoterol FumarateHumansAdrenergic beta-AgonistsAlbuterolBronchodilator AgentsEthanolaminesFormoterol FumarateMethacholine Chloride

Identifiers

PMID16168062
PMCPMC1266400

What OpenQuestion holds

Textmetadata
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.