Evidence map›Paper›PMID 24524222›Full record

Trial reportThe Journal of asthma : official journal of the Association for the Care of Asthma2014

Fixed airflow obstruction in asthma: a descriptive study of patient profiles and effect on treatment responses.

Donald P Tashkin, Bradley E Chipps, Frank Trudo, James G Zangrilli

2 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of asthma : official journal of the Association for the Care of Asthma, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 29% 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.

NCT00651651 phase3completednot on this map

A 12 Week Randomized, Double-blind, Double-Dummy, Placebo-controlled Trial of Symbicort TM (160/4.5mcg) Versus Its Mono-Products (Budesonide and Formoterol) in Children (at Least 6years of Age) and Adults With Asthma-SPRUCE 80/4.5

TypeinterventionalSponsorAstraZenecaRan2002 to 2003Enrolled450ConditionsAsthmaArmsbudesonide/formoterol, budesonide, formoterol
NCT00652002 phase3completednot on this map

A 12 Week, Randomized, Double-blind, Double-dummy, Placebo-controlled Trial of Symbicort TM (160/4.5mcg) Versus Its Mono-products (Budesonide and Formoterol) in Adolescents (at Least 12 Years of Age) and Adults With Asthma - SPRUCE 160/4.5

TypeinterventionalSponsorAstraZenecaRan2002 to 2004Enrolled450ConditionsAsthmaArmsbudesonide/formoterol, budesonide, formoterol
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 36 citations in OpenAlex.

  1. Persistent airway obstruction in severe eosinophilic asthma: targeting interleukin-5 and eosinophils.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Sex and gender in asthma.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
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

4 authors at 3 institutions in 3 countries.

Donald P TashkinDavid Geffen School of Medicine at UCLA, Division of Pulmonary & Critical Care Medicine, University of California , Los Angeles, CA , USA .
Bradley E Chipps
Frank Trudo
James G Zangrilli
AstraZeneca (Germany) · DEAstraZeneca (United Kingdom) · GBCapital Allergy and Respiratory Disease Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of fixed airflow obstruction (FAO) in asthma is unclear.

objectiveTo assess the relationship between FAO and clinical features of asthma and the effect of FAO on treatment response.

methodsPost hoc descriptive analysis of data stratified by FAO category (screening post-albuterol FEV1/FVC <lower limit of normal [LLN] [FAO+] or ≥LLN [FAO-]) from two 12-week, randomized, placebo-controlled studies of budesonide/formoterol or the monocomponents in mild-moderate (study I; aged ≥6 years; NCT00651651; placebo run-in) or moderate-severe (study II; ≥12 years; NCT00652002; budesonide run-in) asthma patients.

resultsAt baseline, FAO+ versus FAO- patients were more likely male and had longer asthma duration and worse pulmonary function. During the treatment period, lung function and asthma control measures with placebo were generally worse in FAO+ versus FAO- patients. Budesonide was effective on most end points in both FAO+ and FAO- patients. In contrast to FAO- patients, FAO+ patients were unresponsive to formoterol monotherapy in both study populations. Consistently greater improvements in most end points (including worsening of asthma as predefined by specific lung function parameters or clinical symptoms) were observed moving from formoterol to budesonide to budesonide/formoterol in both FAO+ and FAO- patients, with generally greater than additive effects on lung function with budesonide/formoterol in FAO+ patients.

conclusionsFAO+ patients tended to be more impaired and at greater risk for an asthma event versus FAO- patients. While FAO+ patients were non-responsive to formoterol monotherapy, they retained responsiveness to budesonide and had the greatest lung function and control responses to budesonide/formoterol that were similar to or greater than responses of FAO- patients.

Indexed as

AdolescentAdultAirway ObstructionAlbuterolAsthmaBronchodilator AgentsBudesonideChildDouble-Blind MethodEthanolaminesFormoterol FumarateHumansMiddle AgedRespiratory Function TestsSeverity of Illness IndexSex FactorsAlbuterolBronchodilator AgentsBudesonideEthanolaminesFormoterol FumarateAirflow limitationairway inflammationbudesonidecombination therapyformoterolinhaled corticosteroidlung function

Identifiers

PMID24524222
PMCPMC4162502
OpenAlexW2045185638

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.