Evidence map›Paper›PMID 20159245›Full record

Trial reportThe Journal of allergy and clinical immunology2010

Predictors of remitting, periodic, and persistent childhood asthma.

Ronina A Covar, Robert Strunk, Robert S Zeiger, Laura A Wilson, Andrew H Liu, Scott Weiss, James Tonascia, Joseph D Spahn, Stanley J Szefler, Childhood Asthma Management Program Research Group

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

41 citing papers in PubMed, 107 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Observational
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Remission of persistent childhood asthma: Early predictors of adult outcomes.The Journal of allergy and clinical immunology · 2019
    Article
  16. Review
  17. Review
  18. Modeling asynchronous event sequences with RNNs.Journal of biomedical informatics · 2018
    Article
  19. Article
  20. 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

10 authors at 6 institutions in 1 country.

Ronina A CovarNational Jewish Health, Denver, CO 80206, USA. covarr@njhealth.org
Robert Strunk
Robert S Zeiger
Laura A Wilson
Andrew H Liu
Scott Weiss
James Tonascia
Joseph D Spahn
Stanley J Szefler
Childhood Asthma Management Program Research Group
University of Colorado Denver · USJohns Hopkins University · USBrigham and Women's Hospital · USNational Jewish Health · USSt. Louis Children's Hospital · USUniversity of California, San Diego · US

Funding

ZOPOLRESTAT PHARMACOKINETICS IN DIABETICS WITH VARYING RENAL FUNCTIONM01RR000051 · NCRR · UNIVERSITY OF COLORADO DENVER · PI KOSMISKI, LISA A. · 1985 to 2008
$52.6M
YOGA FOR THE MANAGEMENT OF HIV-METABOLIC SYNDROMESM01RR000036 · NCRR · WASHINGTON UNIVERSITY · PI NEWCOMER, JOHN W. · 1985 to 2007
$25.4M
ZINC THERAPY FOR SCLERODERMA--PHASE I STUDYM01RR002719 · NCRR · JOHNS HOPKINS UNIVERSITY · PI EARLEY, CHRISTOPHER J · 1986 to 2007
$20.2M
CLINICAL CENTER FOR CAMPN01HR016049 · HR · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 1991 to 2000
$1.0M
CLINICAL COORDINATING CENTER FOR CAMPN01HR016044 · HR · JOHNS HOPKINS UNIVERSITY · PI TONASCIA, JAMES A · 1991 to 2006
$729k
CLINICAL CENTER FOR CAMPN01HR016050 · HR · ASTHMA, INC. · PI SHAPIRO, GAIL G · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016051 · HR · WASHINGTON UNIVERSITY · PI STRUNK, ROBERT C · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016052 · HR · JOHNS HOPKINS UNIVERSITY · PI ADKINSON, N FRANKLIN · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016045 · HR · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI ZEIGER, ROBERT S · 1991 to 2001
$0k
CLINICAL CENTER FOR CAMPN01HR016046 · HR · UNIVERSITY OF NEW MEXICO · PI KELLY, H W · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016047 · HR · HOSPITAL FOR SICK CHLDRN (TORONTO) · PI MACLUSKY, IAN B · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016048 · HR · NATIONAL JEWISH HEALTH · PI SZEFLER, STANLEY J · 1991 to 2000
$0k
NCRR NIH HHS M01 RR000036NCRR NIH HHS M01 RR000051NCRR NIH HHS M01RR00051NCRR NIH HHS M01 RR002719NCRR NIH HHS M01RR0099718-24NCRR NIH HHS M01RR02719-14NCRR NIH HHS RR00036NHLBI NIH HHS N01 HR016044NHLBI NIH HHS N01-HR-16044NHLBI NIH HHS N01-HR-16045NHLBI NIH HHS N01-HR-16046NHLBI NIH HHS N01-HR-16047NHLBI NIH HHS N01-HR-16048NHLBI NIH HHS N01-HR-16049NHLBI NIH HHS N01-HR-16050NHLBI NIH HHS N01-HR-16051NHLBI NIH HHS N01-HR-16052
6 · The paper itself

Abstract

backgroundThe course of mild to moderate persistent asthma in children is not clearly established.

objectiveTo determine the rate and predictors for remitting, periodic, and persistent asthma in adolescence.

methodsThe Childhood Asthma Management Program (CAMP) was a 4.3-year randomized, double-masked, multicenter trial in children with mild to moderate persistent asthma that compared continuous therapy with either budesonide or nedocromil, each to placebo, followed by a 4-year observational follow-up period. Asthma activity during the observation period included remitting (no asthma activity in the last year), persistent (asthma activity in every quarter), and periodic asthma (neither remitting nor persistent).

resultsAsthma was identified as remitting in 6%, periodic in 39%, and persistent in 55% of the 909 participants, with no effect noted from earlier anti-inflammatory treatment during the CAMP trial. Within all 3 asthma activity categories, improvements in airway hyperresponsiveness, eosinophilia, and asthma morbidity were observed over time. Features at entry into CAMP associated with remitting versus persistent asthma were lack of allergen sensitization and exposure to indoor allergens (odds ratio [OR], 3.23; P < .001), milder asthma (OR, 2.01; P = .03), older age (OR, 1.23; P = .01), less airway hyperresponsiveness (higher log methacholine FEV(1) PC(20) (OR, 1.39; P = .03), higher prebronchodilator FEV(1) percent predicted (OR, 1.05; P = .02), and lower forced vital capacity percent predicted (OR, 0.96; P = .04).

conclusionRemission of asthma in adolescence is infrequent and not affected by 4 years of anti-inflammatory controller therapy. Factors such as sensitization and exposure, low lung function, and airway greater hyperresponsiveness decrease the likelihood of remitting asthma.

Indexed as

AdolescentAnti-Asthmatic AgentsAsthmaBudesonideChildChild, PreschoolDouble-Blind MethodFemaleHumansMaleNedocromilRespiratory Function TestsTreatment OutcomeAnti-Asthmatic AgentsBudesonideNedocromil

Identifiers

PMID20159245
PMCPMC2844768
OpenAlexW2064196306

What OpenQuestion holds

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Registered trials

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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.