Evidence map›Paper›PMID 36291452›Full record

ArticleChildren (Basel, Switzerland)2022

Risk Factors for Lung Function Decline in Pediatric Asthma under Treatment: A Retrospective, Multicenter, Observational Study.

Shingo Yamada, Takao Fujisawa, Mizuho Nagao, Hiroshi Matsuzaki, Chikako Motomura, Hiroshi Odajima, Toshinori Nakamura, Takanori Imai, Ken-Ichi Nagakura, Noriyuki Yanagida and 7 more

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

17 authors at 6 institutions in 1 country.

Shingo YamadaAllergy Center, National Hospital Organization Mie National Hospital, Tsu 514-0125, Japan.ORCID 0000-0001-9250-6241
Takao FujisawaAllergy Center, National Hospital Organization Mie National Hospital, 357 Ozato-kubota, Tsu 514-0125, Japan.ORCID 0000-0002-9196-9436
Mizuho NagaoAllergy Center, National Hospital Organization Mie National Hospital, Tsu 514-0125, Japan.
Hiroshi MatsuzakiDepartment of Pediatrics, National Hospital Organization Fukuoka National Hospital, Fukuoka 811-1394, Japan.
Chikako MotomuraDepartment of Pediatrics, National Hospital Organization Fukuoka National Hospital, Fukuoka 811-1394, Japan.ORCID 0000-0001-9199-1302
Hiroshi OdajimaDepartment of Pediatrics, National Hospital Organization Fukuoka National Hospital, Fukuoka 811-1394, Japan.
Toshinori NakamuraDepartment of Pediatrics, Showa University School of Medicine, Tokyo 142-8666, Japan.ORCID 0000-0002-5176-8277
Takanori ImaiDepartment of Pediatrics, Showa University School of Medicine, Tokyo 142-8666, Japan.ORCID 0000-0002-6003-4996
Ken-Ichi NagakuraDepartment of Pediatrics, National Hospital Organization Sagamihara National Hospital, Sagamihara 252-0392, Japan.
Noriyuki YanagidaDepartment of Pediatrics, National Hospital Organization Sagamihara National Hospital, Sagamihara 252-0392, Japan.
Masatoshi MitomoriDepartment of Pediatrics, National Hospital Organization Sagamihara National Hospital, Sagamihara 252-0392, Japan.
Motohiro EbisawaDepartment of Pediatrics, National Hospital Organization Sagamihara National Hospital, Sagamihara 252-0392, Japan.
Shigenori KabashimaAllergy Center, National Center for Child Health and Development, Tokyo 157-8535, Japan.
Yukihiro OhyaAllergy Center, National Center for Child Health and Development, Tokyo 157-8535, Japan.ORCID 0000-0002-1560-3942
Chizu HabukawaDepartment of Pediatric Allergy, National Hospital Organization Minami Wakayama Medical Center, Tanabe 656-8558, Japan.
Minako TomiitaCenter of Pediatric Allergy and Rheumatology, National Hospital Organization Shimoshizu National Hospital, Yotsukaido 284-0003, Japan.
Masahiro HirayamaDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
National Hospital Organization · JPNational Sagamihara Hospital · JPNational Mie Hospital · JPNational Center For Child Health and Development · JPShowa University · JPMie University · JP

Funding

grant-in-aid from the Environmental Restoration and Conservation Agency of Japa not applicable
6 · The paper itself

Abstract

Background: Childhood asthma is a major risk for low lung function in later adulthood, but what factors in asthma are associated with the poor lung function during childhood is not known. Objective: To identify clinical factors in children with asthma associated with low or declining lung function during the treatment. Methods: We enrolled children with asthma who had been treated throughout three age periods, i.e., 6−9, 10−12, and 13−15 years old, at seven specialized hospitals in Japan. Clinical information and lung function measurements were retrieved from the electronic chart systems. To characterize the lung function trajectories during each age period, we evaluated the forced expiratory volume 1 (FEV1) with % predicted values and individual changes by the slope (S) from linear regression. We defined four trajectory patterns: normal (Group N) and low (Group L), showing %FEV1 ≥80% or <80% throughout all three periods; upward (Group U) and downward (Group D), showing S ≥ 0 or S < 0%. Logistic regression analysis was performed to compare factors associated with the unfavorable (D/L) versus favorable (N/U) groups. Results: Among 273 eligible patients, 197 (72%) were classified into Group N (n = 150)/U (n = 47), while 76 (28%) were in Group D (n = 66)/L (n = 10). A history of poor asthma control, long-acting beta2 agonist use, and a lower height Z-score during 13−15 years were associated with an unfavorable outcome (Group D/L). Conversely, inhaled corticosteroid (ICS) use during 10−12 years and high-dose ICS use during 13−15 years were associated with a favorable outcome (Group N/U). Conclusion: We identified several factors that are associated with unfavorable lung function changes in pediatric asthma. Attention should be paid to the possible relationship between yearly changes in lung function and poor asthma control, use of ICS (and its dose) and use of LABA.

Indexed as

asthmaasthma controlchildhood and adolescenceinhaled corticosteroidslung functionrisk factors

Identifiers

PMID36291452
PMCPMC9600699
OpenAlexW4303627958

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.