Evidence map›Paper›PMID 30350255›Full record

ArticleQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2019

Development and construct validation of a parent-proxy quality of life instrument in children with bronchopulmonary dysplasia aged 4-8 years old.

Lysbert Meijer-Schaap, Anthony E J Dubois, Boudewijn J Kollen, Jet Tijmens-van der Hulst, Bertine M J Flokstra-de Blok, Elianne J L E Vrijlandt

Abstract read
In one paragraph

Article in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2019. 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
–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

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

  1. Quality of life of patients and caregivers affected by bronchopulmonary dysplasia: a systematic review.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2023
    Pooled it
  2. Review
  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

6 authors.

Lysbert Meijer-SchaapDepartment of Pulmonary Diseases and Tuberculosis, University Medical Center Groningen, University of Groningen, Hanzeplein 1, Postbus 30.001, 9700 RB, Groningen, The Netherlands. l.schaap@umcg.nl.ORCID http://orcid.org/0000-0002-2925-5619
Anthony E J DuboisDepartment of Pediatrics, Division of Pediatric Pulmonology and Allergy, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Boudewijn J KollenDepartment of General Practice, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Jet Tijmens-van der HulstDepartment of Pediatrics, Division of Pediatric Pulmonology and Allergy, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Bertine M J Flokstra-de BlokGRIAC Research Institute, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Elianne J L E VrijlandtDepartment of Pediatrics, Division of Pediatric Pulmonology and Allergy, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Funding

Stichting Astma Bestrijding SAB 2012/028
6 · The paper itself

Abstract

purposeChildren with bronchopulmonary dysplasia often develop complications that affect them well into adult life. Very little is known about how this affects their quality of life, since no sensitive instrument is available to measure health-related quality of life in this population. In this study, a Dutch parent-proxy instrument was developed for this purpose.

methodsA list of items was generated after literature search and interviews with both parents of patients and clinical experts. Clinically relevant items were selected with the clinical impact method and item analysis. Results of clinical tests to measure complications in children with bronchopulmonary dysplasia were correlated with these items to select the items that show construct validity. Cronbach's alpha was calculated to estimate internal consistency of the items in the final questionnaire.

resultsIn total, 92 children and their parents and 7 clinicians participated. Of 130 identified items, 47 showed clinical relevance. Spirometry, the Child Behavior Checklist, mean arterial pressure, and body mass index were used to determine construct validity of 33 items. These items were structured within five domains: pulmonary complaints, school functioning, growth and nutrition, exercise and locomotion, emotional functioning and health care concerns. The questionnaire showed excellent internal consistency with Cronbach's alpha of 0.919.

conclusionThis study developed a disease-specific parent-proxy instrument to measure health-related quality of life in children with bronchopulmonary dysplasia aged 4-8 years old, the BPD-QoL. All included items show construct validity and internal consistency reliability. Future research should focus on further validation and analysis of responsiveness and reliability.

Indexed as

Bronchopulmonary DysplasiaChildChild, PreschoolFemaleHumansMalePsychometricsQuality of LifeReproducibility of ResultsSurveys and QuestionnairesBronchopulmonary dysplasiaChildrenHealth-related quality of lifeInstrument development

Identifiers

PMID30350255
PMCPMC6373528

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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.