Evidence map›Paper›PMID 34143539›Full record

ArticlePediatric pulmonology2021

Hyperinflation is associated with increased respiratory rate and is a more sensitive measure of cystic fibrosis lung disease during infancy compared to forced expiratory measures.

Heather N Muston, James E Slaven, Christina Tiller, Charles Clem, Thomas W Ferkol, Sarath Ranganathan, Stephanie D Davis, Clement L Ren

Open access · bronzeAbstract read
In one paragraph

Article in Pediatric pulmonology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Observational
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

8 authors at 4 institutions in 2 countries.

Heather N MustonDivision of Pediatric Pulmonology, Allergy and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID 0000-0001-8369-3110
James E SlavenDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Christina TillerDivision of Pediatric Pulmonology, Allergy and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Charles ClemDivision of Pediatric Pulmonology, Allergy and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Thomas W FerkolDepartment of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
Sarath RanganathanDepartment of Paediatrics, Murdoch Children's Research Institute, University of Melbourne, Melbourne, Australia.
Stephanie D DavisDepartment of Pediatrics, The University of North Carolina, Chapel Hill, North Carolina, USA.
Clement L RenDivision of Pediatric Pulmonology, Allergy and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID 0000-0003-4431-0644
Indiana University School of MedicineThe University of Melbourne · AUUniversity of North Carolina at Chapel Hill · USWashington University in St. Louis · US

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Viral Pathogenesis of Early Cystic Fibrosis Lung DiseaseR01HL116211 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI DAVIS, STEPHANIE DUGGINS, FERKOL, THOMAS W · 2012 to 2015
$2.2M
NCATS NIH HHS UL1 TR001108NHLBI NIH HHS R01 HL116211
6 · The paper itself

Abstract

backgroundThe goal of this study was to identify clinical features associated with abnormal infant pulmonary function tests (iPFTs), specifically functional residual capacity (FRC), in infants with cystic fibrosis (CF) diagnosed via newborn screen (NBS). We hypothesized that poor nutritional status in the first 6-12 months would be associated with increased FRC at 12-24 months.

methodsThis study utilized a combination of retrospectively and prospectively collected data from ongoing research studies and iPFTs performed for clinical indications. Demographic and clinical features were obtained from the electronic medical record. Forced expiratory flows and volumes were obtained using the raised volume rapid thoracoabdominal technique (RVRTC) and FRC was measured via plethysmography.

resultsA total of 45 CF NBS infants had iPFTs performed between 12 and 24 months. Mean forced vital capacity, forced expiratory volume in 0.5 s, and forced expiratory flows were all within normal limits. In contrast, the mean FRC z-score was 2.18 (95% confidence interval [CI] = 1.48, 2.88) and the mean respiratory rate (RR) z-score was 1.42 (95% CI = 0.95, 1.89). There was no significant association between poor nutritional status and abnormal lung function. However, there was a significant association between higher RR and increased FRC, and a RR cutoff of 36 breaths/min resulted in 92% sensitivity to detect hyperinflation with 32% specificity.

conclusionThese results suggest that FRC is a more sensitive measure of early CF lung disease than RVRTC measurements and that RR may be a simple, noninvasive clinical marker to identify CF NBS infants with hyperinflation.

Indexed as

Cystic FibrosisForced Expiratory VolumeHumansInfantInfant, NewbornLungRespiratory RateRetrospective StudiesVital Capacitycystic fibrosisinfant pulmonary functionpulmonary function testingpulmonary physiology

Identifiers

PMID34143539
PMCPMC8373786
OpenAlexW3167741896

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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.