Home Cough Monitoring Reveals Higher Nighttime Cough Burden in Children With Cystic Fibrosis Compared With Healthy Children

A passive cough monitor detected nighttime cough in cwCF and HC. CwCF with preserved lung function have more nights with cough than HC despite being on elexacator/tezacaftor/ivacaftor (ETI).

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Publication Details

Journal
Pediatric Pulmonology
Published
2025-11-01
DOI
https://doi.org/10.1002/ppul.71351
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.00
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article

Home Cough Monitoring Reveals Higher Nighttime Cough Burden in Children With Cystic Fibrosis Compared With Healthy Children

Edith T. Zemanick, Tim Vigers, Jordana E. Hoppe, Scott D. Sagel et al.
Pediatric Pulmonology
Cystic Fibrosis Research Advances
article

Home Cough Monitoring Reveals Higher Nighttime Cough Burden in Children With Cystic Fibrosis Compared With Healthy Children

Edith T. Zemanick, Tim Vigers, Jordana E. Hoppe, Scott D. Sagel, E. Hanley, Amanda I. Messinger, L. Melzer
article en

Abstract

A passive cough monitor detected nighttime cough in cwCF and HC. CwCF with preserved lung function have more nights with cough than HC despite being on elexacator/tezacaftor/ivacaftor (ETI).

Pediatric PulmonologyVol. 60(11)
Children's Hospital Colorado (US), Barbara Bush Children’s Hospital (US), University of Colorado Anschutz Medical Campus (US), University of Colorado Denver (US)
Openalex Percentile: Top 50%
Cystic Fibrosis Research Advances
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