Volume 56, Issue 7 pp. 2036-2042
ORIGINAL ARTICLE

Bronchodilator responsiveness in cystic fibrosis children treated for pulmonary exacerbations

Mordechai Pollak MD, MSc

Mordechai Pollak MD, MSc

Division of Respiratory Medicine, Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

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Michelle Shaw MSc

Michelle Shaw MSc

Translational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

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David Wilson BSc

David Wilson BSc

Division of Respiratory Medicine, Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

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Melinda Solomon MD

Melinda Solomon MD

Division of Respiratory Medicine, Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

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Felix Ratjen MD, PhD

Felix Ratjen MD, PhD

Division of Respiratory Medicine, Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

Translational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

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Hartmut Grasemann MD

Corresponding Author

Hartmut Grasemann MD

Division of Respiratory Medicine, Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

Translational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

Correspondence Hartmut Grasemann, MD, Hospital for Sick Children, 555 University Ave, Toronto, ON M5G 1X8, Canada.

Email: [email protected]

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First published: 08 April 2021

Abstract

Background

Cystic fibrosis (CF) pulmonary exacerbations (PEx) are associated with a significant drop in pulmonary function. The clinical value of measuring bronchodilator (BD) responsiveness during treatment for PEx to monitor or predict recovery of lung function is unclear.

Methods

A retrospective analysis of spirometry with BD response testing obtained during hospital admissions for PEx in pediatric CF patients. Repeated events were included for patients with BD testing during multiple admissions.

Results

Two hundred forty-nine spirometries with BD testing in 102 patients were completed around Day 7 (Days 4–10) of hospital admission for treatment of CF PEx. Median (IQR) forced expiratory volume in 1 s (FEV1) was 70.6% predicted (58.1, 84.6) before the PEx event (best FEV1 in 6 months before admission), 54.4% (41.5, 66.9) at admission, 62.3% (48.4, 74.7) around Day 7 of admission and 67.1% predicted (53.8, 78.2) at the end of treatment. BD response around Day 7 correlated poorly with FEV1 before PEx (r = −.16, p = .02) and did not correlate with recovery to baseline FEV1 at end of treatment (r = .08, p = .22). Only 23/249 (9%) individual tests had a BD response in FEV1 of ≥12% and 200 ml. BD response was not related to age or severity of lung disease and led to an immediate change in clinical management in only four cases.

Conclusions

Significant BD response in CF patients treated for PEx is rare, shows poor correlation with baseline pulmonary function and does not correlate with the recovery of FEV1 with treatment. These data suggest that routine testing for BD response is not indicated during PEx.

DATA ACCESSIBILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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