Therapies Used by Children With Primary Ciliary Dyskinesia: A Natural History Study
- PMID: 39575633
- PMCID: PMC11750599
- DOI: 10.1002/ppul.27412
Therapies Used by Children With Primary Ciliary Dyskinesia: A Natural History Study
Abstract
Introduction: Primary ciliary dyskinesia (PCD) management has not been systematically evaluated and is largely empirical.
Methods: Pediatric participants with PCD were enrolled in a prospective, longitudinal, multicenter, observational study. Therapies were recorded at annual visits and categorized by type. Age-related trends in prevalence of therapies were described by serial cross-sectional analyses. Generalized estimating equations analyzed covariates affecting prevalence of certain therapies and whether these covariates impacted oral antibiotic courses.
Results: A total of 137 participants completed 897 visits over 13 years. All but one received ≥ 1 antibiotic courses during study participation, most often cephalosporins (74%) or amoxicillin-clavulanate (73%). Thirty-one percent reported chronic azithromycin use. Per participant, there was an average of 2.3 (SD = 2.2) oral antibiotic courses annually. The rate of reported antibiotic courses at the 6 United States sites was 2.6 times higher compared to the Canadian site (p < 0.001). As patients got older, they were more likely to report use of amoxicillin-clavulanate (p < 0.001), chronic azithromycin (p < 0.001), fluroquinolones (p < 0.001), inhaled steroids with long-acting beta-agonists (p = 0.010), and hypertonic saline (p < 0.001). Compared to outer dynein arm defects, those with inner dynein arm/microtubular disorganization defects reported increased use of chronic azithromycin (p = 0.011) and inhaled steroids (p = 0.015).
Discussion: Older participants and those with inner dynein arm/microtubular disorganization defects reported more therapies likely due to disease progression and more severe phenotypes, respectively. We report that a wide range of therapies are used in PCD without disease-specific studies defining benefits and risks.
Keywords: natural history; primary ciliary dyskinesia; therapy.
© 2024 Wiley Periodicals LLC.
Conflict of interest statement
Conflict of interest statement: Disclosures according to the International Committee of Medical Journal Editors can be found through the supplemental documents.
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- UM1 HG006504/HG/NHGRI NIH HHS/United States
- U2C TR002818/TR/NCATS NIH HHS/United States
- Funding support for research was provided by US NIH/ORDR/NCATS/NHLBI grant U54HL096458; NIH/NCATS Colorado CTSA Grant UM1TR004399; US NIH/NHLBI grant R01HL071798. The Genetic Disorders of Mucociliary Clearance Consortium (U54HL096458) is part of the National Center for Advancing Translational Sciences (NCATS) Rare Diseases Clinical Research Network (RDCRN) and supported by the RDCRN Data Management and Coordinating Center (DMCC) (U2CTR002818). RDCRN is an initiative of the Office of Rare Diseases Research (ORDR) funded through a collaboration between NCATS and National Heart, Lung, and Blood Institute (NHLBI).
- U54 HL096458/HL/NHLBI NIH HHS/United States
- R01 HL071798/HL/NHLBI NIH HHS/United States
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