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Multicenter Study
. 2022 Nov;19(11):1865-1870.
doi: 10.1513/AnnalsATS.202202-116OC.

Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia

Affiliations
Multicenter Study

Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia

Wallace B Wee et al. Ann Am Thorac Soc. 2022 Nov.

Abstract

Rationale: Primary ciliary dyskinesia (PCD), an inherited lung disease, is characterized by abnormal ciliary function leading to progressive bronchiectasis. There is wide variability in respiratory disease severity at birth and later in life. Objectives: To evaluate the association between neonatal hospital length of stay (neonatal-LOS) and supplemental oxygen duration (SuppO2) with lung function in pediatric PCD. We hypothesized that longer neonatal-LOS and SuppO2 are associated with worse lung function (i.e., forced expiratory volume in 1 second percent predicted [FEV1pp]). Methods: We performed a secondary analysis of the Genetic Disorders of Mucociliary Clearance Consortium prospective longitudinal multicenter cohort study. Participants enrolled, during 2006-2011, were <19 years old with a confirmed PCD diagnosis and followed annually for 5 years. The exposure variables were neonatal-LOS and SuppO2, counted in days since birth. The outcome, FEV1pp, was measured annually by spirometry. The associations of neonatal-LOS and SuppO2 with FEV1pp were evaluated with a linear mixed-effects model with repeated measures and random intercepts, adjusted for age and ciliary ultrastructural defects. Results: Included were 123 participants (male, 47%; mean enrollment age, 8.3 yr [range, 0 to 18 yr]) with 578 visits (median follow-up, 5 yr). The median neonatal-LOS was 9 d (range, 1 to 90 d), and median SuppO2 was 5 d (range, 0 to 180 d). Neonatal-LOS was associated with worse lung function (-0.27 FEV1pp/d [95% confidence interval, -0.53 to -0.01]; P = 0.04). SuppO2 was not associated with lung function. Conclusions: Neonatal-LOS is associated with worse lung function in pediatric PCD, independent of age and ultrastructural defects. Future research on the mechanisms of neonatal respiratory distress and its management may help us understand the variability of lung health outcomes in PCD.

Keywords: lung function; neonatal; pediatric; primary ciliary dyskinesia.

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Figures

Figure 1.
Figure 1.
Flowchart of participant enrollment. FEV1pp = forced expiratory volume in 1 second percent predicted; PCD = primary ciliary dyskinesia.
Figure 2.
Figure 2.
Number of participants with a given neonatal hospital length of stay

References

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