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Clinical features and management of children with primary ciliary dyskinesia in England.

Authors :
Rubbo B
Best S
Hirst RA
Shoemark A
Goggin P
Carr SB
Chetcuti P
Hogg C
Kenia P
Lucas JS
Moya E
Narayanan M
O'Callaghan C
Williamson M
Walker WT
Source :
Archives of disease in childhood [Arch Dis Child] 2020 Aug; Vol. 105 (8), pp. 724-729. Date of Electronic Publication: 2020 Mar 10.
Publication Year :
2020

Abstract

Objective: In England, the National Health Service commissioned a National Management Service for children with primary ciliary dyskinesia (PCD). The aims of this study were to describe the health of children seen in this Service and compare lung function to children with cystic fibrosis (CF).<br />Design: Multi-centre service evaluation of the English National Management PCD Service.<br />Setting: Four nationally commissioned PCD centres in England.<br />Patients: 333 children with PCD reviewed in the Service in 2015; lung function data were also compared with 2970 children with CF.<br />Results: Median age at diagnosis for PCD was 2.6 years, significantly lower in children with situs inversus (1.0 vs 6.0 years, p<0.001). Compared with national data from the CF Registry, mean (SD) %predicted forced expiratory volume in one second (FEV <subscript>1</subscript> ) was 76.8% in PCD (n=240) and 85.0% in CF, and FEV <subscript>1</subscript> was lower in children with PCD up to the age of 15 years. Approximately half of children had some hearing impairment, with 26% requiring hearing aids. Children with a lower body mass index (BMI) had lower FEV <subscript>1</subscript> (p<0.001). One-third of children had positive respiratory cultures at review, 54% of these grew Haemophilus influenzae .<br />Conclusions: We provide evidence that children with PCD in England have worse lung function than those with CF. Nutritional status should be considered in PCD management, as those with a lower BMI have significantly lower FEV <subscript>1</subscript> . Hearing impairment is common but seems to improve with age. Well-designed and powered randomised controlled trials on management of PCD are needed to inform best clinical practice.<br />Competing Interests: Competing interests: JL reports grants, personal fees and non-financial support from Aerocrine/ Circassia, grants and personal fees from Vertex, grants from Parion, outside the submitted work. SC reports grants, personal fees and non-financial support from Vertex Pharmaceuticals, grants and other from Chiesi Pharmaceuticals, other from Pharmaxis Pharmaceuticals, personal fees from Actavis Pharmaceuticals, other from Profile Pharma, outside the submitted work.<br /> (© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
1468-2044
Volume :
105
Issue :
8
Database :
MEDLINE
Journal :
Archives of disease in childhood
Publication Type :
Academic Journal
Accession number :
32156696
Full Text :
https://doi.org/10.1136/archdischild-2019-317687