Impact of the transition period from childhood to adulthood in cystic fibrosis

被引:2
作者
Louage, A. [1 ]
Knoop, C. [2 ]
Hanssens, L. [1 ]
机构
[1] Univ Libre Bruxelles, Hop Univ Enfants Reine Fabiola ULB, Inst Mucoviscidose, Brussels, Belgium
[2] Univ Libre Bruxelles, Hop Univ Erasme ULB, Inst Mucoviscidose, Brussels, Belgium
关键词
Cystic fibrosis; Transition; Childhood; Adulthood; Lung function; HEALTH OUTCOMES; CARE; ADOLESCENTS; LUNG; SOCIETY;
D O I
10.1016/j.rmr.2019.11.650
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction. The aim of this study was to evaluate the impact of the transition period from childhood to adulthood in patients with cystic fibrosis (CF) being followed up in our reference center. Methods. The clinical, functional, inflammatory and microbiological parameters of all transition patients were compared two years before (T-2) and two years after the transfer (T + 2) from paediatric to adult centers and further analysed according to whether the transition conditions were optimal or suboptimal. Results. Twenty-eight patients were included. The mean age at the transfer visit was 19.5 years (+/-3.5). There were no deaths during the study period. Consultations were more numerous at T-2 [14.5 (+/-5.9) vs. 12.0 (+/-5.1). P`0.004] Chronic colonization with Pseudomonas aeruginosa was more frequent at T+ 2 (46.4% vs. 17.9%, P=0.021). A progressive decrease in FEV1 and FVC was observed between T-2 and T + 2. The number of pulmonary exacerbations was lower in the optimal transition group. Conclusion. The period of transition from childhood to adulthood in patients with CF appears to be associated with functional and microbiological changes. (C) 2019 SPLF. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:235 / 242
页数:8
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