Real-world assessment of LCI following lumacaftor-ivacaftor initiation in adolescents and adults with cystic fibrosis

被引:5
|
作者
Reix, Philippe [1 ,2 ]
Tatopoulos, Aurelie [3 ]
Ioan, Iulia [4 ]
Le Bourgeois, Muriel [5 ]
Bui, Stephanie [6 ,7 ]
Choukroun, Marie Luce [8 ]
Bessaci-Kabouya, Katia [9 ,10 ]
Gerardin, Michele [11 ]
Bokov, Plamen [12 ,13 ]
Da Silva, Jennifer [14 ,15 ,16 ]
Paillasseur, Jean-Louis [17 ]
Burgel, Pierre Regis [14 ,15 ,18 ,19 ]
机构
[1] Hosp Civils Lyon, Cyst Fibrosis Ctr, Lyon, France
[2] Univ Claude Bernard Lyon 1, UMR 5558, Equipe EMET, CNRS, Lyon, France
[3] CHU Nancy, Hop Enfants, Pediat Cyst Fibrosis Ctr, Nancy, France
[4] CHU Nancy, Hop Enfants, Serv Explorat Fonctionnelles Pediat, Nancy, France
[5] Hop Univ Necker Enfants Malad, Pediat Resp Dis & Cyst Fibrosis Ctr, Natl Reference Cyst Fibrosis Reference Ctr, Paris, France
[6] CHU Bordeaux, Pediat Resp Dis & Cyst Fibrosis Ctr, Bordeaux, France
[7] CHU Bordeaux, CIC 1401, Bordeaux, France
[8] CHU Bordeaux, Serv Explorat Fonctionnelles Resp Pediat, Bordeaux, France
[9] Amer Mem Hosp, Dept Pediat A, Reims, France
[10] Amer Mem Hosp, Cyst Fibrosis Ctr, Reims, France
[11] Hop Robert Debre, AP HP, Pediat Cyst Fibrosis Ctr, Paris, France
[12] Hop Robert Debre, AP HP, Serv Physiol Pediat, Paris, France
[13] Univ Paris, UMR1141, Equipe NeoPhen, INSERM Cotutelle, Paris, France
[14] Univ Paris, Paris U1016, Inst Cochin, INSERM, Paris, France
[15] ERN Lung CF Network, Paris, France
[16] Hop Cochin, AP HP, URC CIC Paris Descartes Necker Cochin, Paris, France
[17] Effi Stat, Paris, France
[18] Cochin Hosp, AP HP, Resp Med, Paris, France
[19] Cochin Hosp, AP HP, Natl Cyst Fibrosis Reference Ctr, Paris, France
关键词
Lumacaftor; CFTR modulators; Cystic fibrosis; Multiple breath washout; LUNG CLEARANCE INDEX; AGED; 6-11; YEARS;
D O I
10.1016/j.jcf.2021.06.002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Lung clearance index (LCI) is a biomarker of ventilation inhomogeneity. Data are scarce on its usefulness in daily practice for monitoring the effects of treatments in older children and adults with CF. In this French observational study of lumacaftor-ivacaftor, 63 of 845 patients (7.5%) had available LCI performed at baseline and at six (M6; n = 34) or 12 months (M12; n = 46) after lumacaftor-ivacaftor initiation. At inclusion, median [IQR] age was 16 years [13-17], ppFEV 1 was 72.8 [59.6-80.7], and LCI was 12.3 [10.315.0]. At both M6 and M12, no statistically significant LCI increases of 0.13 units or 1.34% (95% CI: 4.85-7.53) and 0.6 units or 6.66% (95% CI: -0.03-13.5) were observed. Discordant results between LCI and ppFEV 1 were observed in one-third of the patients. In daily practice, LCI monitoring in adolescents and young adults with moderate lung disease gives results that are more heterogenous than those reported in children with milder disease.
引用
收藏
页码:155 / 159
页数:5
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