Lung clearance index evaluation in detecting nocturnal hypoxemia in cystic fibrosis patients: Toward a new diagnostic tool
- PMID: 32217291
- DOI: 10.1016/j.rmed.2020.105906
Lung clearance index evaluation in detecting nocturnal hypoxemia in cystic fibrosis patients: Toward a new diagnostic tool
Abstract
Background: Nocturnal hypoxemia adversely affects outcomes in patients with cystic fibrosis (CF). Although an early detection of this abnormality may be desirable, still its predictability remains uncertain. The Lung Clearance Index (LCI) is a measure of lung ventilation distribution obtained from a multiple-breath washout technique (MBW), recently implemented in patients with CF. This study aimed to establish whether the LCI predicts nocturnal hypoxemia in patients with stable CF, with mild to moderate disease, and normal diurnal gas exchange.
Methods: 31 stable patients (15 males, mean age 17.4 ± 5.2 years) with mild to moderate CF, normoxic when awake, were enrolled. In all patients we performed nocturnal cardio-respiratory polygraphy, lung function measurement, and MBW test to derive LCI values.
Results: LCI was abnormal in most of the patients and inversely correlated with mean nocturnal SpO2 (r = -0.880 p < 0.01). A receiver operating characteristic (ROC) analysis, performed to assess whether LCI predicted nocturnal hypoxemia, revealed a high predictive accuracy of LCI for nocturnal desaturation (AUC = 0.96; Youden index = 0.79). Forced expiratory volume in 1 s (FEV1) was predictive only in patients with more severe airway obstruction, with a moderate degree of accuracy (AUC 0.71).
Conclusions: The LCI showed a high effectiveness in predicting nocturnal hypoxemia in stable patients with CF, particularly when compared with a traditional parameter of lung function such as FEV1.
Keywords: Cystic fibrosis; Lung clearance index; Lung function test; Nocturnal hypoxemia.
Copyright © 2020 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors have no conflicts of interest to disclose that could be perceived as prejudicing the impartiality of the research reported.
Similar articles
-
Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.Thorax. 2008 Feb;63(2):129-34. doi: 10.1136/thx.2007.077784. Epub 2007 Aug 3. Thorax. 2008. PMID: 17675316
-
Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls.Ann Am Thorac Soc. 2020 Sep;17(9):1085-1093. doi: 10.1513/AnnalsATS.201905-375OC. Ann Am Thorac Soc. 2020. PMID: 32603187 Free PMC article.
-
Determining presence of lung disease in young children with cystic fibrosis: lung clearance index, oxygen saturation and cough frequency.J Cyst Fibros. 2012 May;11(3):223-30. doi: 10.1016/j.jcf.2011.12.003. Epub 2012 Jan 23. J Cyst Fibros. 2012. PMID: 22265603
-
[Lung clearance index in cystic fibrosis].Rev Mal Respir. 2019 Mar;36(3):377-395. doi: 10.1016/j.rmr.2018.03.007. Epub 2019 Jan 25. Rev Mal Respir. 2019. PMID: 30686561 Review. French.
-
Lung clearance index in the assessment of airways disease.Respir Med. 2009 Jun;103(6):793-9. doi: 10.1016/j.rmed.2009.01.025. Epub 2009 Feb 25. Respir Med. 2009. PMID: 19246184 Review.
Cited by
-
Sleep Respiratory Disorders in Children and Adolescents with Cystic Fibrosis and Primary Ciliary Dyskinesia.Children (Basel). 2023 Oct 20;10(10):1707. doi: 10.3390/children10101707. Children (Basel). 2023. PMID: 37892370 Free PMC article. Review.
-
Effects of Elexacaftor/Tezacaftor/Ivacaftor on Cardiorespiratory Polygraphy Parameters and Respiratory Muscle Strength in Cystic Fibrosis Patients with Severe Lung Disease.Genes (Basel). 2023 Feb 9;14(2):449. doi: 10.3390/genes14020449. Genes (Basel). 2023. PMID: 36833376 Free PMC article.
-
Effect of Dornase Alfa on the Lung Clearance Index in Children with Cystic Fibrosis: A Lesson from a Case Series.Children (Basel). 2022 Oct 26;9(11):1625. doi: 10.3390/children9111625. Children (Basel). 2022. PMID: 36360353 Free PMC article.
-
Nocturnal non invasive ventilation in normocapnic cystic fibrosis patients: a pilot study.Acta Biomed. 2021 May 12;92(2):e2021164. doi: 10.23750/abm.v92i2.11261. Acta Biomed. 2021. PMID: 33988138 Free PMC article.
-
Toward the Establishment of New Clinical Endpoints for Cystic Fibrosis: The Role of Lung Clearance Index and Cardiopulmonary Exercise Testing.Front Pediatr. 2021 Feb 25;9:635719. doi: 10.3389/fped.2021.635719. eCollection 2021. Front Pediatr. 2021. PMID: 33718306 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
