Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis

被引:19
|
作者
Laube, Beth L. [1 ]
Sharpless, Gail [1 ]
Carson, Kathryn A. [1 ]
Kelly, Amber [1 ]
Mogayzel, Peter J., Jr. [1 ]
机构
[1] Johns Hopkins Med Inst, Eudowood Div Pediat Resp Sci, Baltimore, MD 21287 USA
来源
BMC PULMONARY MEDICINE | 2011年 / 11卷
基金
美国国家卫生研究院;
关键词
Cystic Fibrosis; Hypertonic Saline; Mucociliary Clearance; Sputum Induction; Airway Surface Liquid;
D O I
10.1186/1471-2466-11-45
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Little is known of how mucociliary clearance (MCC) in children with cystic fibrosis (CF) and normal pulmonary function compares with healthy adults, or how an acute inhalation of 7% hypertonic saline (HS) aerosol affects MCC in these same children. Methods: We compared MCC in 12 children with CF and normal pulmonary function after an acute inhalation of 0.12% saline (placebo), or HS, admixed with the radioisotope 99 mtechnetium sulfur colloid in a double-blind, randomized, cross-over study. Mucociliary clearance on the placebo day in the children was also compared to MCC in 10 healthy, non-CF adults. Mucociliary clearance was quantified over a 90 min period, using gamma scintigraphy, and is reported as MCC at 60 min (MCC60) and 90 min (MCC90). Results: Median [interquartile range] MCC60 and MCC90 in the children on the placebo visit were 15.4 [12.4-24.5]% and 19.3 [17.3-27.8%]%, respectively, which were similar to the adults with 17.8 [6.4-28.7]% and 29.6 [16.1-43.5]%, respectively. There was no significant improvement in MCC60 (2.2 [-6.2-11.8]%) or MCC90 (2.3 [-1.2-10.5]%) with HS, compared to placebo. In addition, 5/12 and 4/12 of the children showed a decrease in MCC60 and MCC90, respectively, after inhalation of HS. A post hoc subgroup analysis of the change in MCC90 after HS showed a significantly greater improvement in MCC in children with lower placebo MCC90 compared to those with higher placebo MCC90 (p = 0.045). Conclusions: These data suggest that percent MCC varies significantly between children with CF lung disease and normal pulmonary functions, with some children demonstrating MCC values within the normal range and others showing MCC values that are below normal values. In addition, although MCC did not improve in all children after inhalation of HS, improvement did occur in children with relatively low MCC values after placebo. This finding suggests that acute inhalation of hypertonic saline may benefit a subset of children with low MCC values.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Numerical and experimental investigation of mucociliary clearance breakdown in cystic fibrosis
    Chatelin, Robin
    Anne-Archard, Dominique
    Murris-Espin, Marlene
    Thiriet, Marc
    Poncet, Philippe
    JOURNAL OF BIOMECHANICS, 2017, 53 : 56 - 63
  • [32] Glutathione and bicarbonate nanoparticles improve mucociliary transport in cystic fibrosis epithelia
    Cho, Do Yeon
    Rivers, Nicholas J.
    Lim, Dong-Jin
    Zhang, Shaoyan
    Skinner, Daniel
    Yang, Lydia
    Menon, Adithya J.
    Kelly, Olivia Jo
    Jones, Martin P.
    Bicknell, Brenton T.
    Grayson, Jessica W.
    Harris, Elex
    Rowe, Steven M.
    Woodworth, Bradford A.
    INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2024, 14 (06) : 1026 - 1035
  • [33] Effect of hypertonic saline on mucociliary clearance and clinical outcomes in chronic bronchitis
    Bennett, William D.
    Henderson, Ashley G.
    Ceppe, Agathe
    Zeman, Kirby L.
    Wu, Jihong
    Gladman, Christine
    Fuller, Fred
    Gazda, Stephen
    Button, Brian
    Boucher, Richard C.
    Donaldson, Scott H.
    ERJ OPEN RESEARCH, 2020, 6 (03)
  • [34] Lung Clearance Index as an Outcome Measure for Clinical Trials in Young Children with Cystic Fibrosis A Pilot Study Using Inhaled Hypertonic Saline
    Subbarao, Padmaja
    Stanojevic, Sanja
    Brown, Meghan
    Jensen, Renee
    Rosenfeld, Margaret
    Davis, Stephanie
    Brumback, Lyndia
    Gustafsson, Per
    Ratjen, Felix
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2013, 188 (04) : 456 - 460
  • [35] Rationale for hypertonic saline therapy for cystic fibrosis lung disease
    Tarran, Robert
    Donaldson, Scott
    Boucher, Richard C.
    SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 28 (03) : 295 - 302
  • [36] Inhaled hypertonic saline increases sputum expectoration in cystic fibrosis
    Riedler, J
    Reade, T
    Button, B
    Robertson, CF
    JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 1996, 32 (01) : 48 - 50
  • [37] Effectiveness of hypertonic saline nebulization in airway clearance in children with non-cystic fibrosis bronchiectasis: A randomized control trial
    Anuradha, Kodippilikande W. D. A.
    Gunathilaka, Paththini K. Ganganath
    Wickramasinghe, Vithanage P.
    PEDIATRIC PULMONOLOGY, 2021, 56 (02) : 509 - 515
  • [38] Tolerance of 7% Hypertonic Saline in Pediatric Cystic Fibrosis Patients
    Guevara, Maria Talamo
    McColley, Susanna A.
    Rychlik, Karen
    Savant, Adrienne P.
    PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY, 2020, 33 (02) : 63 - 68
  • [39] Tromethamine improves mucociliary clearance in cystic fibrosis pigs
    Ash, Jamison J.
    Hilkin, Brieanna M.
    Gansemer, Nicholas D.
    Hoffman, Eric A.
    Zabner, Joseph
    Stoltz, David A.
    Abou Alaiwa, Mahmoud H.
    PHYSIOLOGICAL REPORTS, 2022, 10 (17):
  • [40] Elastic mucus strands impair mucociliary clearance in cystic fibrosis pigs
    Pino-Argumedo, Maria, I
    Fischer, Anthony J.
    Hilkin, Brieanna M.
    Gansemer, Nicholas D.
    Allen, Patrick D.
    Hoffman, Eric A.
    Stoltz, David A.
    Welsh, Michael J.
    Abou Alaiwa, Mahmoud H.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2022, 119 (13)