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
  • [11] Timing of hypertonic saline inhalation for cystic fibrosis
    Elkins, Mark
    Dentice, Ruth
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2020, (02):
  • [12] THE IMPACT OF HYPERTONIC SALINE INHALATION ON MUCOCILIARY CLEARANCE AND NASAL NITRIC OXIDE
    Bencova, A.
    Vidan, J.
    Rozborilova, E.
    Kocan, I.
    JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2012, 63 (03): : 309 - 313
  • [13] USE OF PEP IN COMBINATION WITH HYPERTONIC SALINE INHALATION IN CHILDREN AND ADOLESCENTS WITH CYSTIC FIBROSIS
    Elliott, A. B.
    Pendlebury, C.
    Cooper, P.
    PEDIATRIC PULMONOLOGY, 2012, 47 : 365 - 365
  • [14] Inhalation of hypertonic saline aerosol enhances mucociliary clearance in asthmatic and healthy subjects
    Daviskas, E
    Anderson, SD
    Gonda, I
    Eberl, S
    Meikle, S
    Seale, JP
    Bautovich, G
    EUROPEAN RESPIRATORY JOURNAL, 1996, 9 (04) : 725 - 732
  • [15] The impact of hypertonic saline inhalation on nasal nitric oxide levels and mucociliary clearance
    Bencova, Alica
    Vidan, Jaroslav
    Rozborilova, Eva
    EUROPEAN RESPIRATORY JOURNAL, 2013, 42
  • [16] A four week trial of hypertonic saline in children with mild cystic fibrosis lung disease: Effect on mucociliary clearance and clinical outcomes
    Donaldson, Scott H.
    Samulski, T. Danielle
    LaFave, Caroline
    Zeman, Kirby
    Wu, Jihong
    Trimble, Aaron
    Ceppe, Agathe
    Bennett, William D.
    Davis, Stephanie D.
    JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (06) : 942 - 948
  • [17] Mucus clearance and lung function in cystic fibrosis with hypertonic saline
    Donaldson, SH
    Bennett, WD
    Zeman, KL
    Knowles, MR
    Tarran, R
    Boucher, RC
    NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (03): : 241 - 250
  • [18] Mucociliary clearance and buffered hypertonic saline solution
    Talbot, AR
    Herr, TM
    Parsons, DS
    LARYNGOSCOPE, 1997, 107 (04): : 500 - 503
  • [19] Characterizing mucociliary clearance in young children with cystic fibrosis
    Laube, Beth L.
    Carson, Kathryn A.
    Evans, Christopher M.
    Aksit, Melis A.
    Collaco, Joseph M.
    Richardson, Vanessa L.
    Sharpless, Gail
    Zeitlin, Pamela L.
    Cutting, Garry R.
    Mogayzel, Peter J.
    PEDIATRIC RESEARCH, 2022, 91 (03) : 612 - 620
  • [20] Mucociliary clearance in cystic fibrosis
    Robinson, M
    Bye, PTB
    PEDIATRIC PULMONOLOGY, 2002, 33 (04) : 293 - 306