Eltgol Acutelly Improves Airway Clearance and Reduces Static Pulmonary Volumes in Adult Cystic Fibrosis Patients

被引:7
|
作者
Guimaraes, Fernando Silva [1 ,2 ]
Lopes, Agnaldo Jose [3 ]
Ribeiro Moco, Vanessa Joaquim [1 ]
de Souza, Felipe Cavalcanti [1 ]
Silveira de Menezes, Sara Lucia [1 ,2 ]
机构
[1] Augusto Motta Univ Ctr UNISUAM, Rehabil Sci Grad Program, BR-21041021 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Phys Therapy Dept, BR-21941 Rio De Janeiro, Brazil
[3] Univ Estado Rio De Janeiro, Physiol Resp Lab, Rio De Janeiro, Brazil
关键词
Chest physiotherapy; Cystic fibrosis; ELTGOL; MUCUS CLEARANCE; PHYSIOTHERAPY; DRAINAGE;
D O I
10.1589/jpts.26.813
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
[Purpose] Chest physical therapy techniques are essential in order to reduce the frequency of recurrent pulmonary infections that progressively affect lung function in cystic fibrosis patients. Recently, ELTGOL (L'Expiration Lente Totale Glotte Ouverte en d cubitus Lat ral) emerged as an inexpensive and easy to perform therapeutic option. The aim of this study was to compare the acute effects of ELTGOL and the Flutter valve in stable adult patients with cystic fibrosis. [Subjects and Methods] This was a randomized, crossover study with a sample of cystic fibrosis outpatients. The subjects underwent two protocols (Flutter Valve and ELTGOL interventions, referred to as ELTGOL and FLUTTER) in a randomized order with a one-week washout interval between them. The main outcomes were pulmonary function variables and expectorated sputum dry weight. [Results] ELTGOL cleared 0.34 g more of secretions than FLUTTER (95% CI 0.11 to 0.57). When comparing the physiological effects of ELTGOL and FLUTTER, the first was superior in improving airway resistance (-0.51 cmH2O/L/s; 95% CI -0.88 to -0.14) and airway conductance (0.016 L/s/cmH2O; 95% CI 0.008 to 0.023). [Conclusion] ELTGOL promoted higher secretion removal and improvement in airway resistance and conductance than the Flutter valve. These techniques were equivalent in reducing the pulmonary hyperinflation and air trapping in cystic fibrosis patients.
引用
收藏
页码:813 / 816
页数:4
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