Oscillating devices for airway clearance in people with cystic fibrosis

被引:33
作者
Morrison, Lisa [1 ]
Agnew, Jennifer [2 ]
机构
[1] Gartnavel Royal Hosp, W Scotland Adult CF Unit, Glasgow G12 0YN, Lanark, Scotland
[2] Hosp Sick Children, Chest & Cyst Fibrosis Clin, Toronto, ON M5G 1X8, Canada
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2009年 / 01期
关键词
POSITIVE EXPIRATORY PRESSURE; CHEST-WALL OSCILLATION; INTRAPULMONARY PERCUSSIVE VENTILATOR; METAANALYSIS COMBINING PARALLEL; OVER CLINICAL-TRIALS; FLUTTER DEVICE; HOSPITALIZED-PATIENTS; PULMONARY-FUNCTION; PHYSICAL-THERAPY; LUNG-DISEASE;
D O I
10.1002/14651858.CD006842.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Chest physiotherapy is widely prescribed to assist the clearance of airway secretions in people with cystic fibrosis (CF). Oscillating devices generate intra-or extra-thoracic oscillations orally or external to the chest wall. Internally they create variable resistances within the airways, generating controlled oscillating positive pressure which mobilises mucus. Extra-thoracic oscillations are generated by forces outside the respiratory system, e. g. high frequency chest wall oscillation. Objectives To determine the effectiveness and acceptability of oscillating devices compared to other forms of physiotherapy to improve respiratory function, mucus clearance and other outcomes in people with CF. Search strategy We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register comprising references identified from comprehensive electronic database searches and hand searches of relevant journals and abstract books of conference proceedings. Most recent search of the Cystic Fibrosis Trials Register: November 2008. Selection criteria Randomised controlled studies and controlled clinical studies of oscillating devices compared with any other form of physiotherapy in people with CF. Data collection and analysis Two authors independently applied the inclusion criteria to publications and assessed the quality of the included studies. Main results Two hundred and sixty-five studies were identified; thirty studies (total of 708 participants) met the inclusion criteria. Single treatment interventions (therapy technique used only once in the comparison) were excluded. Studies varied in duration from up to one week to one year in duration. Nineteen of the studies were cross-over in design. Data were not published in sufficient detail in most of these studies to perform meta-analysis. Forced expiratory volume in one second (FEV1) was the most frequently measured outcome. Results did not show significant difference in effect between oscillating devices and other methods of airway clearance on FEV1 or other lung function parameters. Where there has been a small but significant change in secondary outcome variables such as sputum volume or weight this has not been wholly in favour of oscillating devices. Participant satisfaction was reported in eleven studies, but this was not specifically in favour of an oscillating device as some participants preferred breathing techniques or techniques used prior to the study interventions. The results for the remaining outcome measures were not examined or reported in sufficient detail to provide any high level evidence. Authors' conclusions There was no clear evidence that oscillation was a more or less effective intervention overall than other forms of physiotherapy. More adequately-powered long-term randomised controlled trials are needed.
引用
收藏
页数:110
相关论文
共 50 条
[41]   Postnatal airway growth in cystic fibrosis piglets [J].
Adam, Ryan J. ;
Abou Alaiwa, Mahmoud H. ;
Bouzek, Drake C. ;
Cook, Daniel P. ;
Gansemer, Nicholas D. ;
Taft, Peter J. ;
Powers, Linda S. ;
Stroik, Mallory R. ;
Hoegger, Mark J. ;
McMenimen, James D. ;
Hoffman, Eric A. ;
Zabner, Joseph ;
Welsh, Michael J. ;
Meyerholz, David K. ;
Stoltz, David A. .
JOURNAL OF APPLIED PHYSIOLOGY, 2017, 123 (03) :526-533
[42]   Development of characteristic airway bifurcations in cystic fibrosis [J].
Bass, Karl ;
Thomas, Morgan L. ;
Kemner-van de Corput, Mariette P. C. ;
Tiddens, Harm A. W. M. ;
Longest, P. Worth .
AEROSOL SCIENCE AND TECHNOLOGY, 2021, 55 (10) :1143-1164
[43]   An update on targeting airway inflammation in cystic fibrosis [J].
Mullen, Eamon ;
Murphy, Mark ;
Bateman, Georgia ;
Casey, Michelle ;
Gunaratnam, Cedric ;
McElvaney, Noel G. .
EXPERT REVIEW OF RESPIRATORY MEDICINE, 2025,
[44]   Tromethamine improves mucociliary clearance in cystic fibrosis pigs [J].
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)
[45]   Characterizing mucociliary clearance in young children with cystic fibrosis [J].
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
[46]   Effectiveness of hypertonic saline nebulization in airway clearance in children with non-cystic fibrosis bronchiectasis: A randomized control trial [J].
Anuradha, Kodippilikande W. D. A. ;
Gunathilaka, Paththini K. Ganganath ;
Wickramasinghe, Vithanage P. .
PEDIATRIC PULMONOLOGY, 2021, 56 (02) :509-515
[47]   Inhibition of airway proteases in cystic fibrosis lung disease [J].
Griese, M. ;
Kappler, M. ;
Gaggar, A. ;
Hartl, D. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 32 (03) :783-795
[48]   Development of an airway mucus defect in the cystic fibrosis rat [J].
Birket, Susan E. ;
Davis, Joy M. ;
Fernandez, Courtney M. ;
Tuggle, Katherine L. ;
Oden, Ashley M. ;
Chu, Kengyeh K. ;
Tearney, Guillermo J. ;
Fanucchi, Michelle V. ;
Sorscher, Eric J. ;
Rowe, Steven M. .
JCI INSIGHT, 2018, 3 (01)
[49]   Cystic fibrosis airway epithelium remodelling: involvement of inflammation [J].
Adam, Damien ;
Roux-Delrieu, Jacqueline ;
Luczka, Emilie ;
Bonnomet, Arnaud ;
Lesage, Julien ;
Merol, Jean-Claude ;
Polette, Myriam ;
Abely, Michel ;
Coraux, Christelle .
JOURNAL OF PATHOLOGY, 2015, 235 (03) :408-419
[50]   Airway disease phenotypes in animal models of cystic fibrosis [J].
Alexandra McCarron ;
Martin Donnelley ;
David Parsons .
Respiratory Research, 19