A randomised crossover trial of chest physiotherapy in non-cystic fibrosis bronchiectasis

被引:131
|
作者
Murray, M. P. [1 ]
Pentland, J. L. [2 ]
Hill, A. T. [1 ]
机构
[1] Royal Infirm Edinburgh NHS Trust, Dept Resp Med, Edinburgh EH16 4SA, Midlothian, Scotland
[2] Royal Infirm Edinburgh NHS Trust, Dept Physiotherapy Resp Med, Edinburgh EH16 4SA, Midlothian, Scotland
关键词
Bronchiectasis; physiotherapy; LEICESTER COUGH QUESTIONNAIRE; GEORGES RESPIRATORY QUESTIONNAIRE; OBSTRUCTIVE PULMONARY-DISEASE; HEALTH-STATUS; STABLE BRONCHIECTASIS; POSTURAL DRAINAGE; ACTIVE CYCLE; THERAPY; VALIDATION; CLEARANCE;
D O I
10.1183/09031936.00055509
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Regular chest physiotherapy is advocated in non-cystic fibrosis bronchiectasis despite little evidence supporting its routine use. This study aimed to establish the efficacy of regular chest physiotherapy in non-cystic fibrosis bronchiectasis compared with no regular chest physiotherapy. 20 patients not practising regular chest physiotherapy were enrolled in a randomised crossover trial of 3 months of twice daily chest physiotherapy using an oscillatory positive expiratory pressure device compared with 3 months of no chest physiotherapy. The primary end-point was the Leicester Cough Questionnaire (LCQ). Additional outcomes included 24-h sputum volume, forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), forced expiratory flow at 25-75% of FVC (FEF25-75%), maximum inspiratory pressure (MIP), maximum expiratory pressure (MEP), exercise capacity, sputum microbiology and St George's Respiratory Questionnaire (SGRQ). The treatment effect was estimated using the differences of the pairs of observations from each patient. There was a significant improvement in all domains and total LCQ score with regular chest physiotherapy (median (interquartile range) total score improvement 1.3 (-0.17-3.25) units; p=0.002). 24-h sputum volume increased significantly with regular chest physiotherapy (2 (06) mL; p=0.02), as did exercise capacity (40 (15-80) m; p=0.001) and SGRQ total score (7.77 (-0.99-14.5) unit improvement; p=0.004). No significant differences were seen in sputum bacteriology, FEV1, FVC, FEF25-75%, MIP or MEP. Regular chest physiotherapy in non-cystic fibrosis bronchiectasis has small, but significant benefits.
引用
收藏
页码:1086 / 1092
页数:7
相关论文
共 50 条
  • [41] A review of non-cystic fibrosis pediatric bronchiectasis
    Boren, Eric J.
    Teuber, Suzanne S.
    Gershwin, M. Eric
    CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2008, 34 (02) : 260 - 273
  • [42] Evaluation of the Cases with Non-Cystic Fibrosis Bronchiectasis
    Korkmaz, Serpil
    Canitez, Yakup
    Cekic, Sukru
    Efe, Hulya Poyraz
    Ocakoglu, Gokhan
    Sapan, Nihat
    GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, 2018, 16 (02): : 106 - 116
  • [43] Surgical management of non-cystic fibrosis bronchiectasis
    Hiramatsu, Miyako
    Shiraishi, Yuji
    JOURNAL OF THORACIC DISEASE, 2018, 10 : S3436 - S3445
  • [44] IMMUNOLOGICAL TESTING IN NON-CYSTIC FIBROSIS BRONCHIECTASIS
    Dwarakanath, A.
    JOURNAL OF THE ROYAL COLLEGE OF PHYSICIANS OF EDINBURGH, 2011, 41 (04): : 380 - 380
  • [45] The pulmonary microbiome in non-cystic fibrosis bronchiectasis
    Mac Aogain, Micheal
    Lim, Albert Yick Hou
    Low, Teck Boon
    Tan, Gan Liang
    Yii, Anthony Chau
    Chandrasekaran, Ravishankar
    Poh, Tuang Yeow
    Ng, Amanda Hui Qi
    Bertrand, Denis
    Koh, Jia Yu
    Leong, Carrie Kah-Lai
    Nagarajan, Niranjan
    Abisheganaden, John
    Koh, Mariko
    Chotirmall, Sanjay Haresh
    EUROPEAN RESPIRATORY JOURNAL, 2017, 50
  • [46] Treatment of paediatric non-cystic fibrosis bronchiectasis
    Edwards, EA
    Twiss, J
    Byrnes, CA
    EXPERT OPINION ON PHARMACOTHERAPY, 2004, 5 (07) : 1471 - 1484
  • [47] Antimicrobial treatment of non-cystic fibrosis bronchiectasis
    Grimwood, Keith
    Bell, Scott C.
    Chang, Anne B.
    EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2014, 12 (10) : 1277 - 1296
  • [48] Patterns Of Pharmacotherapy For Non-Cystic Fibrosis Bronchiectasis
    Henkle, E.
    Daley, C. L.
    Griffith, D. E.
    Walsh, J. W.
    Leitman, P.
    Malanga, E.
    Aksamit, T. R.
    O'Donnell, A. E.
    Thomashow, B.
    Olivier, K. N.
    Knowles, M. R.
    Barker, A. F.
    Metersky, M. L.
    Tino, G.
    Eden, E.
    Salathe, M.
    Johnson, M.
    Wilkins, T.
    Prieto, D.
    Winthrop, K. L.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191
  • [49] Bronchial Hyperreactivity in Non-Cystic Fibrosis Bronchiectasis
    Benan, Musellim
    Isil, Uzel
    Sermin, Borekci
    Bulent, Tutluoglu
    Gokhan, Aygun
    Hatice, Yasar
    Nigar, Halis
    Muzeyyen, Erk
    JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE, 2013, 4 (03) : 224 - 227
  • [50] Aerosolized antibiotics for non-cystic fibrosis bronchiectasis
    Rubin, Bruce K.
    JOURNAL OF AEROSOL MEDICINE AND PULMONARY DRUG DELIVERY, 2008, 21 (01) : 71 - 76