Airway clearance physiotherapy and health-related quality of life in cystic fibrosis

被引:3
|
作者
Gursli, Sandra [1 ]
Quittner, Alexandra [2 ]
Jahnsen, Reidun Birgitta [3 ,4 ]
Skrede, Bjorn [5 ]
Stuge, Britt [6 ]
Bakkeheim, Egil [1 ]
机构
[1] Oslo Univ Hosp, Natl Resource Ctr Cyst Fibrosis, Oslo, Norway
[2] Miami Childrens Res Inst, Miami, FL USA
[3] Oslo Univ Hosp, Dept Neurosci Children, Oslo, Norway
[4] Univ Oslo, Inst Hlth & Soc, CHARM, Oslo, Norway
[5] Oslo Univ Hosp, Dept Pulm Med, Oslo, Norway
[6] Oslo Univ Hosp, Div Orthopaed Surg, Dept Res & Dev, Oslo, Norway
来源
PLOS ONE | 2022年 / 17卷 / 10期
关键词
LONG-TERM; QUESTIONNAIRE; THERAPY; CF;
D O I
10.1371/journal.pone.0276310
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Airway clearance physiotherapy is recommended in cystic fibrosis, but limited evidence exists to suggest how much treatment is enough. As a secondary analysis of a prior study investigating the safety, efficacy, and participants' perceptions of a novel airway clearance technique, specific cough technique (SCT) compared to forced expiration technique (FET), we aimed to evaluate whether the intervention was associated with changes in health-related quality of life (HRQoL). Methods We conducted randomised, controlled individual trials with six adults (N-of-1 RCTs). Each trial included eight weeks of treatment, twice a week, using saline inhalation in horizontal positions, one with SCT and one with FET, in random order. Efficacy was measured by sputum wet weight (g) after each session. Perceived usefulness and preference were self-reported at the end of the study. Lung function was assessed at baseline and at the end of study. HRQoL was measured using the Cystic Fibrosis Questionnaire-Revised (CFQ-R) at baseline (week 1) and at completion of the study (week 8). Individual HRQoL scores (0-100) were coded and analysed using CFQ-R Software Program, version 2.0. Results Patient-reported outcomes were completed by all subjects. Individual CFQ-R-Respiratory Symptoms Scores (CFQ-R-RSS) showed a positive change, meeting the minimal important difference (MID) >= 4 points in five participants and a negative change in one individual. A strong correlation (r = 0.94 (p<0.01) was found between total sputum weight (g) and the positive changes in CFQ-R-RSS, and between changes in lung function and CFQ-R-RSS (r = 0.84 (p = 0.04). Conclusion The airway clearance intervention was associated with clinically meaningful changes in patient-reported symptoms on the CFQ-R in the majority of the participants. This finding warrants further investigation regarding treatment, duration and frequency. A long-term study may reveal beneficial effects on other clinically meaningful endpoints, such as pulmonary exacerbations, high-resolution computed tomography scores and HRQoL.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Health-related quality of life in cystic fibrosis
    Royce, Frederick H.
    Carl, John C.
    [J]. CURRENT OPINION IN PEDIATRICS, 2011, 23 (05) : 535 - 540
  • [2] GENETIC MODIFIERS OF HEALTH-RELATED QUALITY OF LIFE IN CYSTIC FIBROSIS
    Barbato, E. S.
    Darrah, R.
    [J]. PEDIATRIC PULMONOLOGY, 2019, 54 : S244 - S244
  • [3] Health-related quality of life of Spanish children with cystic fibrosis
    Groeneveld, Iris F.
    Sosa, Elena S.
    Perez, Margarita
    Fiuza-Luces, Carmen
    Gonzalez-Saiz, Laura
    Gallardo, Cristian
    Lopez-Mojares, Luis M.
    Ruiz, Jonatan R.
    Lucia, Alejandro
    [J]. QUALITY OF LIFE RESEARCH, 2012, 21 (10) : 1837 - 1845
  • [4] Health-related quality of life of Spanish children with cystic fibrosis
    Iris F. Groeneveld
    Elena S. Sosa
    Margarita Pérez
    Carmen Fiuza-Luces
    Laura Gonzalez-Saiz
    Cristian Gallardo
    Luis M. López-Mojares
    Jonatan R. Ruiz
    Alejandro Lucia
    [J]. Quality of Life Research, 2012, 21 : 1837 - 1845
  • [5] THE IMPACT OF CYSTIC FIBROSIS-RELATED DIABETES ON HEALTH-RELATED QUALITY OF LIFE
    Kwong, E.
    Chong, L.
    Lee, K.
    Zheng, J.
    Wilcox, P. G.
    Quon, B. S.
    [J]. PEDIATRIC PULMONOLOGY, 2018, 53 : 403 - 403
  • [6] The impact of cystic fibrosis-related diabetes on health-related quality of life
    Kwong, Eugenie
    Desai, Sameer
    Chong, Louise
    Lee, Kathleen
    Zheng, Jie
    Wilcox, Pearce G.
    Quon, Bradley S.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2019, 18 (05) : 734 - 736
  • [7] Longitudinal Trends in Health-Related Quality of Life in Adults With Cystic Fibrosis
    Dill, Edward J.
    Dawson, Ree
    Sellers, Deborah E.
    Robinson, Walter M.
    Sawicki, Gregory S.
    [J]. CHEST, 2013, 144 (03) : 981 - 989
  • [8] Measuring health-related quality of life in clinical trials in cystic fibrosis
    Abbott, J.
    Hart, A.
    Havermans, T.
    Matossian, A.
    Goldbeck, L.
    Barreto, C.
    Bergsten-Brucefors, A.
    Besier, T.
    Catastini, P.
    Lupi, F.
    Staab, D.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2011, 10 : S82 - S85
  • [9] Health-related quality of life in adults with cystic fibrosis: The role of coping
    Abbott, Janice
    Hart, Anna
    Morton, Alison
    Gee, Louise
    Conway, Steven
    [J]. JOURNAL OF PSYCHOSOMATIC RESEARCH, 2008, 64 (02) : 149 - 157
  • [10] HEALTH-RELATED QUALITY OF LIFE AMONG ADULT CYSTIC FIBROSIS PATIENTS
    Anderson, P. J.
    Sherman, A. C.
    Campbell, D.
    Reddy, R. M.
    Kumar, S.
    O'Brien, C. E.
    Simonton, S.
    [J]. PEDIATRIC PULMONOLOGY, 2011, : 421 - 421