| Literature DB >> 36068015 |
Craig A Williams1,2, Alan R Barker1, Sarah Denford3,4,5, Samantha B van Beurden6, Mayara S Bianchim7, Jessica E Caterini8,9, Narelle S Cox10,11, Kelly A Mackintosh12, Melitta A McNarry12, Sarah Rand13, Jane E Schneiderman14,15, Greg D Wells8, Peter Anderson16, Daniel Beever17, Z Beverley18, Ronan Buckley19, Brenda Button20,21, Adam J Causer22, Máire Curran23,24,25, Tiffany J Dwyer26,27, Warren Gordon16, Mathieu Gruet28, Ryan A Harris29, Elpis Hatziagorou30, H J Erik Hulzebos31, Asterios Kampouras30,32, Lisa Morrison33, Marietta N Cámara34,35, Clare M Reilly19, Abbey Sawyer36,37, Zoe L Saynor38, James Shelley12, Grace Spencer39, Gemma E Stanford18,40, Don S Urquhart41,42, Rachel Young43, Owen W Tomlinson1,2.
Abstract
BACKGROUND: The roles of physical activity (PA) and exercise within the management of cystic fibrosis (CF) are recognised by their inclusion in numerous standards of care and treatment guidelines. However, information is brief, and both PA and exercise as multi-faceted behaviours require extensive stakeholder input when developing and promoting such guidelines.Entities:
Keywords: clinical practice; health; lifestyle; respiratory disease
Mesh:
Year: 2022 PMID: 36068015 PMCID: PMC9459449 DOI: 10.1177/14799731221121670
Source DB: PubMed Journal: Chron Respir Dis ISSN: 1479-9723 Impact factor: 3.115
Figure 1.Flowchart detailing process involved in establishing consensus document. ACPCF, Association of Chartered Physiotherapists in Cystic Fibrosis; ACSM, American College of Sports Medicine; CDC, Centre for Disease Control; CF, cystic fibrosis; ECFS, European Cystic Fibrosis Society; NICE, National Institute for Health and Care Excellence; PPI, public and patient involvement; SRC, Strategic Research Centre.
Characteristics of the expert group.
| Participant characteristics | Number |
|---|---|
| Country ( | United Kingdom (23), Australia (4), Canada (3), Ireland (3), Greece (2), Chile (1), France (1), Netherlands (1), United States of America (1) |
| SRC/External/PPI, | 14/23/2 |
| Female/Male, | 24/15 |
| Academic/HCP/PPI, | 22/15/2 |
| HCP Positions, | Physiotherapist (7), Consultant/Professor (4), kinesiologist/exercise physiologist (1), clinical researcher (1), pulmonologist (1), technical instructor (1) |
| ECR/Non-ECR †, | 18/19 |
| Experience in CF (years, mean ± SD) | 13 ± 9 years (range = 0–36 years*) |
| Experience in CF (cumulative total, years) | 479 years |
CF: cystic fibrosis; ECR: Early Career Researcher/Professional; HCP: healthcare professional; PPI: public and patient involvement; SRC: Members of ‘Youth Activity Unlimited’ Strategic Research Centre. †Identity as an ECR was self-selected (Supplementary File 1). Academic and clinicians only included within this breakdown of ECR numbers (no PPI included). *Experience in completed number of years.
Sub-themes identified for development within the consensus.
| Main theme | Sub-theme |
|---|---|
| Rationale for physical activity and exercise | Patient oriented
outcomes |
| Health benefits of physical activity and exercise | Lung health |
| Measurement of physical activity and exercise | Measurement of physical
activity |
| Prescription of physical activity and exercise | Optimal training modes and
styles |
| Clinical considerations for physical activity and exercise | Airway
clearance |
Final consensus statements and associated agreement from group members.
| Statement | Agree | Do not agree | Abstain | |
|---|---|---|---|---|
| The rationale for physical activity and exercise in CF – Why are these factors important for people with CF? | ||||
| 1 | Physical activity and exercise contribute to increased survival in people with cystic fibrosis and can also improve an individual’s sense of overall well-being | 36 (95) | 2 (5) | 0 (0) |
| 2 | Engagement in physical activity and exercise has the potential to positively influence the cost associated with hospitalisations, exacerbations, and antibiotic use | 34 (89) | 3 (8) | 1 (3) |
| Health benefits of physical activity and exercise in CF – How does changing these factors benefit people with cystic fibrosis? | ||||
| 3 | Physical activity and exercise can improve cardiovascular health in people with cystic fibrosis, however there is limited research on this topic | 33 (87) | 3 (8) | 2 (5) |
| 4 | Resistance training improves limb muscle strength in people with cystic fibrosis | 35 (92) | 2 (5) | 1 (3) |
| 5 | Exercise of adequate frequency and progressive intensity improves fitness in people with cystic fibrosis | 36 (95) | 2 (5) | 0 (0) |
| 6 | Health-related quality of life is an important and holistic outcome measure that should be included in physical activity and exercise intervention research, but the clinical effectiveness of physical activity and exercise interventions on the different domains of health-related quality of life remains unclear | 36 (95) | 0 (0) | 2 (5) |
| Measurement of physical activity and exercise in CF – How do we monitor these factors? | ||||
| 7 | Accelerometers provide accurate information regarding the volume and accumulation of physical activity, particularly when tailored for use in people with cystic fibrosis, but self-report data is still required to provide contextual, and complementary, information | 34 (89) | 2 (5) | 2 (5) |
| 8 | There are many safe, effective, and informative options for exercise testing in people with cystic fibrosis regardless of age or disease severity | 37 (97) | 1 (3) | 0 (0) |
| 9 | Lab-based tests provide greater insights to the determinants of exercise capacity, but field-based tests can provide useful information if lab-based tests are not available | 35 (92) | 2 (5) | 1 (3) |
| 10 | Standardised methods of exercise testing and physical activity assessment should be utilised to enable within- and between-person comparisons, facilitating the individualisation of physical activity promotion and/or exercise prescription | 36 (95) | 1 (3) | 1 (3) |
| Prescription of physical Activity and exercise in CF – How do we facilitate change and get people with cystic fibrosis moving (more)? | ||||
| 11 | An individualised and comprehensive training program, undertaken at a moderate intensity or higher, as part of the ongoing therapeutic routine is recommended in people with cystic fibrosis | 35 (92) | 2 (5) | 1 (3) |
| 12 | Lifelong adherence to habitual physical activity and exercise across the lifespan is important and challenging, due to the many competing and time-consuming activities | 34 (89) | 4 (11) | 0 (0) |
| 13 | The provision of exercise within cystic fibrosis care is becoming increasingly important and requires additional staffing and expertise at the level required to offer annual exercise testing and prescription, including the option of cardiopulmonary exercise testing. Standardisation of the education, training and roles and responsibilities of exercise specialists and other healthcare professionals responsible for the provision of exercise services is required | 36 (95) | 2 (5) | 0 (0) |
| 14 | Exercise training delivered remotely by video calling is feasible and acceptable to people with cystic fibrosis in a small number of pilot studies, and clinical teams could consider its use as a supplement to face-to-face contact | 37 (97) | 1 (3) | 0 (0) |
| Clinical considerations for physical activity and exercise in CF – What must we also consider when prescribing activity and exercise for people with cystic fibrosis | ||||
| 15 | Exercise with huff or cough improves mucus clearance, however there is no medium- or long-term evidence if exercise can adequately replace airway clearance techniques in people with cystic fibrosis | 38 (100) | 0 (0) | 0 (0) |
| 16 | The clinical efficacy of CFTR modulator therapy on the fitness and physical activity behaviours of people with cystic fibrosis warrants further study. Including exercise testing measurements as standard alongside routinely collected clinical data within cystic fibrosis registries may begin to allow a better understanding of the physiological effects of modulator therapies | 32 (84) | 3 (8) | 3 (8) |
| 17 | Physical activity and exercise are strongly recommended for people with cystic fibrosis. Although the risk is minimal, guidance should be provided to all people with cystic fibrosis around hydration, nutrition, exercise intensity and duration, based on the specific activity | 36 (95) | 1 (3) | 1 (3) |
| 18 | Both energy intake and hydration should be adjusted to meet the elevated caloric and fluid needs of an active person with cystic fibrosis. Every exercise/diet plan should be discussed with the physician and dietician to meet the individual’s body mass index targets, caloric goals, and diet preferences | 34 (89) | 2 (5) | 2 (5) |
| Future directions for physical activity and exercise in CF | ||||
| 19 | The prescription of physical activity and exercise should be individualised for people with cystic fibrosis. All aspects of disease management and personal patient preferences should be considered | 36 (95) | 1 (3) | 1 (3) |
| 20 | Clinical trials in cystic fibrosis should include outcomes associated with physical activity and exercise to understand how lifestyle parameters can be affected by pharmaceutical and non-pharmaceutical interventions | 36 (97) | 1 (3) | 0 (0) |
| 21 | Future trials of physical activity and exercise should seek to include outcomes that are currently under-reported, such as cardiovascular health, mental health, endocrine, inflammatory function, and patient reported outcomes, to help further evaluate the effects of physical activity and exercise upon overall health status | 38 (100) | 0 (0) | 0 (0) |
| 22 | Future research should examine: A. Whether
exercise can adequately replace airway clearance
techniques. | a) 32 (84) | — | — |
All values are presented in percentages, following voting process whereby n =38 group members cast votes. Totals may not always equal 100% due to rounding. Excluded statements provided in Supplemental File 3.