Survey of exercise testing and training in cystic fibrosis clinics in the UK: a decade of progress

被引:1
作者
Tomlinson, Owen William [1 ,2 ,3 ]
Saynor, Zoe L. [4 ]
Stevens, Daniel [5 ,6 ]
Antoun, Joe [4 ]
Urquhart, Don S. [7 ,8 ]
Williams, Craig Anthony [1 ,2 ]
机构
[1] Univ Exeter, Dept Publ Hlth & Sport Sci, Childrens Hlth & Exercise Res Ctr, Exeter, England
[2] Royal Devon Univ Healthcare NHS Fdn Trust, Acad Dept Resp Med, Exeter, England
[3] Univ Exeter, Dept Clin & Biomed Sci, Exeter, England
[4] Univ Portsmouth, Sch Sport Hlth & Exercise Sci, Fac Sci & Hlth, Phys Act Hlth & Rehabil Themat Res Grp, Portsmouth, England
[5] Dalhousie Univ, Sch Hlth & Human Performance, Div Kinesiol, Halifax, NS, Canada
[6] Dalhousie Univ, Div Respirol, Dept Pediat, Fac Med, Halifax, NS, Canada
[7] Royal Hosp Children & Young People, Dept Paediat Resp & Sleep Med, Edinburgh, Scotland
[8] Univ Edinburgh, Dept Child Life & Hlth, Edinburgh, Scotland
关键词
D O I
10.1136/bmjopen-2023-072461
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectivesRegular exercise testing is recommended for people with cystic fibrosis (pwCF), as is the provision and regular review of exercise training programmes. A previous survey on exercise testing and training for pwCF in the UK was conducted over a decade ago. With the landscape of CF changing considerably during this time, this survey aimed to evaluate UK-based exercise testing and training practices for pwCF a decade on.DesignCross-sectional, online survey.ParticipantsA survey was distributed electronically to UK CF clinics and completed by the individual primarily responsible for exercise services. Descriptive statistics and qualitative analyses were undertaken.ResultsIn total, 31 CF centres participated, representing similar to 50% of UK specialist clinics. Of these, 94% reported using exercise testing, 48% of which primarily use cardiopulmonary exercise testing. Exercise testing mostly occurs at annual review (93%) and is most often conducted by physiotherapists (62%). A wide variation in protocols, exercise modalities, normative reference values and cut-offs for exercise-induced desaturation are currently used. All centres reportedly discuss exercise training with pwCF; 94% at every clinic appointment. However, only 52% of centres reportedly use exercise testing to inform individualised exercise training. Physiotherapists typically lead discussions around exercise training (74%).ConclusionsThese data demonstrate that the majority of respondent centres in the UK now offer some exercise testing and training advice for pwCF, representing a marked improvement over the past decade. However, continued efforts are now needed to standardise exercise practices, particularly regarding field testing practices and the translation of test results into personalised training programmes for pwCF.
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共 43 条
[11]   Promotion of physical activity for adolescents with cystic fibrosis: a qualitative study of UK multi disciplinary cystic fibrosis teams [J].
Denford, S. ;
Mackintosh, K. A. ;
McNarry, M. A. ;
Barker, A. R. ;
Williams, C. A. ;
Williams, Craig ;
Barker, Alan ;
Denford, Sarah ;
Oades, Patrick ;
McNarry, Melitta ;
Mackintosh, Kelly ;
Main, Eleanor ;
Rand, Sarah ;
Bryon, Mandy ;
Wells, Greg ;
Schneidermann, Jane ;
Holland, Anne ;
Eldridge, Bev ;
Cox, Narelle ;
O'Halloran, Paul .
PHYSIOTHERAPY, 2020, 106 :111-118
[12]   Increasing response rates to postal questionnaires: systematic review [J].
Edwards, P ;
Roberts, I ;
Clarke, M ;
DiGuiseppi, C ;
Pratap, S ;
Wentz, R ;
Kwan, I .
BRITISH MEDICAL JOURNAL, 2002, 324 (7347) :1183-1185
[13]   Physiotherapy service provision in a specialist adult cystic fibrosis service: A pre-post design study with the inclusion of an allied health assistant [J].
Hall, Kathleen ;
Maxwell, Lyndal ;
Cobb, Robyn ;
Steele, Michael ;
Chambers, Rebecca ;
Roll, Mark ;
Bell, Scott Cameron ;
Kuys, Suzanne .
CHRONIC RESPIRATORY DISEASE, 2021, 18
[14]   Toward the Establishment of New Clinical Endpoints for Cystic Fibrosis: The Role of Lung Clearance Index and Cardiopulmonary Exercise Testing [J].
Hatziagorou, Elpis ;
Kampouras, Asterios ;
Avramidou, Vasiliki ;
Toulia, Ilektra ;
Chrysochoou, Elisavet-Anna ;
Galogavrou, Maria ;
Kirvassilis, Fotios ;
Tsanakas, John .
FRONTIERS IN PEDIATRICS, 2021, 9
[15]   Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic Fibrosis [J].
Hebestreit, Helge ;
Hulzebos, Erik H. J. ;
Schneiderman, Jane E. ;
Karila, Chantal ;
Boas, Steven R. ;
Kriemler, Susi ;
Dwyer, Tiffany ;
Sahlberg, Margareta ;
Urquhart, Don S. ;
Lands, Larry C. ;
Ratjen, Felix ;
Takken, Tim ;
Varanistkaya, Liobou ;
Ruecker, Viktoria ;
Hebestreit, Alexandra ;
Usemann, Jakob ;
Radtke, Thomas ;
Junge, Sibylle ;
Smaczny, Christine ;
Rand, Sarah ;
Dawson, Charlotte .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2019, 199 (08) :987-995
[16]   Statement on Exercise Testing in Cystic Fibrosis [J].
Hebestreit, Helge ;
Arets, Hubertus G. M. ;
Aurora, Paul ;
Boas, Steve ;
Cerny, Frank ;
Hulzebos, Erik H. J. ;
Karila, Chantal ;
Lands, Larry C. ;
Lowman, John D. ;
Swisher, Anne ;
Urquhart, Don S. .
RESPIRATION, 2015, 90 (04) :332-351
[17]   Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial [J].
Heijerman, Harry G. M. ;
McKone, Edward F. ;
Downey, Damian G. ;
Van Braeckel, Eva ;
Rowe, Steven M. ;
Tullis, Elizabeth ;
Mall, Marcus A. ;
Welter, John J. ;
Ramsey, Bonnie W. ;
Mckee, Charlotte M. ;
Marigowda, Gautham ;
Moskowitz, Samuel M. ;
Waltz, David ;
Sosnay, Patrick R. ;
Simard, Christopher ;
Ahluwalia, Neil ;
Xuan, Fengjuan ;
Zhang, Yaohua ;
Taylor-Cousar, Jennifer L. ;
Mccoy, Karen S. .
LANCET, 2019, 394 (10212) :1940-1948
[18]   Charter to establish clinical exercise physiology as a recognised allied health profession in the UK: a call to action [J].
Jones, Helen ;
George, Keith P. ;
Scott, Andrew ;
Buckley, John P. ;
Watson, Paula M. ;
Oxborough, David L. ;
Thijssen, Dick H. ;
Graves, Lee E. F. ;
Whyte, Greg P. ;
McGregor, Gordon ;
Naylor, Louise H. ;
Rosenberg, Michael ;
Askew, Christopher D. ;
Green, Daniel J. .
BMJ OPEN SPORT & EXERCISE MEDICINE, 2021, 7 (03)
[19]   USE OF EXERCISE IN THE MANAGEMENT OF CYSTIC-FIBROSIS - SHORT COMMUNICATION ABOUT A SURVEY OF CYSTIC-FIBROSIS REFERRAL CENTERS [J].
KAPLAN, TA ;
ZEBRANEK, JD ;
MCKEY, RM .
PEDIATRIC PULMONOLOGY, 1991, 10 (03) :205-207
[20]   Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele [J].
Middleton, P. G. ;
Mall, M. A. ;
Drevinek, P. ;
Lands, L. C. ;
McKone, E. F. ;
Polineni, D. ;
Ramsey, B. W. ;
Taylor-Cousar, J. L. ;
Tullis, E. ;
Vermeulen, F. ;
Marigowda, G. ;
Mckee, C. M. ;
Moskowitz, S. M. ;
Nair, N. ;
Savage, J. ;
Simard, C. ;
Tian, S. ;
Waltz, D. ;
Xuan, F. ;
Rowe, S. M. ;
Jain, R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 381 (19) :1809-1819