Literature DB >> 11948041

Effects of an intensive 4-week summer camp on cystic fibrosis: pulmonary function, exercise tolerance, and nutrition.

Hannah Blau1, Huda Mussaffi-Georgy, Gershon Fink, Chaim Kaye, Amir Szeinberg, Shimon A Spitzer, Jacob Yahav.   

Abstract

STUDY
OBJECTIVES: Cystic fibrosis (CF) patients prefer exercise to most other forms of therapy, although objective improvement remains controversial. Israeli CF patients have attended a summer program in Switzerland for many years with subjective improvement. However, CF camps worldwide have been cancelled recently, due to fears of cross-infection with resistant organisms. Therefore, we evaluated the effect of attending the camp on pulmonary function, exercise tolerance, and nutritional state in CF patients.
DESIGN: Weight, resting pulmonary function, incremental exercise test results, and sputum culture findings were assessed before and after a 4-week intensive summer camp.
SETTING: Davos, Switzerland (altitude, 1,500 m). PATIENTS: Thirteen Israeli CF patients (seven women and six men) with an age range of 9 to 25 years who had mild-to-moderate lung disease. No patients had Burkholderia cepacia detected in their sputum.
INTERVENTIONS: The program included a high-calorie diet, chest physiotherapy, daily mountain climbing, and indoor activities. Arterial oxygen saturation (SaO(2)) was maintained at > 88% during exertion.
RESULTS: Exercise tolerance improved significantly. The peak work capacity increased by 12.7%, the maximal oxygen uptake increased by 10%, and minute ventilation increased by 18.5% (p < 0.0005). Of the calculated parameters, the anaerobic threshold improved by 17%. Ventilation was always the limiting factor during exercise, although it improved. There was no significant change in resting lung function and pulse or in SaO(2) decline at maximal exercise. The mean weight gain was 1 kg. No patient acquired B cepacia.
CONCLUSIONS: An intensive summer camp improved exercise tolerance and nutrition in CF patients. This may explain improved patient well-being despite unchanged values for resting lung function. The reinstitution of summer camps, with special care to avoid cross-infection, should be considered.

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Year:  2002        PMID: 11948041     DOI: 10.1378/chest.121.4.1117

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  8 in total

1.  Relationship between breath-hold time and physical performance in patients with cystic fibrosis.

Authors:  Maria Barnai; Istvan Laki; Kalman Gyurkovits; Lajos Angyan; Gyöngyi Horvath
Journal:  Eur J Appl Physiol       Date:  2005-07-09       Impact factor: 3.078

2.  Changes in perceived health of children with congenital heart disease after attending a special sports camp.

Authors:  P Moons; C Barrea; D De Wolf; M Gewillig; M Massin; L Mertens; C Ovaert; B Suys; T Sluysmans
Journal:  Pediatr Cardiol       Date:  2006 Jan-Feb       Impact factor: 1.655

3.  Exercise intensity self-regulation using the OMNI scale in children with cystic fibrosis.

Authors:  Linda W Higgins; Robert J Robertson; Sheryl F Kelsey; Marian B Olson; Leslie A Hoffman; Paul J Rebovich; Luke Haile; David M Orenstein
Journal:  Pediatr Pulmonol       Date:  2012-09-19

Review 4.  Epidemiology, Biology, and Impact of Clonal Pseudomonas aeruginosa Infections in Cystic Fibrosis.

Authors:  Michael D Parkins; Ranjani Somayaji; Valerie J Waters
Journal:  Clin Microbiol Rev       Date:  2018-08-29       Impact factor: 26.132

5.  Rehabilitation Programs for Cystic Fibrosis - View from a CF Center.

Authors:  M Griese; P Busch; D Caroli; B Mertens; C Eismann; M Harari; H Staudter; M Kappler
Journal:  Open Respir Med J       Date:  2010-01-07

6.  Tele-Exercise as a Promising Tool to Promote Exercise in Children With Cystic Fibrosis.

Authors:  Jen Jen Chen; Dan M Cooper; Fadia Haddad; Anna Sladkey; Eliezer Nussbaum; Shlomit Radom-Aizik
Journal:  Front Public Health       Date:  2018-09-28

7.  Handgrip Strength: Associations with Clinical Variables, Body Composition, and Bone Mineral Density in Adults with Cystic Fibrosis.

Authors:  Victoria Contreras-Bolívar; Casilda Olveira; Ignacio Ruiz-García; Nuria Porras; Maria García-Olivares; Francisco José Sánchez-Torralvo; Maria Victoria Girón; Silvia P Alonso-Gallardo; Gabriel Olveira
Journal:  Nutrients       Date:  2021-11-16       Impact factor: 5.717

Review 8.  Infection, inflammation and exercise in cystic fibrosis.

Authors:  Pauline Barbera van de Weert-van Leeuwen; Hubertus Gerardus Maria Arets; Cornelis Korstiaan van der Ent; Jeffrey Matthijn Beekman
Journal:  Respir Res       Date:  2013-03-06
  8 in total

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