Témata prací (Výběr práce)Témata prací (Výběr práce)(verze: 336)
Detail práce
   Přihlásit přes CAS
Možnosti fyzické zátěže u dětí s cystickou fibrózou ve školním věku
Název práce v češtině: Možnosti fyzické zátěže u dětí s cystickou fibrózou ve školním věku
Název v anglickém jazyce: Possibilities of Physical Exercise in School- Age Patients with Cystic Fibrosis
Klíčová slova: cystická fibróza, zátěžové testování, fyzická zátěž, aerobní zdatnost
Klíčová slova anglicky: cystic fibrosis, exercise testing, physical exercise, aerobic exercise capacity
Akademický rok vypsání: 2016/2017
Typ práce: bakalářská práce
Jazyk práce: čeština
Ústav: Klinika rehabilitace a tělovýchovného lékařství (13-432)
Vedoucí / školitel: Mgr. Jana Plešková
Řešitel: skrytý - zadáno vedoucím/školitelem
Datum přihlášení: 17.05.2017
Datum zadání: 20.04.2018
Datum potvrzení stud. oddělením: 17.05.2018
Datum a čas obhajoby: 22.05.2018 08:00
Datum odevzdání elektronické podoby:23.04.2018
Datum odevzdání tištěné podoby:23.04.2018
Datum proběhlé obhajoby: 22.05.2018
Oponenti: doc. PaedDr. Libuše Smolíková, Ph.D.
 
 
 
Seznam odborné literatury
AKKERMAN, Moniek, VAN BRUSSEL, Marco, BONGERS, Bart C., HULZEBOS, Erik H.J., HELDERS, Paul J.M a TAKKEN, Tim, © 2010. Oxygen Uptake Efficiency Slope in Healthy Children. Pediatric Exercise Science [online]. HUMAN KINETICS JOURNALS, 22(3), 431-441 [cit. 2018-03-15]. DOI: 10.1123/pes.22.3.431. eISSN 1543-2920. Dostupné z: http://journals.humankinetics.com/doi/10.1123/pes.22.3.431.
ALMAJED, Athari a LANDS, Larry C., © 2012. The evolution of exercise capacity and its limiting factors in Cystic Fibrosis. Pediatric Respiratory Reviews [online]. Elsevier, 13(4), s. 195-199 [cit. 2017-02-01]. DOI: 10.1016/j.prrv.2012.01.001. ISSN 1526-0542. Dostupné z: databáze ScienceDirect.
ALPERN, Adrianne N., BRUMBACK, Lyndia C., RATJEN, Felix, ROSENFELD, Margaret, DAVIS, Stephanie D. a QUITTNER, Alexandra L., 2015. Initial evaluation of the Parent Cystic Fibrosis Questionnaire—Revised (CFQ-R) in infants and young children. Journal of Cystic Fibrosis [online]. Elsevier B. V., 14(3), s. 403-411 [cit. 2018-03-20]. DOI: 10.1016/j.jcf.2014.11.002. eISSN 1873-5010. Dostupné z: http://www.cysticfibrosisjournal.com/article/S1569-1993(14)00263-X/fulltext.
ARIKAN, Hulya, YATAR, İlker, CALIK-KUTUKCU, Ebru et al., © 2015. A comparison of respiratory and peripheral muscle strength, functional exercise capacity, activities of daily living and physical fitness in patients with cystic fibrosis and healthy subjects. Research in Developmental Disabilities [online]. Elsevier, 45-46, s. 147-156 [cit. 2018-01-04]. DOI: 10.1016/j.ridd.2015.07.020. ISSN 0891-4222. Dostupné z: databáze ScienceDirect.
BARRY, Sinead C. a GALLAGHER, Charles G., 2003. Corticosteroids and skeletal muscle function in cystic fibrosis. Journal of Applied Physiology [online]. The American Physiological Society, 95(4), s. 1379-1384 [cit. 2018-04-02]. DOI: 10.1152/japplphysiol.00506.2002. ISSN 8750-7587. Dostupné z: http://www.physiology.org/doi/10.1152/japplphysiol.00506.2002.
BIANCHI, Maria Luisa, ROMANO, Giovanna, SARAIFOGER, Silvia, COSTANTINI, Diana, LIMONTA, Cristina a COLOMBO, Carla, 2006. BMD and Body Composition in Children and Young Patients Affected by Cystic Fibrosis. JOURNAL OF BONE AND MINERAL RESEARCH [online]. American Society for Bone and Mineral Research, 21(3), [cit. 2018-03-22]. DOI: 10.1359/JBMR.051106. ISSN 0884-0431.
BLOCK, J K, VANDEMHEEN, K L, TULLIS, E et al., 2006. Predictors of pulmonary exacerbations in patients with cystic fibrosis infected with multi-resistant bacteria. Thorax [online]. BMJ Publishing Group, 2006, 61(11), s. 969-974 [cit. 2018-03-20]. DOI: 10.1136/thx.2006.061366. ISSN 0040-6376. Dostupné z: http://thorax.bmj.com/content/thoraxjnl/61/11/969.full.pdf.
BOHANNON, Richard W., BUBELA, Deborah J., WANG, Ying-Chih, MAGASI, Susan S. a GERSHON, Richard C., 2015. Six-Minute Walk Test Vs. Three-Minute Step Test for Measuring Functional Endurance. Journal of Strength and Conditioning Research [online]. Lippincott Williams & Wilkins, 29(11), s. 3240–3244 [cit. 2018-02-26]. DOI: 10.1519/JSC.0000000000000253. eISSN 1533-4287. Dostupné z: http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC4004706&blobtype=pdf .
BONGERS, BART C., WERKMAN, MAARTEN S., ARETS, H. G. M. , TAKKEN, TIM a HULZEBOS, H. J. , © 2015. A Possible Alternative Exercise Test for Youths with Cystic Fibrosis. Medicine & Science in Sports & Exercise: Official Journal of the American College of Sports Medicine [online]. Lippincott Williams & Wilkins, 47(3), s. 485-492 [cit. 2017-08-05]. DOI: 10.1249/MSS.0000000000000440. eISSN 1530-0315. Dostupné z: https://journals.lww.com/acsm-msse/Fulltext/2015/03000/A_Possible_Alternative_Exercise_Test_for_Youths.5.aspx.
CYSTIC FIBROSIS FOUNDATION, ©2017. Cystic Fibrosis Foundation Patient Registry 2016 Annual Data Report [online]. Bethesda, Maryland. Dostupné z: https://www.cff.org/Research/Researcher-Resources/Patient-Registry/2016-Patient-Registry-Annual-Data-Report.pdf.
DANIELS, Tracey, MORRISON, Lisa, HARNETT Nuala et al., 2017. Standards of care and Good Clinical Practice for the Physiotherapy Management of Cystic Fibrosis [online]. Cystic Fibrosis Trust [cit. 2017-12-27]. Dostupné z: https://www.cysticfibrosis.org.uk/~/media/documents/life-with-cf/publications/consensus-on-physiotherapy-management--third-edition-2017.ashx?la=en.
DE JONG, Wietze, KAPTEIN, Adrian A., VAN DER SCHANS, Cees P., MANNES, Gregor P.M. , VAN AALDEREN, Wim M.C., GREVINK, René G. a KOËTER, Gerard H., 1997. Quality of Life in Patients With Cystic Fibrosis. PEDIATRIC PULMONOLOGY. Wiley- Liss, 23(2), s. 95-100. ISSN 8755-6863.
DONADIO, Márcio V. F., HEINZMANN-FILHO, João P., VENDRUSCULO, Fernanda M., FRASSON, Patrícia X. H. a MAROSTICA, Paulo J.C., March 2017. Six-Minute Walk Test Results Predict Risk of Hospitalization for Youths with Cystic Fibrosis: A 5-Year Follow-Up Study. THE JOURNAL OF PEDIATRICS [online]. Elsevier, 182, s. 204-209 [cit. 2018-01-07]. DOI: 10.1016/j.jpeds.2016.11.071. eISSN 1097-6833. Dostupné z: databáze ScienceDirect.
DORFMAN, Ruslan et al., 2017. CFMDB Statistics. Cystic Fibrosis Mutation Database [databáze online]. [Toronto]: [Hospital for Sick Children], [aktualizováno 2017-09-09] [cit. 2018-04-11]. Dostupné z: http://www.genet.sickkids.on.ca/StatisticsPage.html.
ECFS [EUROPEAN CYSTIC FIBROSIS SOCIETY], 2017. ECFS PATIENTS REGISTRY, © 2018. [databáze online]. EUROPEAN CYSTIC FIBROSIS SOCIETY, aktualizováno 2017-01-01 [cit. 2018-04-11]. Dostupné z: https://www.ecfs.eu/ecfspr.
FILA, Libor, 2014. Cystická fibróza u dospělých. Interní medicína pro praxi. Solen, 16(2), s. 54-60. ISSN 1212-7299.
FOSTER, Karla, HUANG, Guixia, ZHANG, Nanhua, CRISALLI, Joseph, CHINI, Barbara, AMIN, Raouf a ELDER, Deborah, © 2018. Relationship between exercise capacity and glucose tolerance in cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley Periodicals, 53(2), s. 154-161 [cit. 2018-03-19]. DOI: 10.1002/ppul.23906. eISSN 1099-0496. Dostupné z: Wiley Online Library.
GEORGE, P. M., BANYA, W., PAREEK, N., BILTON, D., CULLINAN, P., HODSON, M. E. a SIMMONDS, N. J., 2011. Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007. British Medical Journal [online]. BMJ Publishing Group, 342,[cit. 2018-03-20]. DOI: 10.1136/bmj.d1008. Dostupné z: https://www.bmj.com/content/bmj/342/bmj.d1008.full.pdf.
GIACCHI, Valentina, ROTOLO, Novella, AMATO, Barbara, DI DIO, Giovanna, BETTA, Pasqua, LA ROSA, Mario, LEONARDI, Salvatore a SCIACCA, Pietro, 2015. Heart Involvement in Children and Adults with Cystic Fibrosis: Correlation with Pulmonary Indexes and Inflammation Markers. Heart, Lung and Circulation [online]. Elsevier, 24(10), s. 1002-1010 [cit. 2018-04-02]. DOI: 10.1016/j.hlc.2015.03.006. eISSN 1444-2892. Dostupné z: databáze ScienceDirect.
GRUBER, W., ORENSTEIN, D.M., BRAUMANN, K.M. a HÜLS, G., © 2008. Health-related fitness and trainability in children with cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley- Liss, 43(10), s. 953-964 [cit. 2018-03-11]. DOI: 10.1002/ppul.20881. ISSN 8755-6863. Dostupné z: Wiley Online Library.
GRUBER, Wolfgang, ORENSTEIN, David M., BRAUMANN, Klaus Michael, PAUL, Karl a HÜLS, Gerd, 2011. Effects of an Exercise Program in Children with Cystic Fibrosis: Are There Differences between Females and Males?. THE JOURNAL OF PEDIATRICS [online]. Elsevier, 158(1), s. 58-63 [cit. 2017-02-04]. DOI: 10.1016/j.jpeds.2010.07.033. ISSN 0022-3476. Dostupné z: databáze ScienceDirect.
GRUET, Mathieu, DECORTE, Nicolas, MELY, Laurent, VALLIER, Jean-Marc, CAMARA, Boubou, QUETANT, Sébastien, WUYAM, Bernard a VERGES, Samuel, 2016. Skeletal muscle contractility and fatigability in adults with cystic fibrosis. Journal of Cystic Fibrosis [online]. Elsevier B. V., 15(1), e1-e8 [cit. 2017-02-01]. DOI: 10.1016/j.jcf.2015.05.004 Dostupné z: databáze ScienceDirect.
GRUET, Mathieu, TROOSTERS, Thierry a VERGES, Samuel, 2017. Peripheral muscle abnormalities in cystic fibrosis: Etiology, clinical implications and response to therapeutic interventions. Journal of Cystic Fibrosis [online]. Elsevier B. V., 16(5), s. 538-552 [cit. 2018-04-02]. DOI: 10.1016/j.jcf.2017.02.007. eISSN 1873-5010. Dostupné z: databáze ScienceDirect.
HEBESTREIT, H., KIESER, S., JUNGE, S. et al., 2010. Long-term effects of a partially supervised conditioning programme in cystic fibrosis. EUROPEAN RESPIRATORY JOURNAL [online]. The European Respiratory Society, 35(3), s. 578-583 [cit. 2017-10-15]. DOI: 10.1183/09031936.00062409. ISSN 0903-1936. Dostupné z: http://erj.ersjournals.com/cgi/doi/10.1183/09031936.00062409.
HEBESTREIT, Helge, ARETS, Hubertus G.M., AURORA, Paul et al., © 2015. Statement on Exercise Testing in Cystic Fibrosis. Respiration [online]. Karger, 90(4), s. 332-351 [cit. 2017-07-16]. DOI: 10.1159/000439057. eISSN 1423-0356. Dostupné z: https://www.karger.com/Article/FullText/439057.
HEBESTREIT, Helge, SCHMID, Kerstin, KIESER, Stephanie et al., 2014. Quality of life is associated with physical activity and fitness in cystic fibrosis. BMC Pulmonary Medicine [online]. BioMed Central, 2014, 14(26) [cit. 2018-04-03]. DOI: 10.1186/1471-2466-14-26. ISSN 1471-2466. Dostupné z: http://bmcpulmmed.biomedcentral.com/articles/10.1186/1471-2466-14-26.
HOLLAND, A. E., RASEKABA, T., WILSON, J. W. a BUTTON, B. M., August 2011. Desaturation During the 3-Minute Step Test Predicts Impaired 12-Month Outcomes in Adult Patients With Cystic Fibrosis. RESPIRATORY CARE [online]. Daedalus Enterprises, 56(8), s. 1137-1142 [cit. 2018-03-01]. DOI: 10.4187/respcare.01016. ISSN 0020-1324. Dostupné z: http://rc.rcjournal.com/cgi/doi/10.4187/respcare.01016.
HOMMERDING, P. X., BAPTISTA, R. R., MAKAREWICZ, G. T., SCHINDEL, C. S., DONADIO, M. V., PINTO, L. A. a MAROSTICA, P. J., January 2015. Effects of an Educational Intervention of Physical Activity for Children and Adolescents With Cystic Fibrosis: A Randomized Controlled Trial. RESPIRATORY CARE [online]. Daedalus Enterprises, 60(1), s. 81-87 [cit. 2018-02-06]. DOI: 10.4187/respcare.02578. eISSN 1943-3654. Dostupné z: http://rc.rcjournal.com/cgi/doi/10.4187/respcare.02578.
HOMOLA, Lukáš, 2014. Cystická fibróza 2013. Postgraduální medicína. Vzácná onemocnění. Mladá fronta a. s., 16(1), s. 11-20. ISSN 1212-4184.
HULZEBOS, Erik H. J., BOMHOF-ROORDINK, Hanna, VAN DE WEERT-VAN LEEUWEN, Pauline B., TWISK, Jos W. R., ARETS, H. G. M., VAN DER ENT, Cornelis K. a TAKKEN, Tim, © 2014. Prediction of Mortality in Adolescents with Cystic Fibrosis. Medicine & Science in Sports & Exercise: Official Journal of the American College of Sports Medicine [online]. Lippincott Williams & Wilkins, 46(11), s. 2047-2052 [cit. 2018-01-07]. DOI: 10.1249/MSS.0000000000000344. eISSN 1530-0315. Dostupné z: https://journals.lww.com/acsm-msse/Fulltext/2014/11000/Prediction_of_Mortality_in_Adolescents_with_Cystic.2.aspx
CHELABI, Riyadh, SOUMAGNE, Thibaud, GUILLIEN, Alicia, PUYRAVEAU, Marc a DEGANO, Bruno, 2018. In cystic fibrosis, lung clearance index is sensitive to detecting abnormalities appearing at exercise in children with normal spirometry. Respiratory Physiology & Neurobiology [online]. Elsevier B. V., 247, s. 9-11 [cit. 2018-01-04]. DOI: 10.1016/j.resp.2017.08.017. eISSN 1878-1519. Dostupné z: databáze ScienceDirect.
CHLUMSKÝ, J., 2016. Doporučený postup pro indikaci, provedení a hodnocení spiroergometri (CPET). Pneumologie.cz [online]. Česká pneumologická a ftizeologická společnosti ČLS JEP [cit. 2018-03-19]. Dostupné z: http://www.pneumologie.cz/upload/1463401653.pdf.
JAKUBEC, Petr, 2006. Cystická fibróza. Interní medicína pro praxi. Solen, 8(5), s. 235-239. ISSN 1212-7299.
KELLY, Andrea, SCHALL, Joan, STALLINGS, Virginia A. a ZEMEL, Babette S., 2016. Trabecular and cortical bone deficits are present in children and adolescents with cystic fibrosis. Bone [online]. Elsevier, 90, s. 7-14 [cit. 2018-03-16]. DOI: 10.1016/j.bone.2016.04.030. ISSN 1873-2763. Dostupné z: databáze ScienceDirect.
KING, S. J., TOPLISS, D. J., KOTSIMBOS, T., NYULASI, I. B., BAILEY, M., EBELING, P. R. a WILSON, J. W., 2005. Reduced bone density in cystic fibrosis: ΔF508 mutation is an independent risk factor. EUROPEAN RESPIRATORY JOURNAL [online]. The European Respiratory Society, 25(1), s. 54-61 [cit. 2018-03-22]. DOI: 10.1183/09031936.04.00050204. ISSN 0903-1936. Dostupné z: http://erj.ersjournals.com/cgi/doi/10.1183/09031936.04.00050204.
KOUCKÝ, Vladimír a POHUNEK, Petr, 2016. Využití metody vícedechového vyplavování inertního plynu z plic ve funkční plicní diagnostice u dětí. STUDIA PNEUMOLOGICA ET PHTHISEOLOGICA. Česká pneumologická a ftizeologická společnost, 76(2), s. 56-66. ISSN 1213-810X.
KRIEMLER, Susi, KIESER, Stephanie, JUNGE, Sibylle, BALLMANN, Manfred, HEBESTREIT, Alexandra, SCHINDLER, Christian, STÜSSI, Christoph a HEBESTREIT, Helge, © 2013. Effect of supervised training on FEV1 in cystic fibrosis: A randomised controlled trial. Journal of Cystic Fibrosis [online]. Elsevier B. V., 12(6), s. 714-720 [cit. 2017-10-28]. DOI: 10.1016/j.jcf.2013.03.003. eISSN 1873-5010. Dostupné z: http://www.cysticfibrosisjournal.com/article/S1569-1993(13)00039-8/fulltext.
KRIEMLER, Susi, RADTKE, Thomas, CHRISTEN, Gregor, KERSTAN-HUBER, Marta a HEBESTREIT, Helge, 2016. Short-Term Effect of Different Physical Exercises and Physiotherapy Combinations on Sputum Expectoration, Oxygen Saturation, and Lung Function in Young Patients with Cystic Fibrosis. LUNG [online]. Springer, 194(4), s. 659-664 [cit. 2017-02-01]. DOI: 10.1007/s00408-016-9888-x. Dostupné z: http://link.springer.com/10.1007/s00408-016-9888-x.
LAMHONWAH, Anne-Marie, BEAR, Christine E., HUAN, Ling Jun, CHIAW, Patrick Kim, ACKERLEY, Cameron A. a TEIN, Ingrid, © 2010. Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise. Annals of Neurology: An Official Journal of the American Neurological Association and the Child Neurology Society [online]. Wiley- Liss, 67(6), s. 802-808 [cit. 2018-04-02]. DOI: 10.1002/ana.21982. ISSN 0364-5134. Dostupné z: Wiley Online Library.
LAMMERS, A E, HISLOP, A A, FLYNN, Y a G HAWORTH, S, 2008. The 6-minute walk test: normal values for children of 4-11 years of age. Archives of Disease in Childhood [online]. BMJ Publishing Group, 93(6), s. 464-468 [cit. 2018-03-25]. DOI: 10.1136/adc.2007.123653. ISSN 0003-9888. Dostupné z: databáze BMJ Journals.
LANNEFORS, L. Physical Excercise. In INTERNATIONAL PHYSIOTHERAPY GROUP FOR CYSTIC FIBROSIS. Physiotherapy for people with Cystic Fibrosis: from infant to adult. 2009, 4th edition . Dostupné z: https://www.ecfs.eu/files/webfm/webfiles/File/Physiotherapy%20WebPages/blue%20booklet%202009%20website%20version%20+1.pdf.
LESSER, Daniel J., FLEMING, Margaret M., MAHER, Carolyn A., KIM, Stephanie B., WOO, Marlyn S. a KEENS, Thomas G., © 2010. Does the 6-min walk test correlate with the exercise stress test in children?. PEDIATRIC PULMONOLOGY [online]. Wiley- Liss, 45(2), s. 135-140 [cit. 2018-02-25]. DOI: 10.1002/ppul.21125. Dostupné z: Wiley Online Library.
MÁČEK, Jiří, ©2011. Pohybová aktivita a sport v dětském věku. In MÁČEK, Miloš, RADVANSKÝ, Jiří et al. FYZIOLOGIE A KLINICKÉ ASPEKTY POHYBOVÉ AKTIVITY. První vydání. Praha: Galén, s. 127-139. ISBN 978-80-7262-695-3.
MOORCROFT, A. J., DODD, M. E. a WEBB, A. K., 1998. Exercise limitations and training for patients with cystic fibrosis. Disability and Rehabilitation [online]. Taylor & Francis, 20(6-7), s. 247-253 [cit. 2017-02-13]. DOI: 10.3109/09638289809166735. ISSN 0963-8288. Dostupné z: databáze Taylor & Francis Online.
MURRAY, Robert K., BENDER, David A., BOTHAM, Kathleen M., KENNELLY, Peter J., RODWELL, Victor W., WEIL, Victor W. Přeložil MATOUŠ, Bohuslav et al., 2012. Harperova ilustrovaná biochemie. 5. české vyd., 1. v nakl. Galén. Praha: Galén. ISBN 978-80-7262-907-7.
NEUMANNOVÁ, Kateřina, JANURA, Miroslav, KOVÁČIKOVÁ, Zuzana, SVOBODA, Zdeněk a JAKUBEC, Lukáš, 2015. Analýza chůze u osob s chronickou obstrukční plicní nemocí. Olomouc: Univerzita Palackého v Olomouci. ISBN 978-80-244-4704-9.
NIXON, Patricia A., ORENSTEIN, David M. , KELSEY, Sheryl F. a DOERSHUK, Carl F., 1992. The Prognostic Value of Exercise Testing in Patients with Cystic Fibrosis. NEW ENGLAND JOURNAL OF MEDICINE [online]. Massachusetts Medical Society, 327(25), s. 1785-1788 [cit. 2018-04-12]. DOI: 10.1056/NEJM199212173272504. Dostupné z: http://www.nejm.org/doi/abs/10.1056/NEJM199212173272504.
OWENS, C. M., AURORA, P., STANOJEVIC, S. et al., 2011. Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF. Thorax [online]. BMJ Publishing Group, 2011, 66(6), s. 481-488 [cit. 2018-04-01]. DOI: 10.1136/thx.2010.150375. eISSN 1468-3296. Dostupné z: http://thorax.bmj.com/cgi/doi/10.1136/thx.2010.150375.
PARAZZI, Paloma Lopes Francisco, MARSON, Fernando Augusto de Lima, RIBEIRO, Maria Angela Gonçalves de Oliveira et al., 2015. Ventilatory abnormalities in patients with cystic fibrosis undergoing the submaximal treadmill exercise test. BMC Pulmonary Medicine [online]. BioMed Central, 15(63) [cit. 2018-01-07]. DOI: 10.1186/s12890-015-0056-5. eISSN 1471-2466. Dostupné z: https://bmcpulmmed.biomedcentral.com/articles/10.1186/s12890-015-0056-5.
PEDERSEN, B. K. a SALTIN, B., © 2015. Exercise as medicine - evidence for prescribing exercise as therapy in 26 different chronic diseases. SCANDINAVIAN JOURNAL OF MEDICINE & SCIENCE IN SPORTS [online]. Wiley, 25(Suppl. 3), s. 1-72 [cit. 2017-02-06]. DOI: 10.1111/sms.12581. eISSN 1600-0838. Dostupné z: http://doi.wiley.com/10.1111/sms.12581.
PÉREZ, Margarita, GROENEVELD, Iris F., SANTANA-SOSA, Elena, FIUZA-LUCES, Carmen, GONZALEZ-SAIZ, Laura, VILLA-ASENSI, José R., LÓPEZ-MOJARES, Luis M., RUBIO, Margarita a LUCIA, Alejandro, © 2014. Aerobic fitness is associated with lower risk of hospitalization in children with cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley Periodicals, 49(7), s. 641-649 [cit. 2018-03-20]. DOI: 10.1002/ppul.22878. eISSN 1099-0496. Dostupné z: Wiley Online Library.
PIANOSI, Paul, LEBLANC, John a ALMUDEVAR, Anthony, © 2005. Relationship between FEV1 and peak oxygen uptake in children with cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley- Liss, 40(4), 324-329 [cit. 2018-03-29]. DOI: 10.1002/ppul.20277. eISSN 8755-6863. Dostupné z: Wiley Online Library.
POULIOU, Eleni, NANAS, Serafim, PAPAMICHALOPOULOS, Antonios, KYPRIANOU, Theodoros, PERPATI, Georgia, MAVROU, Irini a ROUSSOS, Charis, 2001. Prolonged Oxygen Kinetics During Early Recovery From Maximal Exercise in Adult Patients With Cystic Fibrosis. CHEST [online]. American College of Chest Physicians, 119(4), s. 1073-1078 [cit. 2017-07-16]. DOI: 10.1378/chest.119.4.1073. ISSN 0012-3692. Dostupné z: databáze ScienceDirect.
QUITTNER et al., 2002. Cystic Fibrosis Questionnaire Revised. American Thoracic Society.
RADTKE, Thomas, HEBESTREIT, Helge, PUHAN, Milo A. a KRIEMLER, Susi, © 2017. The 1-min sit-to-stand test in cystic fibrosis — Insights into cardiorespiratory responses. Journal of Cystic Fibrosis: The Official Journal of the European Cystic Fibrosis Society [online]. Elsevier B. V., 16(6), s. 744–751 [cit. 2018-01-27]. DOI: 10.1016/j.jcf.2017.01.012. eISSN 1873-5010. Dostupné z: databáze ScienceDirect.
RADTKE, Thomas, Sarah J NOLAN, Sarah J, HEBESTREIT, Helge a KRIEMLER, Susi, 2015. Physical exercise training for cystic fibrosis. Cochrane Database of SystematicReviews [online]. WILEY, (6) [cit. 2017-02-06]. DOI: 10.1002/14651858.CD002768.pub3. eISSN 1361-6137. Dostupné z: Cochrane Library.
RADTKE, Thomas, STEVENS, Daniel, BENDEN, Christian a Craig A. WILLIAMS, ©2009. Clinical Exercise Testing in Children and Adolescents with Cystic Fibrosis. Pediatric Physical Therapy [online]. Lippincott Williams & Wilkins, 21(3), s. 275-281 [cit. 2018-01-06]. DOI: 10.1097/PEP.0b013e3181b15445. eISSN 0898-5669/109/2103-0275. Dostupné z: https://journals.lww.com/pedpt/Fulltext/2009/02130/Clinical_Exercise_Testing_in_Children_and.9.aspx#O18-9 .
RADVANSKÝ, Jiří, ©2009. FUNKČNÍ ZÁTĚŽOVÉ VYŠETŘENÍ NEMOCNÝCH S KARDIORESPIRAČNÍ PORUCHOU. In KOLÁŘ, Pavel et al. REHABILITACE V KLINICKÉ PRAXI. První vydání. Praha: Galén, s. 548- 554. ISBN 978-80-7262-657-1.
RADVANSKÝ, Jiří, ©2011a. Zátěž maximální intenzity. In MÁČEK, Miloš, RADVANSKÝ, Jiří et al. FYZIOLOGIE A KLINICKÉ ASPEKTY POHYBOVÉ AKTIVITY. První vydání. Praha: Galén, s. 17-19. ISBN 978-80-7262-695-3.
RADVANSKÝ, Jiří, ©2011b. Zátěžové vyšetření. In MÁČEK, Miloš, RADVANSKÝ, Jiří et al. FYZIOLOGIE A KLINICKÉ ASPEKTY POHYBOVÉ AKTIVITY. První vydání. Praha: Galén, s. 63-65. ISBN 978-80-7262-695-3.
REYCHLER, Gregory, DEBATISSE, Margaux, LEBECQUE, Patrick, PIETERS, Thierry, LIISTRO, Giuseppe a GOHY, Sophie, © 2016. Variability of gait speed during six minutes walking test in COPD and cystic fibrosis patients. GAIT & POSTURE [online]. Elsevier B. V., 49, 36-40 [cit. 2018-02-07]. DOI: 10.1016/j.gaitpost.2016.06.007. eISSN 1879-2219. Dostupné z: ScienceDirect. ROBINSON, Paul D., COOPER, Peter, VAN ASPEREN, Peter, FITZGERALD, Dominic a SELVADURAI, Dominic, © 2009. Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley- Liss, 44(8), s. 733-742 [cit. 2018-03-29]. DOI: 10.1002/ppul.20956. eISSN 8755-6863. Dostupné z: Wiley Online Library. ROVEDDER, Paula Maria Eidt, FLORES, Josani, ZIEGLER, Bruna, CASAROTTO, Fernanda, JAQUES, Patrícia, BARRETO, Sergio Saldanha Menna a DALCIN, Paulo de Tarso Roth, 2014. Exercise programme in patients with cystic fibrosis: A randomized controlled trial. RESPIRATORY MEDICINE [online]. Elsevier, 108(8), s. 1134-1140 [cit. 2018-04-16]. DOI: 10.1016/j.rmed.2014.04.022. eISSN 1532-3064. Dostupné z: http://www.resmedjournal.com/article/S0954-6111(14)00228-5/fulltext.
SAGLAM, Melda, VARDAR-YAGLI, Naciye, SAVCI, Sema et al., © 2016. Six minute walk test versus incremental shuttle walk test in cystic fibrosis. PEDIATRICS INTERNATIONAL: Official Journal of the Japan Pediatric Society [online]. Wiley, 58(9), s. 887-893 [cit. 2018-02-06]. DOI: 10.1111/ped.12919. eISSN 1442-200X. Dostupné z: Wiley Online Library.
SANTANA- SOSA, ELENA, GROENEVELD, IRIS F., GONZALEZ-SAIZ, LAURA et al., © 2012. Intrahospital Weight and Aerobic Training in Children with Cystic Fibrosis. Medicine & Science in Sports & Exercise: Official Journal of the American College of Sports Medicine [online]. Lippincott Williams & Wilkins, 44(1), s. 2-11 [cit. 2017-09-22]. DOI: 10.1249/MSS.0b013e318228c302. eISSN 1530-0315. Dostupné z: https://journals.lww.com/acsm-msse/Fulltext/2012/01000/Intrahospital_Weight_and_Aerobic_Training_in.2.aspx.
SANTANA-SOSA, Elena, GONZALEZ-SAIZ, Laura, GROENEVELD, Iris F et al., 2014. Benefits of combining inspiratory muscle with ‘whole muscle’ training in children with cystic fibrosis: a randomised controlled trial. British Journal of Sports Medicine [online]. BMJ Publishing Group, 48(20), s. 1513-1517 [cit. 2018-02-06]. DOI: 10.1136/bjsports-2012-091892. eISSN 1473-0480. Dostupné z: http://bjsm.bmj.com/lookup/doi/10.1136/bjsports-2012-091892.
SAYNOR, Zoe L., BARKER, Alan R., OADES, Patrick J. a WILLIAMS, Craig A., © 2013. A protocol to determine valid VO2max in young cystic fibrosis patients. Journal of Science and Medicine in Sport [online]. Elsevier, 16(6), s. 539-544 [cit. 2017-02-13]. DOI: 10.1016/j.jsams.2013.01.010. eISSN 1878-1861. Dostupné z: databáze ScienceDirect.
SAYNOR, ZOE LOUISE, BARKER, ALAN ROBERT, OADES, PATRICK JOHN a WILLIAMS, CRAIG ANTHONY, © 2016. Impaired Pulmonary V˙O2 Kinetics in Cystic Fibrosis Depend on Exercise Intensity. Medicine & Science in Sports & Exercise: Official Journal of the American College of Sports Medicine [online]. Lippincott Williams & Wilkins, 48(11), 2090-2099 [cit. 2018-01-07]. DOI: 10.1249/MSS.0000000000001004. eISSN 1530-0315. Dostupné z: databáze Ovid.
SELVADURAI, H.C., BLIMKIE, C.J., MEYERS, N., MELLIS, C.M., COOPER, P.J. a VAN ASPEREN, P.P., ©2002. Randomized controlled study of in-hospital exercise training programs in children with cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley- Liss, 33(3), s. 194-200 [cit. 2017-01-14]. DOI: 10.1002/ppul.10015. ISSN 8755-6863. Dostupné z: Wiley Online Library.
SERMET-GAUDELUS, Isabelle, BIANCHI, Maria Luisa, GARABÉDIAN, Michèle et al., © 2011. European cystic fibrosis bone mineralisation guidelines. Journal of Cystic Fibrosis: The Official Journal of the European Cystic Fibrosis Society [online]. Elsevier B. V., 10, S16-S23 [cit. 2018-04-16]. DOI: 10.1016/S1569-1993(11)60004-0. Dostupné z: databáze ScienceDirect.
SERMET-GAUDELUS, Isabelle, SOUBERBIELLE, Jean Claude, RUIZ, Jean Charles et al., 2007. Low Bone Mineral Density in Young Children with Cystic Fibrosis. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE [online]. American Thoracic Society, 175(9), s. 951-957 [cit. 2018-03-22]. DOI: 10.1164/rccm.200606-776OC. ISSN 1073-449X. Dostupné z: http://www.atsjournals.org/doi/abs/10.1164/rccm.200606-776OC.
SHEAD, Elizabeth F., HAWORTH, Charles S., BARKER, Helen, BILTON, Diana a COMPSTON, Juliet E., © 2010. Osteoclast function, bone turnover and inflammatory cytokines during infective exacerbations of cystic fibrosis. Journal of Cystic Fibrosis: The Official Journal of the European Cystic Fibrosis Society [online]. Elsevier B. V., 9(2), s. 93-98 [cit. 2018-03-22]. DOI: 10.1016/j.jcf.2009.11.007. ISSN 1569-1993. Dostupné z: http://www.cysticfibrosisjournal.com/article/S1569-1993(09)00154-4/fulltext.
SCHMIDT, Anne Mette, JACOBSEN, Ulla, BREGNBALLE, Vibeke, OLESEN, Hanne Vebert, INGEMANN-HANSEN, Thorsten, THASTUM, Mikael a OLUF SCHIØTZ, Peter, 2011. Exercise and quality of life in patients with cystic fibrosis: A 12-week intervention study. Physiotherapy Theory and Practice [online]. Taylor & Francis Group, 27(8), s. 548-556 [cit. 2017-02-13]. DOI: 10.3109/09593985.2010.545102. ISSN 0959-3985. Dostupné z: http://www.tandfonline.com/doi/full/10.3109/09593985.2010.545102.
SCHNEIDERMAN-WALKER, Jane, POLLOCK, Susan L., COREY, Mary, WILKES, Donna D., CANNY, Gerard J., PEDDER, Linda a REISMAN, J.Joseph, March 2000. A randomized controlled trial of a 3-year home exercise program in cystic fibrosis. The Journal of Pediatrics [online]. Elsevier, 136(3), s. 304-310 [cit. 2018-02-06]. DOI: 10.1067/mpd.2000.103408. ISSN 0022-3476. Dostupné z: databáze ScienceDirect.
SMITH, Laurie, REILLY, Charles C., MACBEAN, Victoria, JOLLEY, Caroline J., ELSTON, Caroline, MOXHAM, John a RAFFERTY, Gerrard F., © 2017. Physiological markers of exercise capacity and lung disease severity in cystic fibrosis. Respirology: Official Journal of the Asian Pacific Society of Respirology [online]. WILEY, 22(4), s. 714-720 [cit. 2018-02-19]. DOI: 10.1111/resp.12954. eISSN 1440-1843. Dostupné z: Wiley Online Library.
SMITH, Nathan, LIM, Angelina, YAP, Matthew, KING, Louise, JAMES, Simon, JONES, Alicia, RANGANATHAN, Sarath a SIMM, Peter, © 2017. Bone mineral density is related to lung function outcomes in young people with cystic fibrosis-A retrospective study. PEDIATRIC PULMONOLOGY [online]. Wiley Periodicals, 52(12), s. 1558-1564 [cit. 2018-02-07]. DOI: 10.1002/ppul.23894. eISSN 1099-0496. Dostupné z: Wiley Online Library.
TAKKEN, Tim, BONGERS, Bart C., VAN BRUSSEL, Marco, HAAPALA, Eero A. a HULZEBOS, Erik H. J., © 2017. Cardiopulmonary Exercise Testing in Pediatrics. Annals of the American Thoracic Society [online]. American Thoracic Society, 14(Supplement 1), S123-S128 [cit. 2018-03-28]. DOI: 10.1513/AnnalsATS.201611-912FR. eISSN 2325-6621 Dostupné z: http://www.atsjournals.org/doi/10.1513/AnnalsATS.201611-912FR.
THOMPSON, James S., THOMPSON, Margaret Wilson, NUSSBAUM, Robert L., WILLARD, Huntington F. a MCINNES, Roderick R., 2004. Klinická genetika: Thompson & Thompson : 6. vyd. Praha: Triton. ISBN 80-7254-475-6.
TOMLINSON, OWEN WILLIAM, BARKER, ALAN ROBERT, OADES, PATRICK JOHN a WILLIAMS, CRAIG ANTHONY, © 2017. Scaling the Oxygen Uptake Efficiency Slope for Body Size in Cystic Fibrosis. Medicine & Science in Sports & Exercise: Official Journal of the American College of Sports Medicine [online]. Lippincott Williams & Wilkins, 49(10), s. 1980-1986 [cit. 2018-04-01]. DOI: 10.1249/MSS.0000000000001314. eISSN 1530-0315. Dostupné z: databáze Ovid.
ULRICH, Silvia, HILDENBRAND, Florian F, TREDER, Ursula, FISCHLER, Manuel, KEUSCH, Stephan, SPEICH, Rudolf a FASNACHT, Margrit, ©2013. Reference values for the 6-minute walk test in healthy children and adolescents in Switzerland. BMC Pulmonary Medicine [online]. BioMed Central, 13(49) [cit. 2018-03-25]. DOI: 10.1186/1471-2466-13-49. ISSN 1471-2466. Dostupné z: http://bmcpulmmed.biomedcentral.com/articles/10.1186/1471-2466-13-49.
URQUHART, Donald, SELL, Zoe, DHOUIEB, Elaine, BELL, Gillian, OLIVER, Sarah, BLACK, Ryan a TALLIS, Matthew, © 2012. Effects of a supervised, outpatient exercise and physiotherapy programme in children with cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley Periodicals, 47(12), s. 1235-1241 [cit. 2017-02-09]. DOI: 10.1002/ppul.22587. eISSN 1099-0496. Dostupné z: Wiley Online Library.
URQUHART, Ds, 2011. Exercise testing in cystic fibrosis: Why (and how)?. Journal of the Royal Society of Medicine [online]. The Royal Society of Medicine, 104(Supplement 1), s6-s14 [cit. 2018-01-04]. DOI: 10.1258/jrsm.2011.s11102. ISSN 0141-0768. Dostupné z: http://journals.sagepub.com/doi/10.1258/JRSM.2011.S11102.
VAN DE WEERT-VAN LEEUWEN, P.B., SLIEKER, M.G., HULZEBOS, H.J., KRUITWAGEN, C.L.J.J., VAN DER ENT, C.K. a ARETS, H.G.M., 2012. Chronic infection and inflammation affect exercise capacity in cystic fibrosis. EUROPEAN RESPIRATORY JOURNAL [online]. The European Respiratory Society, 39(4), s. 893-898 [cit. 2018-04-02]. DOI: 10.1183/09031936.00086211. ISSN 0903-1936. Dostupné z: http://erj.ersjournals.com/lookup/doi/10.1183/09031936.00086211.
VAN DE WEERT-VAN LEEUWEN, Pauline B., HULZEBOS, Hendrikus J., WERKMAN, Maarten S. et al., 2014. Chronic inflammation and infection associate with a lower exercise training response in cystic fibrosis adolescents. RESPIRATORY MEDICINE [online]. Elsevier, 108(3), s. 445-452 [cit. 2018-04-03]. DOI: 10.1016/j.rmed.2013.08.012. Dostupné z: http://www.resmedjournal.com/article/S0954-6111(13)00313-2/fulltext.
VAN ITERSON, Erik H., WHEATLEY, Courtney M., BAKER, Sarah E., OLSON, Thomas P., MORGAN, Wayne J., SNYDER, Eric M. a GONZÁLEZ, Germán E., December 20, 2016. The Coupling of Peripheral Blood Pressure and Ventilatory Responses during Exercise in Young Adults with Cystic Fibrosis. PLoS ONE [online]. Public Library of Science, 11(12) [cit. 2018-01-07]. DOI: 10.1371/journal.pone.0168490. ISSN 1932-6203. Dostupné z: http://dx.plos.org/10.1371/journal.pone.0168490.
VANDEKERCKHOVE, Kristof, KEYZER, Michiel, CORNETTE, Jasper, et al., 2017. Exercise performance and quality of life in children with cystic fibrosis and mildly impaired lung function: relation with antibiotic treatments and hospitalization. European Journal of Pediatrics [online]. Springer, 176(12), s. 1689-1696 [cit. 2018-01-07]. DOI: 10.1007/s00431-017-3024-7. eISSN 1432-1076. Dostupné z: http://link.springer.com/10.1007/s00431-017-3024-7.
VANÍČEK, Hubert, POZLER, Oldřich a SKALICKÁ, Veronika, 2006. Onemocnění gastrointestinálního traktu a exokrinního pankreatu u cystické fibrózy. In VÁVROVÁ, Věra a kolektiv. Cystická fibróza. Praha: Grada, s. 299-313. ISBN 80-247-0531-1.
VÁVROVÁ, Věra a BARTOŠOVÁ, Jana, 2006. Klinické projevy respiračního onemocnění. In VÁVROVÁ, Věra a kolektiv. Cystická fibróza. Praha: Grada, s. 185-197. ISBN 80-247-0531-1.
VÁVROVÁ, Věra, 2006. Potní žlázy. In VÁVROVÁ, Věra a kolektiv. Cystická fibróza. Praha: Grada, s. 381. ISBN 80-247-0531-1.
WASHINGTON, Reginald L., BRICKER, J. Timothy , ALPERT, Bruce S. et al., 1994. Guidelines for Exercise Testing in the Pediatric Age Group: From the Committee on Atherosclerosis and Hypertension in Children, Council on Cardiovascular Disease in the Young, the American Heart Association. Circulation. American Heart Association, 90(4), s. 2166-2179. ISSN 0009-7322.
WEIR, Elise, BURNS, Paul D, DEVENNY, Anne, YOUNG, David a PATON, James Y, 2017. Cardiopulmonary exercise testing in children with cystic fibrosis: one centre's experience. Archives of Disease in Childhood [online]. BMJ Publishing Group, 102(5), s. 440-444 [cit. 2018-03-16]. DOI: 10.1136/archdischild-2016-310651. eISSN 1468-2044. Dostupné z: databáze BMJ Journal.
WERKMAN, M.S., HULZEBOS, H.J., ARETS, H.G.M., VAN DER NET, J., HELDERS, P.J.M. a TAKKEN, T., © 2011. Is static hyperinflation a limiting factor during exercise in adolescents with cystic fibrosis?. PEDIATRIC PULMONOLOGY [online]. Wiley- Liss, 46(2), s. 119-124 [cit. 2018-02-19]. DOI: 10.1002/ppul.21329. ISBN 10.1002/ppul.21329. ISSN 8755-6863. Dostupné z: Wiley Online Library.
WERKMAN, Maarten, JENESON, Jeroen, HELDERS, Paul et al., 2016. Exercise oxidative skeletal muscle metabolism in adolescents with cystic fibrosis. Experimental Physiology [online]. Wiley- Blackwell, 2016, 101(3), 421-431 [cit. 2018-04-02]. DOI: 10.1113/EP085425. ISSN 1469-445X. Dostupné z: https://physoc.onlinelibrary.wiley.com/doi/full/10.1113/EP085425.
WILLIAMS, Craig A. a STEVENS, Daniel, 2013. Physical activity and exercise training in young people with cystic fibrosis: Current recommendations and evidence. Journal of Sport and Health Science [online]. Elsevier B. V., 2(1), s. 39-46 [cit. 2017-02-01]. DOI: 10.1016/j.jshs.2012.11.002. eISSN 2213-2961. Dostupné z: https://www.sciencedirect.com/science/article/pii/S2095254612000804?via%3Dihub.
WILLIAMS, Craig A., TOMLINSON, Owen W., CHUBBOCK, Lucy V., STEVENS, Daniel, SAYNOR, Zoe L., OADES, Patrick J. a BARKER, Alan R., © 2018. The oxygen uptake efficiency slope is not a valid surrogate of aerobic fitness in cystic fibrosis. PEDIATRIC PULMONOLOGY [online]. Wiley Periodicals, 53(1), s. 36-42 [cit. 2018-01-04]. DOI: 10.1002/ppul.23896. eISSN 1099-0496. Dostupné z: Wiley Online Library.
Předběžná náplň práce
Cystická fibróza se řadí mezi nejčastější fatální genetická onemocnění u bělošské populace. Léčba projevů tohoto onemocnění je komplexní a její nedílnou součástí jsou i metody respirační fyzioterapie. Léčebný přístup k tomuto onemocnění umožnil, aby se pacienti mohli dožít v současnosti i více než 40 let. V minulosti byli pacienti s chronickými chorobami odrazováni od fyzické zátěže, ale nyní je již známo, že pravidelná fyzická aktivita přináší těmto pacientům mnohé benefity a zlepšuje kvalitu jejich života.
Tato bakalářská práce je rozdělena na 2 části- teoretickou a praktickou. Teoretická rešerše shrnuje možnosti testování dětských pacientů s cystickou fibrózou ve vztahu k fyzické zdatnosti a dále přináší nejnovější informace o již studovaných tréninkových programech u této specifické skupiny. Praktická část práce sestává z kazuistiky mladého pacienta s cystickou fibrózou, který se podrobil zátěžovému vyšetření a následně absolvoval navržený desetitýdenní tréninkový program.
Předběžná náplň práce v anglickém jazyce
Cystic fibrosis belongs to the most common fatal genetic diseases of Caucasians. The treatment of cystic fibrosis symptoms is a complex system and its integral parts are methods of respiratory physiotherapy. Therapeutic approach helps clients to live even more than 40 years at the present time. Clients living with chronic diseases were discouraged from physical load in the past. But now, we know these patients benefit from regular physical activity.
This thesis is divided into 2 parts - theoretic and practical. Theoretic research summarizes possibilities of testing the children patients with cystic fibrosis in relation to physical condition and also contains the latest information about already studied training programmes of this specific group. Practical part of this thesis is consist of a young client case study, suffering from the cystic fibrosis. This client underwent a physical examination and implemented designed 10- weeks training program thereafter.
 
Univerzita Karlova | Informační systém UK