Inspiratory muscle training in patients with cystic fibrosis

Little information is available about the effects of inspiratory muscle training in patients with cystic fibrosis (CF). In this study the effects of inspiratory-threshold loading in patients with CF on strength and endurance of the inspiratory muscles, pulmonary function, exercise capacity, dyspnoea...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Respiratory medicine 2001-01, Vol.95 (1), p.31-36
Hauptverfasser: DE JONG, W, VAN AALDEREN, W.M.C, KRAAN, J, KOËTER, G.H, VAN DER SCHANS, C.P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 36
container_issue 1
container_start_page 31
container_title Respiratory medicine
container_volume 95
creator DE JONG, W
VAN AALDEREN, W.M.C
KRAAN, J
KOËTER, G.H
VAN DER SCHANS, C.P
description Little information is available about the effects of inspiratory muscle training in patients with cystic fibrosis (CF). In this study the effects of inspiratory-threshold loading in patients with CF on strength and endurance of the inspiratory muscles, pulmonary function, exercise capacity, dyspnoea, and fatigue were evaluated. Sixteen patients were assigned to one of two groups using the minimization method: eight patients in the training group and eight patients in the control group.The training was performed using an inspiratory-threshold loading device. Patients were instructed to use the threshold trainer 20 min a day, 5 days a week for 6 weeks. Patients in the training group trained at inspiratory threshold loads up to 40% of maximal static inspiratory pressure (Pimax) and patients in the control group got ‘sham’ training at a load of 10% of Pimax. No significant differences were found among the two groups in gender, age, weight, height, pulmonary function, exercise capacity, inspiratory-muscle strength and inspiratory-muscle endurance before starting the training programme. Mean (SD) age in the control group was 19 (5·5) years, mean (SD) age in the training group was 17 (5·2) years. Mean FEV1in both groups was 70% predicted, mean inspiratory-muscle strength in both groups was above 100% predicted. All patients except one, assigned to the training group, completed the programme. After 6 weeks of training, mean inspiratory-muscle endurance (% Pimax) in the control group increased from 50% to 54% (P=0·197); in the training group mean inspiratory muscle endurance (% Pimax) increased from 49% to 66% (P=0·003). Statistical analysis showed that the change in inspiratory-muscle endurance (% Pimax) in the training group was significantly higher than in the control group (P=0·012). After training, in the training group there was a tendency of improvement in Pimax with an increase from 105 to 123% predicted, which just fell short of statistical significance (P=0·064). After training no significant differences were found in changes from baseline in pulmonary function, exercise capacity, dyspnoea and fatigue. It is concluded that low-intensity inspiratory-threshold loading at 40% of Pimax was sufficient to elicit an increased inspiratory-muscle endurance in patients with CF.
doi_str_mv 10.1053/rmed.2000.0966
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70598385</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0954611100909661</els_id><sourcerecordid>70598385</sourcerecordid><originalsourceid>FETCH-LOGICAL-c408t-940b6636fb78ea76adc2344f63d37858f12b86c0901296305e0961b3df501d9e3</originalsourceid><addsrcrecordid>eNp10MtKxDAUgOEgio6jW5dSENx1PGkubcCNDF4GBtzoOqRpqpHeTFJl3t6UKbNzlUW-HE5-hK4wrDAwcudaU60yAFiB4PwILTAjWUqA02O0AMFoyjHGZ-jc-6-oBKVwis4wziAHTBfoftP5wToVerdL2tHrxiTBKdvZ7iOxXTKoYE0XfPJrw2eidz5YndS2dL23_gKd1Krx5nI-l-j96fFt_ZJuX58364dtqikUIRUUSs4Jr8u8MCrnqtIZobTmpCJ5wYoaZ2XBNQjAmeAEmIl_wSWpaga4EoYs0e1-7uD679H4IFvrtWka1Zl-9DIHJgpSsAhXe6jjft6ZWg7OtsrtJAY59ZJTLzn1klOv-OB6njyW082Bz4EiuJmB8lo1tVOdtv7gBFCgWVTFXplY4ccaJ72O2bSprDM6yKq3_23wBybLhRo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70598385</pqid></control><display><type>article</type><title>Inspiratory muscle training in patients with cystic fibrosis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>DE JONG, W ; VAN AALDEREN, W.M.C ; KRAAN, J ; KOËTER, G.H ; VAN DER SCHANS, C.P</creator><creatorcontrib>DE JONG, W ; VAN AALDEREN, W.M.C ; KRAAN, J ; KOËTER, G.H ; VAN DER SCHANS, C.P</creatorcontrib><description>Little information is available about the effects of inspiratory muscle training in patients with cystic fibrosis (CF). In this study the effects of inspiratory-threshold loading in patients with CF on strength and endurance of the inspiratory muscles, pulmonary function, exercise capacity, dyspnoea, and fatigue were evaluated. Sixteen patients were assigned to one of two groups using the minimization method: eight patients in the training group and eight patients in the control group.The training was performed using an inspiratory-threshold loading device. Patients were instructed to use the threshold trainer 20 min a day, 5 days a week for 6 weeks. Patients in the training group trained at inspiratory threshold loads up to 40% of maximal static inspiratory pressure (Pimax) and patients in the control group got ‘sham’ training at a load of 10% of Pimax. No significant differences were found among the two groups in gender, age, weight, height, pulmonary function, exercise capacity, inspiratory-muscle strength and inspiratory-muscle endurance before starting the training programme. Mean (SD) age in the control group was 19 (5·5) years, mean (SD) age in the training group was 17 (5·2) years. Mean FEV1in both groups was 70% predicted, mean inspiratory-muscle strength in both groups was above 100% predicted. All patients except one, assigned to the training group, completed the programme. After 6 weeks of training, mean inspiratory-muscle endurance (% Pimax) in the control group increased from 50% to 54% (P=0·197); in the training group mean inspiratory muscle endurance (% Pimax) increased from 49% to 66% (P=0·003). Statistical analysis showed that the change in inspiratory-muscle endurance (% Pimax) in the training group was significantly higher than in the control group (P=0·012). After training, in the training group there was a tendency of improvement in Pimax with an increase from 105 to 123% predicted, which just fell short of statistical significance (P=0·064). After training no significant differences were found in changes from baseline in pulmonary function, exercise capacity, dyspnoea and fatigue. It is concluded that low-intensity inspiratory-threshold loading at 40% of Pimax was sufficient to elicit an increased inspiratory-muscle endurance in patients with CF.</description><identifier>ISSN: 0954-6111</identifier><identifier>EISSN: 1532-3064</identifier><identifier>DOI: 10.1053/rmed.2000.0966</identifier><identifier>PMID: 11207014</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Breathing Exercises ; Child ; Cystic Fibrosis - complications ; Cystic Fibrosis - physiopathology ; Cystic Fibrosis - rehabilitation ; cytic fibrosis ; Dyspnea - etiology ; Exercise Tolerance - physiology ; Fatigue - etiology ; Female ; Forced Expiratory Volume - physiology ; Humans ; Inhalation - physiology ; inspiratory muscle endurance ; inspiratory muscle strength ; inspiratory muscle training ; inspiratory threshold ; Male ; Medical sciences ; Pneumology ; pulmonary function ; Respiratory Muscles - physiopathology ; Respiratory system : syndromes and miscellaneous diseases ; Vital Capacity - physiology</subject><ispartof>Respiratory medicine, 2001-01, Vol.95 (1), p.31-36</ispartof><rights>2001 Harcourt Publishers Ltd</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-940b6636fb78ea76adc2344f63d37858f12b86c0901296305e0961b3df501d9e3</citedby><cites>FETCH-LOGICAL-c408t-940b6636fb78ea76adc2344f63d37858f12b86c0901296305e0961b3df501d9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/rmed.2000.0966$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,4010,27904,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=904042$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11207014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DE JONG, W</creatorcontrib><creatorcontrib>VAN AALDEREN, W.M.C</creatorcontrib><creatorcontrib>KRAAN, J</creatorcontrib><creatorcontrib>KOËTER, G.H</creatorcontrib><creatorcontrib>VAN DER SCHANS, C.P</creatorcontrib><title>Inspiratory muscle training in patients with cystic fibrosis</title><title>Respiratory medicine</title><addtitle>Respir Med</addtitle><description>Little information is available about the effects of inspiratory muscle training in patients with cystic fibrosis (CF). In this study the effects of inspiratory-threshold loading in patients with CF on strength and endurance of the inspiratory muscles, pulmonary function, exercise capacity, dyspnoea, and fatigue were evaluated. Sixteen patients were assigned to one of two groups using the minimization method: eight patients in the training group and eight patients in the control group.The training was performed using an inspiratory-threshold loading device. Patients were instructed to use the threshold trainer 20 min a day, 5 days a week for 6 weeks. Patients in the training group trained at inspiratory threshold loads up to 40% of maximal static inspiratory pressure (Pimax) and patients in the control group got ‘sham’ training at a load of 10% of Pimax. No significant differences were found among the two groups in gender, age, weight, height, pulmonary function, exercise capacity, inspiratory-muscle strength and inspiratory-muscle endurance before starting the training programme. Mean (SD) age in the control group was 19 (5·5) years, mean (SD) age in the training group was 17 (5·2) years. Mean FEV1in both groups was 70% predicted, mean inspiratory-muscle strength in both groups was above 100% predicted. All patients except one, assigned to the training group, completed the programme. After 6 weeks of training, mean inspiratory-muscle endurance (% Pimax) in the control group increased from 50% to 54% (P=0·197); in the training group mean inspiratory muscle endurance (% Pimax) increased from 49% to 66% (P=0·003). Statistical analysis showed that the change in inspiratory-muscle endurance (% Pimax) in the training group was significantly higher than in the control group (P=0·012). After training, in the training group there was a tendency of improvement in Pimax with an increase from 105 to 123% predicted, which just fell short of statistical significance (P=0·064). After training no significant differences were found in changes from baseline in pulmonary function, exercise capacity, dyspnoea and fatigue. It is concluded that low-intensity inspiratory-threshold loading at 40% of Pimax was sufficient to elicit an increased inspiratory-muscle endurance in patients with CF.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Breathing Exercises</subject><subject>Child</subject><subject>Cystic Fibrosis - complications</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Cystic Fibrosis - rehabilitation</subject><subject>cytic fibrosis</subject><subject>Dyspnea - etiology</subject><subject>Exercise Tolerance - physiology</subject><subject>Fatigue - etiology</subject><subject>Female</subject><subject>Forced Expiratory Volume - physiology</subject><subject>Humans</subject><subject>Inhalation - physiology</subject><subject>inspiratory muscle endurance</subject><subject>inspiratory muscle strength</subject><subject>inspiratory muscle training</subject><subject>inspiratory threshold</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pneumology</subject><subject>pulmonary function</subject><subject>Respiratory Muscles - physiopathology</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Vital Capacity - physiology</subject><issn>0954-6111</issn><issn>1532-3064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MtKxDAUgOEgio6jW5dSENx1PGkubcCNDF4GBtzoOqRpqpHeTFJl3t6UKbNzlUW-HE5-hK4wrDAwcudaU60yAFiB4PwILTAjWUqA02O0AMFoyjHGZ-jc-6-oBKVwis4wziAHTBfoftP5wToVerdL2tHrxiTBKdvZ7iOxXTKoYE0XfPJrw2eidz5YndS2dL23_gKd1Krx5nI-l-j96fFt_ZJuX58364dtqikUIRUUSs4Jr8u8MCrnqtIZobTmpCJ5wYoaZ2XBNQjAmeAEmIl_wSWpaga4EoYs0e1-7uD679H4IFvrtWka1Zl-9DIHJgpSsAhXe6jjft6ZWg7OtsrtJAY59ZJTLzn1klOv-OB6njyW082Bz4EiuJmB8lo1tVOdtv7gBFCgWVTFXplY4ccaJ72O2bSprDM6yKq3_23wBybLhRo</recordid><startdate>200101</startdate><enddate>200101</enddate><creator>DE JONG, W</creator><creator>VAN AALDEREN, W.M.C</creator><creator>KRAAN, J</creator><creator>KOËTER, G.H</creator><creator>VAN DER SCHANS, C.P</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200101</creationdate><title>Inspiratory muscle training in patients with cystic fibrosis</title><author>DE JONG, W ; VAN AALDEREN, W.M.C ; KRAAN, J ; KOËTER, G.H ; VAN DER SCHANS, C.P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-940b6636fb78ea76adc2344f63d37858f12b86c0901296305e0961b3df501d9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Breathing Exercises</topic><topic>Child</topic><topic>Cystic Fibrosis - complications</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Cystic Fibrosis - rehabilitation</topic><topic>cytic fibrosis</topic><topic>Dyspnea - etiology</topic><topic>Exercise Tolerance - physiology</topic><topic>Fatigue - etiology</topic><topic>Female</topic><topic>Forced Expiratory Volume - physiology</topic><topic>Humans</topic><topic>Inhalation - physiology</topic><topic>inspiratory muscle endurance</topic><topic>inspiratory muscle strength</topic><topic>inspiratory muscle training</topic><topic>inspiratory threshold</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pneumology</topic><topic>pulmonary function</topic><topic>Respiratory Muscles - physiopathology</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Vital Capacity - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DE JONG, W</creatorcontrib><creatorcontrib>VAN AALDEREN, W.M.C</creatorcontrib><creatorcontrib>KRAAN, J</creatorcontrib><creatorcontrib>KOËTER, G.H</creatorcontrib><creatorcontrib>VAN DER SCHANS, C.P</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Respiratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DE JONG, W</au><au>VAN AALDEREN, W.M.C</au><au>KRAAN, J</au><au>KOËTER, G.H</au><au>VAN DER SCHANS, C.P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inspiratory muscle training in patients with cystic fibrosis</atitle><jtitle>Respiratory medicine</jtitle><addtitle>Respir Med</addtitle><date>2001-01</date><risdate>2001</risdate><volume>95</volume><issue>1</issue><spage>31</spage><epage>36</epage><pages>31-36</pages><issn>0954-6111</issn><eissn>1532-3064</eissn><abstract>Little information is available about the effects of inspiratory muscle training in patients with cystic fibrosis (CF). In this study the effects of inspiratory-threshold loading in patients with CF on strength and endurance of the inspiratory muscles, pulmonary function, exercise capacity, dyspnoea, and fatigue were evaluated. Sixteen patients were assigned to one of two groups using the minimization method: eight patients in the training group and eight patients in the control group.The training was performed using an inspiratory-threshold loading device. Patients were instructed to use the threshold trainer 20 min a day, 5 days a week for 6 weeks. Patients in the training group trained at inspiratory threshold loads up to 40% of maximal static inspiratory pressure (Pimax) and patients in the control group got ‘sham’ training at a load of 10% of Pimax. No significant differences were found among the two groups in gender, age, weight, height, pulmonary function, exercise capacity, inspiratory-muscle strength and inspiratory-muscle endurance before starting the training programme. Mean (SD) age in the control group was 19 (5·5) years, mean (SD) age in the training group was 17 (5·2) years. Mean FEV1in both groups was 70% predicted, mean inspiratory-muscle strength in both groups was above 100% predicted. All patients except one, assigned to the training group, completed the programme. After 6 weeks of training, mean inspiratory-muscle endurance (% Pimax) in the control group increased from 50% to 54% (P=0·197); in the training group mean inspiratory muscle endurance (% Pimax) increased from 49% to 66% (P=0·003). Statistical analysis showed that the change in inspiratory-muscle endurance (% Pimax) in the training group was significantly higher than in the control group (P=0·012). After training, in the training group there was a tendency of improvement in Pimax with an increase from 105 to 123% predicted, which just fell short of statistical significance (P=0·064). After training no significant differences were found in changes from baseline in pulmonary function, exercise capacity, dyspnoea and fatigue. It is concluded that low-intensity inspiratory-threshold loading at 40% of Pimax was sufficient to elicit an increased inspiratory-muscle endurance in patients with CF.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>11207014</pmid><doi>10.1053/rmed.2000.0966</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0954-6111
ispartof Respiratory medicine, 2001-01, Vol.95 (1), p.31-36
issn 0954-6111
1532-3064
language eng
recordid cdi_proquest_miscellaneous_70598385
source MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adolescent
Adult
Biological and medical sciences
Breathing Exercises
Child
Cystic Fibrosis - complications
Cystic Fibrosis - physiopathology
Cystic Fibrosis - rehabilitation
cytic fibrosis
Dyspnea - etiology
Exercise Tolerance - physiology
Fatigue - etiology
Female
Forced Expiratory Volume - physiology
Humans
Inhalation - physiology
inspiratory muscle endurance
inspiratory muscle strength
inspiratory muscle training
inspiratory threshold
Male
Medical sciences
Pneumology
pulmonary function
Respiratory Muscles - physiopathology
Respiratory system : syndromes and miscellaneous diseases
Vital Capacity - physiology
title Inspiratory muscle training in patients with cystic fibrosis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T14%3A47%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inspiratory%20muscle%20training%20in%20patients%20with%20cystic%20fibrosis&rft.jtitle=Respiratory%20medicine&rft.au=DE%20JONG,%20W&rft.date=2001-01&rft.volume=95&rft.issue=1&rft.spage=31&rft.epage=36&rft.pages=31-36&rft.issn=0954-6111&rft.eissn=1532-3064&rft_id=info:doi/10.1053/rmed.2000.0966&rft_dat=%3Cproquest_cross%3E70598385%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70598385&rft_id=info:pmid/11207014&rft_els_id=S0954611100909661&rfr_iscdi=true