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Effects of noninvasive ventilation on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis: Randomized controlled trial

Summary Background Dyspnea and exercise intolerance are the symptoms that most affect the quality of life of children and adolescents with respiratory disorders resulting from cystic fibrosis (CF). Objective To evaluate the effect of noninvasive ventilation (NIV) on treadmill 6-min walk distance and...

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Published in:Respiratory medicine 2014-10, Vol.108 (10), p.1460-1468
Main Authors: Lima, Cibelle Andrade, de Andrade, Armèle de Fátima Dornelas, Campos, Shirley Lima, Brandão, Daniella Cunha, Fregonezi, Guilherme, Mourato, Ianny Pereira, Aliverti, Andrea, de Britto, Murilo Carlos Amorim
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creator Lima, Cibelle Andrade
de Andrade, Armèle de Fátima Dornelas
Campos, Shirley Lima
Brandão, Daniella Cunha
Fregonezi, Guilherme
Mourato, Ianny Pereira
Aliverti, Andrea
de Britto, Murilo Carlos Amorim
description Summary Background Dyspnea and exercise intolerance are the symptoms that most affect the quality of life of children and adolescents with respiratory disorders resulting from cystic fibrosis (CF). Objective To evaluate the effect of noninvasive ventilation (NIV) on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis patients. Method Crossover clinical trial, randomized, controlled and open with 13 children and adolescents with CF, aged 7–16 years, with pulmonary impairment (NTC01987271). The patients performed a treadmill walking test (TWT) during 6 min, with and without NIV on a BiLEVEL mode, an interval of 24–48 h between tests. Before and after each test, patients were assessed by spirometry and optoelectronic plethysmography. Results Walking distance in TWT with NIV was significantly higher that without ventilatory support (mean ± sd: 0.41 ± 0.08 vs . 0.39 ± 0.85 km, p  = 0.039). TWT with NIV increase forced expiratory volume on 1 s (FEV1 ; p  = 0.036), tidal volume (Vt; p  = 0.005), minute ventilation (MV; p  = 0.013), pulmonary rib cage volume (Vrcp; p  = 0.011), and decrease the abdominal volume (Vab; p  = 0.013) after test. There was a significant reduction in oxygen saturation ( p  = 0.018) and permanent increase in respiratory rate after 5 min ( p  = 0.021) after the end test without NIV. Conclusion During the walking test on the treadmill, the NIV change thoracoabdominal kinematics and lung function in order to optimized ventilation and tissue oxygenation, with improvement of walk distance. Consequently, NIV is an effective tool to increase functional capacity in children and adolescents with cystic fibrosis.
doi_str_mv 10.1016/j.rmed.2014.04.006
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Objective To evaluate the effect of noninvasive ventilation (NIV) on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis patients. Method Crossover clinical trial, randomized, controlled and open with 13 children and adolescents with CF, aged 7–16 years, with pulmonary impairment (NTC01987271). The patients performed a treadmill walking test (TWT) during 6 min, with and without NIV on a BiLEVEL mode, an interval of 24–48 h between tests. Before and after each test, patients were assessed by spirometry and optoelectronic plethysmography. Results Walking distance in TWT with NIV was significantly higher that without ventilatory support (mean ± sd: 0.41 ± 0.08 vs . 0.39 ± 0.85 km, p  = 0.039). TWT with NIV increase forced expiratory volume on 1 s (FEV1 ; p  = 0.036), tidal volume (Vt; p  = 0.005), minute ventilation (MV; p  = 0.013), pulmonary rib cage volume (Vrcp; p  = 0.011), and decrease the abdominal volume (Vab; p  = 0.013) after test. There was a significant reduction in oxygen saturation ( p  = 0.018) and permanent increase in respiratory rate after 5 min ( p  = 0.021) after the end test without NIV. Conclusion During the walking test on the treadmill, the NIV change thoracoabdominal kinematics and lung function in order to optimized ventilation and tissue oxygenation, with improvement of walk distance. Consequently, NIV is an effective tool to increase functional capacity in children and adolescents with cystic fibrosis.</description><identifier>ISSN: 0954-6111</identifier><identifier>EISSN: 1532-3064</identifier><identifier>DOI: 10.1016/j.rmed.2014.04.006</identifier><identifier>PMID: 25195137</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adolescent ; Airway management ; Body mass index ; Child ; Cross-Over Studies ; Cystic fibrosis ; Cystic Fibrosis - physiopathology ; Dyspnea - physiopathology ; Exercise ; Exercise - physiology ; Exercise Test ; Exercise tolerance ; Female ; Fitness equipment ; Forced Expiratory Volume - physiology ; Heart rate ; Humans ; Male ; Mortality ; Noninvasive Ventilation ; Plethysmography - methods ; Pulmonary/Respiratory ; Spirometry ; Standard deviation ; Tidal Volume - physiology ; Variables ; Ventilation ; Vital Capacity - physiology</subject><ispartof>Respiratory medicine, 2014-10, Vol.108 (10), p.1460-1468</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Oct 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c553t-a7010e895a69321e3fcb2a00d3b2cffe746eaed095841e88c109d4d1cb763c143</citedby><cites>FETCH-LOGICAL-c553t-a7010e895a69321e3fcb2a00d3b2cffe746eaed095841e88c109d4d1cb763c143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25195137$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lima, Cibelle Andrade</creatorcontrib><creatorcontrib>de Andrade, Armèle de Fátima Dornelas</creatorcontrib><creatorcontrib>Campos, Shirley Lima</creatorcontrib><creatorcontrib>Brandão, Daniella Cunha</creatorcontrib><creatorcontrib>Fregonezi, Guilherme</creatorcontrib><creatorcontrib>Mourato, Ianny Pereira</creatorcontrib><creatorcontrib>Aliverti, Andrea</creatorcontrib><creatorcontrib>de Britto, Murilo Carlos Amorim</creatorcontrib><title>Effects of noninvasive ventilation on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis: Randomized controlled trial</title><title>Respiratory medicine</title><addtitle>Respir Med</addtitle><description>Summary Background Dyspnea and exercise intolerance are the symptoms that most affect the quality of life of children and adolescents with respiratory disorders resulting from cystic fibrosis (CF). Objective To evaluate the effect of noninvasive ventilation (NIV) on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis patients. Method Crossover clinical trial, randomized, controlled and open with 13 children and adolescents with CF, aged 7–16 years, with pulmonary impairment (NTC01987271). The patients performed a treadmill walking test (TWT) during 6 min, with and without NIV on a BiLEVEL mode, an interval of 24–48 h between tests. Before and after each test, patients were assessed by spirometry and optoelectronic plethysmography. Results Walking distance in TWT with NIV was significantly higher that without ventilatory support (mean ± sd: 0.41 ± 0.08 vs . 0.39 ± 0.85 km, p  = 0.039). TWT with NIV increase forced expiratory volume on 1 s (FEV1 ; p  = 0.036), tidal volume (Vt; p  = 0.005), minute ventilation (MV; p  = 0.013), pulmonary rib cage volume (Vrcp; p  = 0.011), and decrease the abdominal volume (Vab; p  = 0.013) after test. There was a significant reduction in oxygen saturation ( p  = 0.018) and permanent increase in respiratory rate after 5 min ( p  = 0.021) after the end test without NIV. Conclusion During the walking test on the treadmill, the NIV change thoracoabdominal kinematics and lung function in order to optimized ventilation and tissue oxygenation, with improvement of walk distance. 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Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Respiratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lima, Cibelle Andrade</au><au>de Andrade, Armèle de Fátima Dornelas</au><au>Campos, Shirley Lima</au><au>Brandão, Daniella Cunha</au><au>Fregonezi, Guilherme</au><au>Mourato, Ianny Pereira</au><au>Aliverti, Andrea</au><au>de Britto, Murilo Carlos Amorim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of noninvasive ventilation on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis: Randomized controlled trial</atitle><jtitle>Respiratory medicine</jtitle><addtitle>Respir Med</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>108</volume><issue>10</issue><spage>1460</spage><epage>1468</epage><pages>1460-1468</pages><issn>0954-6111</issn><eissn>1532-3064</eissn><abstract>Summary Background Dyspnea and exercise intolerance are the symptoms that most affect the quality of life of children and adolescents with respiratory disorders resulting from cystic fibrosis (CF). Objective To evaluate the effect of noninvasive ventilation (NIV) on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis patients. Method Crossover clinical trial, randomized, controlled and open with 13 children and adolescents with CF, aged 7–16 years, with pulmonary impairment (NTC01987271). The patients performed a treadmill walking test (TWT) during 6 min, with and without NIV on a BiLEVEL mode, an interval of 24–48 h between tests. Before and after each test, patients were assessed by spirometry and optoelectronic plethysmography. Results Walking distance in TWT with NIV was significantly higher that without ventilatory support (mean ± sd: 0.41 ± 0.08 vs . 0.39 ± 0.85 km, p  = 0.039). TWT with NIV increase forced expiratory volume on 1 s (FEV1 ; p  = 0.036), tidal volume (Vt; p  = 0.005), minute ventilation (MV; p  = 0.013), pulmonary rib cage volume (Vrcp; p  = 0.011), and decrease the abdominal volume (Vab; p  = 0.013) after test. There was a significant reduction in oxygen saturation ( p  = 0.018) and permanent increase in respiratory rate after 5 min ( p  = 0.021) after the end test without NIV. Conclusion During the walking test on the treadmill, the NIV change thoracoabdominal kinematics and lung function in order to optimized ventilation and tissue oxygenation, with improvement of walk distance. Consequently, NIV is an effective tool to increase functional capacity in children and adolescents with cystic fibrosis.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25195137</pmid><doi>10.1016/j.rmed.2014.04.006</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Airway management
Body mass index
Child
Cross-Over Studies
Cystic fibrosis
Cystic Fibrosis - physiopathology
Dyspnea - physiopathology
Exercise
Exercise - physiology
Exercise Test
Exercise tolerance
Female
Fitness equipment
Forced Expiratory Volume - physiology
Heart rate
Humans
Male
Mortality
Noninvasive Ventilation
Plethysmography - methods
Pulmonary/Respiratory
Spirometry
Standard deviation
Tidal Volume - physiology
Variables
Ventilation
Vital Capacity - physiology
title Effects of noninvasive ventilation on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis: Randomized controlled trial
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