The six-minute walking test in children with cystic fibrosis: Reliability and validity
There is a need to judge general exercise tolerance in children with cystic fibrosis (CF) under normal daily activity conditions and—when more extensive testing is required—in an exercise laboratory in a specialized center. We investigated the reproducibility, validity, and criterion for a 6‐minute...
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description | There is a need to judge general exercise tolerance in children with cystic fibrosis (CF) under normal daily activity conditions and—when more extensive testing is required—in an exercise laboratory in a specialized center. We investigated the reproducibility, validity, and criterion for a 6‐minute walking test, which simulates normal childhood activities. In Part A, we evaluated the reproducibility of a 6‐minute walking test in 23 children (12 girls and 11 boys; ages 11.1 ± 2.2 years; range, 8.2 15.6 years) with mild symptoms of CF [forced expiratory volume in 1 second (FEV1) 94.4 ± 16.5% of predicted values (range, 60.6–129.7); body weight Z‐score −0.71 ± 0.81 (range, −1.73–0.93)]. The subjects performed two standardized 6‐minute walking tests with 1 week between tests. There was no significant difference between the two walking distances reached (737 ± 85 versus 742 ± 90 meters; P = 0.56), and there was a strong correlation between the two walking distances reached by the individuals (r = 0.90, P < 0.0001).
In Part B, the validity of the walking test was evaluated in 15 children (6 girls and 9 boys; ages 14.5 ± 2.0 years; range, 10.2–16.9 years) with moderate symptoms of CF [FEV1 = 58 ± 16.0% of predicted values, (range, 41.1–89.4); RV/TLC ratio = 46.3 ± 6.5% (range, 31.6–57.2); body weight Z‐score: −1.29 ± 0.60 (range, −2.20–0.14)]. They underwent standardized maximum incremental exercise testing on a cycle ergometer and a 6‐minute walking test. Postexertional lactate values exceeded threshold values (as described in the literature) in all patients but one. Correlation analysis (Pearson) showed a significant correlation between the walking distance reached (WD = 697 ± 104 meters), and the maximum workload (Wmax = 118 ± 44 Watt; r = 0.76, P < 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P < 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P < 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P < 0.001) for Wmax and RV/TLC % as the independent variables vs. WD as the dependent variable. We conclude that the 6‐minute walking test is a valid and useful test in children with mild to moderate symptoms of CF to assess their exercise tolerance and endurance. Exercise test results correlated negatively with pulmonary hyperinflation expressed by the RV/TLC ratio. Pediatr Pulmonol. 1996;22:85–89. © 1996 Wiley‐Liss, |
doi_str_mv | 10.1002/(SICI)1099-0496(199608)22:2<85::AID-PPUL1>3.0.CO;2-I |
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In Part B, the validity of the walking test was evaluated in 15 children (6 girls and 9 boys; ages 14.5 ± 2.0 years; range, 10.2–16.9 years) with moderate symptoms of CF [FEV1 = 58 ± 16.0% of predicted values, (range, 41.1–89.4); RV/TLC ratio = 46.3 ± 6.5% (range, 31.6–57.2); body weight Z‐score: −1.29 ± 0.60 (range, −2.20–0.14)]. They underwent standardized maximum incremental exercise testing on a cycle ergometer and a 6‐minute walking test. Postexertional lactate values exceeded threshold values (as described in the literature) in all patients but one. Correlation analysis (Pearson) showed a significant correlation between the walking distance reached (WD = 697 ± 104 meters), and the maximum workload (Wmax = 118 ± 44 Watt; r = 0.76, P < 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P < 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P < 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P < 0.001) for Wmax and RV/TLC % as the independent variables vs. WD as the dependent variable. We conclude that the 6‐minute walking test is a valid and useful test in children with mild to moderate symptoms of CF to assess their exercise tolerance and endurance. Exercise test results correlated negatively with pulmonary hyperinflation expressed by the RV/TLC ratio. Pediatr Pulmonol. 1996;22:85–89. © 1996 Wiley‐Liss, Inc.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/(SICI)1099-0496(199608)22:2<85::AID-PPUL1>3.0.CO;2-I</identifier><identifier>PMID: 8875580</identifier><identifier>CODEN: PEPUES</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Biological and medical sciences ; Child ; cystic fibrosis ; Cystic Fibrosis - diagnosis ; Cystic Fibrosis - physiopathology ; Ergometry ; Exercise Test - methods ; exercise testing ; exercise tolerance ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Other diseases. Semiology ; Regression Analysis ; Reproducibility of Results ; Respiratory Function Tests ; Walking</subject><ispartof>Pediatric pulmonology, 1996-08, Vol.22 (2), p.85-89</ispartof><rights>Copyright © 1996 Wiley‐Liss, Inc.</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4281-b6c3b17409ace7a54710caab02f7c04ce4465df70422f1bb79ccc87b641ad2603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291099-0496%28199608%2922%3A2%3C85%3A%3AAID-PPUL1%3E3.0.CO%3B2-I$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291099-0496%28199608%2922%3A2%3C85%3A%3AAID-PPUL1%3E3.0.CO%3B2-I$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3206031$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8875580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gulmans, V.A.M.</creatorcontrib><creatorcontrib>van Veldhoven, N.H.M.J.</creatorcontrib><creatorcontrib>de Meer, K.</creatorcontrib><creatorcontrib>Helders, P.J.M.</creatorcontrib><title>The six-minute walking test in children with cystic fibrosis: Reliability and validity</title><title>Pediatric pulmonology</title><addtitle>Pediatr. Pulmonol</addtitle><description>There is a need to judge general exercise tolerance in children with cystic fibrosis (CF) under normal daily activity conditions and—when more extensive testing is required—in an exercise laboratory in a specialized center. We investigated the reproducibility, validity, and criterion for a 6‐minute walking test, which simulates normal childhood activities. In Part A, we evaluated the reproducibility of a 6‐minute walking test in 23 children (12 girls and 11 boys; ages 11.1 ± 2.2 years; range, 8.2 15.6 years) with mild symptoms of CF [forced expiratory volume in 1 second (FEV1) 94.4 ± 16.5% of predicted values (range, 60.6–129.7); body weight Z‐score −0.71 ± 0.81 (range, −1.73–0.93)]. The subjects performed two standardized 6‐minute walking tests with 1 week between tests. There was no significant difference between the two walking distances reached (737 ± 85 versus 742 ± 90 meters; P = 0.56), and there was a strong correlation between the two walking distances reached by the individuals (r = 0.90, P < 0.0001).
In Part B, the validity of the walking test was evaluated in 15 children (6 girls and 9 boys; ages 14.5 ± 2.0 years; range, 10.2–16.9 years) with moderate symptoms of CF [FEV1 = 58 ± 16.0% of predicted values, (range, 41.1–89.4); RV/TLC ratio = 46.3 ± 6.5% (range, 31.6–57.2); body weight Z‐score: −1.29 ± 0.60 (range, −2.20–0.14)]. They underwent standardized maximum incremental exercise testing on a cycle ergometer and a 6‐minute walking test. Postexertional lactate values exceeded threshold values (as described in the literature) in all patients but one. Correlation analysis (Pearson) showed a significant correlation between the walking distance reached (WD = 697 ± 104 meters), and the maximum workload (Wmax = 118 ± 44 Watt; r = 0.76, P < 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P < 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P < 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P < 0.001) for Wmax and RV/TLC % as the independent variables vs. WD as the dependent variable. We conclude that the 6‐minute walking test is a valid and useful test in children with mild to moderate symptoms of CF to assess their exercise tolerance and endurance. Exercise test results correlated negatively with pulmonary hyperinflation expressed by the RV/TLC ratio. Pediatr Pulmonol. 1996;22:85–89. © 1996 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>cystic fibrosis</subject><subject>Cystic Fibrosis - diagnosis</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Ergometry</subject><subject>Exercise Test - methods</subject><subject>exercise testing</subject><subject>exercise tolerance</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Regression Analysis</subject><subject>Reproducibility of Results</subject><subject>Respiratory Function Tests</subject><subject>Walking</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF9v0zAUxS0EGmXwEZD8gND2kOI_Sex0E9IIUCKqdWId7O3KcRxq5qYjTun67XFI1RcQT5bvOT73-IfQOSVjSgh7c3Jd5MUpJVkWkThLT2iWpUSeMjZh5zKZTC6K99HV1c2MvuVjMs7nZywqHqHR4cFjNJIiSaJUpvwpeub9D0KCltEjdCR7RZIR-rpYGuztQ7SyzaYzeKvcnW2-4874DtsG66V1VWsavLXdEuud76zGtS3btbd-gr8YZ1Vpne12WDUV_qWcrcLlOXpSK-fNi_15jG4-fljkn6LZfFrkF7NIx0zSqEw1L6mISaa0ESqJBSVaqZKwWmgSaxPHaVLVgsSM1bQsRaa1lqJMY6oqlhJ-jF4Pufft-ucmdIaV9do4pxqz3ngQMk4olyIYF4NRh-a-NTXct3al2h1QAj1ugB439PSgpwcDbmAMGMgEIOCGP7iBA4F8HsZFiH25378pV6Y6hO75Bv3VXldeK1e3qtHWH2yckfAJyg94ttaZ3V_V_t_sX8WGQciNhlzrO_NwyFXtHaSCiwS-XU5hmpPbd58vb-Ga_waxw7eG</recordid><startdate>199608</startdate><enddate>199608</enddate><creator>Gulmans, V.A.M.</creator><creator>van Veldhoven, N.H.M.J.</creator><creator>de Meer, K.</creator><creator>Helders, P.J.M.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</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>199608</creationdate><title>The six-minute walking test in children with cystic fibrosis: Reliability and validity</title><author>Gulmans, V.A.M. ; van Veldhoven, N.H.M.J. ; de Meer, K. ; Helders, P.J.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4281-b6c3b17409ace7a54710caab02f7c04ce4465df70422f1bb79ccc87b641ad2603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>cystic fibrosis</topic><topic>Cystic Fibrosis - diagnosis</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Ergometry</topic><topic>Exercise Test - methods</topic><topic>exercise testing</topic><topic>exercise tolerance</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Regression Analysis</topic><topic>Reproducibility of Results</topic><topic>Respiratory Function Tests</topic><topic>Walking</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gulmans, V.A.M.</creatorcontrib><creatorcontrib>van Veldhoven, N.H.M.J.</creatorcontrib><creatorcontrib>de Meer, K.</creatorcontrib><creatorcontrib>Helders, P.J.M.</creatorcontrib><collection>Istex</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>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gulmans, V.A.M.</au><au>van Veldhoven, N.H.M.J.</au><au>de Meer, K.</au><au>Helders, P.J.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The six-minute walking test in children with cystic fibrosis: Reliability and validity</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr. Pulmonol</addtitle><date>1996-08</date><risdate>1996</risdate><volume>22</volume><issue>2</issue><spage>85</spage><epage>89</epage><pages>85-89</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><coden>PEPUES</coden><abstract>There is a need to judge general exercise tolerance in children with cystic fibrosis (CF) under normal daily activity conditions and—when more extensive testing is required—in an exercise laboratory in a specialized center. We investigated the reproducibility, validity, and criterion for a 6‐minute walking test, which simulates normal childhood activities. In Part A, we evaluated the reproducibility of a 6‐minute walking test in 23 children (12 girls and 11 boys; ages 11.1 ± 2.2 years; range, 8.2 15.6 years) with mild symptoms of CF [forced expiratory volume in 1 second (FEV1) 94.4 ± 16.5% of predicted values (range, 60.6–129.7); body weight Z‐score −0.71 ± 0.81 (range, −1.73–0.93)]. The subjects performed two standardized 6‐minute walking tests with 1 week between tests. There was no significant difference between the two walking distances reached (737 ± 85 versus 742 ± 90 meters; P = 0.56), and there was a strong correlation between the two walking distances reached by the individuals (r = 0.90, P < 0.0001).
In Part B, the validity of the walking test was evaluated in 15 children (6 girls and 9 boys; ages 14.5 ± 2.0 years; range, 10.2–16.9 years) with moderate symptoms of CF [FEV1 = 58 ± 16.0% of predicted values, (range, 41.1–89.4); RV/TLC ratio = 46.3 ± 6.5% (range, 31.6–57.2); body weight Z‐score: −1.29 ± 0.60 (range, −2.20–0.14)]. They underwent standardized maximum incremental exercise testing on a cycle ergometer and a 6‐minute walking test. Postexertional lactate values exceeded threshold values (as described in the literature) in all patients but one. Correlation analysis (Pearson) showed a significant correlation between the walking distance reached (WD = 697 ± 104 meters), and the maximum workload (Wmax = 118 ± 44 Watt; r = 0.76, P < 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P < 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P < 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P < 0.001) for Wmax and RV/TLC % as the independent variables vs. WD as the dependent variable. We conclude that the 6‐minute walking test is a valid and useful test in children with mild to moderate symptoms of CF to assess their exercise tolerance and endurance. Exercise test results correlated negatively with pulmonary hyperinflation expressed by the RV/TLC ratio. Pediatr Pulmonol. 1996;22:85–89. © 1996 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8875580</pmid><doi>10.1002/(SICI)1099-0496(199608)22:2<85::AID-PPUL1>3.0.CO;2-I</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Child cystic fibrosis Cystic Fibrosis - diagnosis Cystic Fibrosis - physiopathology Ergometry Exercise Test - methods exercise testing exercise tolerance Female Gastroenterology. Liver. Pancreas. Abdomen Humans Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Other diseases. Semiology Regression Analysis Reproducibility of Results Respiratory Function Tests Walking |
title | The six-minute walking test in children with cystic fibrosis: Reliability and validity |
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