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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Veröffentlicht in:Pediatric pulmonology 1996-08, Vol.22 (2), p.85-89
Hauptverfasser: Gulmans, V.A.M., van Veldhoven, N.H.M.J., de Meer, K., Helders, P.J.M.
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container_start_page 85
container_title Pediatric pulmonology
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creator Gulmans, V.A.M.
van Veldhoven, N.H.M.J.
de Meer, K.
Helders, P.J.M.
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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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 &lt; 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 &lt; 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P &lt; 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P &lt; 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P &lt; 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. 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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 &lt; 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 &lt; 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P &lt; 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P &lt; 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P &lt; 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 &lt; 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 &lt; 0.001) or the maximum oxygen uptake (1,688 ± 495 ml; r = 0.76, P &lt; 0.001), the latter two being determined on a cycle ergometer. RV/TLC% showed a significant negative correlation (r = −0.72, P &lt; 0.01) with WD. Stepwise multiple regression analysis showed a multiple regression coefficient of R = 0.84 (P &lt; 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&lt;85::AID-PPUL1&gt;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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