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Evaluating Changes in Handgrip Strength in Children With Cystic Fibrosis: A Pilot Study

Background Body mass index (BMI) is used to determine nutrition status in children with cystic fibrosis (CF); however, lean body mass (LBM) is more strongly associated with pulmonary function. Handgrip strength (HGS) measures muscle function and is reflective of LBM. The aims of this study were to a...

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Published in:Nutrition in clinical practice 2018-04, Vol.33 (2), p.261-267
Main Authors: Gibson, Hannah T., McDonald, Catherine M., Derrick, Jennifer Willahan, Eggett, Dennis L., Bellini, Sarah Gunnell
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creator Gibson, Hannah T.
McDonald, Catherine M.
Derrick, Jennifer Willahan
Eggett, Dennis L.
Bellini, Sarah Gunnell
description Background Body mass index (BMI) is used to determine nutrition status in children with cystic fibrosis (CF); however, lean body mass (LBM) is more strongly associated with pulmonary function. Handgrip strength (HGS) measures muscle function and is reflective of LBM. The aims of this study were to assess relationships among HGS, nutrition status, and pulmonary function; changes in HGS posthospitalization; and any relationship between HGS and nutrient intake. Methods Twenty‐three children with CF aged 6–18 years participated. BMI z scores, nutrition risk scores, and pulmonary function were assessed about 5 months before, days 5–7 of hospitalization, and about 6 weeks posthospitalization. HGS z scores and arm anthropometrics were measured during and after hospitalization. Nutrient intakes were assessed during hospitalization. Results Mean HGS z score at hospitalization was −1.95 ± 0.92 and posthospitalization was −1.59 ± 1.06 (P = .007). Mean BMI z score prehospitalization was −0.17 ± 0.63, at hospitalization was −0.09 ± 0.64, and posthospitalization was 0.06 ± 0.54 (P = .065). Mean forced expiratory volume in 1 second (FEV1) prehospitalization was 93.52 ± 17.35, at hospitalization was 85.65 ± 21.57, and posthospitalization was 95.63 ± 18.18 (P = .001). No significant relationship was found between HGS z scores and BMI z scores (P = .892) or HGS z scores and FEV1 (P = .340). Conclusions HGS z scores and FEV1 significantly increased at follow‐up. HGS z scores were lower than the standard even though mean BMI z scores classified participants as normal nutrition status.
doi_str_mv 10.1002/ncp.10067
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Handgrip strength (HGS) measures muscle function and is reflective of LBM. The aims of this study were to assess relationships among HGS, nutrition status, and pulmonary function; changes in HGS posthospitalization; and any relationship between HGS and nutrient intake. Methods Twenty‐three children with CF aged 6–18 years participated. BMI z scores, nutrition risk scores, and pulmonary function were assessed about 5 months before, days 5–7 of hospitalization, and about 6 weeks posthospitalization. HGS z scores and arm anthropometrics were measured during and after hospitalization. Nutrient intakes were assessed during hospitalization. Results Mean HGS z score at hospitalization was −1.95 ± 0.92 and posthospitalization was −1.59 ± 1.06 (P = .007). Mean BMI z score prehospitalization was −0.17 ± 0.63, at hospitalization was −0.09 ± 0.64, and posthospitalization was 0.06 ± 0.54 (P = .065). Mean forced expiratory volume in 1 second (FEV1) prehospitalization was 93.52 ± 17.35, at hospitalization was 85.65 ± 21.57, and posthospitalization was 95.63 ± 18.18 (P = .001). No significant relationship was found between HGS z scores and BMI z scores (P = .892) or HGS z scores and FEV1 (P = .340). Conclusions HGS z scores and FEV1 significantly increased at follow‐up. HGS z scores were lower than the standard even though mean BMI z scores classified participants as normal nutrition status.</description><identifier>ISSN: 0884-5336</identifier><identifier>EISSN: 1941-2452</identifier><identifier>DOI: 10.1002/ncp.10067</identifier><identifier>PMID: 29658185</identifier><language>eng</language><publisher>United States</publisher><subject>Adolescent ; Adolescent Nutritional Physiological Phenomena ; anthropometry ; arm anthropometrics ; Body Mass Index ; Child ; Child Nutritional Physiological Phenomena ; cystic fibrosis ; Cystic Fibrosis - physiopathology ; Cystic Fibrosis - therapy ; Female ; Forced Expiratory Volume ; Hand Strength ; handgrip strength ; Hospitalization ; Hospitals, Pediatric ; Humans ; Longitudinal Studies ; Lung - physiopathology ; Male ; Malnutrition - epidemiology ; Malnutrition - etiology ; Malnutrition - physiopathology ; Muscle Weakness - epidemiology ; Muscle Weakness - etiology ; Muscle Weakness - physiopathology ; Nursing ; Nutrition Assessment ; Pilot Projects ; Risk ; Severity of Illness Index ; Utah - epidemiology</subject><ispartof>Nutrition in clinical practice, 2018-04, Vol.33 (2), p.261-267</ispartof><rights>2018 American Society for Parenteral and Enteral Nutrition</rights><rights>2018 American Society for Parenteral and Enteral Nutrition.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3257-656d72cc8816caf085f5a7b5f9517028a215434bff04bbd482d7b0a0725e6a53</citedby><cites>FETCH-LOGICAL-c3257-656d72cc8816caf085f5a7b5f9517028a215434bff04bbd482d7b0a0725e6a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29658185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gibson, Hannah T.</creatorcontrib><creatorcontrib>McDonald, Catherine M.</creatorcontrib><creatorcontrib>Derrick, Jennifer Willahan</creatorcontrib><creatorcontrib>Eggett, Dennis L.</creatorcontrib><creatorcontrib>Bellini, Sarah Gunnell</creatorcontrib><title>Evaluating Changes in Handgrip Strength in Children With Cystic Fibrosis: A Pilot Study</title><title>Nutrition in clinical practice</title><addtitle>Nutr Clin Pract</addtitle><description>Background Body mass index (BMI) is used to determine nutrition status in children with cystic fibrosis (CF); however, lean body mass (LBM) is more strongly associated with pulmonary function. Handgrip strength (HGS) measures muscle function and is reflective of LBM. The aims of this study were to assess relationships among HGS, nutrition status, and pulmonary function; changes in HGS posthospitalization; and any relationship between HGS and nutrient intake. Methods Twenty‐three children with CF aged 6–18 years participated. BMI z scores, nutrition risk scores, and pulmonary function were assessed about 5 months before, days 5–7 of hospitalization, and about 6 weeks posthospitalization. HGS z scores and arm anthropometrics were measured during and after hospitalization. Nutrient intakes were assessed during hospitalization. Results Mean HGS z score at hospitalization was −1.95 ± 0.92 and posthospitalization was −1.59 ± 1.06 (P = .007). Mean BMI z score prehospitalization was −0.17 ± 0.63, at hospitalization was −0.09 ± 0.64, and posthospitalization was 0.06 ± 0.54 (P = .065). Mean forced expiratory volume in 1 second (FEV1) prehospitalization was 93.52 ± 17.35, at hospitalization was 85.65 ± 21.57, and posthospitalization was 95.63 ± 18.18 (P = .001). No significant relationship was found between HGS z scores and BMI z scores (P = .892) or HGS z scores and FEV1 (P = .340). Conclusions HGS z scores and FEV1 significantly increased at follow‐up. HGS z scores were lower than the standard even though mean BMI z scores classified participants as normal nutrition status.</description><subject>Adolescent</subject><subject>Adolescent Nutritional Physiological Phenomena</subject><subject>anthropometry</subject><subject>arm anthropometrics</subject><subject>Body Mass Index</subject><subject>Child</subject><subject>Child Nutritional Physiological Phenomena</subject><subject>cystic fibrosis</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Cystic Fibrosis - therapy</subject><subject>Female</subject><subject>Forced Expiratory Volume</subject><subject>Hand Strength</subject><subject>handgrip strength</subject><subject>Hospitalization</subject><subject>Hospitals, Pediatric</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Lung - physiopathology</subject><subject>Male</subject><subject>Malnutrition - epidemiology</subject><subject>Malnutrition - etiology</subject><subject>Malnutrition - physiopathology</subject><subject>Muscle Weakness - epidemiology</subject><subject>Muscle Weakness - etiology</subject><subject>Muscle Weakness - physiopathology</subject><subject>Nursing</subject><subject>Nutrition Assessment</subject><subject>Pilot Projects</subject><subject>Risk</subject><subject>Severity of Illness Index</subject><subject>Utah - epidemiology</subject><issn>0884-5336</issn><issn>1941-2452</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kDFPwzAQhS0EoqUw8AeQRxhCbceOHbYqailSBZWo1NFyHCc1SpMSJ6D8e1wCbEx39_Tdu9MD4Bqje4wQmVb6cGwifgLGOKY4IJSRUzBGQtCAhWE0AhfOvSGERcjFORiROGICCzYG2_mHKjvV2qqAyU5VhXHQVnCpqqxo7AG-to2pinZ3FJOdLTM_wq31QtK71mq4sGlTO-se4AyubVm3fqXL-ktwlqvSmaufOgGbxXyTLIPVy-NTMlsFOiSMBxGLMk60FgJHWuVIsJwpnrI8ZpgjIhTBjIY0zXNE0zSjgmQ8RQpxwkykWDgBt4PtoanfO-NaubdOm7JUlak7JwnyV2LOaOzRuwHV_l_XmFweGrtXTS8xkscYpY9Rfsfo2Zsf2y7dm-yP_M3NA9MB-LSl6f93ks_JerD8An7Meuw</recordid><startdate>201804</startdate><enddate>201804</enddate><creator>Gibson, Hannah T.</creator><creator>McDonald, Catherine M.</creator><creator>Derrick, Jennifer Willahan</creator><creator>Eggett, Dennis L.</creator><creator>Bellini, Sarah Gunnell</creator><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>201804</creationdate><title>Evaluating Changes in Handgrip Strength in Children With Cystic Fibrosis: A Pilot Study</title><author>Gibson, Hannah T. ; McDonald, Catherine M. ; Derrick, Jennifer Willahan ; Eggett, Dennis L. ; Bellini, Sarah Gunnell</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3257-656d72cc8816caf085f5a7b5f9517028a215434bff04bbd482d7b0a0725e6a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adolescent</topic><topic>Adolescent Nutritional Physiological Phenomena</topic><topic>anthropometry</topic><topic>arm anthropometrics</topic><topic>Body Mass Index</topic><topic>Child</topic><topic>Child Nutritional Physiological Phenomena</topic><topic>cystic fibrosis</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Cystic Fibrosis - therapy</topic><topic>Female</topic><topic>Forced Expiratory Volume</topic><topic>Hand Strength</topic><topic>handgrip strength</topic><topic>Hospitalization</topic><topic>Hospitals, Pediatric</topic><topic>Humans</topic><topic>Longitudinal Studies</topic><topic>Lung - physiopathology</topic><topic>Male</topic><topic>Malnutrition - epidemiology</topic><topic>Malnutrition - etiology</topic><topic>Malnutrition - physiopathology</topic><topic>Muscle Weakness - epidemiology</topic><topic>Muscle Weakness - etiology</topic><topic>Muscle Weakness - physiopathology</topic><topic>Nursing</topic><topic>Nutrition Assessment</topic><topic>Pilot Projects</topic><topic>Risk</topic><topic>Severity of Illness Index</topic><topic>Utah - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gibson, Hannah T.</creatorcontrib><creatorcontrib>McDonald, Catherine M.</creatorcontrib><creatorcontrib>Derrick, Jennifer Willahan</creatorcontrib><creatorcontrib>Eggett, Dennis L.</creatorcontrib><creatorcontrib>Bellini, Sarah Gunnell</creatorcontrib><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>Nutrition in clinical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gibson, Hannah T.</au><au>McDonald, Catherine M.</au><au>Derrick, Jennifer Willahan</au><au>Eggett, Dennis L.</au><au>Bellini, Sarah Gunnell</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluating Changes in Handgrip Strength in Children With Cystic Fibrosis: A Pilot Study</atitle><jtitle>Nutrition in clinical practice</jtitle><addtitle>Nutr Clin Pract</addtitle><date>2018-04</date><risdate>2018</risdate><volume>33</volume><issue>2</issue><spage>261</spage><epage>267</epage><pages>261-267</pages><issn>0884-5336</issn><eissn>1941-2452</eissn><abstract>Background Body mass index (BMI) is used to determine nutrition status in children with cystic fibrosis (CF); however, lean body mass (LBM) is more strongly associated with pulmonary function. Handgrip strength (HGS) measures muscle function and is reflective of LBM. The aims of this study were to assess relationships among HGS, nutrition status, and pulmonary function; changes in HGS posthospitalization; and any relationship between HGS and nutrient intake. Methods Twenty‐three children with CF aged 6–18 years participated. BMI z scores, nutrition risk scores, and pulmonary function were assessed about 5 months before, days 5–7 of hospitalization, and about 6 weeks posthospitalization. HGS z scores and arm anthropometrics were measured during and after hospitalization. Nutrient intakes were assessed during hospitalization. Results Mean HGS z score at hospitalization was −1.95 ± 0.92 and posthospitalization was −1.59 ± 1.06 (P = .007). Mean BMI z score prehospitalization was −0.17 ± 0.63, at hospitalization was −0.09 ± 0.64, and posthospitalization was 0.06 ± 0.54 (P = .065). Mean forced expiratory volume in 1 second (FEV1) prehospitalization was 93.52 ± 17.35, at hospitalization was 85.65 ± 21.57, and posthospitalization was 95.63 ± 18.18 (P = .001). No significant relationship was found between HGS z scores and BMI z scores (P = .892) or HGS z scores and FEV1 (P = .340). Conclusions HGS z scores and FEV1 significantly increased at follow‐up. HGS z scores were lower than the standard even though mean BMI z scores classified participants as normal nutrition status.</abstract><cop>United States</cop><pmid>29658185</pmid><doi>10.1002/ncp.10067</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adolescent Nutritional Physiological Phenomena
anthropometry
arm anthropometrics
Body Mass Index
Child
Child Nutritional Physiological Phenomena
cystic fibrosis
Cystic Fibrosis - physiopathology
Cystic Fibrosis - therapy
Female
Forced Expiratory Volume
Hand Strength
handgrip strength
Hospitalization
Hospitals, Pediatric
Humans
Longitudinal Studies
Lung - physiopathology
Male
Malnutrition - epidemiology
Malnutrition - etiology
Malnutrition - physiopathology
Muscle Weakness - epidemiology
Muscle Weakness - etiology
Muscle Weakness - physiopathology
Nursing
Nutrition Assessment
Pilot Projects
Risk
Severity of Illness Index
Utah - epidemiology
title Evaluating Changes in Handgrip Strength in Children With Cystic Fibrosis: A Pilot Study
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