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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 |
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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 |
format | article |
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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><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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