Beneficial effects of extended growth hormone treatment after hospital discharge in pediatric burn patients
To study the efficacy of growth hormone given to severely burned children from discharge to 12 months after burn and for 12 months after the drug was discontinued. We have previously shown that low-dose recombinant human growth hormone (rhGH), given to children after a severe thermal injury, success...
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Veröffentlicht in: | Annals of surgery 2006-06, Vol.243 (6), p.796-803 |
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description | To study the efficacy of growth hormone given to severely burned children from discharge to 12 months after burn and for 12 months after the drug was discontinued.
We have previously shown that low-dose recombinant human growth hormone (rhGH), given to children after a severe thermal injury, successfully improved lean muscle mass, bone mineral content, and growth. The aim of the present study was to investigate long-term functional improvements after treatment.
Forty-four pediatric patients with over 40% total body surface area burns were studied for 24 months after burn. Patients were randomized to receive either rhGH (0.05 mg/kg body weight) or placebo. Height, weight, body composition, serum hormones, resting energy expenditure, cardiac function, muscle strength, and number of reconstructive procedures performed were measured during rhGH treatment and for 12 months after treatment was discontinued. Statistical analysis used Tukey's multiple comparison test. Significance was accepted at P < 0.05.
Height, weight, lean body mass, bone mineral content, cardiac function, and muscle strength significantly improved during rhGH treatment compared with placebo (P < 0.05). This treatment significantly increased GH, IGF-I, and IGFBP-3, whereas serum cortisol decreased (P < 0.05). The number of operative reconstructive procedures was significantly lower with rhGH (P < 0.05). Improvements in height, bone mineral content, and IGF-1 concentrations persisted after rhGH treatment (P < 0.05). No side effects with rhGH were observed.
Administration of rhGH for 1 year after burn was safe and improved recovery. These salutary effects continued after rhGH treatment was discontinued. |
doi_str_mv | 10.1097/01.sla.0000219676.69331.fd |
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We have previously shown that low-dose recombinant human growth hormone (rhGH), given to children after a severe thermal injury, successfully improved lean muscle mass, bone mineral content, and growth. The aim of the present study was to investigate long-term functional improvements after treatment.
Forty-four pediatric patients with over 40% total body surface area burns were studied for 24 months after burn. Patients were randomized to receive either rhGH (0.05 mg/kg body weight) or placebo. Height, weight, body composition, serum hormones, resting energy expenditure, cardiac function, muscle strength, and number of reconstructive procedures performed were measured during rhGH treatment and for 12 months after treatment was discontinued. Statistical analysis used Tukey's multiple comparison test. Significance was accepted at P < 0.05.
Height, weight, lean body mass, bone mineral content, cardiac function, and muscle strength significantly improved during rhGH treatment compared with placebo (P < 0.05). This treatment significantly increased GH, IGF-I, and IGFBP-3, whereas serum cortisol decreased (P < 0.05). The number of operative reconstructive procedures was significantly lower with rhGH (P < 0.05). Improvements in height, bone mineral content, and IGF-1 concentrations persisted after rhGH treatment (P < 0.05). No side effects with rhGH were observed.
Administration of rhGH for 1 year after burn was safe and improved recovery. These salutary effects continued after rhGH treatment was discontinued.</description><identifier>ISSN: 0003-4932</identifier><identifier>EISSN: 1528-1140</identifier><identifier>DOI: 10.1097/01.sla.0000219676.69331.fd</identifier><identifier>PMID: 16772783</identifier><identifier>CODEN: ANSUA5</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Biological and medical sciences ; Burns - diagnosis ; Burns - drug therapy ; Burns - physiopathology ; Child ; Double-Blind Method ; Female ; Follow-Up Studies ; General aspects ; Human Growth Hormone - therapeutic use ; Humans ; Male ; Medical sciences ; Miscellaneous ; Original ; Outpatients ; Patient Discharge ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Recombinant Proteins - therapeutic use ; Retrospective Studies ; Time Factors ; Trauma Severity Indices ; Treatment Outcome ; Ventricular Function, Left - drug effects</subject><ispartof>Annals of surgery, 2006-06, Vol.243 (6), p.796-803</ispartof><rights>2006 INIST-CNRS</rights><rights>2006 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-7fbb2d17d43599f6059e6c9c3c65fc0f541325ce1d7eda51a7b635a6623575743</citedby><cites>FETCH-LOGICAL-c454t-7fbb2d17d43599f6059e6c9c3c65fc0f541325ce1d7eda51a7b635a6623575743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479605/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479605/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,309,310,314,727,780,784,789,790,885,23930,23931,25140,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17858716$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16772783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PRZKORA, Rene</creatorcontrib><creatorcontrib>HERNDON, David N</creatorcontrib><creatorcontrib>SUMAN, Oscar E</creatorcontrib><creatorcontrib>JESCHKE, Marc G</creatorcontrib><creatorcontrib>MEYER, Walter J</creatorcontrib><creatorcontrib>CHINKES, David L</creatorcontrib><creatorcontrib>MLCAK, Ronald P</creatorcontrib><creatorcontrib>HUANG, Ted</creatorcontrib><creatorcontrib>BARROW, Robert E</creatorcontrib><title>Beneficial effects of extended growth hormone treatment after hospital discharge in pediatric burn patients</title><title>Annals of surgery</title><addtitle>Ann Surg</addtitle><description>To study the efficacy of growth hormone given to severely burned children from discharge to 12 months after burn and for 12 months after the drug was discontinued.
We have previously shown that low-dose recombinant human growth hormone (rhGH), given to children after a severe thermal injury, successfully improved lean muscle mass, bone mineral content, and growth. The aim of the present study was to investigate long-term functional improvements after treatment.
Forty-four pediatric patients with over 40% total body surface area burns were studied for 24 months after burn. Patients were randomized to receive either rhGH (0.05 mg/kg body weight) or placebo. Height, weight, body composition, serum hormones, resting energy expenditure, cardiac function, muscle strength, and number of reconstructive procedures performed were measured during rhGH treatment and for 12 months after treatment was discontinued. Statistical analysis used Tukey's multiple comparison test. Significance was accepted at P < 0.05.
Height, weight, lean body mass, bone mineral content, cardiac function, and muscle strength significantly improved during rhGH treatment compared with placebo (P < 0.05). This treatment significantly increased GH, IGF-I, and IGFBP-3, whereas serum cortisol decreased (P < 0.05). The number of operative reconstructive procedures was significantly lower with rhGH (P < 0.05). Improvements in height, bone mineral content, and IGF-1 concentrations persisted after rhGH treatment (P < 0.05). No side effects with rhGH were observed.
Administration of rhGH for 1 year after burn was safe and improved recovery. These salutary effects continued after rhGH treatment was discontinued.</description><subject>Biological and medical sciences</subject><subject>Burns - diagnosis</subject><subject>Burns - drug therapy</subject><subject>Burns - physiopathology</subject><subject>Child</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>General aspects</subject><subject>Human Growth Hormone - therapeutic use</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Original</subject><subject>Outpatients</subject><subject>Patient Discharge</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Time Factors</subject><subject>Trauma Severity Indices</subject><subject>Treatment Outcome</subject><subject>Ventricular Function, Left - drug effects</subject><issn>0003-4932</issn><issn>1528-1140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV1vFCEYhYmxsWv1LxhionczheFr8MKkNn40aeKNXhMGXnbRmWEFVuu_F-3GVW4I8JxzgIPQc0p6SrS6JLQvs-1JGwPVUsleasZoH_wDtKFiGDtKOXmINg1gHddsOEePS_lCCOUjUY_QOZVKDWpkG_T1DawQoot2xhACuFpwChjuKqwePN7m9KPu8C7lJa2AawZbF1grtqFCbvtlH2vT-ljczuYt4LjiPfhoa44OT4fclrbGJilP0Fmwc4Gnx_kCfX739tP1h-724_ub66vbznHBa6fCNA2eKs-Z0DpIIjRIpx1zUgRHguCUDcIB9Qq8FdSqSTJhpRyYUEJxdoFe3_vuD9MC3rXsbGezz3Gx-adJNpr_T9a4M9v03VCudItrBi-PBjl9O0CpZmnPg3m2K6RDMbL9otBiaOCre9DlVEqG8DeEEvO7K0OoaV2ZU1fmT1cm-CZ-9u81T9JjOQ14cQRscXYO2a4ulhOnRjEqKtkvAF2h3Q</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>PRZKORA, Rene</creator><creator>HERNDON, David N</creator><creator>SUMAN, Oscar E</creator><creator>JESCHKE, Marc G</creator><creator>MEYER, Walter J</creator><creator>CHINKES, David L</creator><creator>MLCAK, Ronald P</creator><creator>HUANG, Ted</creator><creator>BARROW, Robert E</creator><general>Lippincott</general><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><scope>5PM</scope></search><sort><creationdate>20060601</creationdate><title>Beneficial effects of extended growth hormone treatment after hospital discharge in pediatric burn patients</title><author>PRZKORA, Rene ; HERNDON, David N ; SUMAN, Oscar E ; JESCHKE, Marc G ; MEYER, Walter J ; CHINKES, David L ; MLCAK, Ronald P ; HUANG, Ted ; BARROW, Robert E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-7fbb2d17d43599f6059e6c9c3c65fc0f541325ce1d7eda51a7b635a6623575743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Biological and medical sciences</topic><topic>Burns - diagnosis</topic><topic>Burns - drug therapy</topic><topic>Burns - physiopathology</topic><topic>Child</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>General aspects</topic><topic>Human Growth Hormone - therapeutic use</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Original</topic><topic>Outpatients</topic><topic>Patient Discharge</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Recombinant Proteins - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Time Factors</topic><topic>Trauma Severity Indices</topic><topic>Treatment Outcome</topic><topic>Ventricular Function, Left - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PRZKORA, Rene</creatorcontrib><creatorcontrib>HERNDON, David N</creatorcontrib><creatorcontrib>SUMAN, Oscar E</creatorcontrib><creatorcontrib>JESCHKE, Marc G</creatorcontrib><creatorcontrib>MEYER, Walter J</creatorcontrib><creatorcontrib>CHINKES, David L</creatorcontrib><creatorcontrib>MLCAK, Ronald P</creatorcontrib><creatorcontrib>HUANG, Ted</creatorcontrib><creatorcontrib>BARROW, Robert E</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PRZKORA, Rene</au><au>HERNDON, David N</au><au>SUMAN, Oscar E</au><au>JESCHKE, Marc G</au><au>MEYER, Walter J</au><au>CHINKES, David L</au><au>MLCAK, Ronald P</au><au>HUANG, Ted</au><au>BARROW, Robert E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beneficial effects of extended growth hormone treatment after hospital discharge in pediatric burn patients</atitle><jtitle>Annals of surgery</jtitle><addtitle>Ann Surg</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>243</volume><issue>6</issue><spage>796</spage><epage>803</epage><pages>796-803</pages><issn>0003-4932</issn><eissn>1528-1140</eissn><coden>ANSUA5</coden><abstract>To study the efficacy of growth hormone given to severely burned children from discharge to 12 months after burn and for 12 months after the drug was discontinued.
We have previously shown that low-dose recombinant human growth hormone (rhGH), given to children after a severe thermal injury, successfully improved lean muscle mass, bone mineral content, and growth. The aim of the present study was to investigate long-term functional improvements after treatment.
Forty-four pediatric patients with over 40% total body surface area burns were studied for 24 months after burn. Patients were randomized to receive either rhGH (0.05 mg/kg body weight) or placebo. Height, weight, body composition, serum hormones, resting energy expenditure, cardiac function, muscle strength, and number of reconstructive procedures performed were measured during rhGH treatment and for 12 months after treatment was discontinued. Statistical analysis used Tukey's multiple comparison test. Significance was accepted at P < 0.05.
Height, weight, lean body mass, bone mineral content, cardiac function, and muscle strength significantly improved during rhGH treatment compared with placebo (P < 0.05). This treatment significantly increased GH, IGF-I, and IGFBP-3, whereas serum cortisol decreased (P < 0.05). The number of operative reconstructive procedures was significantly lower with rhGH (P < 0.05). Improvements in height, bone mineral content, and IGF-1 concentrations persisted after rhGH treatment (P < 0.05). No side effects with rhGH were observed.
Administration of rhGH for 1 year after burn was safe and improved recovery. These salutary effects continued after rhGH treatment was discontinued.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>16772783</pmid><doi>10.1097/01.sla.0000219676.69331.fd</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Burns - diagnosis Burns - drug therapy Burns - physiopathology Child Double-Blind Method Female Follow-Up Studies General aspects Human Growth Hormone - therapeutic use Humans Male Medical sciences Miscellaneous Original Outpatients Patient Discharge Public health. Hygiene Public health. Hygiene-occupational medicine Recombinant Proteins - therapeutic use Retrospective Studies Time Factors Trauma Severity Indices Treatment Outcome Ventricular Function, Left - drug effects |
title | Beneficial effects of extended growth hormone treatment after hospital discharge in pediatric burn patients |
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