Growth in children with choledochal malformations: effect of the Roux loop

Purpose Excision and biliary reconstruction using a Roux loop is the current standard for choledochal malformation (CM). This is un-physiological, delivering bile beyond the duodenum and excluding a significant length of the jejunum from intestinal absorption. We investigated whether this had an eff...

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Veröffentlicht in:Pediatric surgery international 2015-11, Vol.31 (11), p.1015-1019
Hauptverfasser: Ford, Kathryn E., Cooper, Lilli R. L., Davenport, Mark
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creator Ford, Kathryn E.
Cooper, Lilli R. L.
Davenport, Mark
description Purpose Excision and biliary reconstruction using a Roux loop is the current standard for choledochal malformation (CM). This is un-physiological, delivering bile beyond the duodenum and excluding a significant length of the jejunum from intestinal absorption. We investigated whether this had an effect on post-operative growth. Methods Retrospective case-note analysis of children surgically treated for CM. Growth variables were converted to standard deviation scores (SDS) and compared against population norms. P  
doi_str_mv 10.1007/s00383-015-3759-z
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L. ; Davenport, Mark</creator><creatorcontrib>Ford, Kathryn E. ; Cooper, Lilli R. L. ; Davenport, Mark</creatorcontrib><description>Purpose Excision and biliary reconstruction using a Roux loop is the current standard for choledochal malformation (CM). This is un-physiological, delivering bile beyond the duodenum and excluding a significant length of the jejunum from intestinal absorption. We investigated whether this had an effect on post-operative growth. Methods Retrospective case-note analysis of children surgically treated for CM. Growth variables were converted to standard deviation scores (SDS) and compared against population norms. P  &lt; 0.05 was significant. Results From 1994 to 2014, 135 children (&lt;16 years) were identified. Median age at surgery was 3.3 (IQR 1.5–7) years. Morphology included: type 1 C ystic ( n  = 54, 40 %), type 1 Fusiform ( n  = 58, 43 %) and type 4 (intra and extra-hepatic) ( n  = 22, 16 %). There was pre-operative growth failure [median weight SDS = −0.4 (−1.2 − 0.4), P  = 0.0004] with a similar trend for height [SDS = −0.38 (−1.2 − 0.5), P  = 0.08)]. This correlated with presentation bilirubin ( r s  = −0.24, P  = 0.004), GGT ( r s  = −0.27, P  = 0.002) and AST ( r s  = −0.27, P  = 0.002) but not morphology ( P  = 0.82) or presentation ( P  = 0.4). Median follow-up was 1.9 (0.6–4.7) years, during which time both height ( P  = 0.73) and weight ( P  = 0.45) reverted to normal. Conclusion This is the first report of growth in children with CM following a Roux-loop reconstruction and showed pre-operative growth failure probably attributed to a period of biliary obstruction but catch-up growth when corrected.</description><identifier>ISSN: 0179-0358</identifier><identifier>EISSN: 1437-9813</identifier><identifier>DOI: 10.1007/s00383-015-3759-z</identifier><identifier>PMID: 26266756</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anastomosis, Roux-en-Y ; Bile Ducts - abnormalities ; Bile Ducts - physiopathology ; Bile Ducts - surgery ; Body Height - physiology ; Body Weight - physiology ; Child ; Child Development - physiology ; Child, Preschool ; Female ; Follow-Up Studies ; Humans ; Infant ; Male ; Medicine ; Medicine &amp; Public Health ; Original Article ; Pediatric Surgery ; Pediatrics ; Retrospective Studies ; Surgery ; Treatment Outcome</subject><ispartof>Pediatric surgery international, 2015-11, Vol.31 (11), p.1015-1019</ispartof><rights>Springer-Verlag Berlin Heidelberg 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-c1c21db66caa0416c58f461fb7cf533881d2ab3306515c6f91ef13f6023fd4143</citedby><cites>FETCH-LOGICAL-c442t-c1c21db66caa0416c58f461fb7cf533881d2ab3306515c6f91ef13f6023fd4143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00383-015-3759-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00383-015-3759-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26266756$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ford, Kathryn E.</creatorcontrib><creatorcontrib>Cooper, Lilli R. L.</creatorcontrib><creatorcontrib>Davenport, Mark</creatorcontrib><title>Growth in children with choledochal malformations: effect of the Roux loop</title><title>Pediatric surgery international</title><addtitle>Pediatr Surg Int</addtitle><addtitle>Pediatr Surg Int</addtitle><description>Purpose Excision and biliary reconstruction using a Roux loop is the current standard for choledochal malformation (CM). This is un-physiological, delivering bile beyond the duodenum and excluding a significant length of the jejunum from intestinal absorption. We investigated whether this had an effect on post-operative growth. Methods Retrospective case-note analysis of children surgically treated for CM. Growth variables were converted to standard deviation scores (SDS) and compared against population norms. P  &lt; 0.05 was significant. Results From 1994 to 2014, 135 children (&lt;16 years) were identified. Median age at surgery was 3.3 (IQR 1.5–7) years. Morphology included: type 1 C ystic ( n  = 54, 40 %), type 1 Fusiform ( n  = 58, 43 %) and type 4 (intra and extra-hepatic) ( n  = 22, 16 %). There was pre-operative growth failure [median weight SDS = −0.4 (−1.2 − 0.4), P  = 0.0004] with a similar trend for height [SDS = −0.38 (−1.2 − 0.5), P  = 0.08)]. This correlated with presentation bilirubin ( r s  = −0.24, P  = 0.004), GGT ( r s  = −0.27, P  = 0.002) and AST ( r s  = −0.27, P  = 0.002) but not morphology ( P  = 0.82) or presentation ( P  = 0.4). Median follow-up was 1.9 (0.6–4.7) years, during which time both height ( P  = 0.73) and weight ( P  = 0.45) reverted to normal. 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L.</creator><creator>Davenport, Mark</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20151101</creationdate><title>Growth in children with choledochal malformations: effect of the Roux loop</title><author>Ford, Kathryn E. ; Cooper, Lilli R. L. ; Davenport, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-c1c21db66caa0416c58f461fb7cf533881d2ab3306515c6f91ef13f6023fd4143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Anastomosis, Roux-en-Y</topic><topic>Bile Ducts - abnormalities</topic><topic>Bile Ducts - physiopathology</topic><topic>Bile Ducts - surgery</topic><topic>Body Height - physiology</topic><topic>Body Weight - physiology</topic><topic>Child</topic><topic>Child Development - physiology</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Original Article</topic><topic>Pediatric Surgery</topic><topic>Pediatrics</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ford, Kathryn E.</creatorcontrib><creatorcontrib>Cooper, Lilli R. L.</creatorcontrib><creatorcontrib>Davenport, Mark</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric surgery international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ford, Kathryn E.</au><au>Cooper, Lilli R. L.</au><au>Davenport, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Growth in children with choledochal malformations: effect of the Roux loop</atitle><jtitle>Pediatric surgery international</jtitle><stitle>Pediatr Surg Int</stitle><addtitle>Pediatr Surg Int</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>31</volume><issue>11</issue><spage>1015</spage><epage>1019</epage><pages>1015-1019</pages><issn>0179-0358</issn><eissn>1437-9813</eissn><abstract>Purpose Excision and biliary reconstruction using a Roux loop is the current standard for choledochal malformation (CM). This is un-physiological, delivering bile beyond the duodenum and excluding a significant length of the jejunum from intestinal absorption. We investigated whether this had an effect on post-operative growth. Methods Retrospective case-note analysis of children surgically treated for CM. Growth variables were converted to standard deviation scores (SDS) and compared against population norms. P  &lt; 0.05 was significant. Results From 1994 to 2014, 135 children (&lt;16 years) were identified. Median age at surgery was 3.3 (IQR 1.5–7) years. Morphology included: type 1 C ystic ( n  = 54, 40 %), type 1 Fusiform ( n  = 58, 43 %) and type 4 (intra and extra-hepatic) ( n  = 22, 16 %). There was pre-operative growth failure [median weight SDS = −0.4 (−1.2 − 0.4), P  = 0.0004] with a similar trend for height [SDS = −0.38 (−1.2 − 0.5), P  = 0.08)]. This correlated with presentation bilirubin ( r s  = −0.24, P  = 0.004), GGT ( r s  = −0.27, P  = 0.002) and AST ( r s  = −0.27, P  = 0.002) but not morphology ( P  = 0.82) or presentation ( P  = 0.4). Median follow-up was 1.9 (0.6–4.7) years, during which time both height ( P  = 0.73) and weight ( P  = 0.45) reverted to normal. Conclusion This is the first report of growth in children with CM following a Roux-loop reconstruction and showed pre-operative growth failure probably attributed to a period of biliary obstruction but catch-up growth when corrected.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26266756</pmid><doi>10.1007/s00383-015-3759-z</doi><tpages>5</tpages></addata></record>
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subjects Anastomosis, Roux-en-Y
Bile Ducts - abnormalities
Bile Ducts - physiopathology
Bile Ducts - surgery
Body Height - physiology
Body Weight - physiology
Child
Child Development - physiology
Child, Preschool
Female
Follow-Up Studies
Humans
Infant
Male
Medicine
Medicine & Public Health
Original Article
Pediatric Surgery
Pediatrics
Retrospective Studies
Surgery
Treatment Outcome
title Growth in children with choledochal malformations: effect of the Roux loop
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