Surfactant phosphatidylcholine pool size in human neonates with congenital diaphragmatic hernia requiring ECMO
Objective We measured surfactant phosphatidylcholine (PC) pool size and half-life in human congenital diaphragmatic hernia (CDH) patients who required extracorporeal membrane oxygenation (ECMO). Study design Surfactant PC pool size and half-life were measured by endotracheal administration of deuter...
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Veröffentlicht in: | The Journal of pediatrics 2003-03, Vol.142 (3), p.247-252 |
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creator | Janssen, Daphne J.M.T. Tibboel, Dick Carnielli, Virgilio P. van Emmen, Esther Luijendijk, Ingrid H.T. Darcos Wattimena, J.L. Zimmermann, Luc J.I. |
description | Objective We measured surfactant phosphatidylcholine (PC) pool size and half-life in human congenital diaphragmatic hernia (CDH) patients who required extracorporeal membrane oxygenation (ECMO). Study design Surfactant PC pool size and half-life were measured by endotracheal administration of deuterium-labeled dipalmitoylphosphatidylcholine in 8 neonates with CDH on ECMO (CDH-ECMO), in 7 neonates with meconium aspiration syndrome on ECMO (MAS-ECMO), and in 6 ventilated infants (NON-ECMO). Results Lung PC pool size in the CDH-ECMO group was 73 ± 17 mg/kg (mean ± SEM), which was not significantly different from the MAS-ECMO (50 ± 18 mg/kg) and the NON-ECMO group (69 ± 38 mg/kg). Surfactant PC concentration in tracheal aspirates was not different between groups (~6 mg/mL). However, the percentage of palmitic acid in surfactant PC was significantly lower in the MAS-ECMO (56.3%) and the NON-ECMO (55.8%) group compared with the CDH-ECMO (67.6%) group. Surfactant PC half-life (~24 hours) was not different between the groups. A correlation was found between the surfactant PC half-life and the duration of ECMO. Conclusions These data show no decreased surfactant PC pool size in high risk CDH patients who require ECMO. A shorter half-life of surfactant PC, indicating a faster turnover, may result in a faster improvement of the pulmonary condition during ECMO. (J Pediatr 2003;142:247-52) |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73117205</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022347602403447</els_id><sourcerecordid>73117205</sourcerecordid><originalsourceid>FETCH-LOGICAL-c276t-26d3bd9b02b47b1b9fc660157b51274936168563bed84de8fd285dd328577a633</originalsourceid><addsrcrecordid>eNptkDuP1DAURi0EYoeFih65gQZl8Ct2XKLR8pAWbQHUlmPfTIwSO2s7oOXXk9GMtA3Nvc3R0aeD0GtK9pRI9WFe_J4RwvdaPEE7SrRqZMf5U7QjhLGGCyWv0ItSfhFCtCDkObqiTArCFdmh-H3Ng3XVxoqXMZVltDX4h8mNaQoR8JLShEv4CzhEPK6zjThCirZCwX9CHbFL8QgxVDthH-wyZnucN4XDI-QYLM5wv4Yc4hHfHL7dvUTPBjsVeHX51-jnp5sfhy_N7d3nr4ePt41jStaGSc97r3vCeqF62uvBSUloq_qWMiU0l1R2reQ9-E546AbPutZ7vl2lrOT8Gr07e5ec7lco1cyhOJgmu61fi1GcUsVIu4Hvz6DLqZQMg1lymG1-MJSYU16z5TWnvEaLjX5z0a79DP6RvfTcgLcXwBZnpyHb6EJ55ITstFYnUXvmYIvwO0A2xQWIDnzI4KrxKfx3wD-U1JZK</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73117205</pqid></control><display><type>article</type><title>Surfactant phosphatidylcholine pool size in human neonates with congenital diaphragmatic hernia requiring ECMO</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Janssen, Daphne J.M.T. ; Tibboel, Dick ; Carnielli, Virgilio P. ; van Emmen, Esther ; Luijendijk, Ingrid H.T. ; Darcos Wattimena, J.L. ; Zimmermann, Luc J.I.</creator><creatorcontrib>Janssen, Daphne J.M.T. ; Tibboel, Dick ; Carnielli, Virgilio P. ; van Emmen, Esther ; Luijendijk, Ingrid H.T. ; Darcos Wattimena, J.L. ; Zimmermann, Luc J.I.</creatorcontrib><description>Objective We measured surfactant phosphatidylcholine (PC) pool size and half-life in human congenital diaphragmatic hernia (CDH) patients who required extracorporeal membrane oxygenation (ECMO). Study design Surfactant PC pool size and half-life were measured by endotracheal administration of deuterium-labeled dipalmitoylphosphatidylcholine in 8 neonates with CDH on ECMO (CDH-ECMO), in 7 neonates with meconium aspiration syndrome on ECMO (MAS-ECMO), and in 6 ventilated infants (NON-ECMO). Results Lung PC pool size in the CDH-ECMO group was 73 ± 17 mg/kg (mean ± SEM), which was not significantly different from the MAS-ECMO (50 ± 18 mg/kg) and the NON-ECMO group (69 ± 38 mg/kg). Surfactant PC concentration in tracheal aspirates was not different between groups (~6 mg/mL). However, the percentage of palmitic acid in surfactant PC was significantly lower in the MAS-ECMO (56.3%) and the NON-ECMO (55.8%) group compared with the CDH-ECMO (67.6%) group. Surfactant PC half-life (~24 hours) was not different between the groups. A correlation was found between the surfactant PC half-life and the duration of ECMO. Conclusions These data show no decreased surfactant PC pool size in high risk CDH patients who require ECMO. A shorter half-life of surfactant PC, indicating a faster turnover, may result in a faster improvement of the pulmonary condition during ECMO. (J Pediatr 2003;142:247-52)</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1067/mpd.2003.94</identifier><identifier>PMID: 12640370</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>1,2-Dipalmitoylphosphatidylcholine ; Biological and medical sciences ; Deuterium ; Extracorporeal Membrane Oxygenation ; Female ; Half-Life ; Hernia, Diaphragmatic - complications ; Hernia, Diaphragmatic - metabolism ; Hernias, Diaphragmatic, Congenital ; Humans ; Infant, Newborn ; Isotope Labeling ; Male ; Meconium Aspiration Syndrome - metabolism ; Meconium Aspiration Syndrome - therapy ; Medical sciences ; Phosphatidylcholines - analysis ; Pneumology ; Pulmonary Surfactants - chemistry ; Respiration, Artificial ; Respiratory Insufficiency - etiology ; Respiratory Insufficiency - therapy ; Respiratory system : syndromes and miscellaneous diseases</subject><ispartof>The Journal of pediatrics, 2003-03, Vol.142 (3), p.247-252</ispartof><rights>2003</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c276t-26d3bd9b02b47b1b9fc660157b51274936168563bed84de8fd285dd328577a633</citedby><cites>FETCH-LOGICAL-c276t-26d3bd9b02b47b1b9fc660157b51274936168563bed84de8fd285dd328577a633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1067/mpd.2003.94$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14689974$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12640370$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Janssen, Daphne J.M.T.</creatorcontrib><creatorcontrib>Tibboel, Dick</creatorcontrib><creatorcontrib>Carnielli, Virgilio P.</creatorcontrib><creatorcontrib>van Emmen, Esther</creatorcontrib><creatorcontrib>Luijendijk, Ingrid H.T.</creatorcontrib><creatorcontrib>Darcos Wattimena, J.L.</creatorcontrib><creatorcontrib>Zimmermann, Luc J.I.</creatorcontrib><title>Surfactant phosphatidylcholine pool size in human neonates with congenital diaphragmatic hernia requiring ECMO</title><title>The Journal of pediatrics</title><addtitle>J Pediatr</addtitle><description>Objective We measured surfactant phosphatidylcholine (PC) pool size and half-life in human congenital diaphragmatic hernia (CDH) patients who required extracorporeal membrane oxygenation (ECMO). Study design Surfactant PC pool size and half-life were measured by endotracheal administration of deuterium-labeled dipalmitoylphosphatidylcholine in 8 neonates with CDH on ECMO (CDH-ECMO), in 7 neonates with meconium aspiration syndrome on ECMO (MAS-ECMO), and in 6 ventilated infants (NON-ECMO). Results Lung PC pool size in the CDH-ECMO group was 73 ± 17 mg/kg (mean ± SEM), which was not significantly different from the MAS-ECMO (50 ± 18 mg/kg) and the NON-ECMO group (69 ± 38 mg/kg). Surfactant PC concentration in tracheal aspirates was not different between groups (~6 mg/mL). However, the percentage of palmitic acid in surfactant PC was significantly lower in the MAS-ECMO (56.3%) and the NON-ECMO (55.8%) group compared with the CDH-ECMO (67.6%) group. Surfactant PC half-life (~24 hours) was not different between the groups. A correlation was found between the surfactant PC half-life and the duration of ECMO. Conclusions These data show no decreased surfactant PC pool size in high risk CDH patients who require ECMO. A shorter half-life of surfactant PC, indicating a faster turnover, may result in a faster improvement of the pulmonary condition during ECMO. (J Pediatr 2003;142:247-52)</description><subject>1,2-Dipalmitoylphosphatidylcholine</subject><subject>Biological and medical sciences</subject><subject>Deuterium</subject><subject>Extracorporeal Membrane Oxygenation</subject><subject>Female</subject><subject>Half-Life</subject><subject>Hernia, Diaphragmatic - complications</subject><subject>Hernia, Diaphragmatic - metabolism</subject><subject>Hernias, Diaphragmatic, Congenital</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Isotope Labeling</subject><subject>Male</subject><subject>Meconium Aspiration Syndrome - metabolism</subject><subject>Meconium Aspiration Syndrome - therapy</subject><subject>Medical sciences</subject><subject>Phosphatidylcholines - analysis</subject><subject>Pneumology</subject><subject>Pulmonary Surfactants - chemistry</subject><subject>Respiration, Artificial</subject><subject>Respiratory Insufficiency - etiology</subject><subject>Respiratory Insufficiency - therapy</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkDuP1DAURi0EYoeFih65gQZl8Ct2XKLR8pAWbQHUlmPfTIwSO2s7oOXXk9GMtA3Nvc3R0aeD0GtK9pRI9WFe_J4RwvdaPEE7SrRqZMf5U7QjhLGGCyWv0ItSfhFCtCDkObqiTArCFdmh-H3Ng3XVxoqXMZVltDX4h8mNaQoR8JLShEv4CzhEPK6zjThCirZCwX9CHbFL8QgxVDthH-wyZnucN4XDI-QYLM5wv4Yc4hHfHL7dvUTPBjsVeHX51-jnp5sfhy_N7d3nr4ePt41jStaGSc97r3vCeqF62uvBSUloq_qWMiU0l1R2reQ9-E546AbPutZ7vl2lrOT8Gr07e5ec7lco1cyhOJgmu61fi1GcUsVIu4Hvz6DLqZQMg1lymG1-MJSYU16z5TWnvEaLjX5z0a79DP6RvfTcgLcXwBZnpyHb6EJ55ITstFYnUXvmYIvwO0A2xQWIDnzI4KrxKfx3wD-U1JZK</recordid><startdate>20030301</startdate><enddate>20030301</enddate><creator>Janssen, Daphne J.M.T.</creator><creator>Tibboel, Dick</creator><creator>Carnielli, Virgilio P.</creator><creator>van Emmen, Esther</creator><creator>Luijendijk, Ingrid H.T.</creator><creator>Darcos Wattimena, J.L.</creator><creator>Zimmermann, Luc J.I.</creator><general>Mosby, Inc</general><general>Elsevier</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></search><sort><creationdate>20030301</creationdate><title>Surfactant phosphatidylcholine pool size in human neonates with congenital diaphragmatic hernia requiring ECMO</title><author>Janssen, Daphne J.M.T. ; Tibboel, Dick ; Carnielli, Virgilio P. ; van Emmen, Esther ; Luijendijk, Ingrid H.T. ; Darcos Wattimena, J.L. ; Zimmermann, Luc J.I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c276t-26d3bd9b02b47b1b9fc660157b51274936168563bed84de8fd285dd328577a633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>1,2-Dipalmitoylphosphatidylcholine</topic><topic>Biological and medical sciences</topic><topic>Deuterium</topic><topic>Extracorporeal Membrane Oxygenation</topic><topic>Female</topic><topic>Half-Life</topic><topic>Hernia, Diaphragmatic - complications</topic><topic>Hernia, Diaphragmatic - metabolism</topic><topic>Hernias, Diaphragmatic, Congenital</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Isotope Labeling</topic><topic>Male</topic><topic>Meconium Aspiration Syndrome - metabolism</topic><topic>Meconium Aspiration Syndrome - therapy</topic><topic>Medical sciences</topic><topic>Phosphatidylcholines - analysis</topic><topic>Pneumology</topic><topic>Pulmonary Surfactants - chemistry</topic><topic>Respiration, Artificial</topic><topic>Respiratory Insufficiency - etiology</topic><topic>Respiratory Insufficiency - therapy</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Janssen, Daphne J.M.T.</creatorcontrib><creatorcontrib>Tibboel, Dick</creatorcontrib><creatorcontrib>Carnielli, Virgilio P.</creatorcontrib><creatorcontrib>van Emmen, Esther</creatorcontrib><creatorcontrib>Luijendijk, Ingrid H.T.</creatorcontrib><creatorcontrib>Darcos Wattimena, J.L.</creatorcontrib><creatorcontrib>Zimmermann, Luc J.I.</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><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Janssen, Daphne J.M.T.</au><au>Tibboel, Dick</au><au>Carnielli, Virgilio P.</au><au>van Emmen, Esther</au><au>Luijendijk, Ingrid H.T.</au><au>Darcos Wattimena, J.L.</au><au>Zimmermann, Luc J.I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surfactant phosphatidylcholine pool size in human neonates with congenital diaphragmatic hernia requiring ECMO</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>142</volume><issue>3</issue><spage>247</spage><epage>252</epage><pages>247-252</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><abstract>Objective We measured surfactant phosphatidylcholine (PC) pool size and half-life in human congenital diaphragmatic hernia (CDH) patients who required extracorporeal membrane oxygenation (ECMO). Study design Surfactant PC pool size and half-life were measured by endotracheal administration of deuterium-labeled dipalmitoylphosphatidylcholine in 8 neonates with CDH on ECMO (CDH-ECMO), in 7 neonates with meconium aspiration syndrome on ECMO (MAS-ECMO), and in 6 ventilated infants (NON-ECMO). Results Lung PC pool size in the CDH-ECMO group was 73 ± 17 mg/kg (mean ± SEM), which was not significantly different from the MAS-ECMO (50 ± 18 mg/kg) and the NON-ECMO group (69 ± 38 mg/kg). Surfactant PC concentration in tracheal aspirates was not different between groups (~6 mg/mL). However, the percentage of palmitic acid in surfactant PC was significantly lower in the MAS-ECMO (56.3%) and the NON-ECMO (55.8%) group compared with the CDH-ECMO (67.6%) group. Surfactant PC half-life (~24 hours) was not different between the groups. A correlation was found between the surfactant PC half-life and the duration of ECMO. Conclusions These data show no decreased surfactant PC pool size in high risk CDH patients who require ECMO. A shorter half-life of surfactant PC, indicating a faster turnover, may result in a faster improvement of the pulmonary condition during ECMO. (J Pediatr 2003;142:247-52)</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>12640370</pmid><doi>10.1067/mpd.2003.94</doi><tpages>6</tpages></addata></record> |
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subjects | 1,2-Dipalmitoylphosphatidylcholine Biological and medical sciences Deuterium Extracorporeal Membrane Oxygenation Female Half-Life Hernia, Diaphragmatic - complications Hernia, Diaphragmatic - metabolism Hernias, Diaphragmatic, Congenital Humans Infant, Newborn Isotope Labeling Male Meconium Aspiration Syndrome - metabolism Meconium Aspiration Syndrome - therapy Medical sciences Phosphatidylcholines - analysis Pneumology Pulmonary Surfactants - chemistry Respiration, Artificial Respiratory Insufficiency - etiology Respiratory Insufficiency - therapy Respiratory system : syndromes and miscellaneous diseases |
title | Surfactant phosphatidylcholine pool size in human neonates with congenital diaphragmatic hernia requiring ECMO |
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