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
Hauptverfasser: 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.
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container_end_page 252
container_issue 3
container_start_page 247
container_title The Journal of pediatrics
container_volume 142
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)
doi_str_mv 10.1067/mpd.2003.94
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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. 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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. 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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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