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J Pediatr ; 142(3): 247-52, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12640370

RESUMO

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.


Assuntos
1,2-Dipalmitoilfosfatidilcolina , Oxigenação por Membrana Extracorpórea , Hérnia Diafragmática/metabolismo , Hérnias Diafragmáticas Congênitas , Fosfatidilcolinas/análise , Deutério , Feminino , Meia-Vida , Hérnia Diafragmática/complicações , Humanos , Recém-Nascido , Marcação por Isótopo , Masculino , Síndrome de Aspiração de Mecônio/metabolismo , Síndrome de Aspiração de Mecônio/terapia , Surfactantes Pulmonares/química , Respiração Artificial , Insuficiência Respiratória/etiologia , Insuficiência Respiratória/terapia
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