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1.
Arch Dis Child Fetal Neonatal Ed ; 90(5): F406-10, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15863490

RESUMO

BACKGROUND: Bronchopulmonary dysplasia (BPD) is a common outcome of preterm birth. Experimental animal work has shown that initial ventilation strategies injure the immature lung and may lead to BPD. Studies with asphyxiated babies have shown that, if tidal ventilation at birth is preceded by sustained lung inflation, larger inflation volumes can be achieved, which is thought to lead to clearance of lung fluid and formation of the functional residual capacity (FRC). OBJECTIVE: To see if sustained lung inflation at initial resuscitation of preterm babies would facilitate the removal of lung fluid, establish the FRC, and allow an even distribution of alveolar opening, permitting less aggressive ventilation, leading to a reduction in pulmonary inflammation and subsequent BPD. METHOD: The outcomes of 52 babies of less than 31 weeks gestation, resuscitated at birth using either a sustained lung inflation of five seconds or a conventional lung inflation of two seconds for the first assisted breath of resuscitation, were examined. Evidence of pulmonary inflammation was determined by quantification of interleukins 6, 10, and 1beta and tumour necrosis factor alpha in bronchoalveolar lavage fluid by enzyme linked immunosorbent assay. RESULTS: There were no significant differences in any of the cytokines. Death occurred in 3/26 babies in the conventional group and 6/26 babies in the sustained lung inflation group. Survival without BPD occurred in 13/26 and 14/26 respectively. CONCLUSION: The use of sustained lung inflation at resuscitation did not reduce lung injury, as measured by inflammatory markers.


Assuntos
Asfixia Neonatal/terapia , Displasia Broncopulmonar/prevenção & controle , Doenças do Prematuro/terapia , Respiração Artificial/métodos , Líquido da Lavagem Broncoalveolar/química , Displasia Broncopulmonar/etiologia , Displasia Broncopulmonar/metabolismo , Dióxido de Carbono/sangue , Citocinas/metabolismo , Feminino , Capacidade Residual Funcional , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Doenças do Prematuro/metabolismo , Inalação , Masculino , Pressão Parcial
2.
Arch Dis Child Fetal Neonatal Ed ; 90(5): F401-5, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15863491

RESUMO

BACKGROUND: Bronchopulmonary dysplasia is an inflammatory fibrotic condition produced as a consequence of injurious influences in the neonatal lung. Exposing the premature lung to high concentrations of oxygen is thought to play an important part in lung injury pathogenesis. OBJECTIVE: To see if the amount of oxygen used during resuscitation at birth triggers events that lead to the subsequent lung injury and if a reduction in oxygen used leads to a reduction in lung injury. METHOD: The outcomes of newborn babies less than 31 weeks gestation who were resuscitated using either 50% or 100% oxygen were examined. Eight of the babies receiving 50% oxygen required an increase in their oxygen concentration. Evidence of pulmonary inflammation was determined by quantifying interleukin 6, 1beta, and 10 and tumour necrosis factor alpha in bronchoalveolar lavage fluid by enzyme linked immunosorbent assay. RESULTS: There were no significant differences in any of the cytokines studied in either of the groups. Death occurred in 5/26 (19%) babies who received 100% oxygen and 4/26 (15%) babies who received 50% oxygen. Survival without bronchopulmonary dysplasia at 36 weeks postmenstrual age occurred in 14/26 (54%) and 13/26 (50%). CONCLUSION: Reducing the oxygen to 50% at resuscitation did not influence either short or long term outcomes, but a small benefit could not be excluded. There was no increase in adverse clinical outcomes in babies who received 100% oxygen.


Assuntos
Asfixia Neonatal/terapia , Displasia Broncopulmonar/prevenção & controle , Doenças do Prematuro/terapia , Oxigenoterapia/efeitos adversos , Líquido da Lavagem Broncoalveolar/química , Displasia Broncopulmonar/etiologia , Displasia Broncopulmonar/metabolismo , Dióxido de Carbono/sangue , Citocinas/metabolismo , Feminino , Humanos , Concentração de Íons de Hidrogênio , Recém-Nascido , Recém-Nascido Prematuro , Masculino , Oxigênio/sangue , Oxigenoterapia/métodos , Pressão Parcial , Respiração
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