Protein Metabolism in Critically Ill Surgical Neonates
Protein Metabolism in Critically Ill Surgical Neonates
批准号:
6691319
负责人:
PATRICK J JAVID
金额:
$4.99万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-07-01 至 2004-06-30
关键词:
acute phase protein clinical research clinical trials cortisol critical care dietary supplements extracorporeal circulation glucose glucose clamp technique human subject insulin insulin sensitivity /resistance interleukin 6 longitudinal human study metabolism disorder chemotherapy newborn human (0-6 weeks) nutrition related tag parenteral feedings patient oriented research physiologic stressor postdoctoral investigator protein biosynthesis protein degradation protein metabolism protein quantitation /detection saline stable isotope
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英文摘要
DESCRIPTION (provided by applicant): Neonates on extracorporeal life support (ECLS) have the highest rate of protein catabolism ever reported. Interventions designed to limit this process remain sparsely investigated despite the association between protein loss and increased morbidity and mortality in surgical patients. This proposal seeks to test the hypothesis that the intravenous administration of insulin will improve the extreme protein catabolism in neonates on ECLS. Such an investigation is significant as ECLS is a lifesaving surgical therapy that has been utilized in over 16,000 babies with cardiac and respiratory failure. However, morbidity remains high, and the attendant mortality has stayed constant at 15-20 % over the past decade.
A pilot study of a prospective, randomized, crossover trial is proposed using neonates on ECLS as a model of neonatal critical illness and employing validated stable isotope tracer techniques to quantify protein metabolism. The protocol is designed to determine if the application of a hyperinsulinemic euglycemic clamp in parenterally fed neonates on ECLS will result in an improvement in protein balance. Secondly, the study aims to elucidate the mechanisms of the alteration in protein balance through assessment of both whole body and hepatic insulin sensitivity.
This fundamental metabolic investigation has the potential to improve the management of neonates requiring ECLS and is important in defining how net protein balance may be optimized in a wide range of critically ill surgical neonates.
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