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临床试验/NCT01050660
NCT01050660已完成不适用

Low Dose Parenteral Fat for Prevention of Parenteral Nutrition Associated Cholestasis in Preterm Neonates

Yale University2 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
136
试验地点
2
主要终点
The Presence of Cholestasis at Age of 28 Days or When Full Enteral Nutrition is Achieved, Whichever is Longer.

研究概览

简要总结

The goal of the study is to determine if parenteral nutrition-associated cholestasis (PNAC) is related to the amount of parenteral (intravenous) fat administered to premature babies until full enteral nutrition is achieved.

详细描述

In the neonatal intensive care unit, parenteral nutrition is widely used to provide protein, energy, vitamins and minerals to infants who cannot accept enteral feeds.

Intravenous fat emulsion is an important component of parenteral nutrition because of the important caloric supply that it brings, but also for the essential fatty acids (linoleic and linolenic acid) that it provides. Because intravenous fat emulsion is the only supply of essential fatty acids, at least until the enteral feeds are established, there is a minimum of fat that has to be administered with at least 0.25g/kg /day for preterm babies and 0.1g/kg/day for term infants (Lee EJ, 1993). The maximal dose of intravenous fat safe to administer is difficult to determine. Although in larger preterm infants intravenous fat is tolerated well based on measurement of serum triglycerides, there are still question regarding tolerance in extremely low birth weight infants.

Parenteral nutrition has been associated with the development of liver disease-parenteral nutrition associated liver disease (PNALD). PNALD can range from cholestasis and a transient elevation of liver enzymes to more severe forms including fibrosis, liver cirrhosis and hepatic failure. Cholestasis, defined as hyperbilirubinemia with a direct bilirubin above 2 mg/dL or more than 15% of total bilirubin, is a hepatocellular injury of the liver that manifests after the administration of parenteral nutrition for at least two weeks. The mechanism by which the liver injury occurs is unknown and probably multifactorial. Risk factors associated with the development of PNAC include: prematurity, low birth weight, absence of enteral feeds, bacterial sepsis, necrotizing enterocolitis, prolonged use of parenteral nutrition, and multiple surgical procedures on the gastro-intestinal tract. In addition, many of the nutrients contained in parenteral nutrition, have been linked with the development of cholestasis.

Specific factors associated with intravenous fat emulsions that have been related to PNAC include : phytosterols, the rate of administration of the intravenous emulsion, the total amount of fat administered and toxic metabolites of intravenous fat emulsions.

The total amount of lipids was found to be a risk factor for cholestasis in children on long-term parenteral nutrition and decreased amount of fat was recommended for the prevention of this hepatic complication (Colomb V, 2000). In the adult population parenteral lipid intake of less than 1gr/kg of body weight decreased the risk of cholestasis in parenteral nutrition treated patients (Cavicchi, 2000).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
12 Hours 至 48 Hours(Child)
性别
All
接受健康志愿者

入选标准

  • Preterm infants less than or equal to 29 weeks' gestation
  • Age less than 48 hours

排除标准

  • Congenital intrauterine infection, known to be associated with liver involvement and cholestasis
  • Known structural liver abnormalities that are associated with cholestasis
  • Known genetic disorders: trisomy 21, trisomy 13 and trisomy 18
  • Inborn errors of metabolism
  • Infants meeting the criteria for terminal illness (eg, pH < 6.8 > 2 hours)
  • Inability to obtain informed consent

结局指标

主要结局

The Presence of Cholestasis at Age of 28 Days or When Full Enteral Nutrition is Achieved, Whichever is Longer.

时间窗: 28 days of age or when full enteral nutrition is acheived, whichever is longer

次要结局

  • Incidence of Necrotizing Enterocolitis (NEC)(At discharge from Newborn ICU)
  • Incidence of Retinopathy of Prematurity (ROP)(At discharge from Newborn ICU)
  • Late Onset Sepsis(At the discharge from Newborn ICU)
  • Length of Stay(At discharge from Newborn ICU/death)
  • Anthropometric Measurements(Body Weight)(At age of 28 days and at discharge)
  • Anthropometric Measurements(Length)(At age of 28 days and at discharge)
  • Anthropometric Measurements(Head Circumference)(At age of 28 days and at discharge)
  • Mortality Rate- Death Rate Before Discharge From the Hospital(Discharge from the Newborn ICU)
  • Incidence of Bronchopulmonary Dysplasia (BPD)(36 weeks PMA or discharge home,whichever comes first)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard Ehrenkranz

Professor of Pediatrics

Yale University

研究点 (2)

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