Alberta Research Centre for Health Evidence, University of Alberta, Edmonton, AB, Canada.
JPEN J Parenter Enteral Nutr. 2013 Jan;37(1):44-55. doi: 10.1177/0148607112450300. Epub 2012 Jun 8.
There is growing interest in the use of ω-3 fatty acid (n-3FA) lipid emulsions to prevent complications associated with parenteral nutrition. The authors systematically reviewed the evidence on the benefits and safety of n-3FA compared with standard lipid emulsions in children with intestinal disease, critical illness, trauma, or postoperative complications.
The authors searched 4 bibliographic databases from their inception to March 2011, conference proceedings, trial registries, and reference lists. Two reviewers independently selected studies, assessed methodological quality, and rated the strength of the evidence. One reviewer extracted and a second reviewer verified data. The authors summarized findings qualitatively and conducted meta-analysis when appropriate.
Five randomized controlled trials with unclear risk of bias and 3 high-quality prospective cohort studies were included. The studies examined premature, low birth weight infants (n = 6) and children with heart disease (n = 1) or intestinal failure (n = 1). The strength of evidence was consistently low or very low across all lipid emulsion comparisons and outcomes. In young children, n-3FA emulsions resulted in improvement in some biochemical outcomes of intestinal failure-associated liver disease but no difference in mortality. Few studies examined patient-important outcomes, such as length of hospital and intensive care stay; need for transplantation, growth, and cognitive development; or the long-term effects and potential harms associated with these therapies.
Currently, there is a lack of sufficient high-quality data to support the use of parenteral n-3FA lipid emulsions in children. Future trials examining long-term clinical outcomes and harms are needed.
人们对 ω-3 脂肪酸(n-3FA)脂乳剂的应用越来越感兴趣,希望用它来预防肠外营养相关并发症。作者系统地回顾了 n-3FA 与标准脂乳剂在患有肠道疾病、危重病、创伤或术后并发症的儿童中的益处和安全性的证据。
作者从建库到 2011 年 3 月检索了 4 个文献数据库、会议记录、试验登记处和参考文献列表。两名审查员独立选择研究、评估方法学质量并评估证据的强度。一名审查员提取数据,另一名审查员验证数据。作者对发现进行了定性总结,并在适当的情况下进行了荟萃分析。
纳入了 5 项偏倚风险不确定的随机对照试验和 3 项高质量的前瞻性队列研究。这些研究检查了早产儿、低出生体重儿(n=6)和心脏病(n=1)或肠衰竭(n=1)患儿。所有脂乳剂比较和结局的证据强度始终较低或极低。在幼儿中,n-3FA 乳剂可改善与肠衰竭相关肝病的一些生化结局,但对死亡率无差异。很少有研究检查了对患者重要的结局,如住院和重症监护时间;移植、生长和认知发育的需求;或这些治疗相关的长期影响和潜在危害。
目前,缺乏足够的高质量数据来支持儿童使用肠外 n-3FA 脂乳剂。需要未来的试验来检查长期的临床结局和危害。