首页> 外文期刊>BMC Pediatrics >Lactoferrin infant feeding trial_Canada (LIFT_Canada): protocol for a randomized trial of adding lactoferrin to feeds of very-low-birth-weight preterm infants
【24h】

Lactoferrin infant feeding trial_Canada (LIFT_Canada): protocol for a randomized trial of adding lactoferrin to feeds of very-low-birth-weight preterm infants

机译:Lactoferrin婴儿喂养Trial_Canada(Lift_Canada):加入乳铁蛋白的随机试验的方案,以饲料为极低出生重量的早产儿

获取原文
           

摘要

In Canada alone, almost 3000 VLBW infants are born and treated annually with almost 1200 going onto death or survival with severe brain injury, chronic lung disorders, aggressive retinopathy of prematurity, late-onset sepsis, or significant necrotizing enterocolitis. Lactoferrin is an antimicrobial, antioxidant, anti-inflammatory iron-carrying, bifidogenic glycoprotein found in all vertebrates and in mammalian milk, leukocytes and exocrine secretions. Lactoferrin aids in creating an environment for growth of beneficial bacteria in the gut, thus reducing colonization with pathogenic bacteria. It is hypothesized that oral bovine lactoferrin (bLF), through its antimicrobial, antioxidant and anti-inflammatory properties, will reduce the rate of mortality or major morbidity in very low birth weight preterm infants. Lactoferrin Infant Feeding Trial_Canada (LIFT_Canada) is a multi-centre, double-masked, randomized controlled trial with the aim to enroll 500 infants whose data will be combined with the data of the 1542 infants enrolled from Lactoferrin Infant Feeding Trial_Australia/New Zealand (LIFT_ANZ) in a pooled intention-to-treat analysis. Eligible infants will be randomized and allocated to one of two treatment groups: 1) a daily dose of 200?mg/kg bLF in breast/donor human milk or formula milk until 34?weeks corrected gestation or for a minimum of 2?weeks, whichever is longer, or until discharge home or transfer, if earlier; 2) no bLF with daily feeds. The primary outcome will be determined at 36?weeks corrected gestation for the presence of neonatal morbidity and at discharge for survival and treated retinopathy of prematurity. The duration of the trial is expected to be 36?months. Currently, there continues to be no clear answer related to the benefit of bLF in reducing mortality or any or all of the significant neonatal morbidities in very low birth weight infants. LIFT_Canada is designed with the hope that the pooled results from Australia, New Zealand, and Canada may help to clarify the situation. Clinical Trials.Gov, Identifier: NCT03367013, Registered December 8, 2017.
机译:仅在加拿大,近3000名VLBW婴儿诞生并每年出生,近1200次患有严重的脑损伤,慢性肺病,早期性脓肿或显着的坏死性小肠结肠炎的侵袭性视网膜病变。 Lactoferrin是一种抗微生物,抗氧化剂,抗炎铁,在所有脊椎动物和哺乳动物乳,白细胞和外泌泌分泌物中发现的双离糖蛋白。乳铁蛋白有助于创造肠道中有益细菌生长的环境,从而减少了与致病细菌的殖民化。假设通过其抗微生物,抗氧化剂和抗炎特性,通过其抗微生物,抗氧化剂和抗炎性能来解析口腔牛乳蛋白(BLF)将降低死亡率的死亡率或主要发病率,以极低的出生体重早产。 Lactoferrin婴儿喂养试验_Canada(Lift_Canada)是一个多中心,双掩盖,随机对照试验,旨在注册500名婴儿,其数据将与1542名婴儿的数据相结合,其中1542名婴儿从Lactoferrin婴儿喂养Trial_australia /新西兰(Lift_Anz )在汇集意向治疗分析中。符合条件的婴儿将随机分配并分配给两种治疗组中的一个:1)每日剂量为200?Mg / kg BLF,乳腺/供体牛奶或配方牛奶直至34?周纠正或至少2个?周,如果较早,则以较长者为准,直到放电或转移; 2)没有每日饲料的BLF。主要结果将在36?周内确定纠正新生儿发病率的存在,并在存活下进行存活和治疗早熟的视网膜病变。预计审判的持续时间将是36个月。目前,与BLF在降低死亡率或任何或所有显着的新生儿病症中,继续没有明确的答案,其在非常低的出生体重婴儿中。 LIFT_CANADA旨在希望澳大利亚,新西兰和加拿大的合并结果可能有助于澄清这种情况。临床试验.GOV,标识符:NCT03367013,2017年12月8日注册。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号