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首页> 外文期刊>JMIR Research Protocols >Bovine Lactoferrin to Prevent Neonatal Infections in Low-Birth-Weight Newborns in Pakistan: Protocol for a Three-Arm Double-Blind Randomized Controlled Trial
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Bovine Lactoferrin to Prevent Neonatal Infections in Low-Birth-Weight Newborns in Pakistan: Protocol for a Three-Arm Double-Blind Randomized Controlled Trial

机译:牛乳铁蛋白,以防止巴基斯坦低孕产量新生儿的新生儿感染:三臂双盲随机对照试验的议定书

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Background Sepsis is a common and severe complication in premature neonates, particularly those born with low birth weights (2500 g). Neonatal sepsis is steadily emerging as a leading cause of neonatal mortality in Pakistan. Lactoferrin is a natural product with broad-spectrum antimicrobial properties and glycoprotein that is actively involved in innate immune host responses. Clinical trials have revealed its protective effect on sepsis, but lactoferrin dosage, duration, and role in the prevention of sepsis are still uncertain. Objective We aimed to establish the efficacy of bovine lactoferrin in the prevention of late-onset sepsis and to determine the optimal dose and method of administering bovine lactoferrin that may contribute to improvement in overall survival of low birth weight infants. Methods We will implement the study in 2 phases at the Aga Khan University Hospital. The first phase, which we have completed, was formative research. This phase mainly focused on a qualitative exploration of perceptions about feeding and caring practices of low birth weight newborns and a trial of improved practices for the preparation and administration of bovine lactoferrin to newborns. The second phase is a 3-arm double-blind randomized controlled trial. In this phase, we randomly allocated 2 different daily oral prophylactic doses of bovine lactoferrin (150 mg or 300 mg) and placebo to 300 low–birth weight neonates starting within the first 72 hours of birth and continuing for the first 28 days of life. Results The study protocol was approved by the Ethics Review Committee of Aga Khan University on August 16, 2017. Data collection began in April 2018 and was completed in September 2020. Data analyses are yet to be completed. We expect the results to be published in peer-reviewed journals by autumn of 2021. Conclusions This intervention, if effective, has the potential to be translated into a safe, affordable, and widely utilized treatment to prevent sepsis and, subsequently, may improve the survival outcomes of low birth weight neonates in Pakistan and other low- and middle-income countries.
机译:背景技术败血症是早产儿的常见和严重的并发症,特别是出生出生体重(&lt 2500 g)的常见并发症。新生儿脓毒症是巴基斯坦新生儿死亡率的主要原因。乳铁蛋白是一种具有广谱抗微生物性质和糖蛋白的天然产物,其主动参与先天免疫宿主反应。临床试验揭示了对败血症的保护作用,但在预防败血症中的乳蛋白剂量,持续时间和作用仍然不确定。目的我们旨在建立牛乳铁蛋白在预防后期发病败血症中的疗效,并确定牛乳铁蛋白的最佳剂量和方法,可能有助于改善低出生体重婴儿的总体存活。方法我们将在Aga Khan大学医院实施2阶段的研究。我们已完成的第一阶段是形成性研究。该阶段主要集中探讨了对低出生体重新生儿的喂养和关怀实践的定性探索,以及对牛乳铁蛋白的制备和施用牛乳铁蛋白的改进做法的试验。第二阶段是3手臂双盲随机对照试验。在这种阶段,我们随机分配了2种不同的每日口服预防剂量的牛乳蛋白(150mg或300mg),并在前72小时的出生后开始安慰剂至300个低出生体重的新生儿,并继续前28天。结果2017年8月16日,Aga Khan大学伦理审查委员会批准了研究议定书。数据收集于2018年4月开始,并于2020年9月完成。数据分析尚未完成。我们预计将在2021年秋季在同行评论期刊上发表的结果。结论如果有效,这种干预有可能被翻译成安全,实惠,广泛利用的治疗,以防止败血症,随后,可以改善巴基斯坦和其他低收入国家的低出生体重新生儿的生存结果。

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