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Daily home fortification with iron as ferrous fumarate versus NaFeEDTA: a randomised, placebo-controlled, non-inferiority trial in Kenyan children

机译:每日家用家庭设防用铁作为富马酸铁与NAFEEDTA:肯尼亚儿童随机,安慰剂控制,非劣势试验

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BackgroundWe aimed to show the non-inferiority of home fortification with a daily dose of 3?mg iron in the form of iron as ferric sodium ethylenediaminetetraacetate (NaFeEDTA) compared with 12.5?mg iron as encapsulated ferrous fumarate in Kenyan children aged 12–36 months. In addition, we updated a recent meta-analysis to assess the efficacy of home fortification with iron-containing powders, with a view to examining diversity in trial results. MethodsWe gave chemoprevention by dihydroartemisinin-piperaquine, albendazole and praziquantel to 338 afebrile children with haemoglobin concentration ≥70?g/L. We randomly allocated them to daily home fortification for 30?days with either placebo, 3?mg iron as NaFeEDTA or 12.5?mg iron as encapsulated ferrous fumarate. We assessed haemoglobin concentration (primary outcome), plasma iron markers, plasma inflammation markers and Plasmodium infection in samples collected at baseline and after 30?days of intervention. We conducted a meta-analysis of randomised controlled trials in pre-school children to assess the effect of home fortification with iron-containing powders on anaemia and haemoglobin concentration at end of intervention. ResultsA total of 315 children completed the 30-day intervention period. At baseline, 66.9% of children had inflammation (plasma C-reactive protein concentration >5?mg/L or plasma α 1-acid glycoprotein concentration >1.0?g/L); in those without inflammation, 42.5% were iron deficient. There was no evidence, either in per protocol analysis or intention-to-treat analysis, that home fortification with either of the iron interventions improved haemoglobin concentration, plasma ferritin concentration, plasma transferrin receptor concentration or erythrocyte zinc protoporphyrin-haem ratio. We also found no evidence of effect modification by iron status, anaemia status and inflammation status at baseline. In the meta-analysis, the effect on haemoglobin concentration was highly heterogeneous between trials ( I 2: 84.1%; p value for test of heterogeneity: ConclusionsIn this population, home fortification with either 3?mg iron as NaFeEDTA or 12.5?mg iron as encapsulated ferrous fumarate was insufficiently efficacious to assess non-inferiority of 3?mg iron as NaFeEDTA compared to 12.5?mg iron as encapsulated ferrous fumarate. Our finding of heterogeneity between trial results should stimulate subgroup analysis or meta-regression to identify population-specific factors that determine efficacy. Trial RegistrationThe trial was registered with ClinicalTrials.gov ( NCT02073149 ) on 25 February 2014.
机译:背景技术旨在显示家庭强化的非自卑,每日剂量为铁,以铁的形式为铁,与乙二胺四乙酸铁(Nafeedta)相比,与12.5毫克铁为12.5毫克铁,在12-36个月的肯尼亚儿童封装的富马酸盐。此外,我们还更新了最近的Meta分析,以评估家庭设防与含铁粉末的功效,以期检查试验结果中的多样性。方法网络通过二氢氨基氨苄蛋白 - 哌啶,苯胺唑和普拉齐替雷斯给338个血红蛋白浓度≥70≤1/升。我们随机将它们分配给日常家庭设防30?天用安慰剂,3毫克铁作为Nafeedta或12.5毫克铁作为封装的黑色富马酸盐。我们评估了在基线收集的样品中的血红蛋白浓度(初级结果),血浆铁标记,血浆炎症标志物和疟原虫感染,并在30次干预后30?我们对学龄前儿童进行了随机对照试验进行了荟萃分析,以评估家庭设防与含铁液对贫血和血红蛋白浓度在干预结束时的影响。结果总共315名儿童完成了30天的干预期。在基线时,66.9%的儿童具有炎症(血浆C-反应蛋白浓度> 5→Mg / L或血浆α<亚> 1 - 酸糖蛋白浓度> 1.0?G / L);在没有炎症的那些没有炎症的那些中,42.5%是铁缺乏。没有证据,无论是在每种协议分析还是意图治疗分析中,那么家用的强化与铁干预的任何一种改善血红蛋白浓度,等离子体铁蛋白浓度,血浆转移素受体浓度或红细胞锌原子卟啉-haem比例。我们还发现基线的铁状态,贫血地位和炎症状态没有有效修饰的证据。在荟萃分析中,对试验之间的对血红蛋白浓度的影响(I 2 :84.1%; P值用于异质性的值:结论本群,拥有3毫克铁的家庭设防。 Nafeedta或12.5?镁铁作为封装的黑色富马酸盐不充分地有效地评估3〜mg铁的非较低性,与12.5毫克铁作为封装的铁料。我们在试验结果之间发现异质性应刺激子组分析或元回归识别确定疗效的人口特定因素。试验注册试验在2014年2月25日与Clinicaltrials.gov(NCT02073149)注册。

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