Balanced energy protein supplements

  • 文章类型: Journal Article
    背景:母体营养不足是婴儿生长迟缓的直接危险因素。
    目的:我们评估了哺乳期妇女产后补充平衡能量蛋白(BEP)和婴儿补充阿奇霉素(AZ)对婴儿生长结局的影响。
    方法:在卡拉奇进行了一项哺乳期母亲-新生儿双胎的随机对照优势试验,巴基斯坦。打算母乳喂养中上臂周长小于23厘米的新生儿的母亲和生活在0-6天之间的活婴以1:1:1的比例随机分配到三只手臂之一。控制组的哺乳期母亲接受了纯母乳喂养的标准护理咨询,营养,婴儿免疫接种和健康促进以及补充叶酸铁,直至婴儿6个月大.在干预组1中,母亲每天另外接受两袋75克BEP,在第2组的干预中,以及标准护理和BEP,婴儿在42天的生命中还接受了一剂阿奇霉素(20mg/kg).主要结果是6个月时的婴儿身长速度。总样本量为957(每组319个)。
    结果:从2018年8月1日至2020年5月19日,在每只手臂中随机分配了319个哺乳期母亲-新生儿双胎,最后一次随访于2020年11月20日完成。单独BEP和对照之间的长度速度(cm/月)的平均差为0.01(95%CI:-0.03,0.06),BEP加AZ和对照为0.08(95%CI:0.03,0.13),单独BEP+AZ和BEP之间为0.06(95%CI:0.01,0.11)。试验中有1.46%(14/957)的婴儿死亡,记录了17.9%(171/957)的非致死性事件(可注射治疗和/或住院).
    结论:产后母亲BEP补充和婴儿AZ给药可适度改善婴儿6个月时的生长结局,提示同时解决母婴营养不良的潜在益处。
    该试验于2018年6月21日在ClinicalTrials.govNCT03564652上注册。
    BACKGROUND: Maternal undernutrition is a direct risk factor for infant growth faltering.
    OBJECTIVE: We evaluated the effect of postnatal balanced energy protein (BEP) supplementation in lactating women and azithromycin (AZ) in infants on infant growth outcomes.
    METHODS: A randomized controlled superiority trial of lactating mother-newborn dyads was conducted in Karachi, Pakistan. Mothers intending to breastfeed their newborns with mid-upper arm circumference of <23 cm and live infants between 0 and 6 d of life were randomly assigned to 1 of 3 arms in a 1:1:1 ratio. Lactating mothers in the control arm received standard-of-care counseling on exclusive breastfeeding, nutrition, infant immunization, and health promotion plus iron-folate supplementation until the infant was 6 mo old. In intervention arm 1, mothers additionally received two 75-g sachets of BEP per day. In intervention arm 2, along with the standard-of-care and BEP, the infant also received 1 dose of azithromycin (20 mg/kg) at the age of 42 d . The primary outcome was infant length velocity at 6 mo. The total sample size was 957 (319 in each arm).
    RESULTS: From 1 August, 2018 to 19 May, 2020, 319 lactating mother-newborn dyads were randomly assigned in each arm, and the last follow-up was completed on 20 November, 2020. The mean difference in length velocity (cm/mo) between BEP alone and control was 0.01 (95% confidence interval [CI]: -0.03, 0.06), BEP plus AZ and control was 0.08 (95% CI: 0.03, 0.13), and between BEP + AZ and BEP alone was 0.06 (95% CI: 0.01, 0.11). There were 1.46% (14/957) infant deaths in the trial, and 17.9% (171/957) nonfatal events (injectable treatment and/or hospitalizations) were recorded.
    CONCLUSIONS: Postnatal maternal BEP supplementation and infant AZ administration could modestly improve infant growth outcomes at 6 mo, suggesting potential benefits in simultaneously addressing maternal and infant undernutrition. This trial was registered at clinicaltrials.gov as NCT03564652.
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  • 文章类型: Clinical Trial Protocol
    BACKGROUND: Globally, 45% of under-five deaths are either directly or indirectly attributable to malnutrition, and most of these deaths are in low- and middle-income countries (LMICs). Children are particularly vulnerable in the first 6 months of life. An estimated 4.7 million infants under the age of 6 months are moderately wasted, whereas 3.8 million are severely wasted. Although the children of malnourished women have an increased risk of stunting and wasting, there is little information on this issue.
    METHODS: This is a community-based, open-label, multiarm randomized controlled trial that will include parallel group assignments with a 1:1:1 allocation ratio in low-income squatter settlements in urban Karachi, Pakistan. The women in the control group (control arm) will receive standard counseling only, whereas the lactating women in the first intervention group (intervention arm 1) will receive two sachets of balanced energy protein (BEP) supplementation per day from enrollment until the infant reaches 6 months of age. The lactating women in the second intervention group (intervention arm 2) will receive the same BEP supplementation as those in intervention arm 1 while their babies will also receive a single stat dose (20 mg/kg orally) of azithromycin at 42 days. The primary outcome will be the relative length velocity from 0 to 6 months by intervention arm. The primary analysis will be intention-to-treat analysis.
    BACKGROUND: ClinicalTrials.gov NCT03564652 . Registered on 21 June 2018.
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