首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Randomized clinical trial of behavioral and nutrition treatment to improve energy intake and growth in toddlers and preschoolers with cystic fibrosis.
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Randomized clinical trial of behavioral and nutrition treatment to improve energy intake and growth in toddlers and preschoolers with cystic fibrosis.

机译:行为和营养治疗可改善患有囊性纤维化的学步儿童和学龄前儿童的能量摄入和生长的随机临床试验。

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摘要

OBJECTIVE: To conduct a randomized clinical trial comparing a behavioral and nutrition intervention (BEH) with a usual care control condition (CTL) for children (ages 18 months to 4 years) with cystic fibrosis (CF) and pancreatic insufficiency. This trial was designed to (1) evaluate a randomized comparison of BEH with CTL over 8 weeks, (2) provide a replication of the impact of BEH by inviting the CTL group to receive BEH after 8 weeks, and (3) examine the maintenance of BEH at 3- and 12-month follow-up. METHODS: Of 14 eligible children, 10 were randomly assigned and initiated treatment (71% recruitment rate). Four participants were randomly assigned to BEH, and 6 were assigned to CTL (5 of whom chose to crossover to BEH). BEH included nutrition counseling to increase energy intake (via types of foods and addables/spreadables) and child behavioral management training to teach parents differential attention and contingency management skills. CTL was consistent with the 2002 CF Foundation Consensus Conference Guidelines for nutritional care. RESULTS: BEH led to greater increases in energy intake pre- to posttreatment than CTL as measured by calories per day (842 kcal/day vs -131 kcal/day change). On receiving BEH, the change in energy intake was replicated with the CTL group (892 kcal/day change). At 3- and 12-month follow-up, energy intake was maintained (672 kcal/day increase from baseline and 750 kcal/day increase from baseline, respectively). Children in this study met or exceeded normal weight and height velocities from pretreatment to the 3-month follow-up (mean weight: 1.4 kg/6 months; mean height: 5.1 cm/6 months) and from posttreatment to the 12-month follow-up (mean weight: 2.5 kg/12 months; mean height: 8.3 cm/12 months). CONCLUSIONS: Toddlers and preschoolers who have CF and received BEH were able to meet the energy intake recommendations for this disease and maintain these gains up to 12 months after treatment. In addition, these children demonstrated weight and height velocities from pretreatment to 12-month follow-up, consistent with the goal of normal growth. BEH is a promising, evidence-based, early nutritional intervention for children with CF. An upcoming multisite clinical trial will test BEH versus an attention control condition using a larger sample (N = 100), providing additional evidence about the efficacy of this treatment for energy intake and growth in young children with CF.
机译:目的:进行一项随机临床试验,比较行为和营养干预(BEH)与患有囊性纤维化(CF)和胰腺功能不全的儿童(18个月至4岁)的常规护理控制条件(CTL)。该试验旨在(1)评估BEH与CTL在8周内的随机比较,(2)邀请CTL组在8周后接受BEH,以复制BEH的影响,以及(3)检查维持情况在3个月和12个月的随访中评估BEH。方法:在14名符合条件的儿童中,有10名被随机分配并开始治疗(入组率为71%)。随机将4位参与者分配给BEH,将6位参与者分配给CTL(其中5位选择了过渡到BEH)。 BEH包括营养咨询,以增加能量摄入(通过食物和添加剂/易散剂的种类),以及儿童行为管理培训,以教导父母不同的注意力和应变管理技能。 CTL与2002 CF基金会营养保健会议共识一致。结果:以每天的卡路里来衡量,BEH导致治疗前和治疗后的能量摄入量比CTL更大(842 kcal /天与-131 kcal /天的变化)。接受BEH后,CTL组重复摄取能量的变化(892 kcal /天的变化)。在3个月和12个月的随访中,维持了能量摄入(分别从基线增加672 kcal /天和从基线增加750 kcal /天)。本研究中的儿童从治疗前到随访3个月(平均体重:1.4 kg / 6个月;平均身高:5.1 cm / 6个月)以及从治疗后到随访12个月达到或超过正常体重和身高速度。 -up(平均体重:2.5千克/ 12个月;平均身高:8.3厘米/ 12个月)。结论:患有CF并接受BEH的幼儿和学龄前儿童能够满足该疾病的能量摄入建议,并在治疗后12个月内保持这些收益。此外,这些儿童从预处理到随访12个月表现出体重和身高速度,符合正常生长的目标。 BEH是一种有前景的,有证据的,针对CF儿童的早期营养干预措施。即将进行的一项多站点临床试验将使用更大的样本(N = 100)来测试BEH与注意力控制状况的比较,从而提供有关该治疗对CF患儿能量摄入和生长的功效的其他证据。

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