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用于囊性纤维化患儿的口服蛋白质能量补充剂:CALICO多中心随机对照试验

Oral protein energy supplements for children with cystic fibrosis: CALICO multicentre randomised controlled trial.

作者信息

Poustie Vanessa J, Russell Jayne E, Watling Ruth M, Ashby Deborah, Smyth Rosalind L

机构信息

University of Liverpool Division of Child Health, Royal Liverpool Children's Hospital, Liverpool L12 2AP.

出版信息

BMJ. 2006 Mar 18;332(7542):632-6. doi: 10.1136/bmj.38737.600880.AE. Epub 2006 Feb 8.

DOI:10.1136/bmj.38737.600880.AE
PMID:16467348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1403226/
Abstract

OBJECTIVE

To determine whether oral protein energy supplements, used long term in children with cystic fibrosis who are moderately malnourished, improve nutritional and other outcomes.

DESIGN

Multicentre randomised controlled trial.

SETTING

Seven specialist paediatric cystic fibrosis centres and their associated shared care clinics and seven smaller paediatric cystic fibrosis clinics.

PARTICIPANTS

102 children with cystic fibrosis, aged between 2 and 15 years, who were moderately malnourished.

INTERVENTIONS

Oral protein energy supplements in addition to usual dietary advice compared with dietary advice alone, for 12 months.

MAIN OUTCOME MEASURE

Change in body mass index centile over one year.

RESULTS

Use of supplements was not associated with a change in body mass index centile (mean difference 2.99 centile points, 95% confidence interval -2.70 to 8.68) or other nutritional and spirometric outcomes in this group of children.

CONCLUSIONS

Long term use of oral protein energy supplements did not result in an improvement in nutritional status or other clinical outcomes in children with cystic fibrosis who were moderately malnourished. Oral protein energy supplements should not be regarded as an essential part of the management of this group of children.

TRIAL REGISTRATION

ISRCTN: 95744468.

摘要

目的

确定长期给中度营养不良的囊性纤维化患儿口服蛋白质能量补充剂是否能改善营养状况及其他结局。

设计

多中心随机对照试验。

地点

7家儿科囊性纤维化专科中心及其相关的共享护理诊所和7家规模较小的儿科囊性纤维化诊所。

参与者

102名年龄在2至15岁之间的中度营养不良的囊性纤维化患儿。

干预措施

除常规饮食建议外,口服蛋白质能量补充剂,为期12个月,并与仅接受饮食建议进行比较。

主要结局指标

一年内体重指数百分位的变化。

结果

在这组儿童中,补充剂的使用与体重指数百分位的变化(平均差异2.99个百分位,95%置信区间为-2.70至8.68)或其他营养和肺功能检查结局无关。

结论

长期口服蛋白质能量补充剂并未改善中度营养不良的囊性纤维化患儿的营养状况或其他临床结局。口服蛋白质能量补充剂不应被视为这组患儿治疗的必要组成部分。

试验注册号

ISRCTN:95744468。

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本文引用的文献

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Dietary supplement use is prevalent among children with a chronic illness.慢性病患儿中普遍存在使用膳食补充剂的情况。
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Resting energy expenditure and lung disease in cystic fibrosis.囊性纤维化患者的静息能量消耗与肺部疾病
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Nutrition in patients with cystic fibrosis: a European Consensus.囊性纤维化患者的营养:欧洲共识
J Cyst Fibros. 2002 Jun;1(2):51-75. doi: 10.1016/s1569-1993(02)00032-2.
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Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis.囊性纤维化患儿生长参数的纵向变化与肺功能变化相关。
Pediatrics. 2003 Sep;112(3 Pt 1):588-92. doi: 10.1542/peds.112.3.588.
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Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis.生命早期的生长和营养指标可预测囊性纤维化患者的肺功能。
J Pediatr. 2003 Jun;142(6):624-30. doi: 10.1067/mpd.2003.152.
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Validity of the assessment of dietary intake: problems of misreporting.饮食摄入量评估的有效性:误报问题。
Curr Opin Clin Nutr Metab Care. 2002 Sep;5(5):489-93. doi: 10.1097/00075197-200209000-00006.
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Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project.囊性纤维化患者营养状况与肺功能的关系:来自德国囊性纤维化质量保证(CFQA)项目的横断面和纵向分析
Thorax. 2002 Jul;57(7):596-601. doi: 10.1136/thorax.57.7.596.
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Caloric intake and eating behavior in infants and toddlers with cystic fibrosis.患有囊性纤维化的婴幼儿的热量摄入与饮食行为
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Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry.囊性纤维化患儿生长、营养状况与肺功能之间的纵向关系:来自囊性纤维化基金会国家囊性纤维化患者登记处的分析
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