患有Phenylketonuria的患者的食困难
Alexia Diovana Fernandes da Rocha1, Chenia Caldeira Martinez1,2, Lilia Farret Refosco3
1Universidade Federal de Ciências da Saúde de Porto Alegre - UFCSPA - Porto Alegre (RS), Brasil.
CoDAS
|October 4, 2023
概括
患有基尿症 (PKU) 的儿童表现出与对照人群相似的食困难,但自主性较低,不太可能被母乳养. 他们也更经常使用瓶子.
科学领域:
- 儿科 儿科 儿科
- 营养科学 营养科学
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 基尿 (PKU) 是一种罕见的遗传性疾病,需要饮食管理.
- 患有PKU的儿童的食模式和自主性尚未得到充分了解.
- 早期发现营养困难对于儿童的最佳发育至关重要.
研究的目的:
- 分析一种工具,用于识别患有PKU的儿童的食困难.
- 为了比较患有PKU的儿童的养行为与健康对照.
主要方法:
- 一项横截面,受控的研究,涉及40名患有PKU的儿童和46名健康对照.
- 参与者通过电子方式完成了巴西婴儿食量表 (EBAI).
- 通过社交媒体和门诊邀请方便抽样.
主要成果:
- 在PKU患者 (25%) 和对照 (28.3%) 之间,疑似食困难的频率没有显著差异.
- 患有PKU的儿童的养自主性显著降低 (p=0.005).
- 患有PKU的患者不太可能被母乳养 (p=0.002),更可能使用婴儿奶瓶 (p=0.028).
结论:
- 照顾者报告的食困难在两组之间频率相似.
- 患有PKU的儿童表现出明显的养模式,包括自主能力降低和养方法改变.
- 研究结果强调,需要为患有PKU的儿童提供有针对性的养支持.
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