Abstract
Phenylketonuria (PKU) management aims to control phenylalanine (Phe) intakes. In newborns and infants this implies possible titration of Human milk (HM) with supplementation of Phe-free formula. HM benefits, better if prolonged, are well known in healthy populations, suggesting it may be used in PKU patients. Despite that, the current literature does not define recommendations on how best perform it in such a population. The main purpose of this study was to evaluate nutrition approaches in newborns and infants affected by PKU and to define if differences can influence the duration of breastfeeding. Data from 42 PKU infants were reviewed. Of these, 67% were breastfed with the use of three different approaches. The type of approach used impacted the duration of breastfeeding, which was longer when using a pre-measured amount of Phe-free formula administered prior to HM. This is the first study to suggest a specific method for breastfeeding in PKU. Considering widely known breastfeeding benefits, both for patients and their mothers, our data should encourage adequate awareness on how to choose correct breastfeeding modalities.
Subject
Food Science,Nutrition and Dietetics
Reference38 articles.
1. The complete European guidelines on phenylketonuria: diagnosis and treatment
2. Breast-feeding Success Among Infants With Phenylketonuria
3. Hyperphenylalaninemia: Phenylalanine Hydroxylase Deficiency
https://ommbid.mhmedical.com/content.aspx?bookid=2709§ionid=225081923
4. Newborn Screening Fact Sheets
5. Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system;Jervis;Proc. Soc. Exp. Boil. Med.,1953
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献