Weaning practices in phenylketonuria vary between health professionals in Europe.

dc.contributor.authorPinto, A
dc.contributor.authorAdams, S
dc.contributor.authorAhring, K
dc.contributor.authorAllen, H
dc.contributor.authorAlmeida, M F
dc.contributor.authorGarcia-Arenas, D
dc.contributor.authorArslan, N
dc.contributor.authorAssoun, M
dc.contributor.authorAtik Altınok, Y
dc.contributor.authorBarrio-Carreras, D
dc.contributor.authorBelanger Quintana, A
dc.contributor.authorBernabei, S M
dc.contributor.authorBontemps, C
dc.contributor.authorBoyle, F
dc.contributor.authorBruni, G
dc.contributor.authorBueno-Delgado, M
dc.contributor.authorCaine, G
dc.contributor.authorCarvalho, R
dc.contributor.authorChrobot, A
dc.contributor.authorChyż, K
dc.contributor.authorCochrane, B
dc.contributor.authorCorreia, C
dc.contributor.authorCorthouts, K
dc.contributor.authorDaly, A
dc.contributor.authorDe Leo, S
dc.contributor.authorDesloovere, A
dc.contributor.authorDe Meyer, A
dc.contributor.authorDe Theux, A
dc.contributor.authorDidycz, B
dc.contributor.authorDijsselhof, M E
dc.contributor.authorDokoupil, K
dc.contributor.authorDrabik, J
dc.contributor.authorDunlop, C
dc.contributor.authorEberle-Pelloth, W
dc.contributor.authorEftring, K
dc.contributor.authorEkengren, J
dc.contributor.authorErrekalde, I
dc.contributor.authorEvans, S
dc.contributor.authorFoucart, A
dc.contributor.authorFokkema, L
dc.contributor.authorFrançois, L
dc.contributor.authorFrench, M
dc.contributor.authorForssell, E
dc.contributor.authorGingell, C
dc.contributor.authorGonçalves, C
dc.contributor.authorGökmen Özel, H
dc.contributor.authorGrimsley, A
dc.contributor.authorGugelmo, G
dc.contributor.authorGyüre, E
dc.contributor.authorHeller, C
dc.contributor.authorHensler, R
dc.contributor.authorJardim, I
dc.contributor.authorJoost, C
dc.contributor.authorJörg-Streller, M
dc.contributor.authorJouault, C
dc.contributor.authorJung, A
dc.contributor.authorKanthe, M
dc.contributor.authorKoç, N
dc.contributor.authorKok, I L
dc.contributor.authorKozanoğlu, T
dc.contributor.authorKumru, B
dc.contributor.authorLang, F
dc.contributor.authorLang, K
dc.contributor.authorLiegeois, I
dc.contributor.authorLiguori, A
dc.contributor.authorLilje, R
dc.contributor.authorĻubina, O
dc.contributor.authorManta-Vogli, P
dc.contributor.authorMayr, D
dc.contributor.authorMeneses, C
dc.contributor.authorNewby, C
dc.contributor.authorMeyer, U
dc.contributor.authorMexia, S
dc.contributor.authorNicol, C
dc.contributor.authorOch, U
dc.contributor.authorOlivas, S M
dc.contributor.authorPedrón-Giner, C
dc.contributor.authorPereira, R
dc.contributor.authorPlutowska-Hoffmann, K
dc.contributor.authorPurves, J
dc.contributor.authorRe Dionigi, A
dc.contributor.authorReinson, K
dc.contributor.authorRobert, M
dc.contributor.authorRobertson, L
dc.contributor.authorRocha, J C
dc.contributor.authorRohde, C
dc.contributor.authorRosenbaum-Fabian, S
dc.contributor.authorRossi, A
dc.contributor.authorRuiz, M
dc.contributor.authorSaligova, J
dc.contributor.authorGutiérrez-Sánchez, A
dc.contributor.authorSchlune, A
dc.contributor.authorSchulpis, K
dc.contributor.authorSerrano-Nieto, J
dc.contributor.authorSkarpalezou, A
dc.contributor.authorSkeath, R
dc.contributor.authorSlabbert, A
dc.contributor.authorStraczek, K
dc.contributor.authorGiżewska, M
dc.contributor.authorTerry, A
dc.contributor.authorThom, R
dc.contributor.authorTooke, A
dc.contributor.authorTuokkola, J
dc.contributor.authorvan Dam, E
dc.contributor.authorvan den Hurk, T A M
dc.contributor.authorvan der Ploeg, E M C
dc.contributor.authorVande Kerckhove, K
dc.contributor.authorVan Driessche, M
dc.contributor.authorvan Wegberg, A M J
dc.contributor.authorvan Wyk, K
dc.contributor.authorVasconcelos, C
dc.contributor.authorVelez García, V
dc.contributor.authorWildgoose, J
dc.contributor.authorWinkler, T
dc.contributor.authorŻółkowska, J
dc.contributor.authorZuvadelli, J
dc.contributor.authorMacDonald, A
dc.date.accessioned2025-01-07T15:23:49Z
dc.date.available2025-01-07T15:23:49Z
dc.date.issued2018-11-25
dc.description.abstractIn phenylketonuria (PKU), weaning is considered more challenging when compared to feeding healthy infants. The primary aim of weaning is to gradually replace natural protein from breast milk or standard infant formula with solids containing equivalent phenylalanine (Phe). In addition, a Phe-free second stage L-amino acid supplement is usually recommended from around 6 months to replace Phe-free infant formula. Our aim was to assess different weaning approaches used by health professionals across Europe. A cross sectional questionnaire (survey monkey®) composed of 31 multiple and single choice questions was sent to European colleagues caring for inherited metabolic disorders (IMD). Centres were grouped into geographical regions for analysis. Weaning started at 17-26 weeks in 85% (n = 81/95) of centres, >26 weeks in 12% (n = 11/95) and 26 weeks in 12% (n = 11/95) and 26 weeks. First solids were mainly low Phe vegetables (59%, n = 56/95) and fruit (34%, n = 32/95).A Phe exchange system to allocate dietary Phe was used by 52% (n = 49/95) of centres predominantly from Northern and Southern Europe and 48% (n = 46/95) calculated most Phe containing food sources (all centres in Eastern Europe and the majority from Germany and Austria). Some centres used a combination of both methods.A second stage Phe-free L-amino acid supplement containing a higher protein equivalent was introduced by 41% (n = 39/95) of centres at infant age 26-36 weeks (mainly from Germany, Austria, Northern and Eastern Europe) and 37% (n = 35/95) at infant age > 1y mainly from Southern Europe. 53% (n = 50/95) of centres recommended a second stage Phe-free L-amino acid supplement in a spoonable or semi-solid form. Weaning strategies vary throughout European PKU centres. There is evidence to suggest that different infant weaning strategies may influence longer term adherence to the PKU diet or acceptance of Phe-free L-amino acid supplements; rendering prospective long-term studies important. It is essential to identify an effective weaning strategy that reduces caregiver burden but is associated with acceptable dietary adherence and optimal infant feeding development.
dc.identifier.doi10.1016/j.ymgmr.2018.11.003
dc.identifier.issn2214-4269
dc.identifier.pmcPMC6349955
dc.identifier.pmid30705824
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC6349955/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.ymgmr.2018.11.003
dc.identifier.urihttps://hdl.handle.net/10668/27105
dc.journal.titleMolecular genetics and metabolism reports
dc.journal.titleabbreviationMol Genet Metab Rep
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de la Victoria
dc.organizationSAS - Hospital Universitario Virgen del Rocío
dc.page.number39-44
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectInfant
dc.subjectPhe-free infant formula
dc.subjectPhenylalanine
dc.subjectPhenylketonuria
dc.subjectWeaning
dc.titleWeaning practices in phenylketonuria vary between health professionals in Europe.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number18

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