Literature DB >> 11882785

Barriers to successful dietary control among pregnant women with phenylketonuria.

Amanda Savage Brown1, Paul M Fernhoff, Susan E Waisbren, Dianne M Frazier, Rani Singh, Fran Rohr, Jill M Morris, Aileen Kenneson, Pia MacDonald, Marta Gwinn, Margaret Honein, Sonja A Rasmussen.   

Abstract

PURPOSE: The teratogenic effects of maternal PKU are preventable, yet affected babies continue to be born. This study's purpose was to identify barriers to successful dietary control among pregnant women with PKU.
METHODS: An interview-based study was conducted of women with PKU who were known to metabolic disease clinics in three states and pregnant during 1998 to 2000. Medical records were used to document timing of metabolic control.
RESULTS: Of 24 women in the study, only 8 (33%) initiated the diet before pregnancy. Of 22 medical records received, only 12 (55%) indicated control of blood phenylalanine levels before 10 weeks' gestation. Risk factors for late dietary control included young age and belief that treatment costs complicated the diet. Although all of the women expressed confidence in the metabolic clinic staff, few perceived their obstetricians were knowledgeable about the maternal PKU diet. Of 13 women enrolled in state-based assistance programs, 9 (69%) reported proof of pregnancy was required for eligibility. Many women using private insurance reported their insurers were unwilling to pay for medical foods. When the data were stratified according to state of residence, differences were observed in the rate of live-born infants, prepregnancy medical food use, average travel time to the metabolic clinic, and gestational week when metabolic control was achieved.
CONCLUSION: Our study's findings may be used to target educational messages to women with PKU and to direct future research directions. For example, obstetric knowledge of maternal PKU needs further evaluation. Discrepancies should be resolved between maternal PKU medical recommendations and the policies of third party-payers. The disparities in financial assistance and services available to pregnant women with PKU residing in different states should be examined further.

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Year:  2002        PMID: 11882785     DOI: 10.1097/00125817-200203000-00006

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  10 in total

1.  Use of Gastrostomy Tube to Prevent Maternal PKU Syndrome.

Authors:  Jessica A Scott Schwoerer; Lisa Obernolte; Sandra Van Calcar; Susan Heighway; Heather Bankowski; Phillip Williams; Gregory Rice
Journal:  JIMD Rep       Date:  2012-01-31

2.  Sapropterin hydrochloride: enzyme enhancement therapy for phenylketonuria.

Authors:  Robin Lachmann
Journal:  Ther Adv Endocrinol Metab       Date:  2011-06       Impact factor: 3.565

3.  Newborn screening: complexities in universal genetic testing.

Authors:  Nancy S Green; Siobhan M Dolan; Thomas H Murray
Journal:  Am J Public Health       Date:  2006-03-29       Impact factor: 9.308

4.  Domino liver transplant from a donor with maple syrup urine disease into a recipient with phenylketonuria.

Authors:  Vikram K Raghu; Steven F Dobrowolski; Rakesh Sindhi; Kevin A Strauss; George V Mazariegos; Jerry Vockley; Kyle Soltys
Journal:  Mol Genet Metab Rep       Date:  2022-04-21

Review 5.  The truth of treating patients with phenylketonuria after childhood: the need for a new guideline.

Authors:  F J van Spronsen; P Burgard
Journal:  J Inherit Metab Dis       Date:  2008-08-12       Impact factor: 4.982

6.  The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings.

Authors:  F Rohr; A Munier; D Sullivan; I Bailey; M Gennaccaro; H Levy; H Brereton; S Gleason; B Goss; E Lesperance; K Moseley; R Singh; L Tonyes; H Vespa; S Waisbren
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

Review 7.  The complete European guidelines on phenylketonuria: diagnosis and treatment.

Authors:  A M J van Wegberg; A MacDonald; K Ahring; A Bélanger-Quintana; N Blau; A M Bosch; A Burlina; J Campistol; F Feillet; M Giżewska; S C Huijbregts; S Kearney; V Leuzzi; F Maillot; A C Muntau; M van Rijn; F Trefz; J H Walter; F J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2017-10-12       Impact factor: 4.123

8.  Promoting psychological well-being in women with phenylketonuria: Pregnancy-related stresses, coping strategies and supports.

Authors:  Rachel M Roberts; Tamara Muller; Annabel Sweeney; Drago Bratkovic; Anne Gannoni
Journal:  Mol Genet Metab Rep       Date:  2014-04-17

9.  Dietary management of maternal phenylketonuria with glycomacropeptide and amino acids supplements: A case report.

Authors:  A Pinto; M F Almeida; A Cunha; C Carmona; S Rocha; A Guimas; R Ribeiro; C R Mota; E Martins; A MacDonald; J C Rocha
Journal:  Mol Genet Metab Rep       Date:  2017-10-18

10.  First Japanese case of maternal phenylketonuria treated with sapropterin dihydrochloride and the normal growth and development of the child.

Authors:  Hiromi Nyuzuki; Taro Yamazaki; Megumi Saito; Akira Ohtake
Journal:  Mol Genet Metab Rep       Date:  2019-11-01
  10 in total

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