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. 1980 May;70(5):498–503. doi: 10.2105/ajph.70.5.498

Diet discontinuation policies and practices of PKU clinics in the United States.

V E Schuett, R F Gurda, E S Brown
PMCID: PMC1619429  PMID: 7377420

Abstract

Marked diversity in policies and practices for discontinuation of the PKU diet in the U.S. was found in a nationwide survey. Seventy-two of the 78 identified clinical centers treating PKU provided data. No clinicians are currently considering diet discontinuation at ages earlier than their present policy or practice. A definite trend toward later discontinuation of diet was identified. A few clinicians have always recommended indefinite diet continuation while many clinics have experience with children ages 9--12 who have discontinued the diet. Clinics with seven or more children off diet in this age range are significantly more likely than smaller clinics to be considering a later age for diet discontinuation. There were 151 children approximately age 10 or older, who remain on a low phenylalanine diet. These children are followed by 29 clinics, but over one-half of them are followed by five clinics which have had long-standing policies of indefinite diet continuation. Factors associated with success in long-term management are a firm clinic policy supporting continued diet treatment; frequent, supportive contacts with the family; open discussion by staff with families and establishment of a trusting relationship; teaching children to accept responsibility for diet management from an early age.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Berry H. K., O'Grady D. J., Perlmutter L. J., Bofinger M. K. Intellectual development and academic achievement of children treated early for phenylketonuria. Dev Med Child Neurol. 1979 Jun;21(3):311–320. doi: 10.1111/j.1469-8749.1979.tb01623.x. [DOI] [PubMed] [Google Scholar]
  2. Bickel H., Kaiser-Grubel S. Uber die Phenylketonurie. Psychometrische Erfolgsbeuteilung der phenylalaninarmen Diät bei phenylketonurischen Kindern. Dtsch Med Wochenschr. 1971 Sep 3;96(36):1415–1423. doi: 10.1055/s-0028-1110153. [DOI] [PubMed] [Google Scholar]
  3. Brown E. S., Warner R. Mental development of phenylketonuric children on or off diet after the age of six. Psychol Med. 1976 May;6(2):287–296. doi: 10.1017/s0033291700013842. [DOI] [PubMed] [Google Scholar]
  4. Cabalska B., Duczyńska N., Borzymowska J., Zorska K., Koślacz-Folga A., Bozkowa K. Termination of dietary treatment in phenylketonuria. Eur J Pediatr. 1977 Nov 4;126(4):253–262. doi: 10.1007/BF00477051. [DOI] [PubMed] [Google Scholar]
  5. Holtzman N. A., Welcher D. W., Mellits E. D. Termination of restricted diet in children with phenylketonuria: a randomized controlled study. N Engl J Med. 1975 Nov 27;293(22):1121–1124. doi: 10.1056/NEJM197511272932204. [DOI] [PubMed] [Google Scholar]
  6. Johnson C. F. What is the best age to discontinue the low phenylalanine diet in phenylketonuria? A presentation of some contributory data. Clin Pediatr (Phila) 1972 Mar;11(3):148–156. doi: 10.1177/000992287201100306. [DOI] [PubMed] [Google Scholar]
  7. Moen J. L., Wilcox R. D., Burns J. K. PKU as a factor in the development of self-esteem. J Pediatr. 1977 Jun;90(6):1027–1029. doi: 10.1016/s0022-3476(77)80591-x. [DOI] [PubMed] [Google Scholar]
  8. Murphy D. Termination of dietary treatment of phenylketonuria. Ir J Med Sci. 1969 Apr;8(4):177–183. doi: 10.1007/BF02954680. [DOI] [PubMed] [Google Scholar]
  9. Pueschel S. M., Yeatman S., Hum C. Discontinuing the phenylalamine-restricted diet in young children with PKY. Psychosocial aspects. J Am Diet Assoc. 1977 May;70(5):506–509. [PubMed] [Google Scholar]
  10. Robertson E. F., Hill G. N., Cashel K., Rooney J., Brummitt R., Pollard A. C. Management of phenylketonuria: South Australian experience of 13 cases. Med J Aust. 1976 May 1;1(18):647–650. [PubMed] [Google Scholar]
  11. Singh I. J., Savara B. S., Newman M. T. Growth in the skeletal and non-skeletal components of head width from 9 to 14 years of age. Hum Biol. 1967 May;39(2):182–191. [PubMed] [Google Scholar]
  12. Smith I., Lobascher M. E., Stevenson J. E., Wolff O. H., Schmidt H., Grubel-Kaiser S., Bickel H. Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria. Br Med J. 1978 Sep 9;2(6139):723–726. doi: 10.1136/bmj.2.6139.723. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Williamson M., Koch R., Berlow S. Diet discontinuation in phenylketonuria. Pediatrics. 1979 May;63(5):823–824. [PubMed] [Google Scholar]

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