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Management of early treated adolescents and young adults with phenylketonuria: Development of international consensus recommendations using a modified Delphi approach.
Burton, Barbara K; Hermida, Álvaro; Bélanger-Quintana, Amaya; Bell, Heather; Bjoraker, Kendra J; Christ, Shawn E; Grant, Mitzie L; Harding, Cary O; Huijbregts, Stephan C J; Longo, Nicola; McNutt, Markey C; Nguyen-Driver, Mina D; Santos Pessoa, André L; Rocha, Júlio César; Sacharow, Stephanie; Sanchez-Valle, Amarilis; Sivri, H Serap; Vockley, Jerry; Walterfang, Mark; Whittle, Sarah; Muntau, Ania C.
Afiliación
  • Burton BK; Ann and Robert H. Lurie Children's Hospital and Northwestern University Feinberg School of Medicine, Chicago, IL, USA. Electronic address: bburton@luriechildrens.org.
  • Hermida Á; Clinical University Hospital of Santiago de Compostela, University of Santiago de Compostela, CIBERER, MetabERN, Institute of Clinical Research of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
  • Bélanger-Quintana A; Metabolic Diseases Unit, Department of Paediatrics, Ramon y Cajal Hospital, Madrid, Spain.
  • Bell H; Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Mount Sinai Hospital, Toronto, ON, Canada.
  • Bjoraker KJ; 3:1 Neuropsychology Consultants, PLLC, Minneapolis, MN, USA.
  • Christ SE; Department of Psychological Sciences, University of Missouri, Columbia, MO, USA.
  • Grant ML; Department of Psychiatry, Drexel University College of Medicine, Philadelphia, PA, USA.
  • Harding CO; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
  • Huijbregts SCJ; Leiden Institute for Brain and Cognition, Leiden University, Leiden, the Netherlands.
  • Longo N; Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.
  • McNutt MC; McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX, USA.
  • Nguyen-Driver MD; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
  • Santos Pessoa AL; Pediatric Neurology Service, Albert Sabin Children's Hospital, University of Ceará State, Fortaleza, Ceará, Brazil.
  • Rocha JC; Nutrition and Metabolism, NOVA Medical School, Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Portugal; Neuropsychiatry Unit, Royal Melbourne Hospital, Melbourne, VIC, Australia; Melbourne Neuropsychiatry Centre, University of Melbourne, Melbourne, VIC, Australia.
  • Sacharow S; CINTESIS-Center for Health Technology and Services Research, NOVA Medical School, Lisboa, Portugal; Florey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australia.
  • Sanchez-Valle A; Reference Centre of Inherited Metabolic Diseases, Centro Hospitalar Universitário de Lisboa Central, Lisboa, Portugal.
  • Sivri HS; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.
  • Vockley J; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Walterfang M; Department of Pediatrics, Morsani College of Medicine, University of South Florida, Tampa, FL, USA; Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, Melbourne, VIC, Australia; University Children's Hospital, University Medical Center Hamburg Eppendorf, Hamburg, Ge
  • Whittle S; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Section of Pediatric Metabolism, Ankara, Turkey.
  • Muntau AC; Department of Pediatrics, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Mol Genet Metab ; 137(1-2): 114-126, 2022.
Article en En | MEDLINE | ID: mdl-36027720
ABSTRACT

BACKGROUND:

Early treated patients with phenylketonuria (PKU) often become lost to follow-up from adolescence onwards due to the historical focus of PKU care on the pediatric population and lack of programs facilitating the transition to adulthood. As a result, evidence on the management of adolescents and young adults with PKU is limited.

METHODS:

Two meetings were held with a multidisciplinary international panel of 25 experts in PKU and comorbidities frequently experienced by patients with PKU. Based on the outcomes of the first meeting, a set of statements were developed. During the second meeting, these statements were voted on for consensus generation (≥70% agreement), using a modified Delphi approach.

RESULTS:

A total of 37 consensus recommendations were developed across five areas that were deemed important in the management of adolescents and young adults with PKU (1) general physical health, (2) mental health and neurocognitive functioning, (3) blood Phe target range, (4) PKU-specific challenges, and (5) transition to adult care. The consensus recommendations reflect the personal opinions and experiences from the participating experts supported with evidence when available. Overall, clinicians managing adolescents and young adults with PKU should be aware of the wide variety of PKU-associated comorbidities, initiating screening at an early age. In addition, management of adolescents/young adults should be a joint effort between the patient, clinical center, and parents/caregivers supporting adolescents with gradually gaining independent control of their disease during the transition to adulthood.

CONCLUSIONS:

A multidisciplinary international group of experts used a modified Delphi approach to develop a set of consensus recommendations with the aim of providing guidance and offering tools to clinics to aid with supporting adolescents and young adults with PKU.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenilcetonurias Tipo de estudio: Diagnostic_studies / Guideline / Screening_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenilcetonurias Tipo de estudio: Diagnostic_studies / Guideline / Screening_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2022 Tipo del documento: Article