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International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up.
Welling, Lindsey; Bernstein, Laurie E; Berry, Gerard T; Burlina, Alberto B; Eyskens, François; Gautschi, Matthias; Grünewald, Stephanie; Gubbels, Cynthia S; Knerr, Ina; Labrune, Philippe; van der Lee, Johanna H; MacDonald, Anita; Murphy, Elaine; Portnoi, Pat A; Õunap, Katrin; Potter, Nancy L; Rubio-Gozalbo, M Estela; Spencer, Jessica B; Timmers, Inge; Treacy, Eileen P; Van Calcar, Sandra C; Waisbren, Susan E; Bosch, Annet M.
  • Welling L; Department of Pediatrics, Emma Children's Hospital, Academic Medical Center, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
  • Bernstein LE; Section of Clinical Genetics and Metabolism, Inherited Metabolic Disease Nutrition Department, University of Colorado-Denver School of Medicine, The Children's Hospital Colorado, Aurora, CO, USA.
  • Berry GT; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Burlina AB; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Eyskens F; Department of Pediatrics, Metabolic Unit, University Hospital, University of Padova, Padova, Italy.
  • Gautschi M; Department of Metabolic Disorders in Children, Antwerp University Hospital UZA, Edegem, Belgium.
  • Grünewald S; University Children's Hospital, Pediatric Endocrinology, Diabetes and Metabolism, and Institute of Clinical Chemistry, Inselspital, University of Bern, Bern, Switzerland.
  • Gubbels CS; Metabolic Unit, Great Ormond Street Hospital and Institute of Child Health, University College London, London, UK.
  • Knerr I; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Labrune P; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • van der Lee JH; National Centre for Inherited Metabolic Disorders, Temple St. Children's University Hospital, Dublin, Ireland.
  • MacDonald A; Department of Pediatrics, APHP, Hopital Antoine Béclère, Cedex Clamart, France.
  • Murphy E; Pediatric Clinical Research Office, Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
  • Portnoi PA; Birmingham Children's Hospital, Steelhouse Lane, Birmingham, UK.
  • Õunap K; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
  • Potter NL; Medical Advisory Panel, Galactosemia Support Group UK, West Midlands, UK.
  • Rubio-Gozalbo ME; Department of Pediatrics, University of Tartu, Tartu, Estonia.
  • Spencer JB; Department of Genetics, Tartu University Hospital, Tartu, Estonia.
  • Timmers I; Department of Speech and Hearing Sciences, Washington State University, Spokane, WA, USA.
  • Treacy EP; Department of Pediatrics and Laboratory Genetic Metabolic Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Van Calcar SC; Department of Gynecology and Obstetrics, School of Medicine, Emory University, Atlanta, Georgia.
  • Waisbren SE; Department of Cognitive Neuroscience, Maastricht University, Maastricht, The Netherlands.
  • Bosch AM; National Centre for Inherited Metabolic Disorders, Temple St. Children's University Hospital and Mater Misericordiae University Hospital, Dublin, Ireland.
J Inherit Metab Dis ; 40(2): 171-176, 2017 03.
Article en En | MEDLINE | ID: mdl-27858262
ABSTRACT
Classical galactosemia (CG) is an inborn error of galactose metabolism. Evidence-based guidelines for the treatment and follow-up of CG are currently lacking, and treatment and follow-up have been demonstrated to vary worldwide. To provide patients around the world the same state-of-the-art in care, members of The Galactosemia Network (GalNet) developed an evidence-based and internationally applicable guideline for the diagnosis, treatment, and follow-up of CG. The guideline was developed using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) system. A systematic review of the literature was performed, after key questions were formulated during an initial GalNet meeting. The first author and one of the working group experts conducted data-extraction. All experts were involved in data-extraction. Quality of the body of evidence was evaluated and recommendations were formulated. Whenever possible recommendations were evidence-based, if not they were based on expert opinion. Consensus was reached by multiple conference calls, consensus rounds via e-mail and a final consensus meeting. Recommendations addressing diagnosis, dietary treatment, biochemical monitoring, and follow-up of clinical complications were formulated. For all recommendations but one, full consensus was reached. A 93 % consensus was reached on the recommendation addressing age at start of bone density screening. During the development of this guideline, gaps of knowledge were identified in most fields of interest, foremost in the fields of treatment and follow-up.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Galactosemias Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Galactosemias Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article