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Managing infants with craniofacial malformations - Where to go next?
Poets, Christian F; Abadie, Veronique; Breugem, Corstiaan; Wallis, Colin; Abel, Francois; Chalouhi, Christel; Kruisinga, Frea; Sorg, Anna-Lisa; Wiechers, Cornelia.
Afiliación
  • Poets CF; Interdisciplinary Center for Cleft Palate & Craniofacial Malformations and Department of Neonatology, Tübingen University Hospital, Tübingen, Germany. Electronic address: Christian-f.poets@med.uni-tuebingen.de.
  • Abadie V; Department of General Pediatrics, Reference Center for Rare Diseases "Pierre Robin Sequences and Congenital Sucking-swallowing Troubles", Necker University Hospital, Paris University, France.
  • Breugem C; Department of Plastic Reconstructive and Hand Surgery, Amsterdam UMC, Emma Children's Hospital - Location AMC, University of Amsterdam, the Netherlands.
  • Wallis C; Department of Paediatric Respiratory Medicine, Great Ormond Street Hospital, London, UK.
  • Abel F; Department of Paediatric Respiratory Medicine, Great Ormond Street Hospital, London, UK.
  • Chalouhi C; Department of Plastic Reconstructive and Hand Surgery, Amsterdam UMC, Emma Children's Hospital - Location AMC, University of Amsterdam, the Netherlands.
  • Kruisinga F; Department of Plastic Reconstructive and Hand Surgery, Amsterdam UMC, Emma Children's Hospital - Location AMC, University of Amsterdam, the Netherlands.
  • Sorg AL; Interdisciplinary Center for Cleft Palate & Craniofacial Malformations and Department of Neonatology, Tübingen University Hospital, Tübingen, Germany.
  • Wiechers C; Interdisciplinary Center for Cleft Palate & Craniofacial Malformations and Department of Neonatology, Tübingen University Hospital, Tübingen, Germany.
Semin Fetal Neonatal Med ; 26(6): 101289, 2021 12.
Article en En | MEDLINE | ID: mdl-34548245
ABSTRACT
Treatment of infants with craniofacial malformations, e.g. Robin sequence, is characterized by considerable heterogeneity and a lack of randomized trials to identify an optimal approach. We propose to establish an international register using a common minimal dataset that will better allow for a comparison between key determinants and outcomes in these patients. In infants, this should include an assessment of mandibular micrognathia, glossoptosis, upper airway obstruction, weight gain and mode of feeding. Later on, neurocognition, speech development, hearing and quality of life should also be included. Together, these data will help better to advice parents on which treatment to choose for their baby with a craniofacial malformation.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Pierre Robin / Obstrucción de las Vías Aéreas Tipo de estudio: Clinical_trials Límite: Humans / Infant Idioma: En Revista: Semin Fetal Neonatal Med Asunto de la revista: PEDIATRIA / PERINATOLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Pierre Robin / Obstrucción de las Vías Aéreas Tipo de estudio: Clinical_trials Límite: Humans / Infant Idioma: En Revista: Semin Fetal Neonatal Med Asunto de la revista: PEDIATRIA / PERINATOLOGIA Año: 2021 Tipo del documento: Article