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Recommendations for neuroradiological examinations in children living with achondroplasia: a European Society of Pediatric Radiology and European Society of Neuroradiology opinion paper.
Wright, Jenny; Cheung, Moira; Siddiqui, Ata; Lucas, Jonathan; Calder, Alistair; Argyropoulou, Maria I; Arthurs, Owen J; Caro-Dominguez, Pablo; Thompson, Dominic; Severino, Mariasavina; D'Arco, Felice.
Afiliação
  • Wright J; Department of Radiology, Manchester University NHS Foundation Trust, Oxford Road, Manchester, M13 9WL, UK. drjennywright@doctors.org.uk.
  • Cheung M; Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, Great Ormond Street, London, UK.
  • Siddiqui A; Department of Neuroradiology, Guy's and Saint Thomas' NHS Foundation Trust, London, UK.
  • Lucas J; Paediatric Spinal Surgery, Evelina London Children's Hospital, London, UK.
  • Calder A; Department of Radiology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Argyropoulou MI; NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK.
  • Arthurs OJ; Department of Clinical Radiology and Imaging, Medical School, University of Ioannina, Ioannina, Greece.
  • Caro-Dominguez P; Department of Radiology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Thompson D; NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK.
  • Severino M; Unidad de Radiologia Pediatrica, Servicio de Radiologia, Hospital Universitario Virgen del Rocio, Seville, Spain.
  • D'Arco F; Department of Paediatric Neurosurgery, Great Ormond Street Hospital for Children NHS Foundation Trust, Great Ormond Street, London, UK.
Pediatr Radiol ; 53(12): 2323-2344, 2023 11.
Article em En | MEDLINE | ID: mdl-37674051
ABSTRACT
Children living with achondroplasia are at an increased risk of developing neurological complications, which may be associated with acute and life-altering events. To remediate this risk, the timely acquisition of effective neuroimaging that can help to guide clinical management is essential. We propose imaging protocols and follow-up strategies for evaluating the neuroanatomy of these children and to effectively identify potential neurological complications, including compression at the cervicomedullary junction secondary to foramen magnum stenosis, spinal deformity and spinal canal stenosis. When compiling these recommendations, emphasis has been placed on reducing scan times and avoiding unnecessary radiation exposure. Standardized imaging protocols are important to ensure that clinically useful neuroimaging is performed in children living with achondroplasia and to ensure reproducibility in future clinical trials. The members of the European Society of Pediatric Radiology (ESPR) Neuroradiology Taskforce and European Society of Neuroradiology pediatric subcommittee, together with clinicians and surgeons with specific expertise in achondroplasia, wrote this opinion paper. The research committee of the ESPR also endorsed the final draft. The rationale for these recommendations is based on currently available literature, supplemented by best practice opinion from radiologists and clinicians with subject-specific expertise.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Radiologia / Acondroplasia Tipo de estudo: Guideline Limite: Child / Humans / Infant Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Radiologia / Acondroplasia Tipo de estudo: Guideline Limite: Child / Humans / Infant Idioma: En Ano de publicação: 2023 Tipo de documento: Article