4.2 Article

Consensus guidelines on managing Rett syndrome across the lifespan

Journal

BMJ PAEDIATRICS OPEN
Volume 4, Issue 1, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjpo-2020-000717

Keywords

neurology; genetics; syndrome; rehabilitation; gastroenterology

Categories

Funding

  1. International Rett Syndrome Foundation
  2. Rett Syndrome Research Trust
  3. NIH [U54 HD061222, U54 HD461222]
  4. Blue Bird Circle
  5. Children's Hospital Colorado Foundation Ponzio Family Chair in Neurology Research

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BackgroundRett syndrome (RTT) is a severe neurodevelopmental disorder with complex medical comorbidities extending beyond the nervous system requiring the attention of health professionals. There is no peer-reviewed, consensus-based therapeutic guidance to care in RTT. The objective was to provide consensus on guidance of best practice for addressing these concerns.MethodsInformed by the literature and using a modified Delphi approach, a consensus process was used to develop guidance for care in RTT by health professionals.ResultsTypical RTT presents early in childhood in a clinically recognisable fashion. Multisystem comorbidities evolve throughout the lifespan requiring coordination of care between primary care and often multiple subspecialty providers. To assist health professionals and families in seeking best practice, a checklist and detailed references for guidance were developed by consensus.ConclusionsThe overall multisystem issues of RTT require primary care providers and other health professionals to manage complex medical comorbidities within the context of the whole individual and family. Given the median life expectancy well into the sixth decade, guidance is provided to health professionals to achieve current best possible outcomes for these special-needs individuals.

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