Consensus guidelines on managing Rett syndrome across the lifespan

Author:

Fu Cary,Armstrong Dallas,Marsh Eric,Lieberman David,Motil Kathleen,Witt Rochelle,Standridge Shannon,Nues Paige,Lane Jane,Dinkel Tristen,Coenraads Monica,von Hehn Jana,Jones Mary,Hale Katie,Suter Bernhard,Glaze Daniel,Neul Jeffrey,Percy Alan,Benke TimothyORCID

Abstract

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.

Funder

Blue Bird Circle

International Rett Syndrome Foundation

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Rett Syndrome Research Trust

Children's Hospital Colorado Foundation

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

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