Development of consensus-based guidelines for managing communication of individuals with Rett syndrome. (2nd April 2020)

• Record Type: Journal Article
• Authors: Townend, Gillian S.; Bartolotta, Theresa E.; Urbanowicz, Anna; Wandin, Helena; Curfs, Leopold M.G.
• Is Part Of: Augmentative and alternative communication. Volume 36:Number 2(2020)
• Page Start: 71
• Page End: 81
• Publication Date: 2020-04-02
• Subjects: Augmentative and alternative communication -- clinical practice guidelines -- consensus-based guidelines -- Delphi survey -- expert consensus -- Rett syndrome; People with disabilities -- Means of communication -- Periodicals; Communication devices for people with disabilities -- Periodicals; 616.85503
• DOI: 10.1080/07434618.2020.1785009
• Languages: English
• ISSNs: 0743-4618

Abstract

Abstract: Difficulties with communication have a profound impact on the lives of individuals with Rett syndrome and their caregivers. Globally, many families report difficulty accessing appropriate and timely information and services from professionals with expertise in augmentative and alternative communication (AAC) as it pertains to Rett syndrome. To address this need, international consensus-based guidelines for managing the communication of individuals with Rett syndrome were developed by combining available evidence and lived experience with expert opinion. A two-phase Delphi survey was built on statements and recommendations extracted from a review of over 300 pieces of literature combined with survey responses from communication professionals and caregivers. All statements that reached a pre-determined threshold of ≥70% agreement were incorporated into guidelines that consist of 268 statements and recommendations relating to (a) rights of the individual; (b) beliefs and attitudes of communication partners; (c) professional knowledge and team work; (d) strategies to optimize engagement; (e) assessment; and (f) intervention (targets and goals, techniques), including the use of AAC. To date, this project is the largest of its kind, with 650 participants from 43 countries contributing to development of consensus-based guidelines for Rett syndrome.