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Twenty years of surveillance in Rett syndrome: what does this tell us?

BACKGROUND: The clinical characteristics of children diagnosed with Rett syndrome are well described. Survival and how these characteristics persist or change in adulthood are less well documented. This study aimed to describe overall survival and adult health in those with Rett syndrome. METHODS: U...

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Autores principales: Anderson, Alison, Wong, Kingsley, Jacoby, Peter, Downs, Jenny, Leonard, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078387/
https://www.ncbi.nlm.nih.gov/pubmed/24942262
http://dx.doi.org/10.1186/1750-1172-9-87
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author Anderson, Alison
Wong, Kingsley
Jacoby, Peter
Downs, Jenny
Leonard, Helen
author_facet Anderson, Alison
Wong, Kingsley
Jacoby, Peter
Downs, Jenny
Leonard, Helen
author_sort Anderson, Alison
collection PubMed
description BACKGROUND: The clinical characteristics of children diagnosed with Rett syndrome are well described. Survival and how these characteristics persist or change in adulthood are less well documented. This study aimed to describe overall survival and adult health in those with Rett syndrome. METHODS: Using the Kaplan-Meier method, we estimated survival of individuals registered with the Australian Rett syndrome Database (ARSD) who had been followed for up to 20 years (n = 396). We then conducted logistic and linear regression analyses investigating epilepsy, musculoskeletal, gastrointestinal, autonomic dysfunction and behaviour of individuals aged 18 years and over using cross sectional cohorts from the ARSD (n = 150) and the international database InterRett (n = 273). RESULTS: The likelihood of survival was 77.6% at 20 years, 71.5% at 25 years and 59.8% at 37 years. The median age of the combined cross-sectional cohort was 25 years (range 18 to 54 years), the majority (71%) were living in their parental home and the remainder being cared for in group homes or other institutions. Just over half walked either independently (18%) or with assistance (43%). The majority (86%) had scoliosis with 40% of those having undergone corrective surgery. Almost two-thirds (64%) of the women were taking anti-epileptic medications at the time of data collection. Constipation was highly prevalent (83%) and many experienced bloating (53%). Biliary dyskinesia, inflammation or infection of the gallbladder was reported for 20 women (5%) and of those 13 had undergone gallbladder surgery. Sleep disturbance was relatively common (63%), and adverse mood events and anxiety were slightly more prevalent in those aged 26-30 years in comparison to the younger and older age groups. Other frequently reported medical conditions included urinary tract infections, pneumonia and other respiratory conditions. CONCLUSIONS: Survival in Rett syndrome has now been estimated with the most accurate follow up to date. During adulthood, continuation of multidisciplinary services and programs is necessary to optimise health and wellbeing.
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spelling pubmed-40783872014-07-03 Twenty years of surveillance in Rett syndrome: what does this tell us? Anderson, Alison Wong, Kingsley Jacoby, Peter Downs, Jenny Leonard, Helen Orphanet J Rare Dis Research BACKGROUND: The clinical characteristics of children diagnosed with Rett syndrome are well described. Survival and how these characteristics persist or change in adulthood are less well documented. This study aimed to describe overall survival and adult health in those with Rett syndrome. METHODS: Using the Kaplan-Meier method, we estimated survival of individuals registered with the Australian Rett syndrome Database (ARSD) who had been followed for up to 20 years (n = 396). We then conducted logistic and linear regression analyses investigating epilepsy, musculoskeletal, gastrointestinal, autonomic dysfunction and behaviour of individuals aged 18 years and over using cross sectional cohorts from the ARSD (n = 150) and the international database InterRett (n = 273). RESULTS: The likelihood of survival was 77.6% at 20 years, 71.5% at 25 years and 59.8% at 37 years. The median age of the combined cross-sectional cohort was 25 years (range 18 to 54 years), the majority (71%) were living in their parental home and the remainder being cared for in group homes or other institutions. Just over half walked either independently (18%) or with assistance (43%). The majority (86%) had scoliosis with 40% of those having undergone corrective surgery. Almost two-thirds (64%) of the women were taking anti-epileptic medications at the time of data collection. Constipation was highly prevalent (83%) and many experienced bloating (53%). Biliary dyskinesia, inflammation or infection of the gallbladder was reported for 20 women (5%) and of those 13 had undergone gallbladder surgery. Sleep disturbance was relatively common (63%), and adverse mood events and anxiety were slightly more prevalent in those aged 26-30 years in comparison to the younger and older age groups. Other frequently reported medical conditions included urinary tract infections, pneumonia and other respiratory conditions. CONCLUSIONS: Survival in Rett syndrome has now been estimated with the most accurate follow up to date. During adulthood, continuation of multidisciplinary services and programs is necessary to optimise health and wellbeing. BioMed Central 2014-06-19 /pmc/articles/PMC4078387/ /pubmed/24942262 http://dx.doi.org/10.1186/1750-1172-9-87 Text en Copyright © 2014 Anderson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Anderson, Alison
Wong, Kingsley
Jacoby, Peter
Downs, Jenny
Leonard, Helen
Twenty years of surveillance in Rett syndrome: what does this tell us?
title Twenty years of surveillance in Rett syndrome: what does this tell us?
title_full Twenty years of surveillance in Rett syndrome: what does this tell us?
title_fullStr Twenty years of surveillance in Rett syndrome: what does this tell us?
title_full_unstemmed Twenty years of surveillance in Rett syndrome: what does this tell us?
title_short Twenty years of surveillance in Rett syndrome: what does this tell us?
title_sort twenty years of surveillance in rett syndrome: what does this tell us?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078387/
https://www.ncbi.nlm.nih.gov/pubmed/24942262
http://dx.doi.org/10.1186/1750-1172-9-87
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