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Sleep related rhythmic movement disorder: phenotypic characteristics and treatment response in a paediatric cohort
1School of Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Insights
Sleep related rhythmic movement disorder (SR-RMD) significantly impacts children and families. Extended-release melatonin showed promise in improving symptoms and wellbeing.
Area of Science:
- Pediatric Neurology
- Sleep Medicine
- Developmental Pediatrics
Background:
- Limited research exists on sleep related rhythmic movement disorder (SR-RMD) in children.
- A systematic clinical evaluation was developed to enhance understanding and treatment of SR-RMD.
Purpose of the Study:
- To describe phenotypic and polysomnographic characteristics of pediatric SR-RMD.
- To evaluate the impact of SR-RMD on children and families.
- To assess treatment response in children with SR-RMD.
Main Methods:
- Retrospective chart review of 66 children diagnosed with SR-RMD.
- Utilized validated screening questionnaires for autism spectrum characteristics, behavior, and sensory profiles.
- Collected polysomnography data and standardized questionnaires on sleep quality and wellbeing.
Main Results:
- The study included children aged 0.9-16.3 years, with 51.5% having neurodevelopmental disorders, primarily autism spectrum disorder.
- High rates of behavioral disturbance and sensory processing differences were observed, impacting 72% of children and 75% of family members.
- Extended-release melatonin was prescribed to 52 children, with 24 out of 27 showing improvement.
Conclusions:
- SR-RMD imposes a substantial burden on child and family wellbeing.
- Novel findings include sensory processing differences in this population.
- Parent-reported therapeutic response to extended-release melatonin suggests a potential research avenue.
Objective:
To describe phenotypic, polysomnographic characteristics, impact, and treatment response in children with sleep related rhythmic movement disorder (SR-RMD).
Background:
There is limited research on SR-RMD. We have developed a systematic clinical evaluation of children with SR-RMD to improve understanding and treatment.
Methods:
A retrospective chart review of 66 children at a UK tertiary hospital. Baseline assessment included validated screening questionnaires to study autism spectrum characteristics, general behaviour and sensory profile. A standardised questionnaire assessed impact on sleep quality and daytime wellbeing of child and family. Polysomnography data were collated.
Results:
Children were aged 0.9-16.3 years (78.8% male). 51.5% had a neurodevelopmental disorder, most commonly autism spectrum disorder. High rates of behavioural disturbance and sensory processing differences were reported, not confined to children with neurodevelopmental disorders. Parents reported concerns about risk of injury, loss of sleep and persistence into adulthood. Daytime wellbeing was affected in 72% of children and 75% of other family members. Only 31/48 children demonstrated rhythmic movements during video-polysomnography, occupying on average 6.1% of time in bed. Most clusters occurred in the settling period but also arose from N1, N2 and REM sleep and wake after sleep onset. Melatonin was prescribed to 52 children, all but one were extended-release preparations. 24/27 children with available data were reported to improve with melatonin.
Conclusions:
SR-RMD places a significant burden on child and family wellbeing. Our novel findings of sensory processing differences in this population and parent reported therapeutic response to extended-release melatonin offer potential avenues for future research.
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