Sleep Disturbance in Children with Fetal Alcohol Spectrum Disorder and the Relationship to the Neurodevelopmental Profile

被引:1
|
作者
O'Rourke, Claudia [1 ,2 ]
Horne, Rosemary S. C. [2 ,3 ]
Nixon, Gillian M. [3 ]
Harris, Katrina R. [1 ]
Connelly, Annette [1 ]
Crichton, Alison [1 ,2 ]
机构
[1] Monash Hlth, Monash Childrens Hosp, Victorian Fetal Alcohol Serv, Dev Pediat, Melbourne, Australia
[2] Monash Univ, Dept Pediat, Melbourne, Australia
[3] Monash Hlth, Melbourne Childrens Sleep Ctr, Monash Childrens Hosp, Melbourne, Australia
来源
关键词
FASD; fetal alcohol; sleep; sleep disturbance scale for children; BEHAVIOR; EXPOSURE;
D O I
10.1097/DBP.0000000000001282
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Objective: Sleep disturbance is an important feature of fetal alcohol spectrum disorder (FASD). We sought to describe sleep patterns in school-aged children with FASD, in comparison with a typically developing community group, and investigate the relationship between sleep and neurodevelopmental profiles. Method: The FASD cohort (N = 36) was recruited from a tertiary Australian FASD diagnostic center, and the typically developing group (N = 36) was previously recruited as a control cohort for a separate study. Sleep disturbance was assessed with the caregiver-completed Sleep Disturbance Scale for Children (SDSC) questionnaire. Neurodevelopmental assessment results for the 10 domains impaired in FASD were used for correlations with sleep disturbance. Results: In the FASD group, 80% of children scored above the SDSC cutoff, compared with 22% of the control group (p < 0.001). Statistically significant group differences were seen for all 6 subscales of the SDSC (p < 0.05). The most frequently affected domains in the FASD group related to difficulties with initiating and maintaining sleep (58%), sleep-wake transition disorders (44%), and disorders of arousal (42%). A statistically significant relationship was not found between sleep and the severity of neurodevelopmental impairment or impairment of a particular domain, acknowledging the limitations of our small sample size. Half of the FASD sample (52%) were taking a pharmaceutical agent to support sleep, which was not associated with lower SDSC scores. Conclusion: In this small study, sleep disturbances were frequently reported by carers of children with FASD, independent of the severity of their neurodevelopmental impairments. Persistent sleep disturbance despite the use of sleep medications highlights the need for prospective studies exploring sleep interventions in this population. Integration of behavioral sleep medicine into management is recommended for all children with FASD.
引用
收藏
页码:E358 / E364
页数:7
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