唐氏综合征和自闭症谱系障碍的心理药理学治疗:研究现状和实践考虑。

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY American Journal of Medical Genetics Part C: Seminars in Medical Genetics Pub Date : 2023-12-01 Epub Date: 2023-10-23 DOI:10.1002/ajmg.c.32069
Nicole T Baumer, George Capone
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引用次数: 0

摘要

唐氏综合症(DS)或自闭症谱系障碍(ASD)患者,尤其是同时患有唐氏综合症和同时患有自闭症谱系疾病的患者 + ASD)通常表现出行为和精神症状,这些症状会影响生活质量,并增加护理人员的负担。虽然DS和ASD的主要治疗侧重于教育和行为治疗,但药物治疗可用于减轻症状负担。DS和DS缺乏证据,临床试验有限 + ASD。一些科学证据是可用的,主要是在开放标签研究和案例系列中,可以指导治疗选择。此外,临床决策通常是根据ASD患者的证据和经验推断出来的,或是根据无DS患者的智力残疾推断出来的。本文综述了DS、ASD和DS药物治疗的最新研究 + ASD,综述DS患者同时发生的神经发育和心理健康诊断 + ASD的整个寿命,并描述了精神药理学管理的实用方法。
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Psychopharmacological treatments in Down syndrome and autism spectrum disorder: State of the research and practical considerations.

Individuals with Down syndrome (DS) or Autism Spectrum Disorder (ASD), and especially those with both DS and co-occurring ASD (DS + ASD) commonly display behavioral and psychiatric symptoms that can impact quality of life and places increased burden on caregivers. While the mainstay of treatment in DS and ASD is focused on educational and behavioral therapies, pharmacological treatments can be used to reduce symptom burden. There is a paucity of evidence and limited clinical trials in DS and DS + ASD. Some scientific evidence is available, primarily in open label studies and case series that can guide treatment choices. Additionally, clinical decisions are often extrapolated from evidence and experience from those with ASD, or intellectual disability in those without DS. This article reviews current research in pharmacological treatment in DS, ASD, and DS + ASD, reviews co-occurring neurodevelopmental and mental health diagnoses in individuals with DS + ASD across the lifespan, and describes practical approaches to psychopharmacological management.

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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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