Autism spectrum disorders

自闭症谱系障碍
  • 文章类型: Journal Article
    背景:引入了产前和围产期预测因子的星座作为自闭症谱系障碍(ASD)的预测因子,然而,西方缺乏关于这些预测因子的方向和强度的信息,伊朗。本研究旨在确定该地区儿童ASD的产前和围产期预测因素。
    方法:这项病例对照研究在哈马丹进行,伊朗西部,2022年1月至3月。该研究包括100名自闭症儿童,他们将自闭症中心称为病例组。选择来自卫生服务中心注册系统的100名无ASD儿童作为对照组,并按年龄和居住地与病例相匹配(1:1)。专家小组制定了有关ASD的产前和围产期预测因素的结构化问卷。问卷是通过采访孩子的母亲来进行的。
    结果:男孩性别(OR:3.51,95%CI:1.74-7.10,p值<0.001),小于胎龄(SGA)(3.92,1.64-9.39,0.002),在多变量分析中,母体糖尿病(3.51,1.03~24.95,0.04)和精神障碍家族史(3.64,1.18~11.27,0.04)被确定为显著的预测因子.
    结论:我们的研究强调了筛查和监测男孩ASD的重要性,那些有SGA历史的人,来自有糖尿病史和精神障碍家族史的母亲。提出复制发现强调了进行更大样本量研究的必要性。
    BACKGROUND: The constellation of pre and perinatal predictors are introduced as predictor for autism spectrum disorders (ASD), however, the information about the direction and strength of these predictors are lacking in Western, Iran. The current study aimed to determine the pre and perinatal predictors of ASD among children in this region.
    METHODS: This case-control study was conducted in Hamadan, Western Iran during January to March 2022. The study included 100 children with ASD who referred to the autism center as case group. Hundred children without ASD from registration system of health service centers were selected as control group and were matched (1:1) to cases by age and place of residency. A structured questionnaire about pre and perinatal predictors of ASD was developed by an expert panel. The questionnaire was administered by interviewing the mothers of children.
    RESULTS: Boy gender (OR: 3.51, 95% CI: 1.74-7.10, p-value < 0.001), small for gestational age (SGA) (3.92, 1.64-9.39, 0.002), maternal diabetes (3.51, 1.03-24.95, 0.04) and family history of mental disorders (3.64, 1.18-11.27, 0.04) were identified as significant predictors in a multivariable analysis.
    CONCLUSIONS: Our study emphasizes on the importance of screening and monitoring for ASD in the boys, those with history of SGA, from mothers with history of diabetes and with family history of mental disorders. Proposing the replication of findings emphasizes the necessity of conducting studies with larger sample sizes.
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  • 文章类型: Journal Article
    非典型惯用手的患病率较高(非右撇子或左撇子-,与其他类型的发育障碍患者相比,在被诊断为自闭症谱系障碍(ASD)的个体中反复报道了混合手优势)。然而,这种差异的确切大小以及可能的影响因素仍然未知.这项研究的主要目的是了解护理人员对患有发育障碍的孩子的惯用手的印象及其与使用手偏好量表评估孩子的关系。
    本研究的样本是来自两个国家的1116名发育障碍个体,来自伊朗的541人(51.5%)和来自伊拉克库尔德斯坦地区(KRI)的575人(48.5%)。根据父母报告并使用标准化量表(手偏好演示测试“HPDT”)评估样品的惯用性。
    护理人员对其家属的惯用手能力的报告与有效的手偏好量表的应用之间存在统计学上的显着差异,它们不一定重叠。根据看护者的报告,惯用手与发育障碍类型之间存在统计学上的显着关系,与根据看护者的报告有ID的人相比,患有ASD的人是非右撇子。因此,当应用HDTP作为诊断量表时,ASD组和ID组之间没有看到类似的差异。虽然ASD和ID组的左撇子相似(23-24%),ASD组的混合习惯为38%,而ID组为33%.
    手偏好演示测试(HPDT)是确定患有ASD和ID的个体的手偏好的有效方法。结论是,父母对ASD的手偏爱后代的报告需要通过量表的应用来批准,并且护理人员和专业人员需要更多地了解早期运动症状,例如惯用手。进一步的研究应侧重于惯用手在不同发育障碍儿童的精细运动技能和眼手协调发展中的作用以及这些不同障碍之间的差异。
    UNASSIGNED: A higher rate of atypical handedness prevalence (non-right-handedness or left-, mixed-hand dominance) has been recurrently reported in individuals diagnosed with autism spectrum disorder (ASD) compared to individuals with other types of developmental disabilities. However, the exact magnitude of this difference as well as the presence of possible contributing factors remained unknown. The main aim of this study was to understand caregivers\' impression of the handedness of their child with developmental disabilities and its relationship with assessments of the child using a hand preference scale.
    UNASSIGNED: The sample of the present study was 1116 individuals with developmental disabilities from two countries, 541 (51.5%) individuals from Iran and 575 (48.5%) individuals from the Kurdistan Region of Iraq (KRI). The handedness of the sample was evaluated based on the parental report and utilizing a standardized scale (The Hand-Preference Demonstration Test \"HPDT\").
    UNASSIGNED: There was a statistically significant difference between caregivers\' reports on their dependents\' handedness and the application of a valid hand preference scale and they do not necessarily overlap. There was a statistically significant relationship between handedness and type of developmental disabilities based on caregivers\' reports and individuals with ASD were more non-right-handed compared to individuals with ID based on the caregivers\' report. Hence similar difference was not seen between the ASD and ID groups when HDTP was applied as a diagnostic scale. While left-handedness in the ASD and ID group was similar (23-24%), mixed-handedness in the ASD group was 38% compared to 33% in the ID group.
    UNASSIGNED: The Hand-Preference Demonstration Test (HPDT) was a valid way to determine the hand preference of individuals with ASD and ID. It is concluded that parental reports on their offspring with ASD\'s hand preference need to be approved through the application of a scale and caregivers and professionals need to be more aware of early motor symptoms such as handedness. Further research should focus on the role of handedness in the development of fine motor skills and eye-hand coordination in children with differing developmental disabilities and variations among those differing impairments.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    自闭症谱系障碍(ASDs)是一组发育障碍,其特征是社交交际技能不足以及重复和/或刻板行为的发生。Coffin-Siris综合征(CSS)的典型特征是第五指骨远端指骨或指甲的发育不全或发育不全,不同程度的发育或认知延迟,独特的面部特征,低张力,多毛症/多毛症,和稀疏的头皮头发。在这项研究中,我们详细描述了一名诊断为CSS的男孩的自闭症特征,并进一步讨论了他们的遗传背景。
    一个患有ASD的8岁男孩,先天性异常,在基因检测后,神经系统问题被诊断为Coffin-Siris综合征。遗传检测揭示了ARID1B基因中的杂合的从头致病变异(5类)c.1638_1647del,该变异是Coffin-Siris综合征的病因,也是其他智力障碍(ID)相关疾病的病因,包括自闭症。诊断之前的测试,以及先天性异常和发育问题,进一步描述,试图更好地呈现他的表型。
    自闭症和与ARID1B相关的疾病都在一个范围内。本报告指出了进一步研究这些疾病的遗传背景以了解其复杂病因的重要性和必要性。
    UNASSIGNED: Autism spectrum disorders (ASDs) are a group of developmental disorders characterized by deficits in social communicative skills and the occurrence of repetitive and/or stereotyped behaviors. Coffin-Siris syndrome (CSS) is classically characterized by aplasia or hypoplasia of the distal phalanx or nail of the fifth and additional digits, developmental or cognitive delay of varying degrees, distinctive facial features, hypotonia, hirsutism/hypertrichosis, and sparse scalp hair. In this study, we present a detailed description of autistic traits in a boy diagnosed with CSS and further discuss their genetic backgrounds.
    UNASSIGNED: An 8-year-old boy with ASD, congenital anomalies, and neurological problems had been diagnosed with Coffin-Siris syndrome after genetic testing. Genetic testing revealed a heterozygous de novo pathogenic variant (class 5) c.1638_1647del in the ARID1B gene that is causative of Coffin-Siris syndrome but also other intellectual disability (ID)-related disorders, including autism. Tests that preceded the diagnoses, as well as congenital anomalies and developmental issues, were further described in an attempt to better present his phenotype.
    UNASSIGNED: Both autism and ARID1B-related disorders are on a spectrum. This report points out the importance and necessity of further research regarding the genetic backgrounds of these disorders to understand their complex etiology.
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  • 文章类型: Journal Article
    这项研究的目的是确定自闭症谱系障碍儿童的增强现实是否是基于证据的实践。为此,进行了系统的文献综述,以确定实施增强现实的研究.该审查遵循了系统审查和荟萃分析(PRISMA)指南的首选报告项目。作为审查的结果,使用质量指标分析了9项符合纳入标准的单病例实验设计(SCED)研究.在质量评估结束时,通过使用Tau-U计算了8项SCED研究的效果大小,这些研究被确定为具有强大或足够质量的证据。研究结果表明,增强现实在为自闭症谱系障碍儿童教授新技能方面是一种有前途且非常有效的干预措施(TauU=0.98)。
    The purpose of this study was to determine whether the augmented reality in children with autism spectrum disorder is an evidence-based practice. For this purpose, a systematic literature review was conducted for determining research that implemented the augmented reality. The review followed the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. As a result of the review, nine single-case experimental design (SCED) research that met the inclusion criteria were analyzed using the quality indicators. At the end of the quality evaluation, the effect size of eight SCED research that were determined to have evidence of a strong or adequate quality was calculated by using Tau-U. The results of the study revealed that the augmented reality was a promising and highly effective intervention (Tau U = 0.98) in teaching new skills for children with autism spectrum disorder.
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  • 文章类型: Journal Article
    背景:安乐死审查委员会(RegionaleToetsingscommissiesEuthanasie,RTE)审查所有荷兰安乐死和医生协助自杀(EAS)的案例,以审查是否符合六个法律“应有的照顾”标准,包括“无法忍受的痛苦,没有改善的前景”。如果智力障碍或自闭症谱系障碍(ASD)的人提出EAS要求,则存在显着的复杂性和道德困境。
    目的:描述被授予EAS请求的智障和/或ASD患者的特征和情况;调查导致EAS请求的痛苦的主要原因;并检查医生对请求的回应。
    方法:搜索了927例EAS病例报告(2012-2021)的在线RTE数据库中的智障和/或ASD患者(n=39)。对这些病例报告进行了归纳主题内容分析,使用框架方法。
    结果:与智力障碍和/或ASD直接相关的因素是21%病例中描述的痛苦的唯一原因,也是42%病例中的主要促成因素。EAS请求的原因包括社会孤立和孤独(77%),缺乏韧性或应对策略(56%),缺乏灵活性(僵化的思维或难以适应变化)(44%)和对刺激过度敏感(26%)。在三分之一的案例中,医生指出,由于ASD和智力残疾无法治疗,因此没有改善的前景。
    结论:对与终身残疾相关的痛苦的社会支持的检查,以及围绕这些因素的可接受性的辩论,作为授予EAS的理由,具有国际重要性。
    BACKGROUND: Euthanasia review committees (Regionale Toetsingscommissies Euthanasie, RTE) scrutinise all Dutch cases of euthanasia and physician-assisted suicide (EAS) to review whether six legal \'due care\' criteria are met, including \'unbearable suffering without prospect of improvement\'. There are significant complexities and ethical dilemmas if EAS requests are made by people with intellectual disabilities or autism spectrum disorders (ASD).
    OBJECTIVE: To describe the characteristics and circumstances of people with intellectual disabilities and/or ASD who were granted their EAS request; investigate the main causes of suffering that led to the EAS request; and examine physicians\' response to the request.
    METHODS: The online RTE database of 927 EAS case reports (2012-2021) was searched for patients with intellectual disabilities and/or ASD (n = 39). Inductive thematic content analysis was performed on these case reports, using the framework method.
    RESULTS: Factors directly associated with intellectual disability and/or ASD were the sole cause of suffering described in 21% of cases and a major contributing factor in a further 42% of cases. Reasons for the EAS request included social isolation and loneliness (77%), lack of resilience or coping strategies (56%), lack of flexibility (rigid thinking or difficulty adapting to change) (44%) and oversensitivity to stimuli (26%). In one-third of cases, physicians noted there was \'no prospect of improvement\' as ASD and intellectual disability are not treatable.
    CONCLUSIONS: Examination of societal support for suffering associated with lifelong disability, and debates around the acceptability of these factors as reasons for granting EAS, are of international importance.
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  • 文章类型: Journal Article
    未经批准:尽管等待时间很长,公共儿科发育评估服务对于评估儿童仍然至关重要。评估是一个重要的机会,可以指导支持的放置以改善结果。很少有研究检查临床评估服务如何进行评估,提交结果并向家庭写报告。这项研究检查了发展评估服务机构提供给护理人员的85份报告。评估报告是否(1)满足了护理人员感知的需求,(2)利用现有数据提供有关儿童需求的适当信息,(3)提供可操作和具体需求的建议,(4)具有适当的可读性水平,(5)遵循现有的自闭症评估指南。研究结果表明,临床医生更专注于自闭症的诊断需求,而护理人员更专注于非诊断需求。与自闭症诊断相关的建议是可行的,但是他们很少解决诸如认知障碍或心理健康之类的合并症。例如,只有13%的报告包含自闭症谱系障碍以外的其他疾病的建议,尽管61%的人接受了两种或两种以上的诊断。报告主要遵循自闭症评估指南,但是家庭使用的语言比建议的要复杂。提供了对未来实践的建议,以便可以考虑如何提高参加服务的家庭报告的质量和有效性。
    Despite long wait times, public paediatric developmental assessment services remain crucial for assessment of children. Assessment is a critical opportunity to guide the placement of supports to improve outcomes. There is little research examining how clinical assessment services conduct their assessments, present results and write reports to families. This study examined 85 reports provided to caregivers at a developmental assessment service. Reports were evaluated for whether they (1) addressed caregiver perceived needs, (2) used available data to provide appropriate information about child needs, (3) provided recommendations that were actionable and specific to needs, (4) had appropriate readability levels and (5) followed existing autism assessment guidelines. Findings showed clinicians were more focused on autism diagnostic needs while caregivers were more focused on non-diagnostic needs. Recommendations related to autism diagnoses were actionable, but they rarely addressed comorbidities such as cognitive impairments or mental health. For instance, only 13% of reports contained recommendations for conditions other than autism spectrum disorder, despite 61% of the population receiving two or more diagnoses. Reports largely followed autism assessment guidelines, but the language used was more complex for families than recommended. Recommendations for future practice are provided so that consideration may be given to how to improve the quality and effectiveness of reports for families attending services.
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  • 文章类型: Journal Article
    本报告试图提出与在低收入和中等收入地区为自闭症谱系障碍(ASD)患者建立医疗保健服务相关的挑战。已强调的特定案例是建立日托服务,重点是为ASD患者提供康复和培训服务,以及他们的照顾者和家庭成员,伊拉克库尔德斯坦地区(KRI)根据我的经验,相关的挑战分为三个主要层面:个人、专业,和组织。该报告强调了理解与建立医疗保健服务相关的挑战并希望将其控制的重要性。另外,了解具有ASD经验的个人的医疗服务的文化方面,以解决共享的每个级别的问题。在报告的最后部分得出结论,建立医疗保健质量的关键是了解个人对医疗保健的态度,专业,和组织层面。这种态度决定了对服务的期望,并定义了寻求援助的行为。结果为医疗保健领域的利益相关者提供了洞察力,允许更好地理解和改善可用性和获得质量驱动的医疗保健服务。实行职前和在职培训方法,以解决在KRI中建立个人级别的医疗保健服务的相关挑战。类似的政策可能适用于其他LMIC,那里缺乏专业和熟练的医疗保健服务提供商。
    The present report from the field tries to present challenges associated with establishing healthcare services for individuals with autism spectrum disorders (ASD) in a low- and middle-income area. The given case that has been highlighted is establishing daycare services focusing on rehabilitation and training services for individuals with ASD, and their caregivers and family members, in the Kurdistan Region of Iraq (KRI). Based on my experience, the associated challenges are divided into three primary levels: personal, professional, and organizational. The report highlights the importance of understanding the challenges associated with establishing healthcare services with the desire to put them under control. Plus, understanding the cultural aspects of the healthcare services for individuals with ASD experiences to address the issues at each level shared. It is concluded in the final part of the report that the key to establishing healthcare quality is to understand attitudes toward healthcare at the personal, professional, and organizational levels. This attitude determines the expectation from the services and defines assistance-seeking behaviors. Results offer insight for stakeholders in the healthcare field, allowing for a better understanding and improvement of availability and access to quality-driven healthcare services. A pre- and in-service training approach is practiced to address the associated challenges of establishing healthcare services at the personal level in KRI. A similar policy might be applicable in other LMICs, where there is a lack of professional and skillful healthcare service providers.
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  • 文章类型: Journal Article
    (1)背景:“自我形象”(IOS)是最近开发和评估的15个疗程的艺术治疗计划,以减少“自我意识”中的困难,\'情绪调节\',\'灵活性\',和被诊断患有自闭症谱系障碍(ASD)的儿童的“社会行为”。在本文中,探讨儿童行为的变化是否与治疗师在IOS和15周后的行为相对应。(2)方法:在重复的案例研究设计中,12名儿童和7名治疗师参加了会议。艺术治疗师通过应用两种观察工具来监测自己和孩子的行为:OAT(在艺术治疗中观察自闭症儿童)和EAT(评估与自闭症儿童一起工作时的艺术治疗师行为)。在节目的三个时刻,儿童在艺术创作过程中的行为与治疗师的行为进行了单独和集体比较。(3)结果:考虑到所有OAT分量表,在治疗结束时和治疗后15周,十二个儿童中有十个表现出实质性或中度的积极行为变化。“社会行为”的改善脱颖而出。中途治疗艺术治疗师最突出的表现是对“情绪调节”的支持,\'灵活性\',和“社会行为”。无法确定儿童行为变化与治疗师行为之间的明确一对一关系。(4)结论:该研究通过监测儿童和治疗师的行为,为AT治疗过程提供了新的见解。艺术创作本身和艺术治疗三角形(儿童,艺术创作,治疗师)提供机会来提高孩子的言语和非言语沟通技巧。
    (1) Background: \'Images of Self\' (IOS) is a recently developed and evaluated art therapy program of 15 sessions to reduce difficulties in \'sense of self\', \'emotion regulation\', \'flexibility\', and \'social behavior\' of children diagnosed with Autism Spectrum Disorders (ASD). In this paper, it is explored whether change in the child\'s behaviors corresponds to the therapist\'s actions during IOS and 15 weeks later. (2) Method: In a repeated case study design, twelve children and seven therapists participated. Art therapists monitored their own and the children\'s behavior by applying two observation instruments: the OAT (Observation of a child with autism in Art Therapy) and EAT (Evaluation of Art Therapist\'s behavior when working with a child with autism). Child behaviors during art making were-individually and as a group-compared with therapist\'s actions at three moments during the program. (3) Results: Ten of twelve children showed a substantial or moderate positive behavior change considering all OAT subscales at the end of the program and 15 weeks after treatment. Improvement of \'social behavior\' stood out. Halfway treatment art therapists most prominently showed support of \'emotion regulation\', \'flexibility\', and \'social behavior\'. Clear one-on-one relationships between changes in children\'s behavior and actions of therapists could not be identified. (4) Conclusion: The study provides new insights in the AT treatment process by monitoring children\'s and therapists\' behavior. The art making itself and the art therapy triangle (child, art making, therapist) offer opportunities to improve verbal and nonverbal communication skills of the child.
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  • 文章类型: Journal Article
    快速的技术进步,ASD患者的特征及其对技术的兴趣有望通过各种技术干预措施向自闭症谱系障碍(ASD)患者提供社交技能。机器人干预就是其中之一。然而,尽管机器人技术经常与ASD患者一起使用,关于社交技能指导和方法的评论数量有限。本研究旨在对单案例实验设计进行全面的描述性分析,其中向患有ASD的个人指导社交技能,并将社交机器人作为独立变量。
    在同行评审的期刊上发表的13个单案例实验设计,其中使用社交机器人向患有ASD的个人传授社交技能,并根据以下五个类别进行了全面的描述性分析:(a)关键特征,(b)方法特点,(c)调查结果,(d)数据分析,和(E)单例实验设计中的关键参数。
    社交机器人通常有效地指导社交技能。几种社交技能(例如,眼神交流,社交互动,简单的问候)在研究中得到了指导。通常使用人形机器人和NAO。研究数据主要进行统计学分析。在单例实验设计中,基于基本参数的研究存在几个问题。
    本研究中的研究在几个方面有所不同(例如,结果,数据分析,和因变量)。因此,在社交技能的教学中,仍然需要进行一些机器人研究。这项研究将为目前在教室中使用机器人但不知道在教学中使用哪些技能以及如何在功能上使用它们的教师提供指导,因为它显示了机器人的应用研究。这项研究的结果将表明,与ASD儿童一起工作的实施者可以在康复环境中使用技术工具,教师可以在他们的机器人中占据一席之地,对自闭症儿童进行干预,给他们不同的视角。可以看出,自闭症儿童的教育不仅是1:1,而且与人类,但是机器人也可以提供教育。这样,技术在教学中的力量将变得更加清晰。尤其是在康复方面。最后,这项研究将为教学提供新的选择,特别是对于旨在教授社交技能的教师,并使他们有机会全面检查这些学科的不同研究过程。
    UNASSIGNED: The rapid technological advances, the traits of individuals with ASD and their interest in technology are promising for the instruction of social skills to individuals with autism spectrum disorder (ASD) using various technological interventions. Robotic interventions are among these. However, although robotics is frequently used with individuals with ASD, there is a limited number of reviews on social skills instruction and methods. The present study aimed to conduct a comprehensive descriptive analysis on single-case experimental designs where social skills were instructed to individuals with ASD and social robots were included as independent variables.
    UNASSIGNED: Thirteen single-case experimental designs published in peer-reviewed journals in which social skills were taught to individuals with ASD using social robots were reviewed with a comprehensive descriptive analysis based on five categories: (a) key characteristics, (b) methodological characteristics, (c) findings, (d) data analysis, and (e) key parameters in single-case experimental designs.
    UNASSIGNED: Social robots are generally effective in the instruction of social skills. Several social skills (e.g., making eye contact, social interaction, simple greetings) were instructed in the studies. Humanoid robots and NAO were used generally. The study data were predominantly analyzed statistically. There were several problems in research based on the basic parameters in single-case experimental designs.
    UNASSIGNED: The researches in this study differ in several respects (e.g., results, data analysis, and dependent variable). Thus, there is still a need for several robotics studies in the instruction of social skills. IMPLICATIONS FOR REHABILITATIONThis study will be a guide for teachers who currently use robots in their classrooms but do not know which skills to use in teaching and how to use them functionally, as it shows applied research with robots.The findings of this research will show implementers working with children with ASD that technological tools can be used in rehabilitation environments, and that teachers can take a place in their robots in interventions for children with ASD, giving them a different perspective.It will be seen that the education of children with ASD is not only 1:1 and with humans, but robots can also provide education. In this way, the power of technology in teaching will become clearer. Especially in rehabilitation.Finally, this research will offer new options in teaching especially for teachers who aim at teaching social skills and will give them the opportunity to comprehensively examine the processes of different studies on these subjects.
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