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Editorial 社论
IF 1.2 Q3 Medicine Pub Date : 2020-03-26 DOI: 10.1108/aia-04-2020-055
E. Chaplin, J. McCarthy
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引用次数: 0
Editorial 社论
IF 1.2 Q3 Medicine Pub Date : 2019-12-13 DOI: 10.1108/aia-01-2020-054
E. Chaplin, J. McCarthy
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引用次数: 0
Why caregivers discontinue applied behavior analysis (ABA) and choose communication-based autism interventions 为什么照顾者停止应用行为分析(ABA)而选择基于沟通的自闭症干预
IF 1.2 Q3 Medicine Pub Date : 2019-11-06 DOI: 10.1108/aia-02-2019-0004
Henny Kupferstein
PurposeThe purpose of this paper is to explore why autistic people and their caregivers choose interventions other than applied behavior analysis (ABA), and how their decision impacts them over their lifespan. The focus group was divided into those who pursued augmentative and alternative communication (AAC)-based supports, received ABA, selected other interventions or received no intervention at all. The reported posttraumatic stress symptoms (PTSS) of ABA recipients were compared to non-ABA recipients in order to evaluate the long-term impacts of all intervention types. Using a mixed-method thematic analysis, optional comments submitted alongside a quantitative online survey were reviewed for emergent themes. These comments augmented the survey Likert scores with a qualitative impression of the diverse intervention-related attitudes among participants. Investigating the lived experiences of autism intervention recipients illuminated the scope of the long-term impacts of each intervention that was chosen. Overall, autistics who received no intervention fared best, based on the lowest reported PTSS. These findings may inform the potential redesign of autism interventions based on the firsthand reported experiences and opinions of autistics.Design/methodology/approachThe aim of this study was to conduct research that is both question-driven and data-driven to aid in the analysis of existing data (Van Helden, 2013). In the research question-driven approach, the independent variables were the intervention type and duration of exposure relative to lifespan; the dependent variables were the PTSS severity score and binary indicator of meeting PTSS criteria. The analyses that were conducted included linear regression analyses of severity score on intervention type and duration, and χ2 tests for independence of the probabilities of PTSS criterion satisfaction and intervention type. This experiment was designed to test the data-driven hypothesis that the prevalence and severity of PTSS are dependent on the type of autism intervention and duration of exposure. After reviewing the primary data set, the data-driven inquiry determined that the sample for secondary analysis should be categorized by communication-based vs non-communication-based intervention type in order to best complement the limitations and strengths of the published findings from the primary analysis.FindingsAutistics who received no intervention had a 59 percent lower likelihood of meeting the PTSS criteria when compared to their ABA peers, and they remained 99.6 percent stable in their reported symptoms throughout their lifespan (R2=0.004). ABA recipients were 1.74 times more likely to meet the PTSS criteria when compared to their AAC peers. Within the 23 percent who selected an intervention other than ABA, consisting of psychotherapy, mental health, son-rise and other varying interventions, 63 percent were asymptomatic. This suggests that the combined benefits of communication-
目的探讨自闭症患者及其照顾者选择应用行为分析(ABA)之外的干预措施的原因,以及他们的决定如何影响他们的一生。焦点小组分为寻求辅助和替代沟通(AAC)为基础的支持,接受ABA,选择其他干预或根本不接受干预。为了评估所有干预类型的长期影响,将ABA接受者报告的创伤后应激症状(PTSS)与非ABA接受者进行比较。使用混合方法的主题分析,可选的意见与定量在线调查一起提交,以审查紧急主题。这些评论增加了调查李克特得分与参与者之间的不同干预相关态度的定性印象。调查自闭症干预接受者的生活经历,阐明了所选择的每种干预措施的长期影响范围。总的来说,根据最低的ptsd报告,没有接受干预的自闭症患者表现最好。这些发现可能为基于第一手报道的自闭症经验和观点的自闭症干预措施的重新设计提供信息。设计/方法/方法本研究的目的是进行问题驱动和数据驱动的研究,以帮助分析现有数据(Van Helden, 2013)。在研究问题驱动法中,自变量为相对于寿命的干预类型和暴露持续时间;因变量为PTSS严重程度评分和满足PTSS标准的二元指标。进行的分析包括严重程度评分对干预类型和持续时间的线性回归分析,以及PTSS标准满意度概率与干预类型独立性的χ2检验。本实验旨在验证数据驱动的假设,即ptsd的患病率和严重程度取决于自闭症干预的类型和暴露时间。在审查了主要数据集之后,数据驱动的调查确定了用于二次分析的样本应按基于通信的干预类型与非基于通信的干预类型进行分类,以便最好地补充来自主要分析的已发表结果的局限性和优势。研究发现,与ABA患者相比,未接受干预的自闭症患者达到PTSS标准的可能性低59%,并且在其一生中报告的症状保持99.6%的稳定性(R2=0.004)。ABA接受者与AAC同龄人相比,达到PTSS标准的可能性高出1.74倍。23%的人选择了ABA以外的干预措施,包括心理治疗、心理健康、儿子崛起和其他不同的干预措施,其中63%是无症状的。这表明,基于沟通的干预与行为主义影响的ABA实践的综合效益可能有助于提高生活质量。虽然不能概括出本研究的范围,但从数据中可以看出,没有接受任何干预的自闭症患者在他们的一生中表现最好。研究的局限性/意义二次分析的明显优势是揭示初步研究中可能被忽视的关键发现。初步数据中遗漏的变量使研究人员对至关重要的发现缺乏经验,这可能会通过后续研究中的后续测试来减轻(Cheng和Phillips, 2014, p. 374)。复制了初级分析中所有变量的频率表和交叉表。现有数据的二次分析是从原始研究中使用的设计变量进行的,并应用于二次分析,以产生较少偏差的估计(Lohr, 2010;格劳巴德和科恩,1996)。每个干预组的纳入标准,PTSS评分和暴露时间,继承自最初的分析,以便对与AAC和PTSS有关的核心变量的编码进行战略性判断。460名受访者的数据样本减少到非aba组n=330。外部统计学家对每个被调查者进行评分,并使用Cohen 's κ系数(κ=1)评估相互信度。实际意义在儿童干预的长期规划中包括自闭症的声音对于那些试图满足个人、家庭和社区需求的人来说是至关重要的。父母和自闭症参与者的引用都是直接从可选评论中获得的,以揭示父母退出或坚持自闭症干预的原因。社会影响实践者和干预服务提供者必须考虑那些直接受到干预方式、频率或强度影响的人的反馈。 最近的文献也证实了这种工作的必要性,例如基于社区的参与性研究(Raymaker, 2016)。自闭症患者应该被认为是他们自己经验的专家(Milton, 2014)。社区-学术伙伴关系对于调查自闭症人群的需求是必要的(Meza et al., 2016)。大多数自闭症患者并不认为自闭症是一种精神疾病或行为障碍。我们必须认识到,当伤害行为持续存在,情绪、认知、睡眠模式和注意力紊乱加剧时,这些症状与自闭症无关,而与创伤后应激障碍(PTSD)的诊断标准密切相关。当PTSD未得到充分诊断和治疗时,自闭症个体可能会经历过度觉醒,并被其他令人愉快的刺激所触发。由于自闭症干预通常是围绕高接触、长时间和1:1参与进行的,因此必须重新评估干预的性质,对处于高唤醒状态的自闭症患者来说,这是一个潜在的创伤性事件。任何触发大于帮助的干预措施都应避免并在出现ptsd时停止。
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引用次数: 3
Emotion regulation and intervention in adults with autism spectrum disorder: a synthesis of the literature 成人自闭症谱系障碍的情绪调节与干预:文献综述
IF 1.2 Q3 Medicine Pub Date : 2019-10-25 DOI: 10.1108/aia-12-2018-0050
Jan Mei Lim
PurposeEmotion regulation is an ongoing multiprocess phenomenon and is a challenging developmental task to acquire in individuals with autism spectrum disorder (ASD) who have different neurobiological profiles and emotion regulation problems. The purpose of this paper is to review recent literature to understand the neurobiological and psychological perspective of emotion regulation in ASD, while converging themes of psychosocial interventions and existing best practices on emotion regulation within this heterogeneous population are reviewed and discussed in consideration of intellectual disability (ID).Design/methodology/approachReview of recent literature and common empirically supported interventions addressing emotional regulation implemented in individuals with and without ASD, and with and without ID were included in the electronic database search through PubMed, EBSChost, Science Direct, Wiley Online Library, GALE and SAGE. Search terms used included autism, ID, cognitive control, executive function, sensory processing/intervention, emotion regulation, cognitive behavior therapy, mindfulness, social stories, positive behavior support and behavior therapy.FindingsNeural systems governing emotion regulation can be divided into “top-down” and “bottom-up” processing. Prefrontal cortex, cognitive and attentional control are critical for effective emotion regulation. Individuals with ASD, and with ID show impairments in these areas have problems with emotion regulation. Targeted psychosocial intervention need to consider bottom-up and top-down processes of emotion regulation, and that standardized interventions require adaptations.Originality/valueThere are limited studies looking into understanding the neurobiological and psychological perspective of emotion regulation in ASD and linking them to interventions. This review highlights psychosocial interventions that are important for further research, investigation and development as treatment in this population is limited.
目的情绪调节是一种持续的多过程现象,对于具有不同神经生物学特征和情绪调节问题的自闭症谱系障碍(ASD)患者来说,这是一项具有挑战性的发展任务。本文的目的是回顾最近的文献,以了解ASD情绪调节的神经生物学和心理学观点,同时,考虑到智力残疾(ID),回顾和讨论了心理社会干预的融合主题和该异质人群中情绪调节的现有最佳实践。设计/方法/方法回顾了最近的文献和常见的经验支持的干预措施,这些干预措施解决了在患有和没有ASD的个体中实施的情绪调节,以及通过PubMed、EBSChost、Science Direct、Wiley Online Library、GALE和SAGE进行的电子数据库搜索中包括有和没有ID。使用的搜索术语包括自闭症、ID、认知控制、执行功能、感觉处理/干预、情绪调节、认知行为治疗、正念、社交故事、积极行为支持和行为治疗。发现控制情绪调节的神经系统可以分为“自上而下”和“自下而上”的处理。额前皮层、认知和注意力控制对有效的情绪调节至关重要。患有自闭症谱系障碍和ID的人在这些方面表现出障碍,他们在情绪调节方面存在问题。有针对性的心理社会干预需要考虑自下而上和自上而下的情绪调节过程,而标准化干预需要适应。原创性/价值在理解ASD情绪调节的神经生物学和心理学观点并将其与干预措施联系起来方面,研究有限。这篇综述强调了对进一步研究、调查和发展很重要的心理社会干预措施,因为对这一人群的治疗是有限的。
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引用次数: 2
Applying a SWOT analysis to inform educational provision of learners on the autism spectrum 应用SWOT分析为自闭症谱系学习者提供教育
IF 1.2 Q3 Medicine Pub Date : 2019-09-26 DOI: 10.1108/AIA-03-2018-0011
Claire Sciberras
PurposeRequests for increased support within mainstream school settings within the field of autism tend to take place across most international educational scenarios. In light of such recommendation, the purpose of this paper is to outline how the implementation of a strengths, weaknesses, opportunities and threats (SWOT) analysis within educational settings might be beneficial in order to improve the support provided for learners on the autism spectrum (AS).Design/methodology/approachAlthough a SWOT analysis framework is generally carried out in corporate domains for companies and firms to investigate their competitive impact within the marketplace so as to develop future concepts, this analysis structure may also be usefully applied within educational settings so as to inform practice.FindingsIf implemented in an effective manner, a SWOT analysis will potentially provide a comprehensive synopsis of the issues and concerns which are relevant for considering and evolving the provision of support for students. Indeed, it will enable educational environments to enhance their strengths so as to increase appropriate opportunities and address the weaknesses within their services in order to potentially overcome their barriers and enhance the quality of life of learners on the spectrum.Originality/valueThis paper includes the viewpoint of the author in relation to a SWOT analysis so as to inform practice for learners on the AS.
在大多数国际教育场景中,在主流学校环境中增加自闭症领域支持的请求往往发生。鉴于这些建议,本文的目的是概述如何在教育环境中实施优势、劣势、机会和威胁(SWOT)分析,以改善为自闭症谱系(AS)学习者提供的支持。设计/方法/方法虽然SWOT分析框架通常在公司领域进行,用于公司和公司调查其在市场中的竞争影响,以开发未来的概念,但这种分析结构也可以有效地应用于教育环境中,以便为实践提供信息。如果以有效的方式实施,SWOT分析将有可能提供与考虑和发展为学生提供支持相关的问题和关注点的全面摘要。事实上,它将使教育环境能够增强其优势,从而增加适当的机会,解决其服务中的弱点,从而有可能克服障碍,提高自闭症学习者的生活质量。原创性/价值本文包含了作者关于SWOT分析的观点,以便为学习者在as上的实践提供信息。
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引用次数: 1
Empowering autistic adults through their involvement in the development of a virtual world 让自闭症成年人参与虚拟世界的开发
IF 1.2 Q3 Medicine Pub Date : 2019-09-26 DOI: 10.1108/AIA-01-2019-0001
Yurgos Politis, L. Olivia, Thomas Olivia
PurposePeople with cognitive disabilities have a right to an inclusive society, and to have access to services and products that meet their specific needs. Participatory design (PD) represents a potentially effective way to ensure these rights, because users become influencers of the technological development and design process, are actively involved in the customization of that technology and develop a relationship with the designers/developers. Literature suggests that user involvement in technology development produces better products and has shown that this process offers users a voice and the process is also conducive to mutual learning between researchers and participants. This paper aims to discuss these issues.Design/methodology/approachHere the authors will present the development of a virtual world (VW) platform, having as a starting point a minimally viable initial version. This was followed by the creation of a networking framework to test each feature of the VW, which allowed connected users, most of whom on the autistic spectrum, to interact with each other in real time in the VW, and to see each other’s effects. Stress testing sessions were initiated with a mixed group of 15 users, 8 of whom with autism (7 male and 1 female). Ten of the participants were male and five were female (Figure 1).FindingsEven though the platform is feature-complete, its code is still in development; features can be improved/expanded upon, which necessitates further testing. The most commonly flagged issues from the stress testing were requests for videos/text manuals, the camera controls and chat message errors. These were implemented/fixed or added to the feature roadmap. “Heavy avatar customization” was also suggested, which has conceptual merit, but is not a priority.Practical implicationsPD is an inclusive approach that addresses personal needs and preferences, matching up the person with the tools and environments to ensure equity and inclusion. The VW whose development is described in this paper has been used for communication skills training with autistic young adults. It could be used for other social, life, academic and vocational skills training. This type of training through VR/VW may help enhance the employment-related skills of neurodiverse populations (and thus empower independent living) and has the potential for broader implementation and wider access in terms of distance learning.Originality/valueThis paper adds to the rather limited literature on applying PD approaches in the development of products for people with neurodevelopmental disabilities. The authors will present such a process for the development of a VW with people with autism. Although literature suggests that user involvement produces better outcomes, adopting this approach is not straightforward. The paper will describe in detail not only the contribution the participants made in every phase but also the limitations of applying a PD approach with a neurod
目的认知障碍者有权享受包容性社会,有权获得满足其特定需求的服务和产品。参与式设计(PD)代表了一种确保这些权利的潜在有效方式,因为用户成为技术开发和设计过程的影响者,积极参与该技术的定制,并与设计师/开发者建立关系。文献表明,用户参与技术开发会产生更好的产品,并表明这一过程为用户提供了发言权,这一过程也有利于研究人员和参与者之间的相互学习。本文旨在探讨这些问题。设计/方法论/方法在这里,作者将介绍虚拟世界(VW)平台的开发,并以最小可行的初始版本为起点。随后,他们创建了一个网络框架来测试大众的每一个功能,这使得相互连接的用户(其中大多数是自闭症患者)能够在大众中实时互动,并看到彼此的效果。压力测试是由15名用户组成的混合组开始的,其中8人患有自闭症(7名男性和1名女性)。10名参与者是男性,5名是女性(图1)。尽管该平台功能齐全,但其代码仍在开发中;功能可以改进/扩展,这需要进一步的测试。压力测试中最常见的问题是对视频/文本手册的请求、相机控制和聊天消息错误。这些都被实现/修复或添加到特性路线图中。“重型角色定制”也被提出,这在概念上是有价值的,但不是优先考虑的。实践意义社会发展是一种包容性的方法,解决个人需求和偏好,使人与工具和环境相匹配,以确保公平和包容。本文所描述的大众已被用于自闭症青年的沟通技巧培训。它可以用于其他社会、生活、学术和职业技能培训。这种通过虚拟现实/大众进行的培训可能有助于提高神经多样性人群的就业相关技能(从而增强独立生活能力),并有可能在远程学习方面得到更广泛的实施和更广泛的获取。原创性/价值本文补充了在神经发育障碍患者产品开发中应用PD方法的相当有限的文献。作者将展示这样一个过程,以开发一辆大众与自闭症的人。虽然文献表明用户参与产生更好的结果,但采用这种方法并不简单。本文将详细描述参与者在每个阶段所做的贡献,以及在神经多样性人群中应用PD方法的局限性,以便他们在过程中成为平等的合作伙伴,并以有意义的方式参与。
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引用次数: 4
Effectiveness of video assisted teaching on knowledge, attitude and practice among primary caregivers of children with Autism Spectrum Disorder 视频辅助教学在自闭症谱系障碍儿童主要照顾者中的知识、态度和实践效果
IF 1.2 Q3 Medicine Pub Date : 2019-09-26 DOI: 10.1108/AIA-10-2018-0039
Hena Chandran, K. Jayanthi, S. Prabavathy, K. Renuka, Rajesh Bhargavan
PurposeParents or primary caregivers of children with Autism Spectrum Disorder (ASD) have important role in early recognition of the disorder as well as in the management of the disorder. Knowledge, attitude and practice of primary caregivers towards children with ASD are important factors in promoting health and wellness of such children. The purpose of this paper is to evaluate the effectiveness of video-assisted teaching regarding care of children with ASD on knowledge, attitude and practice among primary caregivers.Design/methodology/approachQuasi-experimental research design with one group pre-test post-test was adopted. A total of 60 primary caregivers were selected through stratified random sampling technique. Video-assisted teaching was given to 60 primary caregivers. Data collection was done before and after the video-assisted teaching programme using structured questionnaire which consists of 57 questions.FindingsThe result of the study showed that the post-test level of knowledge attitude and practice among primary caregivers of children with ASD was significantly high (p<0.0001) when compared to pre-test level by using Wilcoxon Signed Rank Test. The study finding revealed that video-assisted teaching was effective in enhancing the knowledge, developing a positive attitude and good practice among primary caregivers regarding care of children with ASD.Social implicationsFindings of this study will help mental health nurses, psychologists, intellectual disability nurses, teachers, public health, social workers, etc. to know the importance of video-assisted teaching programme regarding care of children with ASD and to motivate the primary caregivers to participate in such teaching programme. The community mental health nurse can plan video-assisted teaching programme in a community regarding care of children with ASD.Originality/valueResults of this study indicate that the video-assisted teaching is effective and helps the primary caregivers to enhance the knowledge, attitude and practice regarding care of children with ASD. So continuous awareness in primary health centre and community area is necessary to improve the knowledge, attitude and practice of primary caregivers.
目的自闭症谱系障碍(ASD)儿童的父母或主要照顾者在早期识别该障碍以及管理该障碍方面发挥着重要作用。主要照顾者对ASD儿童的知识、态度和实践是促进此类儿童健康的重要因素。本文的目的是评估视频辅助教学在主要照顾者的知识、态度和实践方面对ASD儿童护理的有效性。设计/方法论/方法采用一组前测后测的准实验研究设计。通过分层随机抽样技术,共选择了60名主要照顾者。为60名初级护理人员提供了视频辅助教学。在视频辅助教学计划前后,使用由57个问题组成的结构化问卷进行数据收集。研究结果表明,通过使用Wilcoxon符号秩检验,ASD儿童的主要照顾者在测试后的知识、态度和实践水平与测试前的水平相比显著较高(p<0.0001)。研究结果表明,视频辅助教学在提高初级护理人员对ASD儿童护理的知识、培养积极态度和良好实践方面是有效的。社会影响本研究的结果将有助于心理健康护士、心理学家、智障护士、教师、公共卫生、社会工作者,了解视频辅助教学计划对ASD儿童护理的重要性,并激励主要照顾者参与此类教学计划。社区心理健康护士可以在社区规划关于ASD儿童护理的视频辅助教学计划。独创性/价值本研究的结果表明,视频辅助教学是有效的,有助于主要照顾者提高对ASD儿童的护理知识、态度和实践。因此,有必要在初级卫生中心和社区地区不断提高认识,以提高初级护理人员的知识、态度和做法。
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引用次数: 5
The acquisition of the Arabic construct state (CS) constructions by Arabic-speaking children with ASD 阿拉伯语自闭症儿童阿拉伯语构念状态构念的习得
IF 1.2 Q3 Medicine Pub Date : 2019-09-26 DOI: 10.1108/AIA-01-2019-0003
A. R. Altakhaineh, Razan N Alkhatib
PurposeThe purpose of this paper is to investigate whether age plays a role in the acquisition of construct state (CS) constructions in Arabic by 14 children with autism spectrum disorder (ASD). It also examined the challenges faced by children with ASD in producing different types of CS constructions. Finally, the study analysed the sources of difficulties children with ASD encounter during the learning process of the CS.Design/methodology/approachFor the purposes of this study, the participants were asked to orally complete short sentences with the help of illustrative pictures.FindingsResults revealed that the age of the 14 children with ASD plays a role in the acquisition of CS constructions. Children of age 12–15 performed better than those of age 8 and 10. Results also showed that children with ASD performed better in producing phrases rather than compounds. Moreover, the participants performed better on endocentric compounds as opposed to exocentric ones. Finally, analysing the errors produced on the text revealed that the acquisition of head direction precedes definiteness.Originality/valueThe topic of the study has not been investigated yet and the study concluded with some important findings concerning teaching Arabic CS to children with ADS.
目的研究年龄是否在14名自闭症谱系障碍(ASD)儿童习得阿拉伯语结构状态(CS)结构中起作用。它还研究了ASD儿童在产生不同类型的CS结构方面所面临的挑战。最后,该研究分析了自闭症谱系障碍儿童在CS学习过程中遇到的困难来源。设计/方法/方法为了本研究的目的,参与者被要求在插图的帮助下口头完成短句。结果显示,14名ASD儿童的年龄在CS结构的获得中起着一定的作用。12-15岁的儿童比8岁和10岁的儿童表现更好。研究结果还表明,自闭症谱系障碍儿童在产生短语方面比产生化合物表现更好。此外,与外核化合物相比,参与者在内核化合物上表现更好。最后,通过对文本中产生的错误的分析,揭示了头部方向的获取先于确定性。原创性/价值该研究的主题尚未调查,该研究得出了一些关于向患有ADS的儿童教授阿拉伯语CS的重要发现。
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引用次数: 5
Age at death and comorbidity of dementia-related disorders among individuals with autism spectrum disorder 自闭症谱系障碍患者的死亡年龄和痴呆相关疾病的合并症
IF 1.2 Q3 Medicine Pub Date : 2019-09-26 DOI: 10.1108/AIA-11-2018-0045
L. Barnard‐Brak, D. Richman, Zhanxia Yang
PurposeAutism spectrum disorder (ASD) is a lifelong disorder that requires intervention and support services for a growing geriatric population. The purpose of this paper is to examine the mean age at death of individuals with ASD and subsequent comorbidity with Alzheimer’s disease, and any form of dementia, as a whole and according to sex.Design/methodology/approachData consisted of 1,754 individuals who had an ASD listed as one of the causes of deaths from the National Vital Statistics System with data from 1999 to 2015. In the current study, the authors present contradictory results with a mean age at death for individuals with ASD was 68 years by adjusting for changing prevalence rates.FindingsFemales with ASD had a higher mean age at death than males with ASD; consistent with the trend in the sex differences in the general population. The results of the current study also indicate that individuals with ASD were, in fact, less likely than the general population to have Alzheimer’s disease or a form of dementia. However, males with ASD were significantly more likely to have acquired Alzheimer’s disease or a form of dementia as compared to females with ASD.Originality/valueGuan and Li (2017) reported a mean age at death of 36 years old for individuals with ASD, which was subsequently reported in the mass media, most notably CNN. The authors contend that this study provides a more accurate estimate mean age at death.
目的自闭症谱系障碍(ASD)是一种终身障碍,需要为不断增长的老年人口提供干预和支持服务。本文的目的是根据性别,从整体上研究ASD患者以及随后与阿尔茨海默病和任何形式的痴呆症共病患者的平均死亡年龄。设计/方法/方法数据由1754名ASD患者组成,他们被国家生命统计系统列为死亡原因之一,数据来自1999年至2015年。在目前的研究中,作者提出了相互矛盾的结果,通过调整患病率的变化,ASD患者的平均死亡年龄为68岁。发现患有自闭症谱系障碍的女性平均死亡年龄高于患有自闭症的男性;与一般人群性别差异的趋势一致。目前的研究结果还表明,事实上,ASD患者患阿尔茨海默病或一种痴呆症的可能性低于普通人群。然而,与ASD女性相比,患有ASD的男性患阿尔茨海默病或一种痴呆症的可能性明显更高。原创/价值观Guan和Li(2017)报道了ASD患者的平均死亡年龄为36岁,随后在大众媒体上进行了报道,尤其是CNN。作者认为,这项研究提供了一个更准确的平均死亡年龄估计。
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引用次数: 7
Editorial 社论
IF 1.2 Q3 Medicine Pub Date : 2019-09-26 DOI: 10.1108/aia-10-2019-053
J. McCarthy, E. Chaplin
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引用次数: 0
期刊
Advances in Autism
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