The future of care and clinical research in autism - recommendations from the 2021 Lancet Commission.

Medical review (Berlin, Germany) Pub Date : 2022-07-01 eCollection Date: 2022-06-01 DOI:10.1515/mr-2022-0015
Xiang Yu, Xiu Xu
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引用次数: 1

Abstract

At least 78 million people worldwide are affected by autism, a neurodevelopmental disorder characterized by deficits in social interactions, and repetitive behaviors and/or interests. Autism typically manifests in early childhood, and affects social communications and behaviors throughout the lifespan of the individual. Under the umbrella of autism spectrum disorder, it is a highly heterogeneous disorder, with some individuals profoundly affected and needing care every day, while others can live highly independent lives, with some adjustments. The past 60 years has seen a major influx of interest in autism, and significant advances in many areas. However, a large gap remains between current scientific knowledge and the help and support that people with autism and their families need. To address these concerns, the Lancet commissioned a report on the "future of care and clinical research in autism". The Commission calls for government coordination between health-care, education and social sectors, as well as active participation from people with autism and their families. The Commission proposes personalized, evidence-based assessments and intervention, that is accessible and affordable to all, and call for increased appreciation of neurodiversity and prioritization of research that can improve the lives of people with autism and their families. How to support each and every autistic individual and their families is highly challenging. The 64-page Lancet Commission Report, published on December 2021, was written jointly by 32 authors from 6 continents and 13 disciplines, including clinicians, other health-care providers, researchers, advocates, autistic individuals and their parents.

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自闭症护理和临床研究的未来——2021年柳叶刀委员会的建议。
全世界至少有7800万人患有自闭症,这是一种神经发育障碍,其特征是社交互动不足、重复行为和/或兴趣。自闭症通常表现在儿童早期,并在个体一生中影响社会沟通和行为。在自闭症谱系障碍的保护伞下,它是一种高度异质性的障碍,一些人受到严重影响,每天都需要护理,而另一些人可以过上高度独立的生活,并进行一些调整。在过去的60年里,人们对自闭症的兴趣大量涌入,并在许多领域取得了重大进展。然而,目前的科学知识与自闭症患者及其家人所需的帮助和支持之间仍然存在很大差距。为了解决这些问题,《柳叶刀》委托撰写了一份关于“自闭症护理和临床研究的未来”的报告。委员会呼吁政府在医疗保健、教育和社会部门之间进行协调,并呼吁自闭症患者及其家人积极参与。委员会提出了个性化的、循证的评估和干预措施,所有人都可以获得并负担得起,并呼吁提高对神经多样性的认识,并优先考虑可以改善自闭症患者及其家人生活的研究。如何支持每一个自闭症患者及其家人是极具挑战性的。这份64页的《柳叶刀委员会报告》于2021年12月发表,由来自6大洲和13个学科的32位作者共同撰写,其中包括临床医生、其他医疗保健提供者、研究人员、倡导者、自闭症患者及其父母。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
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