Access to services for autistic people across Europe.

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY
Siti Nurnadhirah Binte Mohd Ikhsan, Rosemary Holt, Joyce Man, Tracey Parsons, Rik Schalbroeck, Amber Ruigrok, Aurélie Baranger, Carrie Allison, Mary Doherty, Katrien Van den Bosch, Jerneja Terčon, Pierre Violland, Anjuli Ghosh, James Cusack, Simon Baron-Cohen
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引用次数: 0

Abstract

Background: Autistic communities in Europe continue to face difficulties accessing services despite increasing rates of autism diagnosis in recent years.

Methods: To investigate autistic people's access to services in Europe and reasons for unsuccessful access, we conducted the ACCESS-EU survey comprising of 2322 formally diagnosed autistic people and family carers living within the European Union (EU) and the United Kingdom (UK). The survey also examined age group (adult vs. child) and gender (male vs. female) differences in results.

Results: Overall, autistic people reported access to therapy (33.38%), mental health (29.89%), educational (27.05%), medical (34.28%), financial (26.66%), needs assessment (14.90%), information/referral (14.73%), social care (14.43%), employment (7.54%), housing (6.80%), legal (3.96%), helpline (3.40%) and other services (0.26%), and most (≥ 57.61%) had waited up to 6 months from referral to access most services. Several respondents were also unable to access therapeutic (13.53%), mental health (11.90%), autism diagnostic (5.92%), needs assessment (8.32%), financial (9.62%), educational (8.10%), social care (7.39%), information/referral (6.14%), medical (7.28%), housing (5.92%), employment (5.43%), legal (3.42%), and helpline services (2.34%). Reasons cited by respondents for their unsuccessful service access included service unavailability (23.08%), service unsuitability or participant ineligibility (20.04%), long waitlists (17.42%), service unaffordability (11.80%), and rejection from service due to autism diagnosis (9.87%), along with other reasons not listed in the survey (18.42%). Significant age group and gender differences were observed for successful access to services, waiting time, unsuccessful access and reasons for unsuccessful access. Among the five most represented countries in the survey-the UK (33.33%), Spain (14.04%), Poland (13.87%), France (11.07%) and Germany (6.03%)-overall service access was most inconsistent in Poland and the UK, highest in Germany and Spain but poorest in France.

Limitations: Issues related to survey presentation such as the languages in which the survey was conducted and the phrasing of some questions should be considered, as well as issues regarding subjectivity and ambiguity of data analysis such as translation of non-English responses into English.

Conclusions: Our findings suggest that service access among autistic people in Europe is inconsistent. Significant improvement to current policies is required to enhance access to services across Europe.

为全欧洲的自闭症患者提供服务。
背景:尽管近年来自闭症诊断率不断上升,但欧洲的自闭症社区仍然面临着获得服务的困难。方法:为了调查欧洲自闭症患者获得服务的情况及其不成功的原因,我们对欧盟和英国的2322名正式诊断为自闭症的患者及其家庭照顾者进行了access -EU调查。调查还检查了年龄组(成人与儿童)和性别(男性与女性)在结果上的差异。结果:总体而言,自闭症患者获得了治疗(33.38%)、心理健康(29.89%)、教育(27.05%)、医疗(34.28%)、财务(26.66%)、需求评估(14.90%)、信息/转诊(14.73%)、社会护理(14.43%)、就业(7.54%)、住房(6.80%)、法律(3.96%)、热线(3.40%)和其他服务(0.26%),大多数(≥57.61%)患者从转诊开始等待6个月才能获得大多数服务。一些受访者也无法获得治疗(13.53%)、心理健康(11.90%)、自闭症诊断(5.92%)、需求评估(8.32%)、财务(9.62%)、教育(8.10%)、社会关怀(7.39%)、信息/转诊(6.14%)、医疗(7.28%)、住房(5.92%)、就业(5.43%)、法律(3.42%)和热线服务(2.34%)。受访者表示未能获得服务的原因包括服务不可用(23.08%)、服务不适合或参与者不合格(20.04%)、等待名单长(17.42%)、服务负担不起(11.80%)、因自闭症诊断而拒绝服务(9.87%),以及其他未在调查中列出的原因(18.42%)。在成功获得服务、等待时间、不成功获得服务和不成功获得服务的原因方面,观察到显著的年龄组和性别差异。在调查中最具代表性的五个国家中——英国(33.33%)、西班牙(14.04%)、波兰(13.87%)、法国(11.07%)和德国(6.03%)——波兰和英国的整体服务获取情况最不一致,德国和西班牙最高,法国最低。局限性:需要考虑与调查呈现相关的问题,如调查使用的语言和一些问题的措辞,以及数据分析的主观性和模糊性问题,如将非英语回答翻译成英语。结论:我们的研究结果表明,欧洲自闭症患者的服务获取是不一致的。需要对现行政策进行重大改进,以提高整个欧洲获得服务的机会。
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
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
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