Binte Mohd Ikhsan Siti Nurnadhirah, Holt Rosemary, Man Joyce, Parsons Tracey, Schalbroeck Rik, Ruigrok Amber, Baranger Aurélie, Allison Carrie, Doherty Mary, Van den Bosch Katrien, Terčon Jerneja, Violland Pierre, Ghosh Anjuli, Cusack James, Baron-Cohen Simon
Autism Research Centre, Department of Psychiatry, University of Cambridge, Douglas House, 18B Trumpington Road, Cambridge, CB2 8 AH, UK.
Clinical Neurodevelopmental Sciences, Institute of Education and Child Studies, Faculty of Social and Behavioural Sciences, Leiden University, Leiden, The Netherlands.
Mol Autism. 2025 Jun 14;16(1):35. doi: 10.1186/s13229-025-00664-2.
Autistic communities in Europe continue to face difficulties accessing services despite increasing rates of autism diagnosis in recent years.
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.
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.
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.
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.
尽管近年来欧洲自闭症的诊断率不断上升,但欧洲的自闭症群体在获得服务方面仍面临困难。
为了调查欧洲自闭症患者获得服务的情况以及未能成功获得服务的原因,我们开展了“欧洲服务可及性调查”(ACCESS-EU),该调查涵盖了2322名居住在欧盟(EU)和英国(UK)的经正式诊断的自闭症患者及其家庭护理人员。该调查还研究了结果在年龄组(成人与儿童)和性别(男性与女性)方面的差异。
总体而言,自闭症患者报告能够获得治疗服务(33.38%)、心理健康服务(29.89%)、教育服务(27.05%)、医疗服务(34.28%)、财务服务(26.66%)、需求评估服务(14.90%)、信息/转介服务(14.73%)、社会护理服务(14.43%)、就业服务(7.54%)、住房服务(6.80%)、法律服务(3.96%)、热线服务(3.40%)和其他服务(0.26%),并且大多数(≥57.61%)从转介到获得大多数服务的等待时间长达6个月。一些受访者还无法获得治疗服务(13.53%)、心理健康服务(11.90%)、自闭症诊断服务(5.92%)、需求评估服务(8.32%)、财务服务(9.62%)、教育服务(8.10%)、社会护理服务(7.39%)、信息/转介服务(6.14%)、医疗服务(7.28%)、住房服务(5.92%)、就业服务(5.43%)、法律服务(3.42%)和热线服务(2.34%)。受访者提到的未能成功获得服务的原因包括服务不可用(23.08%)、服务不合适或参与者不符合资格(20.04%)、等待名单过长(17.42%)、服务费用过高(11.80%)、因自闭症诊断而被服务拒绝(9.87%),以及调查中未列出的其他原因(18.42%)。在成功获得服务、等待时间、未能成功获得服务以及未能成功获得服务的原因方面,观察到了显著的年龄组和性别差异。在调查中占比最高的五个国家——英国(33.33%)、西班牙(14.04%)、波兰(13.87%)、法国(11.07%)和德国(6.03%)——总体服务可及性在波兰和英国最不一致,在德国和西班牙最高,但在法国最差。
应考虑与调查呈现相关的问题,如进行调查所使用的语言以及一些问题的措辞,以及与数据分析的主观性和模糊性相关的问题,如将非英语回答翻译成英语。
我们的研究结果表明,欧洲自闭症患者的服务可及性不一致。需要对当前政策进行重大改进,以提高全欧洲的服务可及性。