Introduction: Despite the evidence and expert opinion that many adults with autism spectrum disorder (ASD) face barriers to formal diagnosis, qualitative studies examining adult patients' experience and requirements for better access to the diagnosis are still lacking.
Aims: To qualitatively explore the pre-diagnosis experiences of adults with ASD, the impact of receiving a diagnosis, and the need for improved access to diagnosis both for adults with ASD and for adult psychiatrists.
Methods: Sixteen semi-structured interviews were conducted (11 adults diagnosed with ASD and 5 psychiatrists). A mixed deductive-inductive thematic analysis was employed.
Results: Several factors contributing to delayed diagnosis were identified including difficulties accessing healthcare, limited awareness of ASD among some clinicians, the use of camouflaging behaviors by participants, and family adaptation to their symptoms. Receiving a diagnosis was often described as a relief, allowing participants to understand past social difficulties and seek better acknowledgment and accommodation from their environment. The analysis highlighted the need to reduce wait times and service costs, as well as to enhance clinicians' knowledge of ASD to improve accessibility and satisfaction with diagnosis. Participants also noted the complex interplay between media portrayals of ASD and public understanding of the disorder.
Conclusions: Increased education for mental health professionals and broader public awareness campaigns are necessary to facilitate timely access to appropriate diagnosis and support services.
扫码关注我们
求助内容:
应助结果提醒方式:
