“他们为什么不和我们的女儿谈谈?”: Rett综合征的眼动追踪AAC和医学交流

Usree Bhattacharya , Wisnu A. Pradana , Xing Wei , Bukunmi Ogunsola
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引用次数: 1

摘要

这项调查通过眼动追踪增强和替代通信(AAC)技术的视角,探讨了Rett综合征的医学宣传。Rett综合症是一种罕见的导致言语和手部功能丧失的神经系统疾病。我们收集了五名雷特综合征患者及其护理人员的数据,包括半结构化虚拟访谈、AAC设备使用的视频分析以及AAC页面集截图的检查。研究结果揭示了AAC用于表达不适或疾病的不同策略,并强调了护理人员在处理医疗信息中的关键作用。众所周知的挑战,如成本、医疗环境中的时间限制、培训需求以及缺乏标准化的AAC症状描述,眼动追踪AAC技术有可能增强症状评估,培养患者自主性,并促进个性化医疗。这项研究阐明了AAC技术在医疗通信中的变革力量,展示了其在应对通信挑战方面的前景,并强调了其提高雷特综合征和类似健康状况患者生活质量的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“Why don't they talk to our daughter?”: Eye-tracking AAC and medical communication in Rett syndrome

This investigation explores medical advocacy for Rett syndrome—a rare neurological disorder causing loss of speech and hand function—through the lens of eye-tracking augmentative and alternative communication (AAC) technology. We gathered data from five individuals with Rett syndrome and their caregivers, encompassing semi-structured virtual interviews, video analyses of AAC device usage, and examination of AAC pageset screenshots. The findings reveal diverse AAC strategies employed to express discomfort or illness and highlight caregivers' pivotal role in processing medical information. Notwishstanding challenges like cost, time limitations in medical contexts, training needs, and the lack of standardized AAC symptom descriptions, eye-tracking AAC technology has the potential to enhance symptom assessment, foster patient autonomy, and facilitate personalized medical care. This study illuminates the transformative power of this AAC technology in medical communication, showcasing its promise in tackling communication challenges and underscoring its capacity to enhance quality of life for those with Rett syndrome and similar health conditions.

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