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查尔斯·博内综合征患儿的视幻觉体验——一项定性研究

: children's experiences of visual hallucinations in Charles Bonnet syndrome-a qualitative study.

作者信息

Jones Lee, Ditzel-Finn Lara, McDonald Leanne, Moosajee Mariya

机构信息

Institute of Ophthalmology, University College London, London, UK.

Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

出版信息

Arch Dis Child. 2025 Apr 17;110(5):384-390. doi: 10.1136/archdischild-2024-327811.

Abstract

OBJECTIVE

Charles Bonnet syndrome (CBS) refers to the presence of visual hallucinations occurring secondary to visual impairment. The aim of this study was to understand the phenomenology of CBS in children and assess the emotional impact and support needs of patients and their families.

DESIGN

Semistructured qualitative interview study.

SETTING

UK.

PARTICIPANTS

Children (7-15 years) with an inherited retinal disease living with CBS and their parents.

RESULTS

10 participants were recruited from six families (dyadic interviews n=4; parent-only interviews n=2). Thematic analysis identified five superordinate themes relating to experiences of CBS: (1) diagnosis journey, (2) hallucination phenomenology, (3) impact of hallucinations, (4) understanding and managing hallucinations and (5) experiences of support. The impact of CBS was broad and heterogenous, causing significant disruption to patients' daily life. Limited awareness led to parents expressing largely negative healthcare experiences. Overall, the extent of knowledge and understanding of CBS was an indicator of successful self-management of the condition.

CONCLUSIONS

The journey towards understanding and managing CBS for both parents and children is challenging. Although coping strategies can lead to improved adjustment, visual hallucinations compounded the difficulty of living with a chronic visual impairment. Healthcare providers have an integral role in ensuring patients and families are effectively supported to allay fears and promote psychological well-being.

摘要

目的

查尔斯·邦尼特综合征(CBS)是指继发于视力损害的视幻觉。本研究旨在了解儿童CBS的现象学,并评估患者及其家庭的情感影响和支持需求。

设计

半结构化定性访谈研究。

地点

英国。

参与者

患有CBS的遗传性视网膜疾病儿童(7 - 15岁)及其父母。

结果

从六个家庭招募了10名参与者(二元访谈n = 4;仅父母访谈n = 2)。主题分析确定了与CBS经历相关的五个上位主题:(1)诊断过程,(2)幻觉现象学,(3)幻觉的影响,(4)理解和管理幻觉,以及(5)支持经历。CBS的影响广泛且各异,对患者的日常生活造成了严重干扰。认知有限导致父母表达了主要为负面的医疗保健经历。总体而言,对CBS的了解程度是该疾病成功自我管理的一个指标。

结论

父母和孩子在理解和管理CBS方面面临挑战。尽管应对策略可以改善适应情况,但视幻觉加剧了患有慢性视力损害的生活难度。医疗保健提供者在确保患者和家庭得到有效支持以减轻恐惧和促进心理健康方面起着不可或缺的作用。

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