“他们是令人毛骨悚然的生物,有着类似人类的特征”:查尔斯·邦纳综合征中儿童的视觉幻觉经历——一项定性研究。

IF 4.3 3区 医学 Q1 PEDIATRICS Archives of Disease in Childhood Pub Date : 2025-01-09 DOI:10.1136/archdischild-2024-327811
Lee Jones, Lara Ditzel-Finn, Leanne McDonald, Mariya Moosajee
{"title":"“他们是令人毛骨悚然的生物,有着类似人类的特征”:查尔斯·邦纳综合征中儿童的视觉幻觉经历——一项定性研究。","authors":"Lee Jones, Lara Ditzel-Finn, Leanne McDonald, Mariya Moosajee","doi":"10.1136/archdischild-2024-327811","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Design: </strong>Semistructured qualitative interview study.</p><p><strong>Setting: </strong>UK.</p><p><strong>Participants: </strong>Children (7-15 years) with an inherited retinal disease living with CBS and their parents.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":8150,"journal":{"name":"Archives of Disease in Childhood","volume":" ","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>'They're creepy creatures with human-like features'</i>: children's experiences of visual hallucinations in Charles Bonnet syndrome-a qualitative study.\",\"authors\":\"Lee Jones, Lara Ditzel-Finn, Leanne McDonald, Mariya Moosajee\",\"doi\":\"10.1136/archdischild-2024-327811\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>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.</p><p><strong>Design: </strong>Semistructured qualitative interview study.</p><p><strong>Setting: </strong>UK.</p><p><strong>Participants: </strong>Children (7-15 years) with an inherited retinal disease living with CBS and their parents.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>\",\"PeriodicalId\":8150,\"journal\":{\"name\":\"Archives of Disease in Childhood\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of Disease in Childhood\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1136/archdischild-2024-327811\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PEDIATRICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Disease in Childhood","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1136/archdischild-2024-327811","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

摘要

目的:查尔斯邦纳综合征(CBS)是指继发于视觉障碍的视觉幻觉。本研究的目的是了解儿童CBS的现象学,并评估患者及其家属的情绪影响和支持需求。设计:半结构化定性访谈研究。设置:英国。参与者:患有CBS的遗传性视网膜疾病的儿童(7-15岁)及其父母。结果:从6个家庭中招募了10名参与者(二元访谈n=4;家长访谈n=2)。主题分析确定了与CBS经历相关的五个主要主题:(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,(5)支持体验。CBS的影响是广泛和异质性的,对患者的日常生活造成了显著的干扰。有限的意识导致父母表达了大部分负面的医疗保健经历。总体而言,对CBS的知识和理解程度是病情成功自我管理的一个指标。结论:理解和管理父母和孩子的CBS是具有挑战性的。尽管应对策略可以改善适应能力,但视幻觉加剧了慢性视力障碍患者的生活困难。医疗保健提供者在确保患者和家属得到有效支持以减轻恐惧和促进心理健康方面发挥着不可或缺的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
'They're creepy creatures with human-like features': children's experiences of visual hallucinations in Charles Bonnet syndrome-a qualitative study.

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.80
自引率
3.80%
发文量
291
审稿时长
3-6 weeks
期刊介绍: Archives of Disease in Childhood is an international peer review journal that aims to keep paediatricians and others up to date with advances in the diagnosis and treatment of childhood diseases as well as advocacy issues such as child protection. It focuses on all aspects of child health and disease from the perinatal period (in the Fetal and Neonatal edition) through to adolescence. ADC includes original research reports, commentaries, reviews of clinical and policy issues, and evidence reports. Areas covered include: community child health, public health, epidemiology, acute paediatrics, advocacy, and ethics.
期刊最新文献
How can parents' experience of child death reviews be improved? Gender affirming hormone therapy for individuals with gender dysphoria aged <26 years: a systematic review and meta-analysis. Blood folate level needed for fully effective fortification in the prevention of neural tube defects. Severe accidental poisonings in children: a British Paediatric Surveillance Unit nationwide prospective study. Topical analgesia during needle-related procedures in children: a clinical practice guideline.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1