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Internalized Stigma and its Correlates Among Opioid Agonist Treatment Service Users in Nepal 内化耻辱及其相关的阿片类激动剂治疗服务用户在尼泊尔
Pub Date : 2023-10-10 DOI: 10.1007/s40737-023-00353-4
Sagun Ballav Pant, Suraj Bahadur Thapa, John Howard, Saroj Prasad Ojha, Lars Lien
Abstract Opioid use disorder is associated with high levels of stigma and discrimination, which impact treatment seeking and compliance. Despite extensive evidence as an optimal intervention for opioid use disorder, enrollment in Opioid Agonist Treatment (OAT) in settings like Nepal, is accompanied by moral judgements and stigma with a broad narrative of it being merely a replacement of ‘one addiction with another’. Stigma is eventually internalized by many service users impacting enrollment and maintenance in OAT, and quality of life. This study aimed to assess internalized stigma among OAT service users in Nepal and to explore its association with sociodemographic characteristics, lifetime mental disorders and quality of life. A cross-sectional study was conducted among 231 OAT service users, the survey instrument included the Mini-International Neuropsychiatric Interview for DSM-5, Internalized Stigma of Mental Illness Inventory (ISMI) and the World Health Organization Quality of Life –BREF. Factors associated with quality of life and internalized stigma were investigated using bivariate and multivariate analyses. More than half (56.28%) of respondents reported having high internalized stigma with a mean ISMI score of 2.71 ± 0.64. All 29 ISMI items were found to have a mean score greater than 2.5 indicating a high burden of internalized stigma. Service users reporting higher internalized stigma had significantly lower quality of life across all domains, greater medical co-morbidity, lifetime anxiety and depressive disorder and alcohol use disorder. To lessen stigma and its impacts, our findings recommend a national initiative targeting stigma reduction interventions for existing OAT services and beneficiaries.
阿片类药物使用障碍与高水平的耻辱感和歧视相关,影响治疗寻求和依从性。尽管有大量证据表明阿片类药物使用障碍是一种最佳干预措施,但在尼泊尔等地,阿片类药物激动剂治疗(OAT)的登记伴随着道德判断和耻辱,人们普遍认为它只是“一种成瘾与另一种成瘾”的替代。耻辱感最终被许多服务使用者内化,影响了OAT的登记和维持,以及生活质量。本研究旨在评估尼泊尔OAT服务使用者的内化污名,并探讨其与社会人口学特征、终生精神障碍和生活质量的关系。对231名OAT服务使用者进行了横断面研究,调查工具包括DSM-5的迷你国际神经精神病学访谈、精神疾病内化污名量表(ISMI)和世界卫生组织生活质量量表(bref)。使用双变量和多变量分析调查了与生活质量和内化耻辱相关的因素。超过一半(56.28%)的受访者报告有较高的内化耻辱感,平均ISMI得分为2.71±0.64。所有29个ISMI项目的平均得分均大于2.5,表明内化污名负担较高。报告内化污名较高的服务使用者在所有领域的生活质量都明显较低,医疗合并症较高,终生焦虑和抑郁障碍以及酒精使用障碍。为了减少耻辱感及其影响,我们的研究结果建议针对现有OAT服务和受益人的耻辱感减少干预措施的国家倡议。
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引用次数: 0
Involvement of People with Intellectual Disabilities and Their Carers in Research 智障人士及其照顾者参与研究
Pub Date : 2023-10-10 DOI: 10.1007/s40737-023-00371-2
Sarah Rabbitte, Shagufta Adam
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引用次数: 0
Supporting Carers Within a Forensic Intellectual Disability Community Team: The Development of a Carers Strategy 支援智障法医社区团队的照顾者:制定照顾者策略
Pub Date : 2023-10-06 DOI: 10.1007/s40737-023-00370-3
Charlie Freeman, Gisela Perez-Olivas, Elizabeth Patteril, Verity Chester
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引用次数: 0
“With me and for me”: Perspectives of Service Users with Complex Health and Social Needs on Mental Health Care "与我同在,也为我服务":具有复杂健康和社会需求的服务使用者对精神卫生保健的看法
Pub Date : 2023-10-05 DOI: 10.1007/s40737-023-00372-1
Cara Evans, Nick Kates, Julia Abelson, John Lavis
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引用次数: 0
Diagnostic Overshadowing & Implications on Treatment & Rehabilitation of People with a Genetic Syndrome and Co-existing Psychiatric Conditions: A Case Report of 22q11.2 Duplication Syndrome 诊断性遮蔽对治疗的影响遗传综合征和并存精神疾病患者的康复:22q11.2重复综合征一例报告
Pub Date : 2023-09-19 DOI: 10.1007/s40737-023-00366-z
Ashok Singh, Ayomipo Amiola, Phil Temple, Charlotte Maplanka, Ignatius Gunaratna, Verity Chester
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引用次数: 0
The Role of Play in Developing Social Skills Among Children Diagnosed with Autism Spectrum Disorder in Palestine 游戏在巴勒斯坦自闭症谱系障碍儿童社交技能发展中的作用
Pub Date : 2023-09-17 DOI: 10.1007/s40737-023-00365-0
Sally Abdalhai, Denise Zaya Berte, Fayez Mahamid, Dana Bdier
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引用次数: 0
Developing a Patient and Public Involvement Training Course for People with Intellectual Disabilities: The Leicestershire Experience 为智障人士开发病人和公众参与培训课程:莱斯特郡的经验
Pub Date : 2023-09-15 DOI: 10.1007/s40737-023-00369-w
Samuel Tromans, Rosie Marten, Prabhleen Jaggi, Gemma Lewin, Cath Robinson, Anna Janickyj, Karishma Joshi, Dave Clarke, Reza Kiani, Satheesh Gangadharan
Abstract There is a lack of meaningful involvement of people with intellectual disability in research, outside of the context of study participation. There is a need to develop adapted means of facilitating Patient and Public Involvement when working with people with intellectual disability, that takes account for their level of neurodevelopmental functioning. In this article we describe a Patient and Public Involvement course developed for people with intellectual disability, developed by professionals working with this group, which was subsequently piloted in Leicestershire UK. Different versions of the course were developed for student participants with different levels of neurodevelopmental functioning and communication impairment. For Part 1 of the course (‘What is Research?’), students from Pathway 1 (mild intellectual disability) and Pathway 2 (moderate intellectual disability) both had significantly increased ( p ≤ 0.05) mean knowledge test scores post-course relative to pre-course, with non-significant increases in mean confidence test scores for both pathway groups. For Part 2 of the course (‘Your Involvement in Research’), most participants agreed or strongly agreed with the statement ‘I found this interesting’ (Pathway 1: 8 of 9 students [89%]; Pathway 2: 8 of 10 students [80%]), but less students provided equivalent responses to the statement ‘I want to be involved in research in the future’ (Pathway 1: 2 of 9 students [22%]; Pathway 2: 8 of 10 students [80%]). This training course provides a template to provide basic training for people with intellectual disability with respect to research involvement, but requires further evaluation in larger student samples of diverse demographic and neurodevelopmental characteristics.
在研究参与的背景之外,智力残疾人士在研究中缺乏有意义的参与。在与智障人士一起工作时,有必要制定适应的方法,以促进患者和公众的参与,同时考虑到他们的神经发育功能水平。在这篇文章中,我们描述了一个为智障人士开发的病人和公众参与课程,该课程由与该小组合作的专业人员开发,随后在英国莱斯特郡进行了试点。课程的不同版本是为不同程度的神经发育功能和沟通障碍的学生参与者开发的。对于课程的第一部分(“什么是研究?”),途径1(轻度智力残疾)和途径2(中度智力残疾)的学生在课程后的平均知识测试分数相对于课程前都有显著增加(p≤0.05),两个途径组的平均信心测试分数均无显著增加。对于课程的第二部分(“你对研究的参与”),大多数参与者同意或强烈同意“我觉得这很有趣”(途径1:9名学生中有8名[89%];途径2:8 / 10的学生[80%]),但较少的学生对“我想在未来参与研究”的陈述给出了相同的回答(途径1:2 / 9的学生[22%];途径2:8 / 10的学生[80%])。本培训课程提供了一个模板,为参与研究的智障人士提供基础培训,但需要在更大的不同人口统计学和神经发育特征的学生样本中进行进一步评估。
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引用次数: 0
Rasch Analysis of the Behavioral Assessment Screening Tool for Adolescents (BAST-A) in Mild Traumatic Brain Injury 轻度外伤性脑损伤青少年行为评估筛查工具(BAST-A)的Rasch分析
Pub Date : 2023-09-13 DOI: 10.1007/s40737-023-00364-1
Brittany Wright, Shannon B. Juengst, Karen Brewer-Mixon, C. Munro Cullum, Kristin Wilmoth, Lauren Terhorst
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引用次数: 0
Utilisation of Health Technologies for Physical Health of People with Learning Disabilities: Point of Care Testing 利用健康技术促进学习障碍者的身体健康:护理点测试
Pub Date : 2023-09-12 DOI: 10.1007/s40737-023-00362-3
Dolly Sud, Archana Anandaram, Helen Atkins, Robyn McAskill, Sion Scott
Abstract The World Health Organisation defines health technologies as the “application of organized knowledge and skills in the form of devices, medicines, vaccines, procedures and systems developed to solve a health problem and improve quality of lives.” Innovative health technologies have immense potential to improve human health and well-being. However, their advent does not guarantee equitable health outcomes. Not all individuals have equal access to health technologies resulting in different health outcomes for those individuals. Barriers to adoption, implementation, access, research and design can lead to exclusion and perpetuate the health inequalities already experienced by vulnerable or marginalised groups, for example those with intellectual disabilities (ID). Point of care testing (POCT) is a health technology used to monitor physical health and has been available for almost a decade. POCT is reported to be minimally invasive, can be conducted in a wide range of settings, enables shorter time to clinical decision making, improved self-management of health conditions and patient empowerment. Despite the benefits of POCT, adoption, use, awareness and research of the use of this technology in people with ID to monitor physical health appears to be scant. This article will explore the application of POCT in this group of individuals for whom evidence informs us die up to 25 years earlier when compared to the general population, and physical health disease account for the overwhelming majority of premature deaths. This is a narrative review exploring the use of POCT for physical health of people with ID.
世界卫生组织将卫生技术定义为“为解决健康问题和提高生活质量而开发的设备、药物、疫苗、程序和系统等形式的有组织的知识和技能的应用”。创新卫生技术在改善人类健康和福祉方面具有巨大潜力。然而,它们的出现并不能保证公平的卫生结果。并非所有人都能平等地获得卫生技术,导致这些人的健康结果不同。在采用、实施、获取、研究和设计方面的障碍可能导致弱势群体或边缘群体(例如智力残疾者)已经经历的卫生不平等被排斥并长期存在。护理点检测(POCT)是一种用于监测身体健康的卫生技术,已有近十年的历史。据报道,POCT具有微创性,可在广泛的环境中进行,缩短临床决策时间,改善健康状况的自我管理和患者赋权。尽管POCT有好处,但在身份识别人群中采用、使用、认识和研究使用这项技术来监测身体健康的情况似乎很少。本文将探讨POCT在这组个体中的应用,有证据表明,与一般人群相比,这些个体的死亡时间最长可早25年,而身体健康疾病占绝大多数过早死亡。这是一篇叙述性综述,探讨POCT在ID患者身体健康中的应用。
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引用次数: 0
Psychiatry of Intellectual Disability in the Elderly: A Baseline Audit 老年人智障精神病学:基线审计
Pub Date : 2023-09-11 DOI: 10.1007/s40737-023-00363-2
Ayomipo Amiola, Phil Temple, Ashok Singh, Manilka Brahmana, Meghana Rayala, Ignatius Gunaratna
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引用次数: 0
期刊
Journal of psychosocial rehabilitation and mental health
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