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Integrated Physical-Mental Healthcare Services in Specialist Settings to Improve Outcomes for Older People Living With Mental Health Diagnoses: A Systematic Review 在专业机构中提供身心综合保健服务,以改善患有精神疾病的老年人的生活质量:系统性综述
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-12 DOI: 10.1002/gps.6146
Lucy Beishon, Bethan Hickey, Bhavisha Desai, Tamara Chithiramohan, Rachel Evley, Hari Subramaniam, Gregory Maniatopoulos, Anto P. Rajkumar, Tom Dening, Elizabeta Mukateova-Ladinska, Thompson G. Robinson, Carolyn Tarrant

Background

Many older people are now living with co-occurring physical and mental health disorders, but these often managed separately. The aim of this systematic review was to explore integrated physical-mental health care services available internationally for older people living with mental health diagnoses, and whether these result in improved health outcomes.

Methods

Medline, Embase, CINAHL, PsycINFO and Scopus were searched with a predefined search strategy (PROSPERO: CRD42022383824), generating 6210 articles. Studies were included where an integrated physical-mental health care service model was utilised in a population of older people (aged >60 years) with a mental health diagnosis (including dementia or cognitive impairment) and at least one concomitant physical health condition requiring physical health care input. All studies were assessed for risk of bias (ROB 2.0, ROBINS-I) and results were synthesised narratively.

Results

Nine studies were included across inpatient (n = 6, 1262 patients) and community (n = 3, 466 patients) settings. Studies were rated as low-moderate risk of bias. These covered joint physical-mental health wards, liaison services, embedded physicians in mental health wards, and joint multidisciplinary teams. Services with greater integration (e.g., joint wards) had more benefits for patients and carers. There were few benefits to traditional outcomes (e.g., hospital admissions, mortality), but greater care quality, carer satisfaction, and improved mood and engagement were demonstrated.

Conclusions

Multidisciplinary integrated care resulted in improvement of a range of health outcomes for older people with combined physical and mental health needs. Larger and more robust studies are needed to explore the development of these service models further, with cost-effectiveness analyses.

背景 目前,许多老年人同时患有身体和精神疾病,但这些疾病通常是分开管理的。本系统性综述旨在探讨国际上为患有精神疾病的老年人提供的综合身体和心理健康护理服务,以及这些服务是否能改善健康状况。 方法 采用预先确定的检索策略(PROSPERO:CRD42022383824)对 Medline、Embase、CINAHL、PsycINFO 和 Scopus 进行检索,共检索到 6210 篇文章。纳入的研究都是针对被诊断患有精神疾病(包括痴呆症或认知障碍)并同时患有至少一种需要物理治疗的躯体疾病的老年人(年龄在 60 岁以上)采用的综合物理治疗-心理治疗服务模式。对所有研究进行了偏倚风险评估(ROB 2.0,ROBINS-I),并对结果进行了叙述性综合。 结果 共纳入九项研究,涉及住院环境(n = 6,1262 名患者)和社区环境(n = 3,466 名患者)。研究的偏倚风险被评为中低。这些研究涵盖了联合躯体和精神健康病房、联络服务、精神健康病房的嵌入式医生以及联合多学科团队。整合程度更高的服务(如联合病房)对患者和护理者的益处更大。传统的治疗结果(如入院率、死亡率)几乎没有什么益处,但护理质量、护理者满意度以及情绪和参与度都有所提高。 结论 多学科综合护理改善了合并有身心健康需求的老年人的一系列健康结果。需要开展更大规模、更有力的研究,进一步探索这些服务模式的发展,并进行成本效益分析。
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引用次数: 0
EEG Functional Connectivity Differences Predict Future Conversion to Dementia in Mild Cognitive Impairment With Lewy Body or Alzheimer Disease 脑电图功能连接性差异可预测轻度认知障碍伴路易体或阿尔茨海默病患者未来向痴呆症的转化
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-11 DOI: 10.1002/gps.6138
Jahfer Hasoon, Calum A. Hamilton, Julia Schumacher, Sean Colloby, Paul C. Donaghy, Alan J. Thomas, John-Paul Taylor

Background

Predicting which individuals may convert to dementia from mild cognitive impairment (MCI) remains difficult in clinical practice. Electroencephalography (EEG) is a widely available investigation but there is limited research exploring EEG connectivity differences in patients with MCI who convert to dementia.

Methods

Participants with a diagnosis of MCI due to Alzheimer's disease (MCI-AD) or Lewy body disease (MCI-LB) underwent resting state EEG recording. They were followed up annually with a review of the clinical diagnosis (n = 66). Participants with a diagnosis of dementia at year 1 or year 2 follow up were classed as converters (n = 23) and those with a diagnosis of MCI at year 2 were classed as stable (n = 43). We used phase lag index (PLI) to estimate functional connectivity as well as analysing dominant frequency (DF) and relative band power. The Network-based statistic (NBS) toolbox was used to assess differences in network topology.

Results

The converting group had reduced DF (U = 285.5, p = 0.005) and increased relative pre-alpha power (U = 702, p = 0.005) consistent with previous findings. PLI showed reduced average beta band synchrony in the converting group (U = 311, p = 0.014) as well as significant differences in alpha and beta network topology. Logistic regression models using regional beta PLI values revealed that right central to right lateral (Sens = 56.5%, Spec = 86.0%, −2LL = 72.48, p = 0.017) and left central to right lateral (Sens = 47.8%, Spec = 81.4%, −2LL = 71.37, p = 0.012) had the best classification accuracy and fit when adjusted for age and MMSE score.

Conclusion

Patients with MCI who convert to dementia have significant differences in EEG frequency, average connectivity and network topology prior to the onset of dementia. The MCI group is clinically heterogeneous and have underlying physiological differences that may be driving the progression of cognitive symptoms. EEG connectivity could be useful to predict which patients with MCI-AD and MCI-LB convert to dementia, regardless of the neurodegenerative aetiology.

背景 在临床实践中,预测哪些人可能会从轻度认知障碍(MCI)转为痴呆症仍然是个难题。脑电图(EEG)是一种广泛使用的检查方法,但对MCI患者转化为痴呆症的脑电图连接性差异的研究却很有限。 方法 对诊断为阿尔茨海默病(MCI-AD)或路易体病(MCI-LB)导致的 MCI 患者进行静息状态脑电图记录。每年对他们进行随访,并对临床诊断进行复查(n = 66)。第1年或第2年随访时诊断为痴呆症的参与者被归类为转换者(n = 23),第2年诊断为MCI的参与者被归类为稳定者(n = 43)。我们使用相位滞后指数(PLI)估算功能连接性,并分析主导频率(DF)和相对频带功率。基于网络的统计(NBS)工具箱用于评估网络拓扑结构的差异。 结果 转换组的主导频率降低(U = 285.5,p = 0.005),相对α前功率增加(U = 702,p = 0.005),这与之前的研究结果一致。PLI 显示,转换组的β波段平均同步性降低(U = 311,p = 0.014),α和β网络拓扑结构也存在显著差异。使用区域贝塔PLI值的逻辑回归模型显示,在对年龄和MMSE评分进行调整后,右中央到右外侧(Sens = 56.5%,Spec = 86.0%,-2LL = 72.48,p = 0.017)和左中央到右外侧(Sens = 47.8%,Spec = 81.4%,-2LL = 71.37,p = 0.012)的分类准确性和拟合度最好。 结论 MCI 转为痴呆症的患者在痴呆症发病前的脑电图频率、平均连接性和网络拓扑结构存在显著差异。MCI 组在临床上具有异质性,其潜在的生理差异可能是认知症状进展的驱动因素。无论神经退行性病因如何,脑电图连通性都有助于预测哪些MCI-AD和MCI-LB患者会转变为痴呆症。
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引用次数: 0
The Care of Older People With Depression in Nigeria: Qualitative Exploration of the Experience of Lay Providers in Primary Care Settings 尼日利亚抑郁症老年人的护理:对基层医疗机构非专业医疗人员经验的定性探索。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-05 DOI: 10.1002/gps.6147
Akin Ojagbemi, Stephanie Daley, Yvonne Feeney, Oye Gureje

Objectives

There is a large treatment gap for mental health conditions in sub-Saharan Africa where most patients who receive any care do so from lay primary health care workers (PHCW). We sought to examine the experiences of PHCW who provide care for older people with depression in Nigerian primary health care (PHC) settings.

Methods

Qualitative study design. A total of 24 PHCW participated. Using in-depth key informant interviews (KIIs), we explored the views of 15 PHCW selected from 10 rural and urban PHCs in South-Western Nigeria. An additional focus group discussion comprising nine participants was also conducted to discuss emerging themes from KIIs. Data were analysed using thematic analysis.

Results

Three overall themes were identified: views about depression, treatment options, and community outreach implications. Participants perceived depression in older people as being characterised by a range of mood, behavioural, and cognitive symptoms which made clinical assessments particularly challenging. Common treatment options used by PHCW included general advice and counselling, as well as frequent need to prescribe mild analgesics, vitamins and occasional sedatives in line with patients' expectations. Antidepressants were rarely used even though PHCW are authorised. While home visits are part of their expected work schedule, PHCW rarely implemented these due to non-availability of transport facilities. Mobile technology was identified as a possible way of overcoming this constraint to providing community based mental healthcare for older people.

Conclusion

PHCWs perceived that patients' poor cognitive performance, expectations to prescribe sedatives, analgesics and vitamins, as well as non-existence of community-based services were existing barriers to providing evidenced based continued care for older people with depression in the study settings.

目标:在撒哈拉以南非洲地区,精神疾病的治疗缺口很大,那里的大多数患者都是由非专业的初级卫生保健工作者(PHCW)提供治疗。我们试图研究尼日利亚初级卫生保健(PHC)机构中为老年抑郁症患者提供护理的初级卫生保健工作者的经验:定性研究设计。共有 24 名初级保健工作者参与。通过深入的关键信息提供者访谈(KII),我们探讨了从尼日利亚西南部 10 个农村和城市初级保健中心选出的 15 名初级保健工作者的观点。此外,我们还进行了一次由九名参与者组成的焦点小组讨论,以讨论关键信息访谈中出现的主题。采用主题分析法对数据进行了分析:结果:确定了三个总体主题:对抑郁症的看法、治疗方案和社区外联影响。参与者认为,老年人抑郁症的特征是一系列情绪、行为和认知症状,这使得临床评估特别具有挑战性。初级保健工作者常用的治疗方案包括一般建议和咨询,以及经常需要根据病人的期望开具温和的镇痛剂、维生素和偶尔的镇静剂。尽管初级保健社工获得了授权,但他们很少使用抗抑郁药物。虽然家访是他们预期工作日程的一部分,但由于没有交通设施,初级保健工作者很少进行家访。移动技术被认为是克服这一限制,为老年人提供社区精神医疗服务的可行方法:结论:初级保健社工认为,患者认知能力差,期望开具镇静剂、止痛药和维生素,以及不存在以社区为基础的服务,是在研究环境中为患有抑郁症的老年人提供以证据为基础的持续护理的现有障碍。
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引用次数: 0
Promoting Independence Through Quality Dementia Care at Home (PITCH): An Australian Stepped-Wedge Cluster Randomised Controlled Trial Evaluating a Dementia Training Program for Home Care Workers 通过高质量的家庭痴呆症护理促进独立(PITCH):澳大利亚阶梯式楔形集群随机对照试验,评估针对家庭护理人员的痴呆症培训计划。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-05 DOI: 10.1002/gps.6140
Briony Dow, Steven Savvas, Christa Dang, Frances Batchelor, Colleen Doyle, Claudia Cooper, Gill Livingston, Erica Wise, Esther Tan, Anita Panayiotou, Sue Malta, Philip Clarke, Jason Burton, Lee-Fay Low, Samantha M. Loi, Anne Fairhall, Meg Polacsek, Constantine Lyketsos, Samuel Scherer, David Ames, Lidia Engel, Anita M. Y. Goh

Objectives

The primary aim of this pragmatic stepped-wedge cluster RCT was to determine the efficacy of a co-designed dementia specialist training program (the PITCH program) for home care workers (HCWs) to improve their confidence and knowledge when providing care for clients living with dementia.

Methods

HCWs who provided care to clients with dementia were recruited from seven home care service provider organisations in Australia between July 2019 and May 2022, and randomised into one of 18 clusters. The primary outcome was HCW's sense of self-competence in providing care services to people living with dementia at 6 months post PITCH training measured by the Sense of Competence in Dementia Care Staff (SCIDS) Scale.

Results

Two hundred and thirteen HCWS completed baseline assessment and almost half (48.4%) completed all three study assessments. HCWs in clusters that received PITCH training had significantly higher sense of competence (measured by SCIDS) than those who had not received PITCH training. Post hoc analysis revealed that face-to-face PITCH training consistently resulted in improvements in the HCWs sense of competence, dementia attitudes and knowledge when compared to online training and when compared to no training. PITCH training had no effect on the sense of strain HCWs felt in delivering dementia care.

Conclusions

Given the majority of care for people living with dementia is provided at home by family carers supported by HCWs, it is essential that HCWs receive training that improves their skills in dementia care. This study is an important step towards better care at home for people living with dementia.

研究目的方法:在2019年7月至2022年5月期间,从澳大利亚的7家家庭护理服务提供商组织中招募了为痴呆症患者提供护理服务的家庭护理人员,并将其随机分配到18个群组中的一个。主要结果是,在PITCH培训结束后6个月,痴呆症护理人员在为痴呆症患者提供护理服务时的自我胜任感,采用痴呆症护理人员胜任感量表(SCIDS)进行测量:213 名痴呆症护理人员完成了基线评估,近一半(48.4%)完成了所有三项研究评估。接受过 PITCH 培训的群组中的失智症护理人员的能力感(通过 SCIDS 量表测量)明显高于未接受过 PITCH 培训的人员。事后分析表明,与在线培训和未接受培训相比,面对面的 PITCH 培训能够持续改善医护人员的能力感、对痴呆症的态度和知识。PITCH培训对医护人员在提供痴呆症护理时的压力感没有影响:鉴于大多数痴呆症患者的护理工作都是由家庭护理人员在医护人员的支持下在家中完成的,因此医护人员必须接受培训,以提高他们在痴呆症护理方面的技能。这项研究是朝着更好地为痴呆症患者提供家庭护理迈出的重要一步。
{"title":"Promoting Independence Through Quality Dementia Care at Home (PITCH): An Australian Stepped-Wedge Cluster Randomised Controlled Trial Evaluating a Dementia Training Program for Home Care Workers","authors":"Briony Dow,&nbsp;Steven Savvas,&nbsp;Christa Dang,&nbsp;Frances Batchelor,&nbsp;Colleen Doyle,&nbsp;Claudia Cooper,&nbsp;Gill Livingston,&nbsp;Erica Wise,&nbsp;Esther Tan,&nbsp;Anita Panayiotou,&nbsp;Sue Malta,&nbsp;Philip Clarke,&nbsp;Jason Burton,&nbsp;Lee-Fay Low,&nbsp;Samantha M. Loi,&nbsp;Anne Fairhall,&nbsp;Meg Polacsek,&nbsp;Constantine Lyketsos,&nbsp;Samuel Scherer,&nbsp;David Ames,&nbsp;Lidia Engel,&nbsp;Anita M. Y. Goh","doi":"10.1002/gps.6140","DOIUrl":"10.1002/gps.6140","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>The primary aim of this pragmatic stepped-wedge cluster RCT was to determine the efficacy of a co-designed dementia specialist training program (the PITCH program) for home care workers (HCWs) to improve their confidence and knowledge when providing care for clients living with dementia.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>HCWs who provided care to clients with dementia were recruited from seven home care service provider organisations in Australia between July 2019 and May 2022, and randomised into one of 18 clusters. The primary outcome was HCW's sense of self-competence in providing care services to people living with dementia at 6 months post PITCH training measured by the Sense of Competence in Dementia Care Staff (SCIDS) Scale.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Two hundred and thirteen HCWS completed baseline assessment and almost half (48.4%) completed all three study assessments. HCWs in clusters that received PITCH training had significantly higher sense of competence (measured by SCIDS) than those who had not received PITCH training. Post hoc analysis revealed that face-to-face PITCH training consistently resulted in improvements in the HCWs sense of competence, dementia attitudes and knowledge when compared to online training and when compared to no training. PITCH training had no effect on the sense of strain HCWs felt in delivering dementia care.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Given the majority of care for people living with dementia is provided at home by family carers supported by HCWs, it is essential that HCWs receive training that improves their skills in dementia care. This study is an important step towards better care at home for people living with dementia.</p>\u0000 </section>\u0000 </div>","PeriodicalId":14060,"journal":{"name":"International Journal of Geriatric Psychiatry","volume":null,"pages":null},"PeriodicalIF":3.6,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/gps.6140","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142140052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Doing the Right Thing? General Practitioners' Considerations in Achieving a Timely Dementia Diagnosis 做正确的事?全科医生在及时诊断痴呆症时的考虑因素》(General Practitioners' Considerations in Achieving a Timely Dementia Diagnosis)。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-04 DOI: 10.1002/gps.6142
Fleur C. W. Visser, Marlise E. A. van Eersel, Hester J. van der Zaag-Loonen, Liesbeth Hempenius, Marieke Perry, Barbara C. van Munster

Objectives

Timely detection and diagnosis of dementia are beneficial for providing appropriate, anticipatory care and preventing acute situations. However, initiating diagnostic testing is a complex and dynamic process that requires general practitioners (GPs) to balance competing priorities. Previously identified barriers, such as a lack of time, knowledge, and resources, may not fully represent the challenges involved in this process. Therefore, this study aimed to examine GPs' more implicit considerations on starting the diagnostic trajectory for dementia.

Methods

A qualitative study was conducted using semi-structured interviews with 14 Dutch GPs who were purposively selected through maximum variation sampling. The interview transcripts were inductively analyzed in multiple rounds by a multidisciplinary research team using thematic analysis.

Results

GPs' considerations on starting the diagnostic trajectory for dementia can be summarized in three main themes that are interconnected: (1) ‘the presumed patient's willingness’, that is, facing a dilemma of wanting to respect patient autonomy in cases of denial or an absence of a diagnostic request, while at the same time identifying a problem and feeling the urgency to act; (2) ‘the GP's attempt not to harm’, that is, balancing between not wanting to harm the patient and/or relatives with the burdensome label of dementia and with the possible negative consequences of a late diagnosis; and (3) ‘time, trust, and interprofessional collaboration influence timeliness of diagnostic work-up’, that is, time available for consultations, time as a diagnostic factor, GP's diagnostic confidence, and trustful physician–patient relationship.

Conclusions

This study revealed that important ethical dilemmas regarding patient autonomy and the principle of doing no harm lie behind practical GP barriers to initiating diagnostic testing for dementia. Time, trust, and interprofessional collaboration were found to facilitate GPs in determining the right decision and timing with each individual patient and their relatives. Future research could explore the value of diagnostic decision aids that explicitly involve patients and their relatives in this balancing act.

目的:及时发现和诊断痴呆症有利于提供适当的预见性护理和预防急性病症。然而,启动诊断检测是一个复杂而动态的过程,需要全科医生(GPs)平衡相互竞争的优先事项。以前发现的障碍,如缺乏时间、知识和资源,可能并不能完全代表这一过程中所涉及的挑战。因此,本研究旨在探讨全科医生在开始痴呆诊断过程中更多的隐性考虑因素:本研究采用半结构式访谈法对 14 名荷兰全科医生进行了定性研究。多学科研究小组采用主题分析法对访谈记录进行了多轮归纳分析:结果:全科医生在开始诊断痴呆症时的考虑可归纳为三个相互关联的主题:(1) "推测患者的意愿",即在患者拒绝或没有提出诊断要求的情况下,面临既要尊重患者自主权,又要发现问题并感到迫切需要采取行动的两难境地;(2) "全科医生避免伤害的尝试",即在不希望给患者和/或亲属贴上沉重的痴呆症标签,以及不希望因诊断过晚而可能带来的负面影响之间取得平衡;以及 (3) "时间、信任和跨专业合作影响诊断工作的及时性",即可用于会诊的时间、作为诊断因素的时间、全科医生的诊断信心以及信任的医患关系。结论本研究揭示了全科医生在启动痴呆症诊断检测时面临的重要伦理困境,这些困境涉及患者自主权和 "不伤害 "原则。研究发现,时间、信任和跨专业合作有助于全科医生与每位患者及其亲属共同决定正确的决策和时机。未来的研究可以探索诊断决策辅助工具的价值,让患者及其亲属明确参与到这一平衡行动中来。
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引用次数: 0
Comparison of the Parkinson Anxiety Scale and Other Tools to Screen Anxiety in Patients With Parkinson's Disease 帕金森焦虑量表与其他筛查帕金森病患者焦虑的工具的比较。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-03 DOI: 10.1002/gps.6139
Seong-Hi Park
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引用次数: 0
Validation of the Optimal University of California Los Angeles Loneliness Scale Cutoff Score in Screening for the Prevention of Disability Occurrence Among Older Japanese Adults 验证加利福尼亚大学洛杉矶分校孤独感量表在筛查日本老年人预防残疾发生方面的最佳临界值。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-27 DOI: 10.1002/gps.6137
Kouki Tomida, Takahiro Shimoda, Chika Nakajima, Ayuka Kawakami, Hiroyuki Shimada

Objectives

The association between loneliness and disability is a growing public health priority. While the University of California Los Angeles Loneliness Scale (UCLA-LS) has been internationally used as an indicator for assessing loneliness, its optimal cutoff point in relation to disability occurrence has not yet been examined. Therefore, we aimed to determine the optimal cutoff point of the UCLA-LS regarding future disability.

Methods

This longitudinal cohort study was conducted in Tokai City, Aichi Prefecture, Japan. Overall, 4536 community-dwelling older adults (age: 73.8 ± 5.5 years; females: 55.2%) were followed up for 2 years. The area under the curve of the receiver operating characteristic analysis was calculated to evaluate the optimal cutoff point of the UCLA-LS in relation to future disability occurrence using the Youden index, which maximized the sensitivity and specificity of the UCLAS-LS. A survival analysis was conducted to test this cutoff value's external validity, using the presence or absence of disability occurrence as the dependent variable.

Results

The cutoff score of the UCLA-LS in relation to future disability was 44 points. An association was found between new disability occurrence and loneliness based on this cutoff value (hazard ratio: 1.67, 95% confidence interval: 1.29–2.16).

Conclusions

Although cultural context should be taken into account, the optimal cutoff scores for the loneliness scale related to disability identified in this study may be a useful indicator for early recognition of loneliness as a global public health problem and for promoting social participation as one of the disability prevention strategies.

目的:孤独与残疾之间的关系日益成为公共健康的优先事项。尽管加州大学洛杉矶分校孤独感量表(UCLA-LS)已被国际上用作孤独感的评估指标,但其与残疾发生率的最佳临界点尚未得到研究。因此,我们旨在确定 UCLA-LS 与未来残疾有关的最佳临界点:这项纵向队列研究在日本爱知县东海市进行。共对 4536 名居住在社区的老年人(年龄:73.8 ± 5.5 岁;女性:55.2%)进行了为期 2 年的随访。利用尤登指数计算接收者操作特征分析曲线下面积,以评估 UCLA-LS 与未来残疾发生率相关的最佳截断点,从而最大限度地提高 UCLAS-LS 的灵敏度和特异性。以是否发生残疾为因变量,进行生存分析以检验该临界值的外部有效性:结果:与未来残疾相关的 UCLA-LS 临界值为 44 分。根据这一临界值,发现新残疾发生与孤独之间存在关联(危险比:1.67,95% 置信区间:1.29-2.16):尽管应考虑文化背景,但本研究中确定的与残疾相关的孤独感量表的最佳临界值可能是一个有用的指标,有助于及早认识孤独感这一全球公共卫生问题,并促进社会参与,将其作为预防残疾的策略之一。
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引用次数: 0
An Exploration of the Peri-Diagnostic Experiences of Lesbian, Gay and Bisexual People With Dementia Using the Candidacy Framework 利用候选框架探索痴呆症女同性恋、男同性恋和双性恋患者的诊断前经历。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-21 DOI: 10.1002/gps.6135
J. Hammond, B. Hicks, S. Daley, S. Banerjee

Objectives

How dementia affects lesbian, gay, bisexual, trans, queer people or those with other minoritised sexual/gender identities (LGBTQ+) is not well understood. Furthermore, existing research often excludes the voices of LGBTQ+ people living with dementia and focuses instead on their care partners. This study addresses this evidence gap by drawing on the ESRC/NIHR funded DETERMIND cohort, consisting of 940 newly diagnosed people with dementia, to explore the peri-diagnostic experiences of people living with dementia who identify as LGBTQ+.

Methods

We recruited five people (who identified as lesbian, gay or bisexual [LGB]) and completed semi-structured interviews with them and their partner caregivers (n = 3) discussing their experiences of (1) engaging with dementia health care services, (2) receiving a dementia diagnosis, and (3) the support they were offered after diagnosis. Interviews were shaped by the Candidacy Framework, a theoretical model for understanding accessibility of health services, and an inductive thematic analysis was employed to develop common themes.

Findings

Participants did not routinely disclose their LGBTQ+ identities to health service professionals, despite feeling this was an essential aspect of who they are. They relied on their resilience of overcoming previous experiences of lifetime discrimination to navigate complicated dementia care systems. The importance of ‘chosen families’ as informal support networks for LGBTQ+ people living with dementia was highlighted, particularly given the lack of formal care services they felt comfortable accessing. All participants were concerned about their future care needs and whether they would receive home-based or community-based support that respected their LGBTQ+ identities.

Conclusions

This study adds to the limited evidence base that can be used to inform future research, policy and practice seeking to address inequalities across the dementia care pathway. We only interviewed people who identified as LGB so generalizability to the whole LGBTQ+ population is limited, however our data suggest dementia health care professionals should encourage and support disclosures of LGBTQ+ identities so that inclusive care and support planning can be provided to LGBTQ+ people at every stage of dementia.

目标:人们对痴呆症如何影响女同性恋、男同性恋、双性恋、变性人、同性恋者或具有其他少数性/性别身份(LGBTQ+)的人了解不多。此外,现有的研究往往排除了 LGBTQ+ 痴呆症患者的声音,而将重点放在他们的护理伙伴身上。本研究利用由 ESRC/NIHR 资助的 DETERMIND 队列(由 940 名新诊断出的痴呆症患者组成)来探讨被认定为 LGBTQ+ 的痴呆症患者的围诊断期经历,从而填补这一证据空白:我们招募了五名患者(他们被认定为女同性恋、男同性恋或双性恋 [LGB]),并与他们及其伴侣照顾者(n = 3)完成了半结构化访谈,讨论了他们在以下方面的经历:(1)接触痴呆症医疗服务;(2)接受痴呆症诊断;(3)诊断后获得的支持。访谈以 "候选框架 "为基础,"候选框架 "是理解医疗服务可及性的一个理论模型,访谈采用归纳式主题分析法,以形成共同的主题:研究结果:尽管参与者认为LGBTQ+身份是他们的基本特征之一,但他们并没有经常向医疗服务专业人员透露自己的LGBTQ+身份。他们依靠自己的韧性,克服了以往终生遭受歧视的经历,在复杂的痴呆症护理系统中游刃有余。他们强调了 "被选择的家庭 "作为 LGBTQ+ 痴呆症患者非正式支持网络的重要性,尤其是考虑到他们认为可以轻松获得的正规护理服务的缺乏。所有参与者都担心他们未来的护理需求,以及他们是否会得到尊重其 LGBTQ+ 身份的基于家庭或社区的支持:本研究为有限的证据库增添了新的内容,可为未来的研究、政策和实践提供参考,以解决痴呆症护理过程中的不平等问题。我们只采访了那些被认定为 LGBTQ+ 的人,因此对整个 LGBTQ+ 群体的普适性是有限的,但是我们的数据表明,痴呆症医疗保健专业人员应该鼓励和支持 LGBTQ+ 身份的披露,以便在痴呆症的各个阶段为 LGBTQ+ 提供包容性的护理和支持规划。
{"title":"An Exploration of the Peri-Diagnostic Experiences of Lesbian, Gay and Bisexual People With Dementia Using the Candidacy Framework","authors":"J. Hammond,&nbsp;B. Hicks,&nbsp;S. Daley,&nbsp;S. Banerjee","doi":"10.1002/gps.6135","DOIUrl":"10.1002/gps.6135","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>How dementia affects lesbian, gay, bisexual, trans, queer people or those with other minoritised sexual/gender identities (LGBTQ+) is not well understood. Furthermore, existing research often excludes the voices of LGBTQ+ people living with dementia and focuses instead on their care partners. This study addresses this evidence gap by drawing on the ESRC/NIHR funded DETERMIND cohort, consisting of 940 newly diagnosed people with dementia, to explore the peri-diagnostic experiences of people living with dementia who identify as LGBTQ+.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We recruited five people (who identified as lesbian, gay or bisexual [LGB]) and completed semi-structured interviews with them and their partner caregivers (<i>n</i> = 3) discussing their experiences of (1) engaging with dementia health care services, (2) receiving a dementia diagnosis, and (3) the support they were offered after diagnosis. Interviews were shaped by the Candidacy Framework, a theoretical model for understanding accessibility of health services, and an inductive thematic analysis was employed to develop common themes.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Findings</h3>\u0000 \u0000 <p>Participants did not routinely disclose their LGBTQ+ identities to health service professionals, despite feeling this was an essential aspect of who they are. They relied on their resilience of overcoming previous experiences of lifetime discrimination to navigate complicated dementia care systems. The importance of ‘chosen families’ as informal support networks for LGBTQ+ people living with dementia was highlighted, particularly given the lack of formal care services they felt comfortable accessing. All participants were concerned about their future care needs and whether they would receive home-based or community-based support that respected their LGBTQ+ identities.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>This study adds to the limited evidence base that can be used to inform future research, policy and practice seeking to address inequalities across the dementia care pathway. We only interviewed people who identified as LGB so generalizability to the whole LGBTQ+ population is limited, however our data suggest dementia health care professionals should encourage and support disclosures of LGBTQ+ identities so that inclusive care and support planning can be provided to LGBTQ+ people at every stage of dementia.</p>\u0000 </section>\u0000 </div>","PeriodicalId":14060,"journal":{"name":"International Journal of Geriatric Psychiatry","volume":null,"pages":null},"PeriodicalIF":3.6,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/gps.6135","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142017371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Later Life Food Insecurity and Social Isolation in Ghana: The Importance of Psychological Factors 加纳晚年的粮食不安全和社会隔离:心理因素的重要性》(Later Life Food Insecurity and Social Isolation in Ghana: The Importance of Psychological Factors.
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-21 DOI: 10.1002/gps.6134
Razak M. Gyasi, David R. Phillips, Emelia Aikins, Karl Peltzer, Burnett Tetteh Accam, Foster Frempong, Peter Dwumah, Elizabeth Nana Mbrah Koomson-Yalley, Hubert Bimpeh Asiedu, Kabila Abass, André Hajek

Background

Social isolation (SI) and food insecurity (FI) are important social determinants of health that can negatively impact well-being in old age. While research on the association between FI and SI is limited in LMICs, the mediators of this association are largely unknown. This cross-sectional study examined whether FI is associated with SI among older adults in Ghana and whether psychological factors (i.e., depression, anxiety, and sleep problems) mediated the association.

Methods

Our study consisted of adults aged ≥50 years in the Aging, Health, Well-being, and Health-seeking Behavior Study. SI was assessed with the Berkman-Syme Social Network Index, while FI was assessed with dietary inadequacy-related items. We used an ordinary least squares regression (OLS), logistic regressions, and bootstrapping modeling approach to examine our hypotheses with p < 0.05.

Results

The analysis included 1201 individuals (Mage = 66 [SD = 12], women = 63%). In the full sample (β = 0.21; p < 0.001) and in women (β = 0.30, p < 0.001) but not in men, FI was independently associated with SI. FI was comparably associated with increases in SI for the 50–64 age group (β = 0.21, p < 0.001) and ≥65 age cohort (β = 0.19, p < 0.01). Moreover, FI showed differential associations with specific domains of SI (OR = 1.81 to 1.45, p < 0.001). Finally, the FI-SI association was mediated by depressive symptoms (65.16%), anxiety symptoms (30.16%), and sleep problems (9.50%).

Conclusions

Our data highlight the fundamental role of FI in SI among older adults, and the effect is explained by psychosocial factors. Interventions targeted toward strengthening interpersonal ties in old age should include addressing FI and older adults' psychosocial outcomes.

背景:社会隔离(SI)和粮食不安全(FI)是影响健康的重要社会决定因素,会对老年人的福祉产生负面影响。在低收入和中等收入国家,有关 FI 和 SI 之间关系的研究十分有限,而这种关系的中介因素在很大程度上也不为人所知。这项横断面研究探讨了加纳老年人的 FI 是否与 SI 相关,以及心理因素(即抑郁、焦虑和睡眠问题)是否对这种关联起中介作用:我们的研究对象包括 "老龄化、健康、幸福和寻求健康行为研究 "中年龄≥50 岁的成年人。SI通过Berkman-Syme社交网络指数进行评估,而FI则通过与饮食不足相关的项目进行评估。我们使用普通最小二乘法回归(OLS)、逻辑回归和引导建模方法来检验我们的假设,结果为 p:分析包括 1201 人(年龄 = 66 [SD = 12],女性 = 63%)。在全样本中(β = 0.21; p 结论:我们的数据强调了 FI 的基本作用:我们的数据强调了 FI 在老年人 SI 中的基本作用,而社会心理因素可以解释这种影响。针对加强老年人人际关系的干预措施应包括解决 FI 和老年人的社会心理结果问题。
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引用次数: 0
Problem Adaptation Therapy (PATH) to Treat Depression in Older Adults With Cognitive Impairment: A Systematic Review of Treatment Effects 问题适应疗法(PATH)治疗认知障碍老年人的抑郁症:治疗效果系统回顾》。
IF 3.6 3区 医学 Q2 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-19 DOI: 10.1002/gps.6130
Sarah Collyer, Diana Dorstyn

Objectives

Problem adaptation therapy (PATH) is a relatively new psychotherapy that recognises the importance of simultaneously targeting cognitive impairment and functional disability in the treatment of late-life depression. This is the first systematic review to examine the effectiveness of PATH.

Methods

Ageline, Embase, Medline, PsycINFO, Scopus and ProQuest databases were searched from 2010 until 5 April 2024, for studies that evaluated PATH for older people. Where possible, effect sizes (Hedges' g) with 95% confidence intervals and p values were calculated and pooled using a random effects model. The reporting quality of included studies was assessed using Joanna Briggs Institute Critical Appraisal tools and certainty of the evidence behind each result assessed with The Grading of Recommendations Assessment, Development and Evaluation method.

Results

Twelve papers, from seven independent studies and a pooled sample of 579 older adults with multiple comorbidities, were included in this review. PATH participants experienced immediate reductions in depression symptom ratings (gw = 0.72, p < 0.01, Nstudies = 5), alongside small improvements in disability (gw = 0.61, p = 0.04, Nstudies = 4) compared to peers that received supportive therapy, brief psychoeducation, or usual care. The overall evidence quality was, however, characterised by bias, inconsistency, and imprecision in effect estimates. Positive participant feedback and low dropout rates (15%–31%) suggested treatment satisfaction, although these data were not routinely provided.

Conclusions

PATH may be a viable treatment for older people living with mental and cognitive disorders, however there is a need for more rigorous research incorporating follow-up assessments to consolidate the effectiveness of PATH relative to other treatments. Incorporating measures of treatment fidelity are also critical to interpreting and generalising these data. The protocol for this study was prospectively published on the Open Science Framework (https://osf.io/gx57a).

目的:问题适应疗法(PATH)是一种相对较新的心理疗法,它认识到同时针对认知障碍和功能障碍治疗晚年抑郁症的重要性。这是第一篇研究问题适应疗法有效性的系统性综述:从 2010 年到 2024 年 4 月 5 日,在 Ageline、Embase、Medline、PsycINFO、Scopus 和 ProQuest 数据库中检索了对老年人 PATH 进行评估的研究。在可能的情况下,使用随机效应模型计算效应大小(Hedges'g)、95% 置信区间和 p 值并进行汇总。采用乔安娜-布里格斯研究所(Joanna Briggs Institute)的关键评估工具对纳入研究的报告质量进行评估,并采用建议分级评估、发展和评价方法对每项结果背后的证据的确定性进行评估:本综述共收录了 12 篇论文,分别来自 7 项独立研究和 579 名患有多种并发症的老年人的综合样本。与接受支持疗法、简短心理教育或常规护理的同龄人相比,PATH 参与者的抑郁症状评分立即下降(gw = 0.72,p 研究 = 5),残疾状况也略有改善(gw = 0.61,p = 0.04,N 研究 = 4)。不过,总体证据质量存在偏差、不一致和效果估计不精确等问题。参与者的积极反馈和较低的退出率(15%-31%)表明了治疗的满意度,尽管这些数据并不是常规提供的:PATH对患有精神和认知障碍的老年人来说可能是一种可行的治疗方法,但还需要进行更严格的研究,纳入后续评估,以巩固PATH相对于其他治疗方法的有效性。纳入治疗忠诚度的衡量标准对于解释和推广这些数据也至关重要。本研究的方案已在开放科学框架(https://osf.io/gx57a)上进行了前瞻性发布。
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引用次数: 0
期刊
International Journal of Geriatric Psychiatry
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