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Medication Self-Management for Home Care Users Receiving Multidose Drug Dispensing: Qualitative Interview Study. 接受多剂量配药的家庭护理用户的用药自我管理:定性访谈研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-10-04 DOI: 10.2196/57651
Anette Vik Josendal, Trine Strand Bergmo

Background: Multidose drug dispensing (MDD) is an adherence aid where medicines are machine-dispensed in disposable unit bags, usually for a 14-day period. MDD replaces manually filled dosettes in many home care services in Norway. While evidence suggests that MDD can improve medication adherence and reduce errors, there are few studies on how patients manage MDD at home and how this affects their daily routines.

Objective: The aim of the study is to identify factors influencing medication self-management behavior among MDD users living at home and explore how MDD affects medication self-management.

Methods: We conducted semistructured interviews with 19 MDD users in Oslo between August 2019 and February 2020. The interviews were held at the participants' homes, and the interview transcripts were analyzed thematically.

Results: All participants in the study received some form of assistance with medication management from home care services. This assistance ranged from MDD delivery every other week to actual assistance with medication administration multiple times daily. However, regardless of the level of assistance received, participants primarily managed their MDD medications themselves. Daily medication routines and knowledge about medicines varied among the participants, with some taking an active role in their medication management, while others relied on others to take responsibility. The degree of involvement seemed determined by motivation rather than capability.

Conclusions: MDD can support medication self-management, but its effectiveness varies among patients. The level of medication management by MDD users is not solely determined by their actual capabilities. Factors such as interest in self-care and independence, available support, information, and cognitive capacity all play a role in determining the degree of autonomy.

背景:多剂量配药(MDD)是一种辅助坚持服药的方法,即用机器将药物分装在一次性药袋中,通常为期 14 天。在挪威的许多家庭护理服务中,多剂量配药取代了人工灌药。虽然有证据表明 MDD 可以提高服药依从性并减少错误,但有关患者如何在家中管理 MDD 以及这对其日常生活有何影响的研究却很少:本研究旨在确定影响居家 MDD 使用者药物自我管理行为的因素,并探讨 MDD 如何影响药物自我管理:我们在 2019 年 8 月至 2020 年 2 月期间对奥斯陆的 19 名 MDD 用户进行了半结构化访谈。访谈在参与者家中进行,并对访谈记录进行了专题分析:研究中的所有参与者都接受了家庭护理服务机构提供的某种形式的药物管理协助。这种协助包括每隔一周提供一次 MDD,也包括每天多次实际协助用药。然而,无论接受何种程度的协助,参与者主要还是自己管理 MDD 药物。参与者的日常用药习惯和药物知识各不相同,有些人在药物管理中发挥了积极作用,而有些人则依赖他人来承担责任。参与程度似乎取决于动机而非能力:MDD 可以支持药物自我管理,但其效果因患者而异。MDD 使用者的药物管理水平并不完全取决于他们的实际能力。对自我护理和独立性的兴趣、可获得的支持、信息和认知能力等因素都对自主程度起着决定作用。
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引用次数: 0
Development of a 12-Week Unsupervised Online Tai Chi Program for People With Hip and Knee Osteoarthritis: Mixed Methods Study. 为髋关节和膝关节骨性关节炎患者开发为期 12 周的无监督在线太极课程:混合方法研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-30 DOI: 10.2196/55322
Shiyi Julia Zhu, Kim L Bennell, Rana S Hinman, Jenny Harrison, Alexander J Kimp, Rachel K Nelligan
<p><strong>Background: </strong>Osteoarthritis is a leading contributor to global disability. While evidence supports the effectiveness of Tai Chi in improving symptoms for people with hip/knee osteoarthritis, access to in-person Tai Chi classes may be difficult for many people. An unsupervised online Tai Chi intervention for people with osteoarthritis can help overcome accessibility barriers. The Approach to Human-Centered, Evidence-Driven Adaptive Design (AHEAD) framework provides a practical guide for co-designing such an intervention.</p><p><strong>Objective: </strong>This study aims to develop an unsupervised online Tai Chi program for people with hip/knee osteoarthritis.</p><p><strong>Methods: </strong>An iterative process was conducted using the AHEAD framework. Initially, a panel of Tai Chi instructors and people with osteoarthritis was assembled. A literature review was conducted to inform the content of a survey (survey 1), which was completed by the panel and additional Australian Tai Chi instructors to identify Tai Chi movements for potential inclusion. Selection of Tai Chi movements was based on 3 criteria: those that were appropriate (for people with hip/knee osteoarthritis aged 45+ years), safe (to be performed at home unsupervised), and practical (to be delivered online using prerecorded videos). Movements that met these criteria were then ranked in a second survey (survey 2; using conjoint analysis methodology). Survey findings were discussed in a focus group, and the Tai Chi movements for program use were identified. A draft of the online Tai Chi program was developed, and a final survey (survey 3) was conducted with the panel to rate the appropriateness and safety of the proposed program. The final program was developed, and usability testing (think-aloud protocol) was conducted with people with knee osteoarthritis.</p><p><strong>Results: </strong>The panel consisted of 10 Tai Chi instructors and 3 people with osteoarthritis. The literature review identified Yang Style 24 as a common and effective Tai Chi style used in hip/knee osteoarthritis studies. Surveys 1 (n=35) and 2 (n=27) produced a ranked list of 24 Tai Chi movements for potential inclusion. This list was refined and informed by a focus group, with 10 Tai Chi movements being selected for inclusion (known as the Yang Style 10 form). Survey 3 (n=13) found that 92% (n=12) of the panel members believed that the proposed draft Tai Chi program was appropriate and safe, resulting in its adoption. The final program was produced and hosted on a customized website, "My Joint Tai Chi," which was further refined based on user feedback (n=5). "My Joint Tai Chi" is currently being evaluated in a randomized controlled trial.</p><p><strong>Conclusions: </strong>This study demonstrates the use of the AHEAD framework to develop an unsupervised online Tai Chi intervention ("My Joint Tai Chi") for people with hip/knee osteoarthritis. This intervention is now being tested for effectivenes
背景:骨关节炎是导致全球残疾的主要因素。虽然有证据支持太极拳能有效改善髋关节/膝关节骨关节炎患者的症状,但对于许多人来说,亲临现场参加太极拳课程可能会有困难。针对骨关节炎患者的无监督在线太极拳干预措施有助于克服障碍。以人为本、证据驱动的适应性设计方法(AHEAD)框架为共同设计此类干预措施提供了实用指南:本研究旨在为髋关节/膝关节骨关节炎患者开发一个无监督的在线太极程序:方法:采用 AHEAD 框架进行迭代。首先,组建了一个由太极拳教练和骨关节炎患者组成的小组。小组成员和其他澳大利亚太极拳教练完成了调查(调查 1),以确定可能纳入的太极拳动作。太极拳动作的选择基于 3 个标准:合适(适合 45 岁以上的髋关节/膝关节骨关节炎患者)、安全(可在无人监督的情况下在家中进行)和实用(可使用预先录制的视频在线教授)。然后在第二次调查(调查 2;采用联合分析方法)中对符合这些标准的动作进行排序。焦点小组对调查结果进行了讨论,并确定了程序使用的太极拳动作。在线太极程序的草案已经完成,并与小组成员一起进行了最后一次调查(调查 3),对拟议程序的适宜性和安全性进行评分。最终程序开发完成,并对膝关节骨关节炎患者进行了可用性测试(思考-朗读协议):小组成员包括 10 名太极拳教练和 3 名骨关节炎患者。文献综述发现杨式 24 是髋关节/膝关节骨关节炎研究中常用且有效的太极拳式。调查 1(n=35)和调查 2(n=27)得出了一份 24 式太极拳动作的排序列表,以供纳入研究。焦点小组对这一列表进行了改进,并提供了相关信息,最终选出 10 个太极拳动作供纳入研究(称为 "杨式十式")。调查 3 (n=13) 发现,92%(n=12)的小组成员认为拟议的太极程序草案是适当和安全的,因此予以通过。最终方案被制作并托管在一个定制网站 "我的关节太极 "上,并根据用户反馈(人数=5)进一步完善。目前,"我的关节太极 "正在随机对照试验中进行评估:本研究展示了使用 AHEAD 框架为髋关节/膝关节骨关节炎患者开发的无监督在线太极拳干预措施("我的关节太极拳")。目前正在随机对照试验中测试该干预措施的有效性和安全性。
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引用次数: 0
Developing a Life Story Intervention for Older Adults With Dementia or at Risk of Delirium Who Were Hospitalized: Multistage, Stakeholder-Engaged Co-Design Study. 为住院的老年痴呆症患者或有谵妄风险的老年人开发生活故事干预:多阶段、利益相关者参与的共同设计研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-27 DOI: 10.2196/59306
Sarah J Flessa, James D Harrison, Roniela Turnigan, Megan Rathfon, Michael Chandler, Jay Newton-Small, Stephanie E Rogers
<p><strong>Background: </strong>Older adults with chronic or acute cognitive impairment, such as dementia or delirium, who are hospitalized face unique barriers to person-centered care and a higher risk for negative outcomes stemming from hospitalizations. There is a need for co-designed interventions adapted for these patients to the hospital setting to improve care and outcomes. Patient life storytelling interventions have demonstrated promise in enhancing person-centered care by improving patient-care team relationships and providing information to enable care tailored to individual needs and values.</p><p><strong>Objective: </strong>This study aims to engage patients, care partners, and clinical stakeholders in a co-design process to adapt an existing life storytelling model for use with older adults with dementia and at risk of delirium in the acute care hospital setting.</p><p><strong>Methods: </strong>We recruited patients with dementia or at risk of delirium who were hospitalized, their care partners, clinicians, and informaticists. A 3-stage co-design process that used a mixed methods data collection approach including in-depth interviews and surveys was completed. We used content analysis to analyze qualitative data and descriptive statistics to summarize quantitative data.</p><p><strong>Results: </strong>In total, 27 stakeholder informants (ie, patients, care partners, and interdisciplinary care team [IDT] members) participated. Stakeholders were unanimously interested in using patient life stories as a tool for hospital care through electronic health record (EHR) integration. Stakeholders shared potential topics for life stories to cover, including social support, information on patients' key life events, and favorite activities. Participants provided insights into the logistics of integrating life stories into acute care, including interview arrangement, story-sharing methods, and barriers and facilitators. IDT members shared preferences on EHR integration, resulting in 3 co-designed mock-ups of EHR integration options. Stakeholders shared ways to optimize future acceptability and uptake, including engaging with the care team and promoting awareness of life stories, ensuring suitability to the acute environment (eg, distilling information in an easily digestible way), and addressing concerns for patient capacity and privacy (eg, engaging care partners when appropriate). Thoughts on potential impacts of life stories were also elicited, including improving patient- and care partner-IDT member relationships; humanizing patients; increasing clinical team, patient, and caregiver satisfaction; and enabling more specific, tailored care for patients with dementia and at risk of delirium.</p><p><strong>Conclusions: </strong>This study resulted in a co-designed life storytelling intervention for patients with dementia and at risk for delirium in an acute care hospital setting. Stakeholders provided valuable information to ensure future interve
背景:患有慢性或急性认知障碍(如痴呆或谵妄)并住院治疗的老年人在获得以人为本的护理方面面临着独特的障碍,而且因住院而产生不良后果的风险更高。因此需要针对这些患者的情况,共同设计适合医院环境的干预措施,以改善护理和治疗效果。通过改善患者与护理团队之间的关系,并提供信息以便根据个人需求和价值观提供护理,患者生活故事干预已在加强以人为本的护理方面显示出前景:本研究旨在让患者、护理伙伴和临床利益相关者参与到共同设计过程中,以调整现有的生命故事模式,使其适用于医院急症护理环境中患有痴呆症和有谵妄风险的老年人:我们招募了住院的痴呆症患者或有谵妄风险的患者、他们的护理伙伴、临床医生和信息学家。共同设计过程分为三个阶段,采用混合方法收集数据,包括深度访谈和问卷调查。我们使用内容分析法对定性数据进行分析,并使用描述性统计法对定量数据进行总结:共有 27 位利益相关者(即患者、护理伙伴和跨学科护理团队 [IDT] 成员)参与了此次调查。利益相关者一致希望通过整合电子健康记录(EHR),将患者生命故事作为医院护理的一种工具。利益相关者分享了生命故事可能涉及的主题,包括社会支持、患者关键生命事件的信息以及最喜欢的活动。与会者就将生命故事融入急症护理的后勤工作发表了见解,包括访谈安排、故事分享方法以及障碍和促进因素。IDT 成员分享了对电子病历整合的偏好,并共同设计了 3 个电子病历整合模拟方案。利益相关者分享了优化未来可接受性和吸收率的方法,包括与护理团队合作并提高对生命故事的认识,确保适合急症环境(例如,以易于消化的方式提炼信息),以及解决对患者能力和隐私的担忧(例如,在适当的时候让护理合作伙伴参与进来)。此外,还征求了对生命故事潜在影响的看法,包括改善患者、护理伙伴和 IDT 成员之间的关系;使患者人性化;提高临床团队、患者和护理人员的满意度;为痴呆患者和有谵妄风险的患者提供更具体、更有针对性的护理:这项研究为医院急症护理环境中的痴呆症患者和有谵妄风险的患者提供了共同设计的生命故事干预。利益相关者提供了宝贵的信息,以确保未来干预措施的可接受性和吸收率,包括在急症护理环境中的潜在益处、促进因素和挑战。
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引用次数: 0
Extracting Critical Information from Unstructured Clinicians' Notes Data to Identify Dementia Severity Using a Rule-Based Approach: Feasibility Study. 从非结构化临床医生笔记数据中提取关键信息,利用基于规则的方法识别痴呆症严重程度:可行性研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-24 DOI: 10.2196/57926
Ravi Prakash, Matthew E Dupre, Truls Østbye, Hanzhang Xu
<p><strong>Background: </strong>The severity of Alzheimer disease and related dementias (ADRD) is rarely documented in structured data fields in electronic health records (EHRs). Although this information is important for clinical monitoring and decision-making, it is often undocumented or "hidden" in unstructured text fields and not readily available for clinicians to act upon.</p><p><strong>Objective: </strong>We aimed to assess the feasibility and potential bias in using keywords and rule-based matching for obtaining information about the severity of ADRD from EHR data.</p><p><strong>Methods: </strong>We used EHR data from a large academic health care system that included patients with a primary discharge diagnosis of ADRD based on ICD-9 (International Classification of Diseases, Ninth Revision) and ICD-10 (International Statistical Classification of Diseases, Tenth Revision) codes between 2014 and 2019. We first assessed the presence of ADRD severity information and then the severity of ADRD in the EHR. Clinicians' notes were used to determine the severity of ADRD based on two criteria: (1) scores from the Mini Mental State Examination and Montreal Cognitive Assessment and (2) explicit terms for ADRD severity (eg, "mild dementia" and "advanced Alzheimer disease"). We compiled a list of common ADRD symptoms, cognitive test names, and disease severity terms, refining it iteratively based on previous literature and clinical expertise. Subsequently, we used rule-based matching in Python using standard open-source data analysis libraries to identify the context in which specific words or phrases were mentioned. We estimated the prevalence of documented ADRD severity and assessed the performance of our rule-based algorithm.</p><p><strong>Results: </strong>We included 9115 eligible patients with over 65,000 notes from the providers. Overall, 22.93% (2090/9115) of patients were documented with mild ADRD, 20.87% (1902/9115) were documented with moderate or severe ADRD, and 56.20% (5123/9115) did not have any documentation of the severity of their ADRD. For the task of determining the presence of any ADRD severity information, our algorithm achieved an accuracy of >95%, specificity of >95%, sensitivity of >90%, and an F<sub>1</sub>-score of >83%. For the specific task of identifying the actual severity of ADRD, the algorithm performed well with an accuracy of >91%, specificity of >80%, sensitivity of >88%, and F<sub>1</sub>-score of >92%. Comparing patients with mild ADRD to those with more advanced ADRD, the latter group tended to contain older, more likely female, and Black patients, and having received their diagnoses in primary care or in-hospital settings. Relative to patients with undocumented ADRD severity, those with documented ADRD severity had a similar distribution in terms of sex, race, and rural or urban residence.</p><p><strong>Conclusions: </strong>Our study demonstrates the feasibility of using a rule-based matching algorithm to identif
背景:阿尔茨海默病及相关痴呆症(ADRD)的严重程度很少记录在电子病历(EHR)的结构化数据字段中。虽然这些信息对临床监测和决策非常重要,但它们往往没有记录或 "隐藏 "在非结构化文本字段中,临床医生无法随时采取行动:我们旨在评估使用关键词和基于规则的匹配从电子病历数据中获取 ADRD 严重程度信息的可行性和潜在偏差:我们使用了一个大型学术医疗保健系统的电子病历数据,这些数据包括 2014 年至 2019 年期间根据 ICD-9(国际疾病分类,第九版)和 ICD-10(国际疾病统计分类,第十版)代码主要出院诊断为 ADRD 的患者。我们首先评估了电子病历中是否存在 ADRD 严重程度信息,然后评估了 ADRD 的严重程度。我们根据临床医生的记录来确定 ADRD 的严重程度,该记录基于两个标准:(1) Mini Mental State Examination(迷你精神状态检查)和 Montreal Cognitive Assessment(蒙特利尔认知评估)的评分;(2) ADRD 严重程度的明确术语(如 "轻度痴呆 "和 "晚期阿尔茨海默病")。我们编制了一份常见 ADRD 症状、认知测试名称和疾病严重程度术语的列表,并根据以往的文献和临床专业知识反复进行完善。随后,我们在 Python 中使用标准开源数据分析库进行基于规则的匹配,以确定提及特定单词或短语的上下文。我们估算了有记录的 ADRD 严重程度的患病率,并评估了基于规则的算法的性能:我们纳入了 9115 名符合条件的患者,他们的医疗服务提供者提供了 65,000 多份记录。总体而言,22.93%(2090/9115)的患者记录有轻度 ADRD,20.87%(1902/9115)的患者记录有中度或重度 ADRD,56.20%(5123/9115)的患者没有任何关于 ADRD 严重程度的记录。在确定是否存在任何 ADRD 严重程度信息的任务中,我们算法的准确性>95%,特异性>95%,灵敏度>90%,F1 分数>83%。在识别 ADRD 实际严重程度的特定任务中,该算法表现出色,准确率大于 91%,特异性大于 80%,灵敏度大于 88%,F1 分数大于 92%。将轻度 ADRD 患者与晚期 ADRD 患者进行比较,发现晚期 ADRD 患者往往年龄较大,更可能是女性和黑人,并且是在初级保健或医院环境中得到诊断的。与未记录 ADRD 严重程度的患者相比,记录了 ADRD 严重程度的患者在性别、种族、农村或城市居住地方面的分布相似:我们的研究证明了使用基于规则的匹配算法从非结构化电子病历报告数据中识别 ADRD 严重程度的可行性。然而,我们必须认识到不同医疗系统的记录方法不同可能会造成偏差。
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引用次数: 0
Development of a Dementia Case Management Information System App: Mixed Methods Study. 开发痴呆症病例管理信息系统应用程序:混合方法研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-23 DOI: 10.2196/56549
Huei-Ling Huang, Yi-Ping Chao, Chun-Yu Kuo, Ya-Li Sung, Yea-Ing L Shyu, Wen-Chuin Hsu
<p><strong>Background: </strong>Case managers for persons with dementia not only coordinate patient care but also provide family caregivers with educational material and available support services. Taiwan uses a government-based information system for monitoring the provision of health care services. Unfortunately, scheduling patient care and providing information to family caregivers continues to be paper-based, which results in a duplication of patient assessments, complicates scheduling of follow-ups, and hinders communication with caregivers, which limits the ability of case managers to provide cohesive, quality care.</p><p><strong>Objective: </strong>This multiphase study aimed to develop an electronic information system for dementia care case managers based on their perceived case management needs and what they would like included in an electronic health care app.</p><p><strong>Methods: </strong>Case managers were recruited to participate (N=63) by purposive sampling from 28 facilities representing two types of community-based dementia care centers in Taiwan. A dementia case management information system (DCMIS) app was developed in four phases. Phase 1 assessed what should be included in the app by analyzing qualitative face-to-face or internet-based interviews with 33 case managers. Phase 2 formulated a framework for the app to support case managers based on key categories identified in phase 1. During phase 3, a multidisciplinary team of information technology engineers and dementia care experts developed the DCMIS app: hardware and software components were selected, including platforms for messaging, data management, and security. The app was designed to eventually interface with a family caregiver app. Phase 4 involved pilot-testing the DCMIS app with a second group of managers (n=30); feedback was provided via face-to-face interviews about their user experience.</p><p><strong>Results: </strong>Findings from interviews in phase 1 indicated the DCMIS framework should include unified databases for patient reminder follow-up scheduling, support services, a health education module, and shared recordkeeping to facilitate teamwork, networking, and communication. The DCMIS app was built on the LINE (LY Corporation) messaging platform, which is the mobile app most widely used in Taiwan. An open-source database management system allows secure entry and storage of user information and patient data. Case managers had easy access to educational materials on dementia and caregiving for persons living with dementia that could be provided to caregivers. Interviews with case managers following pilot testing indicated that the DCMIS app facilitated the completion of tasks and management responsibilities. Some case managers thought it would be helpful to have a DCMIS desktop computer system rather than a mobile app.</p><p><strong>Conclusions: </strong>Based on pilot testing, the DCMIS app could reduce the growing challenges of high caseloads faced by ca
背景:痴呆症患者的个案经理不仅要协调患者的护理工作,还要为家庭护理人员提供教育材料和可用的支持服务。台湾使用基于政府的信息系统来监控医疗保健服务的提供情况。遗憾的是,为患者安排护理时间和向家庭照护者提供信息仍然采用纸质方式,这导致了患者评估的重复,使随访时间的安排变得复杂,并阻碍了与照护者的沟通,从而限制了个案管理者提供连贯、优质护理的能力:这项多阶段研究旨在根据痴呆症护理个案管理者的个案管理需求以及他们希望电子医疗应用程序包含的内容,为他们开发一套电子信息系统:通过有目的的抽样,从代表台湾两类社区失智症照护中心的28家机构中招募病例管理者(63人)参与研究。痴呆症病例管理信息系统(DCMIS)应用程序的开发分为四个阶段。第一阶段通过分析与 33 名个案管理者面对面或基于互联网的定性访谈,评估应用程序应包括哪些内容。第 2 阶段根据第 1 阶段确定的关键类别,为应用程序制定了一个框架,以支持个案管理者。在第 3 阶段,由信息技术工程师和痴呆症护理专家组成的多学科团队开发了 DCMIS 应用程序:选择了硬件和软件组件,包括消息传递、数据管理和安全平台。该应用程序的设计目的是最终与家庭护理应用程序对接。第 4 阶段包括对第二组管理人员(人数=30)进行 DCMIS 应用程序的试点测试;通过面对面访谈对他们的用户体验进行反馈:第 1 阶段的访谈结果表明,DCMIS 框架应包括统一的数据库,用于患者提醒随访安排、支持服务、健康教育模块和共享记录保存,以促进团队合作、联网和沟通。DCMIS 应用程序建立在 LINE(LY 公司)信息平台上,该平台是台湾使用最广泛的移动应用程序。开放源码数据库管理系统允许安全输入和存储用户信息和患者数据。病例管理员可以方便地获取有关痴呆症和痴呆症患者护理的教育资料,并将其提供给护理人员。试点测试后对个案经理的访谈表明,DCMIS 应用程序有助于完成任务和管理职责。一些个案经理认为,如果有一个 DCMIS 台式电脑系统,而不是一个移动应用程序,会更有帮助:根据试点测试的结果,DCMIS 应用程序可以减少痴呆症患者个案经理面临的日益增多的高工作量挑战,从而改善护理的连续性。这些研究结果将为台湾全面开发该系统并将其与电子医疗系统整合时提供参考。
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引用次数: 0
Internet Use and Higher-Level Functional Capacity Decline Suppression in Japanese Older Adults With Low Education: JAGES 2016-2019 Longitudinal Study. 日本低学历老年人的互联网使用与高级功能能力下降抑制:JAGES 2016-2019 纵向研究》。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-20 DOI: 10.2196/53384
Atsuko Tajika, Atsushi Nakagomi, Yasuhiro Miyaguni, Chie Koga, Katsunori Kondo, Toshiyuki Ojima

Background: Higher-level functional capacity (HLFC) is crucial for the independent living of older adults. While internet use positively impacts the health of older adults, its effect on HLFC and how this effect varies with educational attainment remains uncertain.

Objective: This longitudinal study aimed to investigate whether internet use could mitigate the risk of HLFC decline and if this benefit extends to older adults with lower levels of education.

Methods: The data were sourced from the Japan Gerontological Evaluation Study (JAGES), encompassing 8050 community-dwelling adults aged 65 years and older from 2016 to 2019. The study focused on those who remained self-sufficient from 2016 to 2019, identifying participants with independent HLFC in 2016. The Tokyo Metropolitan Institute of Gerontology Index of Competence defined HLFC operationally, consisting of 3 subscales, namely instrumental activities of daily living, intellectual activity, and social role. The primary variable was the frequency of internet use in 2016; participants who reported using the internet were classified as internet users, while those who answered "No" were identified as nonusers. The study compared the effects of internet use on HLFC decline across educational levels of ≤9 years, 10-12 years, and ≥13 years using Poisson regression analysis adjusted for robust SE to calculate the risk ratio (RR) and 95% CI for HLFC decline in 2019.

Results: After adjusting for demographic and health condition risk factors, internet use was significantly linked to a decreased risk of HLFC decline in older adults over 3 years, including those with lower educational levels. Internet users with ≤9 years of educational attainment experienced a suppressed decline in the total score (RR 0.57, 95% CI 0.43-0.76; P<.001); instrumental activities of daily living (RR 0.58, 95% CI 0.38-0.91; P=.02), intellectual activity (RR 0.60, 95% CI 0.41-0.89; P=.01), and social role (RR 0.74, 95% CI 0.56-0.97; P=.03) compared with nonusers. Participants with 10-12 years of education showed suppression rates of 0.78 (95% CI 0.63-0.98; P=.03), 0.59 (95% CI 0.39-0.90; P=.01), 0.91 (95% CI 0.63-1.31; P=.61), and 0.82 (95% CI 0.68-1.00; P=.05), respectively, and those with ≥13 years displayed suppression rates of 0.65 (95% CI 0.51-0.85; P=.001), 0.55 (95% CI 0.36-0.83; P=.01), 0.64 (95% CI 0.37-1.10; P=.11), and 0.83 (95% CI 0.64-1.08; P=.17), respectively.

Conclusions: These findings indicate that internet use supports the maintenance of HLFC independence in older adults with higher education and those with lower educational levels. Encouraging internet use among older adults with lower levels of education through future policies could help narrow functional health disparities associated with educational attainment.

背景:高级功能能力(HLFC)对老年人的独立生活至关重要。虽然互联网的使用对老年人的健康有积极影响,但其对 HLFC 的影响以及这种影响如何随受教育程度而变化仍不确定:这项纵向研究旨在调查互联网的使用是否能降低 HLFC 下降的风险,以及这种益处是否会延伸到受教育程度较低的老年人:数据来源于日本老年学评估研究(JAGES),包括2016年至2019年期间8050名65岁及以上居住在社区的成年人。研究的重点是那些从 2016 年到 2019 年一直保持自给自足的人,确定了 2016 年拥有独立 HLFC 的参与者。东京都老年学研究所能力指数对HLFC进行了操作性定义,包括3个分量表,即日常生活工具活动、智力活动和社会角色。主要变量是 2016 年使用互联网的频率;将报告使用互联网的参与者归类为互联网使用者,而将回答 "否 "的参与者归类为非使用者。研究比较了不同教育水平(≤9年、10-12年和≥13年)的互联网使用对HLFC下降的影响,使用经稳健SE调整的泊松回归分析计算2019年HLFC下降的风险比(RR)和95% CI:结果:调整人口统计学和健康状况风险因素后,互联网的使用与老年人3年内HLFC下降的风险显著相关,包括教育水平较低的老年人。教育程度≤9年的互联网用户的总分下降受到抑制(RR为0.57,95% CI为0.43-0.76;PC结论:这些研究结果表明,对于教育程度较高的老年人和教育程度较低的老年人来说,使用互联网有助于保持 HLFC 的独立性。通过未来的政策鼓励教育水平较低的老年人使用互联网,有助于缩小与教育程度相关的功能性健康差异。
{"title":"Internet Use and Higher-Level Functional Capacity Decline Suppression in Japanese Older Adults With Low Education: JAGES 2016-2019 Longitudinal Study.","authors":"Atsuko Tajika, Atsushi Nakagomi, Yasuhiro Miyaguni, Chie Koga, Katsunori Kondo, Toshiyuki Ojima","doi":"10.2196/53384","DOIUrl":"10.2196/53384","url":null,"abstract":"<p><strong>Background: </strong>Higher-level functional capacity (HLFC) is crucial for the independent living of older adults. While internet use positively impacts the health of older adults, its effect on HLFC and how this effect varies with educational attainment remains uncertain.</p><p><strong>Objective: </strong>This longitudinal study aimed to investigate whether internet use could mitigate the risk of HLFC decline and if this benefit extends to older adults with lower levels of education.</p><p><strong>Methods: </strong>The data were sourced from the Japan Gerontological Evaluation Study (JAGES), encompassing 8050 community-dwelling adults aged 65 years and older from 2016 to 2019. The study focused on those who remained self-sufficient from 2016 to 2019, identifying participants with independent HLFC in 2016. The Tokyo Metropolitan Institute of Gerontology Index of Competence defined HLFC operationally, consisting of 3 subscales, namely instrumental activities of daily living, intellectual activity, and social role. The primary variable was the frequency of internet use in 2016; participants who reported using the internet were classified as internet users, while those who answered \"No\" were identified as nonusers. The study compared the effects of internet use on HLFC decline across educational levels of ≤9 years, 10-12 years, and ≥13 years using Poisson regression analysis adjusted for robust SE to calculate the risk ratio (RR) and 95% CI for HLFC decline in 2019.</p><p><strong>Results: </strong>After adjusting for demographic and health condition risk factors, internet use was significantly linked to a decreased risk of HLFC decline in older adults over 3 years, including those with lower educational levels. Internet users with ≤9 years of educational attainment experienced a suppressed decline in the total score (RR 0.57, 95% CI 0.43-0.76; P<.001); instrumental activities of daily living (RR 0.58, 95% CI 0.38-0.91; P=.02), intellectual activity (RR 0.60, 95% CI 0.41-0.89; P=.01), and social role (RR 0.74, 95% CI 0.56-0.97; P=.03) compared with nonusers. Participants with 10-12 years of education showed suppression rates of 0.78 (95% CI 0.63-0.98; P=.03), 0.59 (95% CI 0.39-0.90; P=.01), 0.91 (95% CI 0.63-1.31; P=.61), and 0.82 (95% CI 0.68-1.00; P=.05), respectively, and those with ≥13 years displayed suppression rates of 0.65 (95% CI 0.51-0.85; P=.001), 0.55 (95% CI 0.36-0.83; P=.01), 0.64 (95% CI 0.37-1.10; P=.11), and 0.83 (95% CI 0.64-1.08; P=.17), respectively.</p><p><strong>Conclusions: </strong>These findings indicate that internet use supports the maintenance of HLFC independence in older adults with higher education and those with lower educational levels. Encouraging internet use among older adults with lower levels of education through future policies could help narrow functional health disparities associated with educational attainment.</p>","PeriodicalId":36245,"journal":{"name":"JMIR Aging","volume":"7 ","pages":"e53384"},"PeriodicalIF":5.0,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11452757/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142297320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Requirement Analysis of Different Variants of a Measurement and Training Station for Older Adults at Risk of Malnutrition and Reduced Mobility: Focus Group Study. 针对有营养不良和行动不便风险的老年人的测量和训练站不同变体的需求分析:焦点小组研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-17 DOI: 10.2196/58714
Lisa Happe, Marie Sgraja, Vincent Quinten, Mareike Förster, Rebecca Diekmann

Background: Demographic change is leading to an increasing proportion of older people in the German population and requires new approaches for prevention and rehabilitation to promote the independence and health of older people. Technical assistance systems can offer a promising solution for the early detection of nutritional and physical deficits and the initiation of appropriate interventions. Such a system should combine different components, such as devices for assessing physical and nutritional status, educational elements on these topics, and training and feedback options. The concept is that the whole system can be used independently by older adults (aged ≥70 years) for monitoring and early detection of problems in nutrition or physical function, as well as providing opportunities for intervention.

Objective: This study aims to develop technical and digital elements for a measurement and training station (MuTs) with an associated app. Through focus group discussions, target group requirements, barriers, and favorable components for such a system were identified.

Methods: Older adults (aged ≥70 years) were recruited from a community-based setting as well as from a geriatric rehabilitation center. Focus group interviews were conducted between August and November 2022. Following a semistructured interview guideline, attitudes, requirements, preferences, and barriers for the MuTs were discussed. Discussions were stimulated by videos, demonstrations of measuring devices, and participants' ratings of the content presented using rankings. After conducting 1 focus group in the rehabilitation center and 2 in the community, the interview guide was refined, making a more detailed discussion of identified elements and aspects possible. The interviews were recorded, transcribed verbatim, and analyzed using content analysis.

Results: A total of 21 older adults (female participants: n=11, 52%; mean age 78.5, SD 4.6 years) participated in 5 focus group discussions. There was a strong interest in the independent measurement of health parameters, such as pulse and hand grip strength, especially among people with health problems who would welcome feedback on their health development. Participants emphasized the importance of personal guidance and interaction before using the device, as well as the need for feedback mechanisms and personalized training for everyday use. Balance and coordination were mentioned as preferred training areas in a MuTs. New training options that motivate and invite people to participate could increase willingness to use the MuTs.

Conclusions: The target group is generally open and interested in tracking and optimizing diet and physical activity. A general willingness to use a MuTs independently was identified, as well as a compelling need for guidance and feedback on measurement and training to be part of the station.

背景:人口结构的变化导致德国人口中老年人的比例不断增加,这就需要新的预防和康复方法来促进老年人的独立和健康。技术援助系统可以为早期发现营养和身体缺陷并启动适当的干预措施提供一个很有前景的解决方案。这种系统应结合不同的组成部分,如评估身体和营养状况的设备、有关这些主题的教育要素以及培训和反馈选项。其概念是,整个系统可由老年人(年龄≥70 岁)独立使用,用于监测和早期发现营养或身体功能方面的问题,并提供干预机会:本研究旨在开发测量和训练站(MuTs)的技术和数字元素以及相关应用程序。通过焦点小组讨论,确定了目标群体的要求、障碍以及该系统的有利要素:方法:从社区和老年康复中心招募老年人(年龄≥70 岁)。焦点小组访谈于 2022 年 8 月至 11 月间进行。按照半结构式访谈指南,讨论了对 MuTs 的态度、要求、偏好和障碍。讨论由视频、测量设备演示和参与者对所展示内容的评分排名激发。在康复中心进行了 1 次焦点小组讨论,在社区进行了 2 次焦点小组讨论后,对访谈指南进行了改进,以便对确定的要素和方面进行更详细的讨论。对访谈进行了录音、逐字记录和内容分析:共有 21 名老年人(女性:11 人,占 52%;平均年龄 78.5 岁,标准差 4.6 岁)参加了 5 次焦点小组讨论。与会者对独立测量脉搏和手部握力等健康参数有着浓厚的兴趣,尤其是对那些有健康问题的人来说,他们希望得到有关其健康发展的反馈。与会者强调了在使用设备前个人指导和互动的重要性,以及日常使用中反馈机制和个性化培训的必要性。与会者提到,平衡和协调是 MuTs 的首选训练领域。激励和邀请人们参与的新培训方案可以提高人们使用 MuTs 的意愿:结论:目标群体普遍持开放态度,并对跟踪和优化饮食及体育锻炼感兴趣。结论:目标群体总体上是开放的,对跟踪和优化饮食及体育锻炼感兴趣。他们普遍愿意独立使用 MuTs,同时也非常需要测量和培训方面的指导和反馈,这也是测量站的一部分。
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引用次数: 0
Factors Influencing Malnutrition Among Older Adult Residents in the Western Region of Saudi Arabia: Sex Differential Study. 影响沙特阿拉伯西部地区老年居民营养不良的因素:性别差异研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-16 DOI: 10.2196/55572
Mai Adil Ghabashi, Firas Sultan Azzeh

Background: The global population of older adults is on the rise. As people age, their physical functions gradually decline, leading to a decrease in the overall functioning of different organ systems. Due to these changes, older individuals are at a higher risk of encountering various adverse health outcomes and complications, such as malnutrition.

Objective: This study aims to investigate the prevalence of malnutrition and its associated factors among older adults dwelling in the western region of Saudi Arabia. We have analyzed these factors separately for both men and women to understand any potential sex differences.

Methods: A nonrandomized cross-sectional study was conducted for older adults aged ≥60 years in the western region of Saudi Arabia. Personal information was obtained through a closed questionnaire. The Mini Nutritional Assessment Short Form was used to determine the malnutrition status of older adults. Consequently, the individuals were divided into 2 groups: normal and malnourished. To assess the risk factors related to malnutrition, the odds ratio (OR) and 95% CI were determined using a binary logistic regression.

Results: The prevalence of malnutrition in men and women was around 7% and 5%, respectively. Potential risk factors related to malnutrition in men were higher age (OR 1.263, 95% CI 1.086-1.468; P=.002), being widowed (OR 8.392, 95% CI 1.002-70.258; P=.049), and having dental problems (OR 9.408, 95% CI 1.863-47.514; P=.007). On the other hand, risk factors associated with malnutrition in women were lower BMI (OR 0.843, 95% CI 0.747-0.952; P=.006) and being disabled (OR 18.089, 95% CI 0.747-0.952; P=.006).

Conclusions: The findings of this study provide important insights into the risk factors for malnutrition among older adults in the western region of Saudi Arabia. While the overall prevalence of malnutrition was relatively low, the analysis revealed distinct risk factors for older men and women. Interventions developed based on the identified risk factors may prove effective in addressing the issue of malnutrition within this population.

背景:全球老年人口呈上升趋势。随着年龄的增长,人们的身体机能逐渐衰退,导致不同器官系统的整体功能下降。由于这些变化,老年人出现各种不良健康后果和并发症(如营养不良)的风险较高:本研究旨在调查沙特阿拉伯西部地区老年人营养不良的发生率及其相关因素。我们分别对男性和女性的这些因素进行了分析,以了解任何潜在的性别差异:我们对沙特阿拉伯西部地区年龄≥60 岁的老年人进行了一项非随机横断面研究。个人信息通过封闭式问卷调查获得。迷你营养评估简表用于确定老年人的营养不良状况。因此,这些人被分为两组:正常组和营养不良组。为了评估与营养不良相关的风险因素,采用二元逻辑回归法确定了几率比(OR)和 95% CI:结果:男性和女性营养不良的发生率分别约为 7% 和 5%。与男性营养不良有关的潜在风险因素包括年龄较大(OR 1.263,95% CI 1.086-1.468;P=.002)、丧偶(OR 8.392,95% CI 1.002-70.258;P=.049)和牙齿有问题(OR 9.408,95% CI 1.863-47.514;P=.007)。另一方面,与妇女营养不良相关的风险因素是较低的体重指数(OR 0.843,95% CI 0.747-0.952;P=.006)和残疾(OR 18.089,95% CI 0.747-0.952;P=.006):这项研究的结果为了解沙特阿拉伯西部地区老年人营养不良的风险因素提供了重要依据。虽然营养不良的总体发生率相对较低,但分析结果显示,老年男性和女性存在不同的风险因素。根据所发现的风险因素制定的干预措施可能会有效解决这一人群的营养不良问题。
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引用次数: 0
Nursing Staff's Perspectives of Care Robots for Assisted Living Facilities: Systematic Literature Review. 护理人员对生活辅助设施护理机器人的看法:系统性文献综述。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-16 DOI: 10.2196/58629
Katie Trainum, Jiaying Liu, Elliott Hauser, Bo Xie
<p><strong>Background: </strong>Care robots have been proposed in response to nursing shortages in assisted living facilities (ALFs) and the growing population of older adults. While the use of care robots may improve the general health and well-being of older adults, their introduction changes the work of nursing staff fundamentally, and it has implications for the entire health care system. In developing such technology, it is important to include end users, but so far, the nursing staff's perspectives have largely been ignored.</p><p><strong>Objective: </strong>This study aims to examine the literature on nursing staff's attitudes, needs, and preferences related to the use of care robots in ALFs, in order to discover gaps in the literature and guide future research.</p><p><strong>Methods: </strong>This review follows the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) 2020 protocol. On May 12, 2023, we searched PubMed, CINAHL Plus with Full Text, PsycINFO, the IEEE Xplore Digital Library, and the ACM Digital Library using predetermined search terms. Included publications, written in English, focused on the predevelopment phase, in which information was gathered on nursing staff's attitudes, needs, and preferences regarding care robots for ALFs. Publications were excluded if they did not provide peer-reviewed empirical data. The studies' findings were summarized, coded, and analyzed into major themes using thematic analysis and narrative synthesis. Their quality was assessed using McGill University's Mixed Methods Appraisal Tool and the Joanna Briggs Institute's critical appraisal tools.</p><p><strong>Results: </strong>The final sample included 15 studies. Most of the studies (n=11, 73%) were rated as good quality; however, there was a general lack of reporting on important methodological decisions and sample characteristics. Nursing staff desired care robots that could assist with physically demanding tasks and reduce their workload but had mixed feelings on whether robots could or should assist with social tasks. In addition, nursing staff are concerned about the ethics of care robots, as well as about their safety, accessibility, and operability. The nursing staff's culture, qualification, and role in the facility may influence their perspectives of care robots. The studies lacked theory-driven designs and large sample sizes. Eight (53%) studies mentioned using a participatory design approach, but a lack of established criteria for what constitutes participatory design leads to varying degrees of methodological quality.</p><p><strong>Conclusions: </strong>There was consensus among nursing staff that care robots should serve as nursing assistants to reduce workload. Whether robots could or should assist with social tasks remains a question. Further research is needed to mitigate nursing staff's concerns and understand the socioecological factors that influence their perspectives of care robots and their adoption in
背景:护理机器人是为应对生活辅助设施(ALF)护理人员短缺和老年人口不断增长而提出的。虽然护理机器人的使用可能会改善老年人的总体健康和福祉,但它的引入从根本上改变了护理人员的工作,并对整个医疗保健系统产生了影响。在开发此类技术时,将最终用户纳入其中非常重要,但迄今为止,护理人员的观点在很大程度上被忽视了:本研究旨在考察有关护理人员对在 ALF 中使用护理机器人的态度、需求和偏好的文献,以发现文献中的不足并指导未来的研究:本综述遵循 PRISMA(系统综述和元分析首选报告项目)2020 协议。2023 年 5 月 12 日,我们使用预先确定的检索词检索了 PubMed、CINAHL Plus 全文、PsycINFO、IEEE Xplore 数字图书馆和 ACM 数字图书馆。所纳入的出版物均以英文撰写,重点关注前期开发阶段,收集护理人员对 ALF 护理机器人的态度、需求和偏好等信息。如果没有提供经过同行评审的经验数据,则排除在外。采用主题分析和叙事综合法对研究结果进行总结、编码和主要主题分析。研究质量采用麦吉尔大学的混合方法评估工具和乔安娜-布里格斯研究所的批判性评估工具进行评估:最终样本包括 15 项研究。大多数研究(n=11,73%)被评为质量良好;但普遍缺乏对重要方法决定和样本特征的报告。护理人员希望护理机器人能够协助他们完成体力要求较高的任务,减轻他们的工作量,但对于机器人是否能够或应该协助他们完成社交任务,他们的看法不一。此外,护理人员还关注护理机器人的道德问题,以及其安全性、可及性和可操作性。护理人员的文化、资质和在机构中的角色可能会影响他们对护理机器人的看法。这些研究缺乏理论驱动的设计和大样本量。八项研究(53%)提到使用了参与式设计方法,但由于缺乏参与式设计的既定标准,导致研究方法的质量参差不齐:护理人员一致认为护理机器人应作为护理助手,以减少工作量。机器人是否能够或应该协助完成社交任务仍是一个问题。需要进一步开展研究,以减轻护理人员的担忧,并了解影响他们对护理机器人的看法以及在 ALF 中采用护理机器人的社会生态因素。此外,还需要进行理论驱动和大样本量的研究设计,并努力为相关的参与式设计研究制定明确的标准。
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引用次数: 0
Investigating Acoustic and Psycholinguistic Predictors of Cognitive Impairment in Older Adults: Modeling Study. 调查老年人认知障碍的声学和心理语言学预测因素:模型研究。
IF 5 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-16 DOI: 10.2196/54655
Varsha D Badal, Jenna M Reinen, Elizabeth W Twamley, Ellen E Lee, Robert P Fellows, Erhan Bilal, Colin A Depp

Background: About one-third of older adults aged 65 years and older often have mild cognitive impairment or dementia. Acoustic and psycho-linguistic features derived from conversation may be of great diagnostic value because speech involves verbal memory and cognitive and neuromuscular processes. The relative decline in these processes, however, may not be linear and remains understudied.

Objective: This study aims to establish associations between cognitive abilities and various attributes of speech and natural language production. To date, the majority of research has been cross-sectional, relying mostly on data from structured interactions and restricted to textual versus acoustic analyses.

Methods: In a sample of 71 older (mean age 83.3, SD 7.0 years) community-dwelling adults who completed qualitative interviews and cognitive testing, we investigated the performance of both acoustic and psycholinguistic features associated with cognitive deficits contemporaneously and at a 1-2 years follow up (mean follow-up time 512.3, SD 84.5 days).

Results: Combined acoustic and psycholinguistic features achieved high performance (F1-scores 0.73-0.86) and sensitivity (up to 0.90) in estimating cognitive deficits across multiple domains. Performance remained high when acoustic and psycholinguistic features were used to predict follow-up cognitive performance. The psycholinguistic features that were most successful at classifying high cognitive impairment reflected vocabulary richness, the quantity of speech produced, and the fragmentation of speech, whereas the analogous top-ranked acoustic features reflected breathing and nonverbal vocalizations such as giggles or laughter.

Conclusions: These results suggest that both acoustic and psycholinguistic features extracted from qualitative interviews may be reliable markers of cognitive deficits in late life.

背景:在 65 岁及以上的老年人中,约有三分之一通常患有轻度认知障碍或痴呆症。由于言语涉及言语记忆、认知和神经肌肉过程,因此从谈话中得出的声音和语言心理特征可能具有很高的诊断价值。然而,这些过程的相对衰退可能不是线性的,而且仍未得到充分研究:本研究旨在建立认知能力与语音和自然语言生成的各种属性之间的联系。迄今为止,大多数研究都是横断面研究,主要依赖于结构化互动的数据,而且仅限于文本分析和声音分析:方法:我们以 71 位完成定性访谈和认知测试的社区老年人(平均年龄 83.3 岁,标差 7.0 岁)为样本,调查了与认知缺陷相关的声学和心理语言特征在当时和 1-2 年随访期间(平均随访时间 512.3 天,标差 84.5 天)的表现:声学和心理语言学特征的组合在估计多个领域的认知缺陷方面具有较高的性能(F1-分数为0.73-0.86)和灵敏度(高达0.90)。当声学和心理语言学特征被用于预测后续认知表现时,其性能仍然很高。心理语言学特征能最成功地将认知障碍程度较高的人分类,这些特征反映了词汇的丰富程度、说话的数量和说话的片段,而排名靠前的类似声学特征则反映了呼吸和非语言发声,如咯咯笑或大笑:这些结果表明,从定性访谈中提取的声学和心理语言学特征可能是晚年认知障碍的可靠标记。
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JMIR Aging
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