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Technostress Among Health Professionals - A Multilevel Model and Group Comparisons between Settings and Professions. 卫生专业人员中的技术压力——一个多层次模型和环境与专业之间的群体比较。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-06-02 Epub Date: 2021-03-01 DOI: 10.1080/17538157.2021.1872579
Christoph Golz, Karin A Peter, Sandra M G Zwakhalen, Sabine Hahn

Objective: Health organizations increasingly digitize. However, studies reveal contradictory findings regarding the impact of healthcare information technology on health professionals. Therefore, the aim of this study is to describe the prevalence of technostress among health professionals and elaborate on the influencing factors.

Participants: A secondary analysis was conducted utilizing cross-sectional data from the study, "Work-related stress among health professionals in Switzerland", which included 8,112 health professionals from 163 health organizations in Switzerland.

Methods: ANOVA for group comparisons followed by post-hoc analyses, along with a Multilevel Model to identify influencing factors for technostress ranging from "0" (never/almost never) to "100" (always), were conducted.

Results: Health professionals experienced moderate technostress (mean 39.06, SD 32.54). Technostress differed between settings (p <.001) and health professions (p < .001). The model explains 18.1% of the variance with fixed effects, or 24.7% of the variance with fixed and random effects. Being a physician (β = 12.96), a nurse (β = 6.49), or the presence of an effort-reward-imbalance, increased technostress most (β = 6.11). A professional with no professional qualification (β = -7.94) showed the most reduction.

Conclusion: Health professionals experience moderate technostress. However, decision-makers should consider the cognitive and social aspects surrounding digitalization, to reach a beneficial and sustainable level of usage.

目标:卫生组织日益数字化。然而,关于医疗保健信息技术对卫生专业人员的影响,研究揭示了相互矛盾的发现。因此,本研究的目的是描述技术压力在卫生专业人员中的流行程度,并阐述其影响因素。参与者:利用"瑞士卫生专业人员的工作压力"研究的横截面数据进行了二次分析,该研究包括来自瑞士163个卫生组织的8 112名卫生专业人员。方法:采用方差分析进行分组比较,随后进行事后分析,并采用多层模型确定技术压力的影响因素,范围从“0”(从不/几乎从不)到“100”(总是)。结果:卫生专业人员经历中度技术应激(平均39.06,标准差32.54)。技术压力在不同环境之间存在差异(p结论:卫生专业人员经历适度的技术压力。然而,决策者应该考虑围绕数字化的认知和社会方面,以达到有益和可持续的使用水平。
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引用次数: 9
Users' ambivalent sense of security with humanoid robots in healthcare. 在医疗领域,用户对人形机器人的矛盾安全感。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-06-02 Epub Date: 2021-02-24 DOI: 10.1080/17538157.2021.1883027
Linda Nyholm, Regina Santamäki-Fischer, Lisbeth Fagerström

Humanoid robots have already been shown to be useful in healthcare. To ensure successful interactions with humanoid robots, is it essential that the factors that influence users' sense of security be understood. Ensuring patients' sense of security is considered a key principle of good caring. The aim of this study was to illuminate users' sense of security with humanoid robots in healthcare. Twelve semi-structured interviews were conducted. The participants consisted of five women and seven men aged 24-77. Before being interviewed, the participants were shown a video vignette with Pepper, a fully developed humanoid robot, used in the daily care of patients. The data material was analyzed using qualitative content analysis. Most participants perceived the use of humanoid robots in healthcare to be both positive and negative. The overarching theme was: Ambivalent sense of security with humanoid robots in healthcare. The four categories revealed were: Humanoid robots are both reliable and unreliable, Humanoid robots are both safe and unsafe, Humanoid robots are both likable and scary, and Humanoid robots are both caring and uncaring. Here we increased knowledge of whether patients perceive a sense of security with humanoid robots in healthcare, including which fears users have. This is vital information that should be taken into consideration when further developing and introducing humanoid robots into the healthcare setting.

人形机器人已经被证明在医疗保健方面很有用。为了确保与人形机器人的成功交互,了解影响用户安全感的因素是至关重要的。确保病人的安全感被认为是良好护理的关键原则。本研究的目的是阐明在医疗保健中使用人形机器人的用户安全感。进行了12次半结构化访谈。参与者包括5名女性和7名男性,年龄在24-77岁之间。在接受采访之前,参与者观看了一段视频,视频中有一个完全开发的人形机器人Pepper,用于病人的日常护理。采用定性内容分析法对资料进行分析。大多数参与者认为在医疗保健中使用人形机器人既有积极的一面,也有消极的一面。总体主题是:在医疗保健领域使用人形机器人的矛盾安全感。这四类机器人分别是:类人机器人既可靠又不可靠,类人机器人既安全又不安全,类人机器人既可爱又可怕,类人机器人既关心人又不关心人。在这里,我们增加了对患者是否在医疗保健中感受到人形机器人的安全感的了解,包括用户的恐惧。这是在进一步开发和将人形机器人引入医疗环境时应该考虑的重要信息。
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引用次数: 12
Geographically-explicit Ecological Momentary Assessment (GEMA) Architecture and Components: Lessons Learned from PMOMS. 地理明确的生态瞬时评估(GEMA)体系结构和组件:从pmom获得的经验教训。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-06-02 Epub Date: 2021-02-20 DOI: 10.1080/17538157.2021.1877140
Pedram Gharani, Hassan A Karimi, Meirman Syzdykbayev, Lora E Burke, Stephen L Rathbun, Esa M Davis, Tiffany L Gary-Webb, Dara D Mendez

Geographically explicit Ecological Momentary Assessment (GEMA), an extension of Ecological Momentary Assessment (EMA), allows to record time-stamped geographic location information for behavioral data in the every-day environments of study participants. Considering that GEMA studies are continually gaining the attention of researchers and currently there is no single approach in collecting GEMA data, in this paper, we propose and present a GEMA architecture that can be used to conduct any GEMA study based on our experience developing and maintaining the Postpartum Mothers Mobile Study (PMOMS). Our GEMA client-server architecture can be customized to meet the specific requirements of each GEMA study. Key features of our proposed GEMA architecture include: utilization of widely used smartphones to make GEMA studies practical; alleviation of the burden of activities on participants by designing clients (mobile applications) that are very lightweight and servers that are heavyweight in terms of functionality; utilization of at least one positioning sensor to determine EMA contexts marked with locations; and communication through the Internet. We believe that our proposed GEMA architecture, with the illustrated foundation for GEMA studies in our exemplar study (PMOMS), will help researchers from any field conduct GEMA studies efficiently and effectively.

地理显式生态瞬时评估(GEMA)是生态瞬时评估(EMA)的扩展,允许记录研究参与者在日常环境中的行为数据的时间标记地理位置信息。鉴于GEMA研究不断受到研究人员的关注,目前收集GEMA数据没有单一的方法,在本文中,我们根据我们开发和维护产后母亲移动研究(PMOMS)的经验,提出并提出了一种GEMA架构,可用于开展任何GEMA研究。我们的GEMA客户端-服务器架构可以定制,以满足每个GEMA研究的特定要求。我们提出的GEMA架构的主要特点包括:利用广泛使用的智能手机使GEMA研究具有实用性;通过设计轻量级的客户端(移动应用程序)和功能重量级的服务器来减轻参与者的活动负担;使用至少一个定位传感器来确定标记有位置的EMA环境;以及通过互联网进行交流。我们相信,我们提出的GEMA架构,以及我们范例研究(pmom)中GEMA研究的说明基础,将帮助任何领域的研究人员高效、有效地进行GEMA研究。
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引用次数: 2
A systematic review of rapid response applications based on early warning score for early detection of inpatient deterioration. 基于早期预警评分的快速反应应用对住院患者病情恶化的早期发现的系统回顾。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-06-02 Epub Date: 2021-01-21 DOI: 10.1080/17538157.2021.1873349
Mirza Mansoor Baig, Hamid GholamHosseini, Shereen Afifi, Maria Lindén

Aim: The aim of this study was to investigate the effectiveness of current rapid response applications available in acute care settings for escalation of patient deterioration. Current challenges and barriers, as well as key recommendations, were also discussed.

Methods: We adopted PRISMA review methodology and screened a total of 559 articles. After considering the eligibility and selection criteria, we selected 13 articles published between 2015 and 2019. The selection criteria were based on the inclusion of studies that report on the advancement made to the current practice for providing rapid response to the patient deterioration in acute care settings.

Results: We found that current rapid response applications are complicated and time-consuming for detecting inpatient deterioration. Existing applications are either siloed or challenging to use, where clinicians are required to move between two or three different applications to complete an end-to-end patient escalation workflow - from vital signs collection to escalation of deteriorating patients. We found significant differences in escalation and responses when using an electronic tool compared to the manual approach. Moreover, encouraging results were reported in extensive documentation of vital signs and timely alerts for patient deterioration.

Conclusion: The electronic vital signs monitoring applications are proved to be efficient and clinically suitable if they are user-friendly and interoperable. As an outcome, several key recommendations and features were identified that would be crucial to the successful implementation of any rapid response system in all clinical settings.

目的:本研究的目的是调查当前快速反应应用在急性护理环境中对患者病情恶化升级的有效性。会议还讨论了当前面临的挑战和障碍以及主要建议。方法:采用PRISMA综述方法,共筛选559篇文献。在考虑了资格和评选标准后,我们选择了2015年至2019年间发表的13篇文章。选择标准是基于纳入的研究报告,这些研究报告了在急性护理环境中对患者病情恶化提供快速反应的当前实践的进展。结果:我们发现目前的快速反应应用程序复杂且耗时。现有的应用程序要么是孤立的,要么是难以使用的,临床医生需要在两到三个不同的应用程序之间移动,以完成端到端的患者升级工作流程——从生命体征收集到病情恶化的患者升级。我们发现,与使用手动方法相比,使用电子工具在升级和反应方面存在显著差异。此外,在生命体征的大量记录和患者病情恶化的及时警报方面报告了令人鼓舞的结果。结论:电子生命体征监测在临床应用中具有良好的易用性和可操作性。结果,确定了几项关键建议和特征,这些建议和特征对于在所有临床环境中成功实施任何快速反应系统至关重要。
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引用次数: 4
Development of an internet-delivered program and platform for the treatment of depression and anxiety in patients with ischemic heart disease in eMindYourHeart. eMindYourHeart中缺血性心脏病患者抑郁和焦虑治疗的互联网交付程序和平台的开发。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-06-02 Epub Date: 2021-02-25 DOI: 10.1080/17538157.2021.1878185
Thomas Schmidt, Robin Kok, Christina M Andersen, Søren J Skovbakke, Robert Ahm, Uffe Kock Wiil, Lisbeth Frostholm, Susanne S Pedersen

To design and evaluate a mental health treatment program and internet-based delivery platform for patients with ischemic heart disease (IHD) attending cardiac rehabilitation with the aim of reducing the risks associated with anxiety and/or depression. Patients diagnosed with IHD and comorbid anxiety and/or depression. Participatory design of treatment program and internet platform through staged inclusion of participants in two groups. Group 1 was enrolled as co-researchers with prolonged engagement in the project. Group 2 participated only in the pilot evaluation workshop. Three patients were included in Group 1, two patients in Group 2. Inclusion of patients proved challenging, but the extended collaboration with co-researchers yielded valuable circumstantial insight and resulted in the design of a novel nine-module treatment program. Additionally, the inclusion of two participant groups helped shape the development of an internet platform based on an open-source content management system. Our grouped participation method contributes with several recommendations and reflections of advantages of this approach. Collaboration with co-researchers helped us gain a deeper understanding of the impact of language on self-perception and potential stigma. Prolonged participation led to a higher level of trust and familiarity, which enabled uncovering of issues otherwise hidden.

设计和评估缺血性心脏病(IHD)患者参加心脏康复的心理健康治疗方案和基于互联网的交付平台,旨在降低与焦虑和/或抑郁相关的风险。诊断为IHD并伴有焦虑和/或抑郁的患者。通过分阶段纳入两组参与者,进行治疗方案和互联网平台的参与式设计。第一组被招募为长期参与该项目的共同研究人员。第2组只参加了试点评价讲习班。1组3例,2组2例。纳入患者被证明是具有挑战性的,但与共同研究人员的长期合作产生了宝贵的间接见解,并导致了一个新的九个模块治疗方案的设计。此外,两个参与小组的加入有助于形成基于开源内容管理系统的互联网平台的发展。我们的分组参与方法有助于一些建议和反映这种方法的优势。与共同研究人员的合作帮助我们更深入地了解语言对自我认知和潜在耻辱的影响。长时间的参与导致了更高程度的信任和熟悉,这使得发现原本隐藏的问题成为可能。
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引用次数: 7
Impact of patient access to their electronic health record: systematic review. 患者访问其电子健康记录的影响:系统审查。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-06-02 Epub Date: 2021-04-10 DOI: 10.1080/17538157.2021.1879810
Archana Tapuria, Talya Porat, Dipak Kalra, Glen Dsouza, Sun Xiaohui, Vasa Curcin
<p><p>Patient access to their own electronic health records (EHRs) is likely to become an integral part of healthcare systems worldwide. It has the potential to decrease the healthcare provision costs, improve access to healthcare data, self-care, quality of care, and health and patient-centered outcomes. This systematic literature review is aimed at identifying the impact in terms of benefits and issues that have so far been demonstrated by providing patients access to their own EHRs, via providers' secure patient portals from primary healthcare centers and hospitals. Searches were conducted in PubMed, MEDLINE, CINHAL, and Google scholar. Over 2000 papers were screened and were filtered based on duplicates, then by reading the titles and finally based on their abstracts or full text. In total, 74 papers were retained, analyzed, and summarized. Papers were included if providing patient access to their own EHRs was the primary intervention used in the study and its impact or outcome was evaluated. The search technique used to identify relevant literature for this paper involved input from five experts. While findings from 54 of the 74 papers showed positive outcome or benefits of patient access to their EHRs via patient portals, 10 papers have highlighted concerns, 8 papers have highlighted both and 2 have highlighted absence of negative outcomes. The benefits range from re-assurance, reduced anxiety, positive impact on consultations, better doctor-patient relationship, increased awareness and adherence to medication, and improved patient outcomes (e.g., improving blood pressure and glycemic control in a range of study populations). In addition, patient access to their health information was found to improve self-reported levels of engagement or activation related to self-management, enhanced knowledge, and improve recovery scores, and organizational efficiencies in a tertiary level mental health care facility. However, three studies did not find any statistically significant effect of patient portals on health outcomes. The main concerns have been around security, privacy and confidentiality of the health records, and the anxiety it may cause amongst patients. This literature review identified some benefits, concerns, and attitudes demonstrated by providing patients' access to their own EHRs. This access is often part of government strategies when developing patient-centric self-management elements of a sustainable healthcare system. The findings of this review will give healthcare providers a framework to analyze the benefits offered by promoting patient access to EHRs and decide on the best approach for their own specialties and clinical setup. A robust cost-benefit evaluation of such initiatives along with its impact on major stakeholders within the healthcare system would be essential in understanding the overall impact of such initiatives. Implementation of patient access to their EHRs could help governments to appropriately prioritize the d
患者访问自己的电子健康记录(EHRs)可能成为全球医疗保健系统的一个组成部分。它有可能降低医疗保健提供成本,改善对医疗保健数据的访问、自我保健、护理质量以及健康和以患者为中心的结果。本系统文献综述的目的是确定效益和问题方面的影响,迄今为止,通过提供者从初级卫生保健中心和医院的安全患者门户网站,为患者提供自己的电子病历,证明了这些影响。在PubMed, MEDLINE, CINHAL和Google scholar中进行了搜索。对2000多篇论文进行了筛选,并根据重复内容进行筛选,然后通过阅读标题进行筛选,最后根据摘要或全文进行筛选。共有74篇论文被保留、分析和总结。如果研究中使用的主要干预措施是为患者提供自己的电子病历,并评估了其影响或结果,则纳入论文。检索技术用于识别相关文献为这篇论文涉及输入五位专家。虽然74篇论文中有54篇的研究结果显示了患者通过患者门户访问其电子病历的积极结果或益处,但有10篇论文强调了担忧,8篇论文强调了两者,2篇论文强调了没有负面结果。益处包括安心、减少焦虑、对咨询产生积极影响、改善医患关系、提高对药物的认识和依从性,以及改善患者预后(例如,改善一系列研究人群的血压和血糖控制)。此外,研究发现,在三级精神卫生保健机构中,患者访问其健康信息可以提高自我报告的参与或与自我管理相关的激活水平,增强知识,并提高康复分数和组织效率。然而,三项研究并未发现患者门户网站对健康结果有任何统计学上显著的影响。主要的担忧是健康记录的安全性、隐私性和保密性,以及可能引起患者的焦虑。本文献综述确定了一些利益,关注和态度,通过向患者提供自己的电子病历。在开发可持续医疗保健系统中以患者为中心的自我管理元素时,这种访问通常是政府战略的一部分。本综述的发现将为医疗保健提供者提供一个框架,以分析促进患者使用电子病历所带来的好处,并根据自己的专业和临床设置决定最佳方法。对此类举措及其对医疗保健系统内主要利益相关者的影响进行强有力的成本效益评估,对于理解此类举措的总体影响至关重要。实施患者对其电子病历的访问可以帮助政府适当地优先考虑制定或采用国家标准,同时照顾地方差异并满足人口的医疗保健需求,例如,英国政府的目标是使每个患者都可以在线获得完整的初级保健记录。最终,提高透明度和促进个人责任是为子孙后代建立可持续医疗体系的关键要素。
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引用次数: 41
Mobile applications for emerging adults transitioning to independent diabetes monitoring. 向独立糖尿病监测过渡的新兴成人移动应用程序。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-03-02 Epub Date: 2020-11-26 DOI: 10.1080/17538157.2020.1837839
Jennifer Schindler-Ruwisch, Abby Peters

Access to high-quality mhealth tools for diabetes management is critical. The purpose was to systematically review mobile apps for features relevant to helping emerging adults manage their diabetes as they transition to independent diabetes monitoring. Mobile apps were reviewed for relevance to emerging adults, aged 18-25, living with diabetes. The GooglePlay store was systematically searched to identify diabetes management mobile tools. Of the 29 apps, only one app had any features relevant to emerging adults. In total, 20 apps had a feature to share a copy of diet or blood sugar logs with a family member or provider. Only 9 apps had any interactivity other than tracking. While most apps had graphics, only 5 were deemed high quality. Just one app met all three included Mobile Application Rating Scale (MARS) criteria. This review serves as a starting point to guide educators and patients, especially to aid continuity of care when in-person support is not feasible. Ongoing review of new apps with improved functionality and effectiveness studies of the apps' impact on emerging adults' diabetes management is imperative.

获得高质量的糖尿病管理移动医疗工具至关重要。目的是系统地审查移动应用程序的相关功能,帮助新兴成年人在过渡到独立的糖尿病监测时管理他们的糖尿病。手机应用程序与18-25岁的糖尿病患者的相关性进行了审查。系统地搜索GooglePlay商店以确定糖尿病管理移动工具。在29个应用程序中,只有一个应用程序具有与初成人相关的功能。总共有20个应用程序具有与家庭成员或供应商共享饮食或血糖日志副本的功能。只有9个应用程序除了跟踪之外具有任何交互性。虽然大多数应用程序都有图像,但只有5个被认为是高质量的。只有一款应用满足了所有三项移动应用评级标准(MARS)。本综述可作为指导教育工作者和患者的起点,特别是在现场支持不可行的情况下帮助护理的连续性。不断审查具有改进功能和有效性的新应用程序,研究应用程序对新兴成人糖尿病管理的影响是必要的。
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引用次数: 1
Implications of telehealth and digital care solutions during COVID-19 pandemic: a qualitative literature review. COVID-19大流行期间远程医疗和数字护理解决方案的影响:定性文献综述
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-03-02 Epub Date: 2020-11-29 DOI: 10.1080/17538157.2020.1839467
Bokolo Anthony Jnr

The coronavirus disease 2019 (COVID-19) pandemic has brought changes to the way medical care is delivered to keep health workers safe while simultaneously managing available resources. The well-being of patients and healthcare workers is crucial and has become a topic of debate as the world faces adjusts to the COVID-19 pandemic. Therefore, there is need to consider innovative methods of delivering medical care. Telehealth and digital health care which is the provision of medical care via Information Communication Technology (ICT) with highspeed telecommunications systems, has increasingly becoming popular in providing medical care services can be adopted to reduce infections during quarantine and social distancing practices. Specifically, by means of document and literature review this paper discusses the role of telehealth and digital care solutions, types and application of telehealth, and current policies for COVID-19. More importantly, findings from the article present the human, infrastructure, and institutional determinants that influence the adoption of telehealth and digital care solutions during the pandemic. The findings discuss how telehealth and digital care technologies can benefit the society. This study provides implications to informs medical staffs on the potential of digital technologies to provide support during and after the pandemic.

2019年冠状病毒病(COVID-19)大流行改变了提供医疗服务的方式,以确保卫生工作者的安全,同时管理可用资源。患者和医护人员的福祉至关重要,在世界面临COVID-19大流行的调整之际,这已成为一个争论的话题。因此,有必要考虑提供医疗服务的创新方法。远程保健和数字保健是通过信息通信技术(ICT)和高速电信系统提供的医疗保健,在提供可用于减少隔离和社会距离做法期间感染的医疗保健服务方面越来越受欢迎。具体而言,通过文献和文献综述,本文讨论了远程医疗和数字医疗解决方案的作用、远程医疗的类型和应用以及当前针对COVID-19的政策。更重要的是,本文的研究结果揭示了疫情期间影响远程医疗和数字医疗解决方案采用的人力、基础设施和体制决定因素。研究结果讨论了远程医疗和数字护理技术如何造福社会。这项研究提供了启示,使医务人员了解数字技术在大流行期间和之后提供支持的潜力。
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引用次数: 95
Can caregivers trust information technology in the care of their patients? A systematic review. 护理人员能否信任信息技术来护理患者?系统的回顾。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-03-02 Epub Date: 2020-12-01 DOI: 10.1080/17538157.2020.1834399
Alice Noblin, Barbara Hewitt, Murad Moqbel, Scott Sittig, Lakesha Kinnerson, Vera Rulon

The Health Insurance Portability and Accountability Act of 1996 (HIPAA) requires that healthcare providers allow patients to engage in their healthcare by allowing access to their health records. Often patients need informal caregivers including family members or others to help them with their care. This paper explores whether trust is a key factor for informal caregivers' decision to use health information technologies (HIT) including electronic health records (EHR), patient portals, mobile apps, or other devices to care for their patient. Six reviewers conducted a comprehensive search of four literature databases using terms that pertained to a caregiver and trust to investigate the role trust plays when caregivers use HIT. While trust is a key factor for the use of HIT, it the researchers only identified ten articles that met the research question thresholds. Four main topics of trust surfaced including perceived confidentiality, perceived security, technological malfunction, and trustworthiness of the information. Trust is a critical factor for informal caregivers when using HIT to assist in the care of their patient (child, loved one, parent, or acquaintance). Based on the findings, it is clear that more research on the use of HIT by caregivers is needed.

1996年《健康保险便携性和责任法案》(HIPAA)要求医疗保健提供者允许患者通过访问其健康记录来参与其医疗保健。患者通常需要非正式的护理人员,包括家庭成员或其他人来帮助他们进行护理。本文探讨了信任是否是非正式护理人员决定使用健康信息技术(HIT)的关键因素,包括电子健康记录(EHR)、患者门户网站、移动应用程序或其他设备来护理患者。六位评审员使用与护理人员和信任相关的术语对四个文献数据库进行了全面搜索,以调查护理人员使用HIT时信任所起的作用。虽然信任是使用HIT的关键因素,但研究人员只发现了十篇符合研究问题阈值的文章。信任的四个主要主题浮出水面,包括感知的机密性、感知的安全性、技术故障和信息的可信度。在使用HIT协助照顾患者(孩子、爱人、父母或熟人)时,信任是非正式护理人员的关键因素。根据这些发现,很明显,需要对照顾者使用HIT进行更多的研究。
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引用次数: 5
What YouTube narratives reveal about online support, counseling entrance, and how Black Americans manage depression symptomatology. YouTube的叙述揭示了在线支持,咨询入口,以及美国黑人如何处理抑郁症症状。
IF 2.4 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-03-02 Epub Date: 2021-01-06 DOI: 10.1080/17538157.2020.1865967
Kaprea F Johnson, Dana L Brookover, NeShaun J Borden, Allison K Worth, Peter Temple, Lauren B Mahan

This manuscript explores the depression disease management of Black Americans (N = 50) who post their experiences on YouTube. The narratives garnered five themes: (1) personal and national histories as a barrier to treatment and contributor to depression, (2) utilizing the social network as informal counseling and as the catalyst for formal counseling, (3) long-term undiagnosed depression management and mismanagement, (4) advocating to destigmatize and treat depression, and (5) positive experiences initiating and engaging in treatment. Novel findings include how participants discuss narratives in third person, the importance of the Youtube community, and advocacy to destigmatize and treat depression.

本文探讨美国黑人(N = 50)在YouTube上发布他们的经历的抑郁症管理。这些叙述包含了五个主题:(1)个人和国家历史作为治疗抑郁症的障碍和贡献者;(2)利用社会网络作为非正式咨询和正式咨询的催化剂;(3)长期未确诊的抑郁症管理和管理不善;(4)倡导去污名化和治疗抑郁症;(5)启动和参与治疗的积极经历。新的发现包括参与者如何用第三人称讨论故事,Youtube社区的重要性,以及倡导去污名化和治疗抑郁症。
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引用次数: 5
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