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Catalysts for change: A qualitative study of middle managers' perception of nursing professional competence in primary healthcare. 变革的催化剂:中层管理人员对基层医疗机构护理专业能力的定性研究。
IF 1.9 4区 医学 Q2 NURSING Pub Date : 2024-07-29 DOI: 10.1111/scs.13286
Choi Kristian Wiik, Anne Vifladt, Sevald Høye

Aim: This study aims to explore middle managers' perception of nursing professional competence within the Norwegian primary healthcare service, a sector vital for managing complex patient needs.

Design/methods: Semi-structured interviews were conducted with four middle managers across different municipalities in Norway. Qualitative content analyses, following Graneheim and Lundman, were used for analysing the transcription of the interviews and the data collected.

Findings: The qualitative content analysis revealed three main themes: the significance of advanced competence, challenges related to competence development and the necessity for defining advanced competence. The findings indicate that middle managers recognise the importance of advanced nursing competence in providing comprehensive patient care, notwithstanding challenges in manpower and competence enhancement.

Conclusion: This research underlines the significance of investing in increased competence and improved management in primary healthcare and offers valuable insights for healthcare policy and practice to enhance patient care.

目的:本研究旨在探讨中层管理人员对挪威初级医疗保健服务中护理专业能力的看法:对挪威不同城市的四位中层管理人员进行了半结构化访谈。研究结果:定性内容分析揭示了三个主要问题,即护理人员在管理病人复杂需求方面的作用、护理人员在管理病人复杂需求方面的作用以及护理人员在管理病人复杂需求方面的作用:定性内容分析揭示了三大主题:高级能力的重要性、与能力发展相关的挑战以及界定高级能力的必要性。研究结果表明,尽管在人力和能力提升方面存在挑战,但中层管理人员认识到高级护理能力对提供全面患者护理的重要性:这项研究强调了在初级医疗保健中投资提高能力和改善管理的重要性,并为医疗保健政策和实践提供了宝贵的见解,以加强对患者的护理。
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引用次数: 0
Meaning-oriented thematic analysis grounded in reflective lifeworld research-A holistic approach for caring science research. 以反思性生活世界研究为基础的意义导向主题分析--关爱科学研究的整体方法。
IF 1.9 4区 医学 Q2 NURSING Pub Date : 2024-07-12 DOI: 10.1111/scs.13284
Elisabeth Lindberg, Lina Palmér, Ulrica Hörberg

Background and aim: The aim of the present article is to describe meaning-oriented thematic analysis grounded in reflective lifeworld research and to illustrate how the thematic analysis can be integrated in the research process. The article is a methodological paper, including ontological and epistemological assumptions for lifeworld theory. Research based on lifeworld theory is directed towards lived experiences and meanings in everyday life. Research that is founded on the epistemology of the lifeworld can present existential issues important for caring and qualitative research can in particular contribute to existential knowledge needed to understand the world of the patient.

Design: Theoretical paper.

Results: Starting with a phenomenon of relevance for caring science, the article argues for lifeworld interviews as a data collection method that can contribute to depth and meaning, and then presents a description of how structures of meaning can be outlined through a meaning-oriented thematic analysis. The research of lived experiences in caring science demands an approach that includes a reflective attitude during the methodological considerations. This article highlights the importance of ontological and epistemological considerations when conducting a meaning-oriented thematic analysis.

Conclusion: The article places meaning-oriented thematic analysis in a wider research process, considering all aspects from collection of data to the creation of meaning-oriented themes.

背景与目的:本文旨在描述以反思性生活世界研究为基础的意义导向专题分析,并说明如何将专题分析融入研究过程。本文是一篇方法论论文,包括生活世界理论的本体论和认识论假设。基于生活世界理论的研究以日常生活中的经验和意义为研究对象。建立在生活世界认识论基础上的研究可以提出对护理工作非常重要的存在论问题,定性研究尤其有助于提供理解病人世界所需的存在论知识:设计:理论论文:文章从一个与关爱科学相关的现象入手,论证了生活世界访谈作为一种数据收集方法,可以促进研究的深度和意义,然后介绍了如何通过以意义为导向的主题分析来概述意义结构。关爱科学中的生活经验研究需要一种在方法论考虑中包含反思态度的方法。本文强调了在进行以意义为导向的专题分析时,本体论和认识论考虑的重要性:文章将以意义为导向的主题分析置于更广泛的研究过程中,考虑了从收集数据到创建以意义为导向的主题的各个方面。
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引用次数: 0
Exploring young adults' experiences with food allergy during their teenage years: A practice research study. 探索青少年时期的食物过敏经历:实践研究
IF 1.9 4区 医学 Q2 NURSING Pub Date : 2024-07-11 DOI: 10.1111/scs.13283
Britt Egmose, Lotte Huniche, Carsten Bindslev-Jensen, Dorthe S Nielsen, Charlotte G Mørtz

Introduction: Symptoms of anxiety, eating disorders and social isolation are prevalent among teenagers with food allergy compared to peers without. Treatment of teenagers with food allergy focus on preventing anaphylactic reactions, with little attention to promoting social and emotional well-being. The aim of the study was to explore young adults' perspectives on everyday life with food allergy during their teenage years to improve future clinical practice.

Methods: Critical psychological practice research. During a 2-day camp the perspectives of 10 young adults (18-23 years) were explored through participant observation and informal interviews. Three follow up interviews were conducted. A co-researcher group discussed preliminary results, clinical challenges and ways forward.

Results: Being together with peers with food allergy was crucial, fostering belonging and normalisation. The shift in responsibility of managing the risk feels overwhelming and stressful during teen age. Self-understanding was influenced when managing food allergy in social contexts, inducing feelings of burden and isolation. Acceptance and understanding from social relations became important for all participants, and they all underlined desire for being viewed as individuals rather than being defined by their allergy.

Conclusion: Support from other peers with food allergy is crucial for the participants. Transition to independently managing risks introduces uncertainty and social constraints, affecting self-understanding and interactions. Clinicians should prioritise peer support and empower teenagers in managing the risk and psychosocial challenges.

简介与未患有食物过敏症的青少年相比,患有食物过敏症的青少年普遍存在焦虑、饮食失调和社交孤立等症状。对患有食物过敏症的青少年的治疗重点在于预防过敏反应,而很少关注促进社交和情绪健康。本研究旨在探讨青少年对青少年时期食物过敏日常生活的看法,以改进未来的临床实践:批判性心理实践研究。在为期两天的夏令营中,通过参与观察和非正式访谈,探讨了 10 名青少年(18-23 岁)的观点。还进行了三次后续访谈。共同研究小组讨论了初步结果、临床挑战和前进方向:结果:与患有食物过敏症的同龄人在一起是至关重要的,这可以促进归属感和正常化。在青少年时期,管理风险的责任转变让他们感到难以承受和压力重重。在社会环境中处理食物过敏问题时,自我认识会受到影响,从而产生负担和孤独感。社会关系的接纳和理解对所有参与者来说都很重要,他们都强调希望被视为独立的个体,而不是被过敏症所定义:结论:来自其他患有食物过敏症的同伴的支持对参与者至关重要。过渡到独立管理风险带来了不确定性和社会限制,影响了自我认识和互动。临床医生应优先考虑同龄人的支持,增强青少年应对风险和社会心理挑战的能力。
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引用次数: 0
Factors influencing job satisfaction and professional competencies in clinical practice among internationally educated nurses during the migration journey: A mixed-methods systematic review. 影响受过国际教育的护士在移民过程中的工作满意度和临床实践专业能力的因素:混合方法系统综述。
IF 1.9 4区 医学 Q2 NURSING Pub Date : 2024-07-11 DOI: 10.1111/scs.13280
Floro Cubelo, Fatma Al Jabri, Krista Jokiniemi, Hannele Turunen

Background: The increasing migration of internationally educated nurses (IENs) from developing to developed countries highlights the importance of implementing integration strategies that facilitate their workplace transition, leading to improved job satisfaction and professional competence.

Aim: The mixed-methods systematic review aimed to synthesise the current literature on factors influencing job satisfaction and professional competencies among IENs throughout their transition process, including the pre-migration, migration, and post-migration periods.

Methods: This study conducted a mixed-methods systematic review from 2013 to 2023, using the CINAHL, Scopus, and PubMed databases and employing a Population, Interventions, Comparisons, Outcomes (PICO) framework. Quality assessment employed the Mixed Methods Appraisal Tool (MMAT), and data analysis followed a convergent parallel design. Data synthesis was presented narratively, and the literature review adhered to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.

Results: Out of 565 articles, eleven studies (eight qualitative, two quantitative, and one mixed-method) met the inclusion criteria. Three key themes that influenced job satisfaction and professional competencies among IENs were identified: pre-migration and pre-deployment demands, challenges in workplace integration, and post-migration career challenges and retention strategies.

Limitations: The study primarily focused on IENs recruited from developing countries, potentially limiting the generalisability of the findings to IENs from other regions or countries. Furthermore, the inclusion of nurses from developed countries who also migrated was limited in the available studies, which further restricts the applicability of the research findings.

Conclusions: It is essential to reconsider the pre-migration language requirements and evaluate the feasibility of completing them during the integration period to enhance the job satisfaction and professional competencies of IENs. Additionally, key factors for improving job satisfaction among IENs include providing personalised support, addressing managerial barriers, facilitating career advancement, efficiently managing workloads, and promoting effective communication within the healthcare team.

背景:目的:本研究采用混合方法进行系统综述,旨在总结当前有关影响国际教育护士在整个过渡过程(包括移民前、移民中和移民后)中工作满意度和专业能力的因素的文献:本研究使用 CINAHL、Scopus 和 PubMed 数据库,采用人口、干预、比较、结果(PICO)框架,对 2013 年至 2023 年期间的文献进行了混合方法系统综述。质量评估采用混合方法评估工具(MMAT),数据分析采用会聚平行设计。数据综合以叙述方式呈现,文献综述遵循系统综述和元分析首选报告项目(PRISMA)指南:在 565 篇文章中,有 11 项研究(8 项定性研究、2 项定量研究和 1 项混合方法研究)符合纳入标准。确定了影响 IENs 工作满意度和专业能力的三个关键主题:迁移前和部署前的需求、工作场所融入的挑战以及迁移后的职业挑战和保留策略:研究主要集中于从发展中国家招聘的 IENs,这可能会限制研究结果对其他地区或国家 IENs 的普适性。此外,在现有的研究中,来自发达国家的移民护士人数有限,这进一步限制了研究结果的适用性:有必要重新考虑移民前的语言要求,并评估在融入社会期间完成这些要求的可行性,以提高 IENs 的工作满意度和专业能力。此外,提高 IENs 工作满意度的关键因素还包括提供个性化支持、解决管理障碍、促进职业发展、有效管理工作量以及促进医疗团队内部的有效沟通。
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引用次数: 0
Navigating parenthood in the face of amyotrophic lateral sclerosis: A qualitative exploration of partner experiences. 面对肌萎缩性脊髓侧索硬化症,如何为人父母?对伴侣经历的定性探索。
IF 1.9 4区 医学 Q2 NURSING Pub Date : 2024-07-10 DOI: 10.1111/scs.13282
Anne Kristine Bergem, Trude Aamotsmo

Introduction: Among people diagnosed with Amyotrophic Lateral Sclerosis (ALS), there are parents with children living at home. Children in families experiencing severe illness are exposed to stress and health risks. Since 2010, healthcare personnel in Norway must assess whether patients have children under 18 years of age and make sure the children's needs for support are met. A child's ability to cope with family life affected by a serious illness depends on how the parent without the disease manages the situation. Little is known about how the partner of someone affected by ALS manages being next of kin and a parent simultaneously, and what kind of support they need.

Methods: During 2021-2022, six semi-structured interviews were conducted with partners to persons with ALS, whom had children living at home. The interviews were transcribed verbatim and analysed through qualitative content analysis.

Results: Three themes with subthemes emerged: (1) Together, yet alone; (a) restricted home life, (b) missing the sharing of responsibilities and tasks as equal parents, and (c) caught between children's and partner's needs; (2) Experience of coping while waiting for death; (a) cherishing the moments, (b) sense of coping and concern, and (c) ensuring to get recharged; and (3) Support in times of need; (a) difficult to ask the network for help and (b) the healthcare system does not see the whole family.

Conclusions: Our respondents felt alone, caught between the needs of their children and partner, without necessary support from the services, and were left to handle everyday life with all new challenges on their own. Future healthcare services need to consider the challenges faced by families dealing with life-limiting illnesses. A family-focused perspective is needed, so is peer support and interventions that address both emotional and practical aspects of life with an ill partner.

简介在被确诊为肌萎缩侧索硬化症(ALS)的患者中,有父母与子女同住。重病家庭中的儿童面临着压力和健康风险。自2010年起,挪威的医护人员必须评估患者是否有18岁以下的子女,并确保满足儿童的支持需求。孩子是否有能力应对受重病影响的家庭生活,取决于没有患病的父母是如何处理这种情况的。对于 ALS 患者的伴侣如何同时处理近亲和父母的关系,以及他们需要什么样的支持,人们知之甚少:在 2021-2022 年期间,我们对有子女居住在家中的 ALS 患者伴侣进行了六次半结构化访谈。访谈内容逐字记录,并通过定性内容分析进行分析:结果:出现了三个主题和副主题:(1) 相聚却又孤独;(a) 家庭生活受限,(b) 缺少作为平等父母的责任和任务分担,(c) 在子女和伴侣的需求之间徘徊;(2) 等待死亡时的应对经验;(a) 珍惜时光,(b) 应对和关切意识,(c) 确保充电;(3) 需要时的支持;(a) 难以向网络求助,(b) 医疗系统看不到整个家庭。结论:我们的受访者感到孤独,他们既要满足子女和伴侣的需求,又得不到必要的服务支持,只能独自应对日常生活中的各种新挑战。未来的医疗服务需要考虑患局限性疾病的家庭所面临的挑战。我们需要一个以家庭为中心的视角,还需要同伴支持和干预措施,以解决与患病伴侣共同生活的情感和实际问题。
{"title":"Navigating parenthood in the face of amyotrophic lateral sclerosis: A qualitative exploration of partner experiences.","authors":"Anne Kristine Bergem, Trude Aamotsmo","doi":"10.1111/scs.13282","DOIUrl":"https://doi.org/10.1111/scs.13282","url":null,"abstract":"<p><strong>Introduction: </strong>Among people diagnosed with Amyotrophic Lateral Sclerosis (ALS), there are parents with children living at home. Children in families experiencing severe illness are exposed to stress and health risks. Since 2010, healthcare personnel in Norway must assess whether patients have children under 18 years of age and make sure the children's needs for support are met. A child's ability to cope with family life affected by a serious illness depends on how the parent without the disease manages the situation. Little is known about how the partner of someone affected by ALS manages being next of kin and a parent simultaneously, and what kind of support they need.</p><p><strong>Methods: </strong>During 2021-2022, six semi-structured interviews were conducted with partners to persons with ALS, whom had children living at home. The interviews were transcribed verbatim and analysed through qualitative content analysis.</p><p><strong>Results: </strong>Three themes with subthemes emerged: (1) Together, yet alone; (a) restricted home life, (b) missing the sharing of responsibilities and tasks as equal parents, and (c) caught between children's and partner's needs; (2) Experience of coping while waiting for death; (a) cherishing the moments, (b) sense of coping and concern, and (c) ensuring to get recharged; and (3) Support in times of need; (a) difficult to ask the network for help and (b) the healthcare system does not see the whole family.</p><p><strong>Conclusions: </strong>Our respondents felt alone, caught between the needs of their children and partner, without necessary support from the services, and were left to handle everyday life with all new challenges on their own. Future healthcare services need to consider the challenges faced by families dealing with life-limiting illnesses. A family-focused perspective is needed, so is peer support and interventions that address both emotional and practical aspects of life with an ill partner.</p>","PeriodicalId":48171,"journal":{"name":"Scandinavian Journal of Caring Sciences","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141581199","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
'Staying cool, calm and positive': A dialogical narrative analysis of emotional reactions in narratives about operable lung cancer. 保持冷静、沉着和积极":对可手术肺癌叙事中的情绪反应进行对话式叙事分析。
IF 1.9 4区 医学 Q2 Medicine Pub Date : 2024-06-01 Epub Date: 2024-02-02 DOI: 10.1111/scs.13241
Mai Nanna Schoenau, Malene Missel, Mari Holen

Background: Patients with lung cancer suffer from physical, psychosocial and particularly emotional challenges. Twenty-five percent of patients with lung cancer are offered surgery as a potential cure. Nevertheless, 40% of surgically treated patients will experience recurrence. Paradoxically, research shows a dominant narrative of operable lung cancer patients 'being lucky', which silences other narratives about suffering, worries and emotional challenges.

Aim: To explore narratives about operable lung cancer, particularly emotional reactions to illness and suffering in these narratives.

Methods: A qualitative design was applied. Six women and four men diagnosed with operable lung cancer were included from one university hospital in Denmark and interviewed 1 month after surgery using active interviews. The interviews were subject to dialogical narrative analysis. The theoretical foundation is social constructivism, with socio-narratological inspiration.

Findings: A typology of three emotional narratives emerged: 'staying cool', 'staying calm' and 'staying positive'. All three types of narrative are characterised by managing emotional reactions. Staying cool is characterised by not showing emotional reactions; staying calm narratives acknowledge emotional reactions, but that they need to be managed so that they do not burden relatives; and the last, staying positive, is characterised by managing emotional reactions in a positive direction. Together this typology of three emotional narratives revealed that operable lung cancer patients are under normative pressure from these socially preferred narratives of ideal emotional reactions to lung cancer.

Conclusion: A typology of three emotional narratives were identified and can be called 'feeling rules' that guide patients after lung cancer surgery to manage their emotions. Consequently, if patients do not live up to these three emotional narratives of staying cool, calm and positive, they may be socially isolated and restricted from access to support.

背景:肺癌患者在身体、社会心理,尤其是情感方面都面临挑战。25%的肺癌患者可通过手术治愈。然而,40%接受过手术治疗的患者会复发。矛盾的是,研究表明,可手术肺癌患者 "幸运 "的叙述占主导地位,而其他关于痛苦、担忧和情感挑战的叙述则被压制:方法:采用定性设计。丹麦一所大学医院的六名女性和四名男性被诊断患有可手术肺癌,他们在手术后一个月接受了主动访谈。对访谈内容进行对话式叙事分析。研究的理论基础是社会建构主义,并受到社会叙事学的启发:出现了三种情绪叙事类型:"保持冷静"、"保持镇定 "和 "保持积极"。这三类叙事的特点都是管理情绪反应。保持冷静 "的特点是不表现出情绪反应;"保持冷静 "的叙述承认有情绪反应,但需要加以控制,以免给亲属造成负担;最后一种 "保持积极 "的叙述特点是朝着积极的方向控制情绪反应。这三种情绪叙事类型学共同揭示出,可手术肺癌患者受到这些社会偏好的肺癌理想情绪反应叙事的规范压力:结论:研究发现了三种情绪叙述类型,它们可被称为 "感觉规则",指导肺癌术后患者管理自己的情绪。因此,如果患者不遵守这三种情绪叙述,即保持冷静、沉着和积极,他们可能会被社会孤立,并在获得支持方面受到限制。
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引用次数: 0
The midwife's support during transition to motherhood: A modified Delphi study among care providers and childbearing women. 助产士在向母亲过渡期间的支持:在护理人员和育龄妇女中开展的改良德尔菲研究。
IF 1.9 4区 医学 Q2 Medicine Pub Date : 2024-06-01 Epub Date: 2024-03-07 DOI: 10.1111/scs.13250
Yvonne J Kuipers, Natacha Van de Craen, Laura Van den Branden, Eveline Mestdagh

Objective: To reach consensus between care providers and childbearing women about the midwife's relevant and appropriate domains and elements to support transition to motherhood.

Methods: A modified web-based Delphi study was conducted in Flanders (Belgium). After performing a systematic literature review, searching the grey literature and an online poll, a set of 79 items was generated. In two rounds, the items were presented to an expert panel of (1) care providers from various disciplines providing services to childbearing women and (2) to pregnant women and postpartum women up to 1-year postpartum. Consensus was defined when 70% or more of the experts scored ≥6, 5% or less scored ≤3, and a standard deviation of ≤1.1.

Findings: In the first Delphi round, 91 experts reached consensus on 24 items. Seventeen round one items that met one or two consensus objectives were included in round two and were scored by 64 panel experts, reaching consensus on three additional items. The final 27 items covered seven domains: attributes, liaison, management of care from a woman-centred perspective, management of care from the midwife's focus, informational support, relational support, and the midwife's competencies.

Conclusion: The shared understanding between childbearing women and care providers shows that the midwife's transitional support is multifaceted. Our findings offer midwives a standard of care, criteria, guidance, and advice on how they can support childbearing women during transition to motherhood, beyond the existing recommendations and current provision of transitional care.

目的就助产士支持向母亲过渡的相关和适当领域及要素,在护理提供者和育龄妇女之间达成共识:方法: 在佛兰德斯(比利时)开展了一项经过修改的基于网络的德尔菲研究。在进行了系统的文献回顾、灰色文献搜索和在线投票后,产生了一套 79 个项目。这些项目分两轮提交给由以下人员组成的专家小组:(1) 为育龄妇女提供服务的各学科护理人员;(2) 孕妇和产后 1 年以内的产后妇女。当 70% 或更多的专家评分≥6 分,5% 或更少的专家评分≤3 分,且标准偏差≤1.1 时,即为达成共识:在第一轮德尔菲讨论中,91 位专家就 24 个项目达成了共识。在第一轮中,有 17 个项目达到了一个或两个共识目标,这些项目被纳入第二轮,并由 64 位专家小组专家进行打分,就另外 3 个项目达成了共识。最终的 27 个项目涵盖了七个领域:属性、联络、以妇女为中心的护理管理、助产士关注的护理管理、信息支持、关系支持和助产士的能力:结论:育龄妇女和护理提供者之间的共识表明,助产士的过渡支持是多方面的。我们的研究结果为助产士提供了一个护理标准、准则、指导和建议,使她们能够在现有建议和当前提供的过渡护理之外,为育龄妇女在向母亲过渡期间提供支持。
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引用次数: 0
Components of spirituality in older adults: A phenomenological study through interviews based on dignity therapy. 老年人精神信仰的组成部分:基于尊严疗法的访谈现象学研究。
IF 1.9 4区 医学 Q2 Medicine Pub Date : 2024-06-01 Epub Date: 2024-03-07 DOI: 10.1111/scs.13254
Kyoko Nagata, Koji Tanaka

Aim: A key perspective in examining dignity, which is important for older adults, is spirituality. Therefore, this study aimed to identify the components of spirituality in older adults through interviews based on dignity therapy (DT).

Methodological design and justification: Colaizzi's descriptive phenomenology was applied to understand experiences rooted in the life world of older adults from their own perspective.

Ethical issues and approval: This study was approved by the ethical review committee of the author's university. All participants provided consent to participate.

Research methods: Semi-structured interviews based on DT were conducted with 11 community-dwelling adults aged 65 years or older who were using some form of medical or social services. The interviews were transcribed, and the text was analysed based on Colaizzi's phenomenological method.

Results: Four themes were identified as components of spirituality in older adults: trauma, being silent about hard experiences, forming connections and taking on challenges and discovering one's own spirit. The participants felt a sense of helplessness and frustration as they dealt with traumatic events. Feelings of shame, guilt and/or resignation prevented them from talking about the distress they were experiencing, but they were able to move forward after receiving emotional support and having opportunities to share with others. These processes led to the discovery of a new self.

Study limitations: This study assessed the experiences of older adults in Japan and may therefore have been influenced by the social background and culture of Japan. Future research should target older adults from a variety of social backgrounds as well as those with specific health conditions.

Conclusion: The findings suggest the importance of creating opportunities for healthcare professionals as well as family, friends and community members to help older adults reflect on their lives and talk about their accomplishments and unresolved issues. Doing so should help older adults maintain their dignity while remaining aware of their mortality.

目的:研究尊严的一个重要视角是灵性,这对老年人非常重要。因此,本研究旨在通过基于尊严疗法(DT)的访谈,确定老年人精神生活的组成部分:伦理问题和批准:本研究获得了伦理委员会的批准:本研究获得了作者所在大学伦理审查委员会的批准。所有参与者均同意参与:研究方法:根据 DT 对 11 名 65 岁或以上居住在社区、使用某种形式的医疗或社会服务的成年人进行了半结构式访谈。访谈内容均已转录,并根据科莱兹的现象学方法对文本进行了分析:结果:四个主题被确定为老年人精神信仰的组成部分:创伤、对艰难经历保持沉默、建立联系和接受挑战以及发现自己的精神。参与者在处理创伤事件时感到无助和沮丧。羞耻感、负罪感和/或逆来顺受的感觉阻碍了他们谈论自己所经历的痛苦,但在得到情感支持并有机会与他人分享后,他们能够继续前进。这些过程让他们发现了新的自我:本研究评估的是日本老年人的经历,因此可能会受到日本社会背景和文化的影响。未来的研究应该针对来自不同社会背景的老年人以及有特殊健康状况的老年人:研究结果表明,为医疗保健专业人员以及家人、朋友和社区成员创造机会,帮助老年人反思自己的生活、谈论自己的成就和未解决的问题非常重要。这样做应有助于老年人保持尊严,同时意识到自己的死亡。
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引用次数: 0
Swedish stakeholders' views of the preparatory work needed before introducing the nurse practitioner role in municipal healthcare-A focus group study. 瑞典利益相关者对在市政医疗保健中引入执业护士角色之前所需准备工作的看法——焦点小组研究。
IF 1.9 4区 医学 Q2 Medicine Pub Date : 2024-06-01 Epub Date: 2023-11-20 DOI: 10.1111/scs.13224
Birgitta Ljungbeck, Elisabeth Carlson, Katarina Sjögren Forss

Background: The nurse practitioner role has become important globally in handling the growing healthcare needs of older adults with chronic diseases. Nevertheless, research shows that introducing the role is a complex process, and more studies are needed to prepare for its introduction into different healthcare contexts, such as municipal healthcare.

Aim: The aim is to investigate what Swedish stakeholders identify as the preparatory work needed before introducing the nurse practitioner role into municipal healthcare.

Methods: Data were collected through four focus group interviews conducted virtually on the TEAMS digital platform, with three to six participants in each group and 18 participants total. The transcribed interviews were analysed using a six-step thematic approach: familiarisation with the data, coding the data, generating initial themes, reviewing themes, defining and naming the themes and producing the report.

Findings: The findings are divided into two main themes, each with two sub-themes. In the first, clarifying why the nurse practitioner role is needed, participants stressed the importance of having a clear intention for introducing the role. The second, ensure a national framework to bolster the introduction at the local level, demonstrates the need for collaboration among national actors to clarify the role's mandate and authority before its introduction.

Conclusions: Adding the nurse practitioner role to municipal healthcare can help increase the supply of nursing competence and the quality of patient care, but preparation for introducing the role requires extensive work. The development of the nurse practitioner role requires decision-makers and leaders to take primary responsibility for its introduction. This study can support countries in the early phase of developing the nurse practitioner role by identifying both best practices and pitfalls.

背景:护士从业者的作用已成为重要的处理日益增长的医疗保健需求的老年人慢性疾病全球。然而,研究表明,引入这一角色是一个复杂的过程,需要更多的研究来准备将其引入不同的医疗保健环境,如市政医疗保健。目的:目的是调查瑞典利益相关者确定的准备工作,然后将护士执业角色引入市政医疗保健。方法:通过在TEAMS数字平台上虚拟进行的四次焦点小组访谈收集数据,每组3 - 6人,共18人。采访记录采用六步专题方法进行分析:熟悉数据、对数据进行编码、产生初步主题、审查主题、确定和命名主题以及编写报告。调查结果:调查结果分为两个主题,每个主题又有两个子主题。首先,在澄清为什么需要护士从业员角色时,与会者强调了引入这一角色的明确意图的重要性。第二,确保有一个国家框架来支持在地方一级的采用,这表明需要国家行动者之间进行合作,以便在采用该角色之前澄清其任务和权力。结论:在市级卫生保健中引入执业护士角色有助于提高护理能力的供给和患者护理的质量,但引入执业护士角色的准备工作还需要做大量的准备工作。护士执业角色的发展需要决策者和领导者对其引入承担主要责任。这项研究可以通过确定最佳做法和缺陷,为处于发展护士执业作用早期阶段的国家提供支持。
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引用次数: 0
Undergraduate nursing student's attitudes to learning during clinical practice in different semesters when using a conceptual learning model grounded in a caritative caring perspective - A cross-sectional study. 不同学期护理本科学生在临床实践中使用基于牙科护理观点的概念学习模式的学习态度-一项横断面研究。
IF 1.9 4区 医学 Q2 Medicine Pub Date : 2024-06-01 Epub Date: 2023-12-01 DOI: 10.1111/scs.13229
Maria Koldestam, Bo Rolander, Anders Broström, Gunilla Lindqvist, Susanne Knutsson

Aim: To describe undergraduate nursing students' attitudes to learning during clinical practice in different semesters when using the conceptual learning model, Model for Improvements in Learning Outcomes (MILO) grounded in a caritative caring perspective.

Background: With the intention to support interlinking between theory and praxis and offer understanding and structure to facilitate learning, MILO, theoretically grounded in hermeneutics and a caritative caring perspective based on ethical values, was implemented. MILO consists of four contextual concepts (peer learning, co-clinical teachers, student-centred and student-active supervision) and four intrapersonal concepts (nursing, a reflective approach, a critical approach, quality and safety).

Methods: A descriptive comparative quantitative study design was applied at a Swedish university, 3 hospitals and 13 municipalities in one county. Cross-sectional data collected via a questionnaire developed to assess attitudes to learning related to MILO's contextual and intrapersonal concepts and their applications were used.

Results: 209 students in semester 3, 4 and 6 participated in 6 different clinical practice courses. In comparison, intrapersonal concepts, that is, the student's own characteristics and abilities were viewed to be of greater value for learning than contextual, that is, organisational-related concepts in all semesters. Understanding the needs of others and reflective learning were rated to be of major importance. Students in semester 3 valued the use of the applications the highest. To be supervised in pairs was rated the lowest in semester 6. Some of the concepts and their applications were to great extent not applied.

Conclusions: In all semesters, fundamentals in caritative caring and characteristics and abilities related to the individual student were rated to be of greater importance for learning than environmental support. Providing students opportunities to develop independency seems essential. Use of a learning model such as MILO is dependent on a bearing of a caritative caring culture and a shared understanding between all involved in student learning during clinical practice.

目的:探讨基于龋齿护理视角的概念学习模型——学习成果改善模型(MILO)在不同学期护理本科生临床实习中的学习态度。背景:为了支持理论与实践之间的相互联系,并提供理解和结构以促进学习,MILO在理论上以解释学为基础,并以道德价值观为基础的关爱视角实施。MILO包括四个情境概念(同伴学习、共同临床教师、以学生为中心和学生主动监督)和四个个人概念(护理、反思方法、批判方法、质量和安全)。方法:采用描述性比较定量研究设计,对瑞典一所大学、三所医院和一个县的13个市进行研究。通过问卷调查收集的横截面数据用于评估与MILO的情境和个人概念及其应用相关的学习态度。结果:第3、4、6学期209名学生参加了6门不同的临床实践课程。相比之下,在所有学期中,个人概念(即学生自身的特点和能力)被认为比情境概念(即与组织有关的概念)对学习更有价值。理解他人的需求和反思性学习被认为是最重要的。第三学期的学生对应用程序的评价最高。在第六学期被评为最低的是成对监督。其中一些概念及其应用在很大程度上没有得到应用。结论:在所有学期中,与环境支持相比,龋齿护理的基础知识和与个体学生相关的特征和能力对学习更重要。为学生提供发展独立能力的机会似乎是必不可少的。使用像MILO这样的学习模式取决于在临床实践中所有参与学生学习的人对龋齿护理文化的理解和共同理解。
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引用次数: 0
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Scandinavian Journal of Caring Sciences
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