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Refining the program theory of the nurse-led Rapid Response Team in acute care hospitals: A realist evaluation 精细化急症护理医院护士领导快速反应小组的程序理论:一个现实的评估
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-11-06 DOI: 10.1016/j.ijnurstu.2025.105280
Gitte Bunkenborg , Jesper Frederiksen , Tina C.B. Hansen , Tracey Bucknall

Background

Caring for unstable patients in a general ward is a challenging task for nurses and impacts patients' safety. To assist nurses in detecting and managing patient deterioration, the nurse-led Rapid Response Team has been implemented worldwide for over 25 years with divergent results regarding reduced patient mortality, cardiac arrest rates, and admissions for intensive care. To develop new initiatives targeting well-documented challenges embedded in using the nurse-led Rapid Response Team, research-based knowledge from a broader perspective on the Rapid Response Team is crucial. This study evaluated how and for whom the nurse-led Rapid Response Team works.

Objective

To test initial and alternative program theories of the nurse-led Rapid Response Team in acute care hospitals and further refine the program theories of this complex health care intervention.

Design

A realist evaluation.

Methods

A four-stage cycle process was applied, involving a synthesis of literature of the Rapid Response Team published between 2014-24, and empirical data from six qualitative studies, serving as analytical tools. To explore multiple stakeholders' perceptions of the Rapid Response Team a variety of data-collection methods including participant observations, focus group interviews, and individual interviews were used in the qualitative studies. Intensive care and general ward nurses, physicians in clinical and coordinating roles, and multiple hospital managers across various levels at three acute care hospital in three Danish regions were involved in the six qualitative studies.

Findings

The fourth stage of the realist evaluation resulted in a refined program theory stating, “If Rapid Response Team-nurses use their intensive care skills and competences and collaborate amiably, creating a respectful and calm atmosphere whilst also capturing the needs of both nurses and patients, then the role as a Rapid Response Team-nurse is fulfilled and responsibility between the involved parties is shared. General ward nurses will then choose to call the team for assistance and Rapid Response Team-nurses will choose to engage in future Rapid Response Team calls, which will subsequently lead to clinical actions being taken, patients being helped, and general ward nurses feeling secure whilst also learning new skills”.

Conclusion

The nurse-led Rapid Response Team is perceived to work for patients, general ward nurses, Rapid Response Team-nurses, and the organization, due to Rapid Response Team-nurses' skills, the respect between nurses, and the essential collaboration inherent in intra-professional nursing teamwork across nursing positions and working areas. The primary responsibility for this collaboration lies with the individual Rapid Response Team-nurse and the Rapid Response Team-coordinator.
在普通病房照顾不稳定的病人对护士来说是一项具有挑战性的任务,并影响患者的安全。为了帮助护士发现和管理患者病情恶化,护士领导的快速反应小组在全球范围内实施了25年以上,在降低患者死亡率、心脏骤停率和重症监护入院率方面取得了不同的成果。为了制定新的举措,针对使用护士领导的快速反应小组所面临的充分记录的挑战,从更广泛的角度对快速反应小组进行基于研究的知识至关重要。这项研究评估了护士领导的快速反应小组如何工作以及为谁工作。目的对急症护理医院护士主导快速反应小组的初始和备选方案理论进行检验,进一步完善这一复杂卫生保健干预方案理论。设计一个现实的评估。方法采用四阶段循环流程,综合2014-24年快速反应小组发表的文献和6项定性研究的实证数据,作为分析工具。为了探讨多个利益相关者对快速反应小组的看法,在定性研究中使用了各种数据收集方法,包括参与者观察、焦点小组访谈和个人访谈。丹麦三个地区的三家急症护理医院的重症监护和普通病房护士、临床和协调医生以及不同级别的多名医院管理人员参与了六项定性研究。现实主义评估的第四阶段产生了一个精炼的程序理论,“如果快速反应小组护士使用他们的重症监护技能和能力,友好合作,创造尊重和平静的氛围,同时也捕捉护士和病人的需求,那么作为快速反应小组护士的角色就得到了履行,相关各方之间的责任也得到了分担。”普通病房护士将选择呼叫团队寻求帮助,快速反应小组护士将选择参与未来的快速反应团队呼叫,这将随后导致采取临床行动,患者得到帮助,普通病房护士在学习新技能的同时感到安全。”结论由于快速反应小组护士的技能、护士之间的尊重以及跨护理岗位和工作领域的专业护理团队内在的必要协作,护士领导的快速反应小组被认为是为患者、普通病房护士、快速反应小组护士和组织服务的。这种合作的主要责任在于个人快速反应小组护士和快速反应小组协调员。
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引用次数: 0
Palliative care needs of adults severely affected by sickle cell disease: A mixed-methods systematic review 受镰状细胞病严重影响的成人的姑息治疗需求:一项混合方法的系统综述
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-11-05 DOI: 10.1016/j.ijnurstu.2025.105278
Khulood Alyami , Katherine Bristowe , Elizabeth Dzeng , Oladayo Afolabi , Catherine J. Evans
<div><h3>Background</h3><div>Sickle cell disease is one of the most common inherited monogenetic blood disorders. People living with sickle cell disease experience both acute pain and long-lasting complications, leading to co-morbidities which impact their quality of life. Palliative care is both under-reported and under-utilised for people living with sickle cell disease despite the profound impacts of this illness across their lives.</div></div><div><h3>Objective</h3><div>To synthesise published primary evidence on the palliative care needs and experiences of adults severely affected by sickle cell disease.</div></div><div><h3>Design</h3><div>Mixed method systematic narrative review.</div></div><div><h3>Methods</h3><div>Four databases (Medline, PsycINFO, Embase and CINHAL) were searched from inception to April 2024. Eligibility criteria were adults aged ≥<!--> <!-->18 years with severe sickle cell disease defined in the disease severity classification system as Class II (moderate severity) and Class III (most severe). Data from qualitative and quantitative studies were analysed using data-based convergent synthesis. A best-fit framework synthesis approach was used with the World Health Organization definition of palliative care as the a priori framework. Results were mapped to Bronfenbrenner Ecological Model to pursue interaction between needs across different environmental systems.</div></div><div><h3>Results</h3><div>23 studies met eligibility (12 qualitative and 11 quantitative studies). Needs were evident across the five domains of palliative care, and an additional domain titled experiences of using healthcare services: i) Physical needs included distressing symptoms focusing mainly on pain (n = 22 studies). Pain manifested as both acute and chronic and impacted all aspects of a person's life; ii) Psychological needs encompassed depression, suicidal ideation, coping and stigma related to the disease itself and need for opioids for pain management; iii) Social needs included the impact on social life, functioning, personal relationships, employment and education; iv) Spirituality was described in terms of its use when living with a complex chronic condition; v) Family caregiver needs and the support provided included the family feeling unable to support the person at times, and vi) Experiencing access to healthcare services which included lack of trust in healthcare providers.</div></div><div><h3>Conclusions</h3><div>Synthesised palliative care needs for people severely affected by sickle cell disease are interlinked and impact one another. This is influenced by the unpredictability of the disease itself and its chronic complications such as living with and managing chronic wounds. Stigma associated with the disease impacted the person in multiple ways, notably delaying seeking medical treatment, discrimination in the workplace and social isolation. Sickle cell disease is a multifaceted complex condition. Management requires a dynamic holis
镰状细胞病是最常见的遗传性单基因血液疾病之一。镰状细胞病患者会经历急性疼痛和长期并发症,导致影响其生活质量的合并症。尽管镰状细胞病患者的生活受到这种疾病的深刻影响,但姑息治疗的报告和利用都不足。目的综合已发表的关于成人严重镰状细胞病患者姑息治疗需求和经验的主要证据。设计混合方法系统叙述回顾。方法检索Medline、PsycINFO、Embase和CINHAL数据库,检索时间为建库至2024年4月。入选标准为患有严重镰状细胞病的成年人,年龄≥18岁,疾病严重程度分类系统定义为II类(中度严重)和III类(最严重)。定性和定量研究的数据采用基于数据的收敛综合分析。采用最合适的框架综合方法,将世界卫生组织对姑息治疗的定义作为先验框架。结果被映射到Bronfenbrenner生态模型中,以追求不同环境系统之间需求之间的相互作用。结果23项研究符合条件(12项定性研究,11项定量研究)。在姑息治疗的五个领域以及一个名为使用医疗保健服务的体验的额外领域,需求都很明显:i)身体需求包括主要以疼痛为重点的令人痛苦的症状(n = 22项研究)。疼痛表现为急性和慢性,影响一个人生活的各个方面;(二)心理需求包括与疾病本身有关的抑郁、自杀意念、应对和耻辱,以及对阿片类药物治疗疼痛的需求;iii)社会需求包括对社会生活、功能、人际关系、就业和教育的影响;iv)灵性在患有复杂慢性疾病时的使用;v)家庭照顾者的需求和提供的支持包括家庭有时无法支持该人的感觉,以及vi)获得医疗保健服务的经历,包括对医疗保健提供者缺乏信任。结论镰状细胞病重症患者的综合姑息治疗需求是相互联系、相互影响的。这受到疾病本身的不可预测性及其慢性并发症(如与慢性伤口一起生活和处理)的影响。与该疾病相关的污名以多种方式影响患者,特别是延迟就医、工作场所歧视和社会孤立。镰状细胞病是一种多方面的复杂疾病。管理需要一种动态的整体方法,将人置于疾病之前,并强调家庭参与。普洛斯彼罗注册:(CRD42023392072)。
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引用次数: 0
Nurses' role in deprescribing for older adults: A scoping review 护士在老年人处方描述中的作用:范围回顾
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-11-05 DOI: 10.1016/j.ijnurstu.2025.105274
Giorgia Barbuiani , Stefano Terzoni , Rosario Caruso , Silvia Cilluffo , Luca Pasina , Maura Lusignani

Purpose

To map the evidence on nurses' roles and contributions in deprescribing within the multidisciplinary team across all clinical settings.

Methods

This scoping review was conducted using Arksey and O'Malley's framework and the Joanna Briggs Institute (JBI) methodology, and reported by the PRISMA-ScR 2020 checklist. A systematic search was conducted across CINAHL, Embase, MEDLINE (Ovid), Web of Science, Scopus and Google Scholar, with no time restrictions. Studies in English and Italian were included if they explored the role of nurses in deprescribing in older adults (≥ 65 years) across hospital, home, or community settings. A wide range of study designs was considered, including empirical studies, reviews, and gray literature.

Results

28 studies were included in the review. Nurses played key roles in deprescribing through medication review, adherence assessment, detection of adverse drug effects or drug–drug interactions, patient education, and monitoring. Nurse-led interventions, conducted independently or in collaboration with the multidisciplinary team, were effective in reducing potentially inappropriate medications and improving adherence as primary outcomes. Key facilitators of nurses' views on deprescribing included strong interdisciplinary collaboration, training, and use of decision-support tools. Limited resources, a lack of trust in medication counseling, fragmented care, and patient-related difficulties were the main obstacles.

Conclusions

The changing and crucial role that nurses play in the deprescribing process is highlighted in this scoping review. The medication safety of older adults necessitates empowering nurses through organizational frameworks, technology support, and training. There is a clear need for stronger, high-quality evidence, including randomized controlled trials and rigorously designed implementation studies, to assess outcomes and guide the integration of nurse-led deprescribing interventions into everyday clinical practice.

Registration

Protocol registered on the Open Science Framework (doi:10.17605/OSF.IO/C49BU).
目的在所有临床环境中,绘制护士在多学科团队中描述处方的角色和贡献的证据。方法采用Arksey和O'Malley的框架和乔安娜布里格斯研究所(JBI)的方法进行范围审查,并通过PRISMA-ScR 2020检查表进行报告。系统检索了CINAHL、Embase、MEDLINE (Ovid)、Web of Science、Scopus和谷歌Scholar,没有时间限制。在医院、家庭或社区环境中,如果研究护士在老年人(≥65岁)开处方中的作用,则纳入英语和意大利语研究。我们考虑了广泛的研究设计,包括实证研究、综述和灰色文献。结果共纳入28项研究。护士通过药物审查、依从性评估、发现药物不良反应或药物相互作用、患者教育和监测,在开处方方面发挥了关键作用。护士主导的干预,独立进行或与多学科团队合作,在减少潜在的不适当药物和提高依从性作为主要结果方面是有效的。护士对处方的看法的主要促进因素包括强有力的跨学科合作、培训和决策支持工具的使用。资源有限、对药物咨询缺乏信任、支离破碎的护理和患者相关的困难是主要障碍。结论本综述强调了护士在处方过程中所起的重要作用。老年人的用药安全需要通过组织框架、技术支持和培训来授权护士。显然需要更有力、高质量的证据,包括随机对照试验和严格设计的实施研究,以评估结果,并指导将护士主导的处方化干预措施纳入日常临床实践。RegistrationProtocol注册在开放科学框架上(doi:10.17605/OSF.IO/C49BU)。
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引用次数: 0
Effectiveness of interactive digital health services in non-communicable diseases: An umbrella review and evidence synthesis from 26 meta-analyses 非传染性疾病交互式数字卫生服务的有效性:概括性审查和来自26项荟萃分析的证据综合
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-11-05 DOI: 10.1016/j.ijnurstu.2025.105277
Elina Laukka , Miia Jansson , Petra Suonnansalo , Reetta Ojanperä , Henna Härkönen , Sanna Lakoma , Paulus Torkki

Background

New digital health services are continuously developed, implemented, tested, and refined to meet diverse health and system needs. With the rise in non-communicable diseases, these services are increasingly integrated into care processes. However, the effectiveness of digital health services varies across time and settings, highlighting the need to evaluate their effectiveness longitudinally and in specific settings.

Objective

To synthesize current evidence from meta-analyses on the effectiveness of digital health services in non-communicable diseases.

Design

Umbrella review.

Data sources

A search was conducted in Jun 2025 using Cochrane, Ovid Medline, Scopus, and Web of Science databases.

Review methods

We included only peer-reviewed meta-analyses that synthetized RCTs that compared digital health services with usual care on outcomes in non-communicable diseases. Screening, data extraction, and risk of bias assessment were carried out independently by two researchers. Additionally, the strength of evidence was assessed.

Results

This umbrella review analyses 26 meta-analyses to evaluate the effectiveness of digital health services in 12 non-communicable diseases. Most reviews indicate non-significant difference between digital health services and usual care in the clinical outcomes. Digital health services were associated with better clinical outcomes in type 2 diabetes, hypertension and heart failure. Digital health services were also associated with higher patient satisfaction. The heterogeneity of outcome measures limited possibilities in meta-analysis. Convincing evidence for improved outcomes was found in 3.75 %, highly suggestive evidence in 7.5 %, suggestive in 5.6 %, and weak evidence in 23.75 % of the reviews, respectively.

Conclusions

Digital health services are generally as effective as usual care in managing non-communicable diseases, while in specific patient groups they can yield improved clinical outcomes and, overall, higher patient satisfaction. This underscores the need for cost-effectiveness studies to identify services that deliver comparable outcomes at reduced costs. In addition, more high-quality research with standardized outcome measures is needed, as evidence on digital health services involving patient-professional interaction remains non-significant.
新的数字卫生服务不断开发、实施、测试和改进,以满足不同的卫生和系统需求。随着非传染性疾病的增加,这些服务越来越多地纳入护理过程。然而,数字卫生服务的有效性因时间和环境而异,突出表明需要纵向和在特定环境中评估其有效性。目的综合来自非传染性疾病中数字卫生服务有效性的meta分析的现有证据。DesignUmbrella审查。数据来源检索于2025年6月使用Cochrane、Ovid Medline、Scopus和Web of Science数据库进行。我们只纳入了同行评议的荟萃分析,这些荟萃分析综合了将数字医疗服务与常规医疗服务在非传染性疾病结果方面进行比较的随机对照试验。筛选、数据提取和偏倚风险评估由两名研究人员独立进行。此外,还评估了证据的强度。本综述分析了26项荟萃分析,以评估数字卫生服务在12种非传染性疾病中的有效性。大多数综述表明,在临床结果方面,数字医疗服务与常规护理之间没有显著差异。数字医疗服务与2型糖尿病、高血压和心力衰竭患者更好的临床结果相关。数字医疗服务也与更高的患者满意度相关。结果测量的异质性限制了meta分析的可能性。结果改善的可信证据分别为3.75%,高度暗示性证据为7.5%,暗示性证据为5.6%,弱证据为23.75%。结论:在管理非传染性疾病方面,数字医疗服务通常与常规护理一样有效,而在特定的患者群体中,数字医疗服务可以改善临床结果,总体上提高患者满意度。这强调需要进行成本效益研究,以确定以较低成本提供可比结果的服务。此外,由于涉及患者与专业人员互动的数字卫生服务的证据仍然不显著,因此需要进行更多具有标准化结果测量的高质量研究。
{"title":"Effectiveness of interactive digital health services in non-communicable diseases: An umbrella review and evidence synthesis from 26 meta-analyses","authors":"Elina Laukka ,&nbsp;Miia Jansson ,&nbsp;Petra Suonnansalo ,&nbsp;Reetta Ojanperä ,&nbsp;Henna Härkönen ,&nbsp;Sanna Lakoma ,&nbsp;Paulus Torkki","doi":"10.1016/j.ijnurstu.2025.105277","DOIUrl":"10.1016/j.ijnurstu.2025.105277","url":null,"abstract":"<div><h3>Background</h3><div>New digital health services are continuously developed, implemented, tested, and refined to meet diverse health and system needs. With the rise in non-communicable diseases, these services are increasingly integrated into care processes. However, the effectiveness of digital health services varies across time and settings, highlighting the need to evaluate their effectiveness longitudinally and in specific settings.</div></div><div><h3>Objective</h3><div>To synthesize current evidence from meta-analyses on the effectiveness of digital health services in non-communicable diseases.</div></div><div><h3>Design</h3><div>Umbrella review.</div></div><div><h3>Data sources</h3><div>A search was conducted in Jun 2025 using Cochrane, Ovid Medline, Scopus, and Web of Science databases.</div></div><div><h3>Review methods</h3><div>We included only peer-reviewed meta-analyses that synthetized RCTs that compared digital health services with usual care on outcomes in non-communicable diseases. Screening, data extraction, and risk of bias assessment were carried out independently by two researchers. Additionally, the strength of evidence was assessed.</div></div><div><h3>Results</h3><div>This umbrella review analyses 26 meta-analyses to evaluate the effectiveness of digital health services in 12 non-communicable diseases. Most reviews indicate non-significant difference between digital health services and usual care in the clinical outcomes. Digital health services were associated with better clinical outcomes in type 2 diabetes, hypertension and heart failure. Digital health services were also associated with higher patient satisfaction. The heterogeneity of outcome measures limited possibilities in meta-analysis. Convincing evidence for improved outcomes was found in 3.75 %, highly suggestive evidence in 7.5 %, suggestive in 5.6 %, and weak evidence in 23.75 % of the reviews, respectively.</div></div><div><h3>Conclusions</h3><div>Digital health services are generally as effective as usual care in managing non-communicable diseases, while in specific patient groups they can yield improved clinical outcomes and, overall, higher patient satisfaction. This underscores the need for cost-effectiveness studies to identify services that deliver comparable outcomes at reduced costs. In addition, more high-quality research with standardized outcome measures is needed, as evidence on digital health services involving patient-professional interaction remains non-significant.</div></div>","PeriodicalId":50299,"journal":{"name":"International Journal of Nursing Studies","volume":"174 ","pages":"Article 105277"},"PeriodicalIF":7.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145447443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Associations between healthcare workers' substance use and quality of care: Findings from a one-year Swedish follow-up study 医护人员物质使用与护理质量之间的关系:瑞典一项为期一年的随访研究的结果
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-11-02 DOI: 10.1016/j.ijnurstu.2025.105276
Josefina Peláez Zuberbuhler , Amr Aroub , Emelie Thern , Siw Tone Innstrand , Bodil J. Landstad , Malin Sjöström , Emma Brulin

Background

Problem drinking and illicit drug use among healthcare workers (i.e., physicians and nurses) may impair their attention and cognitive functioning, thereby increasing the risk of medical errors and diminishing the quality of patient care.

Objective

To investigate the association between healthcare workers' problem drinking and illicit drug use with subsequent self-rated quality of care provided.

Design

A two-wave longitudinal observational study.

Methods

Panel data were drawn from the Longitudinal Occupational Health Survey in Healthcare Sweden (LOHHCS), collected in 2022 (baseline) and 2023 (follow-up), encompassing a sample of 3280 healthcare workers. Questionnaires included problem drinking, illicit drug use (cannabis and stimulants), and self-rated quality of care they provide to patients. Logistic regression models analysed relationships between the study variables.

Results

At baseline, the prevalence of problem drinking was 3.8 %, and illicit drug use was 1.3 %. Both problem drinking (OR = 1.93, 95 % CI = 1.28–3.02) and illicit drug use (OR = 2.07, 95 % CI = 1.00–4.29) were significantly associated with lower self-rated quality of care provided at follow-up, after adjustment for confounding variables.

Conclusions

This novel longitudinal study shows that healthcare workers reporting substance use at baseline were about twice as likely to report providing poor quality of care one year later. These findings are of clinical relevance and highlight the need for targeted preventive measures and interventions to safeguard the health and well-being of healthcare workers while maintaining quality standards in patient care.
背景:卫生保健工作者(即医生和护士)的酗酒和非法药物使用问题可能损害他们的注意力和认知功能,从而增加医疗差错的风险,降低病人护理的质量。目的探讨医护人员问题饮酒和非法药物使用与随后提供的自评护理质量的关系。设计:双波纵向观察研究。方法数据来自瑞典卫生保健纵向职业健康调查(LOHHCS),于2022年(基线)和2023年(随访)收集,包括3280名卫生保健工作者样本。调查问卷包括饮酒问题、非法药物使用(大麻和兴奋剂)以及他们向患者提供的自评护理质量。逻辑回归模型分析了研究变量之间的关系。结果基线时,问题饮酒患病率为3.8%,非法药物使用率为1.3%。在调整混杂变量后,饮酒问题(OR = 1.93, 95% CI = 1.28-3.02)和非法药物使用(OR = 2.07, 95% CI = 1.00-4.29)与随访时提供的较低自评护理质量显著相关。结论:这项新颖的纵向研究表明,在基线时报告药物使用的医护人员在一年后报告提供低质量护理的可能性大约是其两倍。这些发现具有临床意义,并强调需要有针对性的预防措施和干预措施,以保障卫生保健工作者的健康和福祉,同时保持患者护理的质量标准。
{"title":"Associations between healthcare workers' substance use and quality of care: Findings from a one-year Swedish follow-up study","authors":"Josefina Peláez Zuberbuhler ,&nbsp;Amr Aroub ,&nbsp;Emelie Thern ,&nbsp;Siw Tone Innstrand ,&nbsp;Bodil J. Landstad ,&nbsp;Malin Sjöström ,&nbsp;Emma Brulin","doi":"10.1016/j.ijnurstu.2025.105276","DOIUrl":"10.1016/j.ijnurstu.2025.105276","url":null,"abstract":"<div><h3>Background</h3><div>Problem drinking and illicit drug use among healthcare workers (i.e., physicians and nurses) may impair their attention and cognitive functioning, thereby increasing the risk of medical errors and diminishing the quality of patient care.</div></div><div><h3>Objective</h3><div>To investigate the association between healthcare workers' problem drinking and illicit drug use with subsequent self-rated quality of care provided.</div></div><div><h3>Design</h3><div>A two-wave longitudinal observational study.</div></div><div><h3>Methods</h3><div>Panel data were drawn from the Longitudinal Occupational Health Survey in Healthcare Sweden (LOHHCS), collected in 2022 (baseline) and 2023 (follow-up), encompassing a sample of 3280 healthcare workers. Questionnaires included problem drinking, illicit drug use (cannabis and stimulants), and self-rated quality of care they provide to patients. Logistic regression models analysed relationships between the study variables.</div></div><div><h3>Results</h3><div>At baseline, the prevalence of problem drinking was 3.8 %, and illicit drug use was 1.3 %. Both problem drinking (OR = 1.93, 95 % CI = 1.28–3.02) and illicit drug use (OR = 2.07, 95 % CI = 1.00–4.29) were significantly associated with lower self-rated quality of care provided at follow-up, after adjustment for confounding variables.</div></div><div><h3>Conclusions</h3><div>This novel longitudinal study shows that healthcare workers reporting substance use at baseline were about twice as likely to report providing poor quality of care one year later. These findings are of clinical relevance and highlight the need for targeted preventive measures and interventions to safeguard the health and well-being of healthcare workers while maintaining quality standards in patient care.</div></div>","PeriodicalId":50299,"journal":{"name":"International Journal of Nursing Studies","volume":"174 ","pages":"Article 105276"},"PeriodicalIF":7.1,"publicationDate":"2025-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145427377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
The influence of workplace experience and professional education on enhancing empathy among doctors, nurses and healthcare students: A comparative cross-sectional study 工作经历和专业教育对医生、护士和卫生保健专业学生共情能力的影响:一项比较横断面研究
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-10-30 DOI: 10.1016/j.ijnurstu.2025.105275
Honghong Cai , Qing Wu , Pei Wang

Background

Empathy is crucial for effective clinical practice, and patient care. Despite its importance, the comparative studies and effectiveness analyses focusing on empathy-training strategies within both medical education and clinical practice are limited, particularly in China. The objective of this study is to compare empathy levels across doctors, nurses, medical students, and nursing students in China, exploring how workplace settings, professional roles, and training stages influence empathy development, to inform targeted empathy education strategies.

Methods

A cross-sectional survey was conducted using the Chinese Version of the Jefferson Scale of Healthcare Professional Empathy (C-JSHPE). Participants included doctors, nurses, medical students and nursing students from primary, secondary, and tertiary hospitals, as well as medical schools located in eastern (economically developed), central (moderately developed), and western (less developed) regions of China.

Results

Qualified professionals (licensed nurses and doctors) exhibited significantly higher empathy scores than healthcare students (doctors vs medical students t = 12.959, p < 0.001; nurses vs nursing students t = 7.135, p < 0.001). Nurses exhibited significantly higher empathy than doctors (t = 4.081, p < 0.001), and nursing students likewise exhibited markedly greater empathy than their medical student counterparts (t = 5.221, p < 0.001). Significant differences in empathy scores were observed between nursing students who participated in internships and those who did not (t = 2.548, p < 0.05). In contrast, no such differences emerged among medical students (t = − 0.228, p > 0.05). Both doctors and nurses with more clinical experience demonstrated higher empathy scores (F physician = 10.696, p < 0.001; F nurse = 30.029, p < 0.001). In contrast, those working in tertiary hospitals reported reduced empathy (F physician = 94.018, p < 0.001; F nurse = 486.586, p < 0.001).

Conclusions

This study underscored the importance of both developing and retaining empathy in qualified professionals and healthcare students, and highlighted the significant role of clinical work environments and stages of professional development in shaping empathic capacity. The findings suggested that empathy was not static, but evolved in response to the demands, pressures, and relational dynamics of different clinical roles. Simulation-based education and other experiential learning approaches represent promising avenues for fostering empathy, particularly when integrated longitudinally throughout training and aligned with authentic clinical contexts. Embedding these strategies into the continuum of medical education may be key to sustaining empathy as a core professional competence in complex healthcare systems.
背景:痴呆对于有效的临床实践和患者护理至关重要。尽管移情训练策略很重要,但在医学教育和临床实践中关注移情训练策略的比较研究和有效性分析有限,特别是在中国。本研究的目的是比较中国医生、护士、医学生和护理学生的共情水平,探讨工作环境、职业角色和培训阶段对共情发展的影响,为有针对性的共情教育策略提供依据。方法采用中文版杰弗逊医疗卫生从业人员共情量表(C-JSHPE)进行横断面调查。参与者包括来自中国东部(经济发达)、中部(中等发达)和西部(欠发达)地区的一、二、三级医院以及医学院的医生、护士、医学生和护理学生。结果合格专业人员(执业护士和医生)的共情得分显著高于保健专业学生(医生vs医学生t = 12.959, p < 0.001;护士vs护生t = 7.135, p < 0.001)。护士的共情表现显著高于医生(t = 4.081, p < 0.001),护生的共情表现也显著高于医学生(t = 5.221, p < 0.001)。实习护生与未实习护生共情得分差异有统计学意义(t = 2.548, p < 0.05)。相比之下,医学生之间没有这种差异(t = - 0.228, p > 0.05)。临床经验越丰富的医生和护士共情得分越高(F医师= 10.696,p < 0.001; F护士= 30.029,p < 0.001)。相比之下,在三级医院工作的人报告共情减少(F医生= 94.018,p < 0.001; F护士= 486.586,p < 0.001)。结论本研究强调了培养和保持合格专业人员和卫生保健学生共情能力的重要性,并强调了临床工作环境和专业发展阶段在塑造共情能力方面的重要作用。研究结果表明,共情不是静态的,而是根据不同临床角色的需求、压力和关系动态而进化的。基于模拟的教育和其他体验式学习方法代表了培养同理心的有希望的途径,特别是在整个培训过程中纵向整合并与真实的临床环境保持一致时。将这些策略嵌入到医学教育的连续体中,可能是在复杂的医疗保健系统中保持同理心作为核心专业能力的关键。
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引用次数: 0
The prevalence and risk factors of shift work disorder among nurses: A systematic review and meta-analysis 护士轮班工作障碍的患病率和危险因素:系统回顾和荟萃分析
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-10-30 DOI: 10.1016/j.ijnurstu.2025.105273
Xiaoyan Zhao , Li Zhang , Xinyue Zhang , Jing Guo , Ruijia Guan , Yuanjuan Cheng , Yong Jia

Background

Shift work disorder is common among nurses, marked by circadian rhythm disruption, excessive sleepiness, and cognitive impairment. It increases the risk of cardiovascular and metabolic diseases and contributes to clinical errors from fatigue, endangering patient safety. Its prevalence is notably higher in nurses than in other shift-working populations.

Objectives

This systematic review and meta-analysis aimed to determine the prevalence of and risk factors for shift work disorder among nurses. The ultimate aim was to provide evidence-based guidance for optimizing scheduling system and developing health intervention strategies.

Methods

Nine databases were comprehensively searched up to February 20, 2025, in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A random-effects model was used for the meta-analysis, which was performed using Stata software. The quality of the studies was evaluated using the Joanna Briggs Institute (JBI) tool, and heterogeneity was assessed using the I2 test. Publication bias was examined using funnel plots and the Egger test.

Results

A total of 24 observational studies involving 15,479 nurses were included for analysis. The pooled prevalence of shift work disorder among nurses was 45.5 % (95 % CI: 39.2–51.8 %). Subgroup analysis revealed that Africa (51.0 %) and Asia (46.5 %) had the highest prevalence rates, with a 61.7 % prevalence among nurses working in a “three-shift” model. Risk factors for shift work disorder included high stress (OR = 1.019, 95 % CI: 1.003–1.036), the number of night shifts in the past year (OR = 1.010, 95 % CI: 1.010–1.020), increasing age (OR = 1.025, 95 % CI: 1.002–1.047), the number of quick shifts (OR = 2.593, 95 % CI: 1.979–3.397), anxiety (OR = 1.073, 95 % CI: 1.039–1.108), depression (OR = 1.178, 95 % CI. 1.135–1.223) and fatigue (OR = 1.145, 95 % CI: 1.096–1.197). Heterogeneity analysis of the assessment tools revealed that scales and questionnaires (54.2 %) yielded higher prevalence rates than did the International Classification of Sleep Disorders − 3 (40.2 %) and International Classification of Sleep Disorders − 2 (32.9 %) criteria.

Conclusions

The prevalence of shift work disorder in the nurse population is high although there is substantial heterogeneity across studies. The risk of shift work disorder should be reduced by decreasing the frequency of rapid shifts and night shifts, optimizing scheduling stability, enhancing mental health support, and using standardized assessment tools. The findings provide key evidence for healthcare organizations to develop evidence-based intervention strategies.

Registration

This review was registered with PROSPERO (CRD 42023494210).
轮班工作障碍在护士中很常见,其特征是昼夜节律紊乱、过度嗜睡和认知障碍。它增加了心血管和代谢疾病的风险,并导致疲劳引起的临床错误,危及患者安全。护士的患病率明显高于其他轮班工作人群。目的本系统综述和荟萃分析旨在确定护士轮班工作障碍的患病率和危险因素。最终目的是为优化调度系统和制定健康干预策略提供循证指导。方法按照PRISMA (Preferred Reporting Items for Systematic Reviews and meta - analysis)指南,对截至2025年2月20日的9个数据库进行全面检索。meta分析采用随机效应模型,meta分析采用Stata软件。采用乔安娜布里格斯研究所(JBI)工具评估研究质量,采用I2检验评估异质性。采用漏斗图和Egger检验检验发表偏倚。结果共纳入24项观察性研究,涉及15479名护士。护士轮班工作障碍的总患病率为45.5% (95% CI: 39.2 - 51.8%)。亚组分析显示,非洲(51.0%)和亚洲(46.5%)的患病率最高,在“三班制”模式下工作的护士中,患病率为61.7%。倒班工作障碍的危险因素包括高压力(OR = 1.019, 95% CI: 1.003 ~ 1.036)、过去一年夜班次数(OR = 1.010, 95% CI: 1.010 ~ 1.020)、年龄增长(OR = 1.025, 95% CI: 1.002 ~ 1.047)、快班次数(OR = 2.593, 95% CI: 1.979 ~ 3.397)、焦虑(OR = 1.073, 95% CI: 1.039 ~ 1.108)、抑郁(OR = 1.178, 95% CI: 1.178)。1.135-1.223)和疲劳(OR = 1.145, 95% CI: 1.096-1.197)。评估工具的异质性分析显示,量表和问卷(54.2%)的患病率高于国际睡眠障碍分类- 3(40.2%)和国际睡眠障碍分类- 2(32.9%)标准。结论轮班工作障碍在护士人群中的患病率很高,尽管各研究之间存在很大的异质性。应通过减少快速轮班和夜班的频率、优化调度稳定性、加强心理健康支持和使用标准化评估工具来降低轮班工作障碍的风险。研究结果为医疗机构制定循证干预策略提供了关键证据。注册本综述已在PROSPERO注册(CRD 42023494210)。
{"title":"The prevalence and risk factors of shift work disorder among nurses: A systematic review and meta-analysis","authors":"Xiaoyan Zhao ,&nbsp;Li Zhang ,&nbsp;Xinyue Zhang ,&nbsp;Jing Guo ,&nbsp;Ruijia Guan ,&nbsp;Yuanjuan Cheng ,&nbsp;Yong Jia","doi":"10.1016/j.ijnurstu.2025.105273","DOIUrl":"10.1016/j.ijnurstu.2025.105273","url":null,"abstract":"<div><h3>Background</h3><div>Shift work disorder is common among nurses, marked by circadian rhythm disruption, excessive sleepiness, and cognitive impairment. It increases the risk of cardiovascular and metabolic diseases and contributes to clinical errors from fatigue, endangering patient safety. Its prevalence is notably higher in nurses than in other shift-working populations.</div></div><div><h3>Objectives</h3><div>This systematic review and meta-analysis aimed to determine the prevalence of and risk factors for shift work disorder among nurses. The ultimate aim was to provide evidence-based guidance for optimizing scheduling system and developing health intervention strategies.</div></div><div><h3>Methods</h3><div>Nine databases were comprehensively searched up to February 20, 2025, in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A random-effects model was used for the meta-analysis, which was performed using Stata software. The quality of the studies was evaluated using the Joanna Briggs Institute (JBI) tool, and heterogeneity was assessed using the I<sup>2</sup> test. Publication bias was examined using funnel plots and the Egger test.</div></div><div><h3>Results</h3><div>A total of 24 observational studies involving 15,479 nurses were included for analysis. The pooled prevalence of shift work disorder among nurses was 45.5 % (95 % CI: 39.2–51.8 %). Subgroup analysis revealed that Africa (51.0 %) and Asia (46.5 %) had the highest prevalence rates, with a 61.7 % prevalence among nurses working in a “three-shift” model. Risk factors for shift work disorder included high stress (OR = 1.019, 95 % CI: 1.003–1.036), the number of night shifts in the past year (OR = 1.010, 95 % CI: 1.010–1.020), increasing age (OR = 1.025, 95 % CI: 1.002–1.047), the number of quick shifts (OR = 2.593, 95 % CI: 1.979–3.397), anxiety (OR = 1.073, 95 % CI: 1.039–1.108), depression (OR = 1.178, 95 % CI. 1.135–1.223) and fatigue (OR = 1.145, 95 % CI: 1.096–1.197). Heterogeneity analysis of the assessment tools revealed that scales and questionnaires (54.2 %) yielded higher prevalence rates than did the International Classification of Sleep Disorders −<!--> <!-->3 (40.2 %) and International Classification of Sleep Disorders −<!--> <!-->2 (32.9 %) criteria.</div></div><div><h3>Conclusions</h3><div>The prevalence of shift work disorder in the nurse population is high although there is substantial heterogeneity across studies. The risk of shift work disorder should be reduced by decreasing the frequency of rapid shifts and night shifts, optimizing scheduling stability, enhancing mental health support, and using standardized assessment tools. The findings provide key evidence for healthcare organizations to develop evidence-based intervention strategies.</div></div><div><h3>Registration</h3><div>This review was registered with PROSPERO (CRD 42023494210).</div></div>","PeriodicalId":50299,"journal":{"name":"International Journal of Nursing Studies","volume":"174 ","pages":"Article 105273"},"PeriodicalIF":7.1,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145397131","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
A framework and practical approach to identify and address ethical issues arising in interventional health systems research 确定和解决介入性卫生系统研究中出现的伦理问题的框架和实用方法
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-10-30 DOI: 10.1016/j.ijnurstu.2025.105263
Edna Mutua , Dorothy Oluoch , Sebastian Fuller , Gloria Ngaiza , Nancy Odinga , Caroline Waithira , Vincent Kagonya , Onesmus Onyango , Naima Nasir , Gulraj Grewal , Abdulazeez Imam , Asma Rababeh , Michuki Maina , Kenneth Karumba , Maureen Kelley , Mike English , Sassy Molyneux

Background

Embedded, interventional health systems research is increasingly promoted to better understand and strengthen the performance of health systems. However, for these forms of research, boundaries between clinical care, quality improvement, and public health can be blurred, and ethical implications and frameworks to draw upon are unclear. While there is evolving ethical guidance, few health systems studies have documented ethical dilemmas experienced post ethics approval, and the value of support processes introduced to manage arising dilemmas. In this discussion paper, we share our approach to handling the ethical dilemmas that arose while conducting embedded interventional health systems research in public-sector newborn units in Kenya.

Methods

Building on our past research, and literature on debriefs, reflective learning, ethics reflection groups and moral case deliberations, we evolved an approach to holding regular structured ethics debriefs to discuss and agree upon how to handle ethical issues experienced during ‘fieldwork’. The research team maintained a ‘living log’ of all discussions, detailing all emerging ethical issues and any agreed actions. To prepare this paper, we conducted a thematic analysis of the living log and associated meeting minutes/recordings, and held a series of wider team meetings to reflect upon our learning.

Findings and discussion

Numerous dilemmas were shared by research staff in our debrief fora. We grouped ethical issues encountered into 1) ‘bystander’ issues (defined here as background issues impacting health system functioning, facility staff, patients or families that were not caused or exacerbated by our research activities), 2) issues for those groups that were ‘research imposed’ and 3) issues related to the ‘comfort and well-being of research team members’. Most dilemmas raised related to feeling like bystanders in highly constrained health systems, complicated by our positionalities as ‘outsiders-within’, whereby as health researchers spending time in facilities we were neither fully ‘outsiders’ nor ‘insiders’ to the health system. There was constant moral labour involved in considering our responsibilities for action, which ranged from immediate action from a safety perspective, through rethinking how the research was conducted, to various forms of engagement and feedback across a web of stakeholders.

Conclusion

The approach we developed offers a framework to assist research team members with the significant ethical dilemmas and challenges that arise over the course of conducting studies. We suggest activities to support working prospectively through emerging ethical dilemmas in future studies.
为了更好地了解和加强卫生系统的绩效,嵌入式、干预性卫生系统研究日益得到促进。然而,对于这些形式的研究,临床护理、质量改进和公共卫生之间的界限可能是模糊的,伦理影响和可借鉴的框架是不明确的。虽然有不断发展的伦理指导,但很少有卫生系统研究记录了伦理批准后经历的伦理困境,以及为管理出现的困境而引入的支持程序的价值。在这篇讨论文件中,我们分享了我们处理在肯尼亚公共部门新生儿单位进行嵌入式介入卫生系统研究时出现的伦理困境的方法。方法基于我们过去的研究,以及关于汇报、反思性学习、伦理反思小组和道德案例审议的文献,我们发展了一种定期举行结构化伦理汇报的方法,以讨论和商定如何处理“实地工作”中遇到的伦理问题。研究小组保留了所有讨论的“生活日志”,详细说明了所有新出现的道德问题和任何商定的行动。为了准备这篇论文,我们对生活日志和相关的会议记录/录音进行了专题分析,并举行了一系列更广泛的团队会议来反思我们的学习。调查结果和讨论在我们的汇报论坛上,研究人员分享了许多困境。我们将遇到的伦理问题分为:1)“旁观者”问题(这里定义为影响卫生系统功能、设施工作人员、患者或家庭的背景问题,这些问题不是由我们的研究活动引起或加剧的),2)“研究强加”群体的问题,以及3)与“研究团队成员的舒适和福祉”相关的问题。提出的大多数困境都与在高度受限的卫生系统中感觉自己是旁观者有关,而我们作为“局外人-内部”的地位使情况更加复杂,因此,作为卫生研究人员,我们既不是卫生系统的完全“局外人”,也不是卫生系统的“内部人士”。考虑到我们的行动责任,包括从安全角度立即采取行动,通过重新思考如何进行研究,以及通过利益相关者网络进行各种形式的参与和反馈,这涉及到不断的道德劳动。我们开发的方法提供了一个框架,以帮助研究团队成员处理在进行研究过程中出现的重大伦理困境和挑战。我们建议通过未来研究中出现的伦理困境来支持前瞻性工作的活动。
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引用次数: 0
Erratum to “Priorities for ‘out-of-hours’ home-based palliative care for professionals, patients, and family caregivers: A qualitative interview study” [Int. J. Nurs. Stud. 171 (2025) 105193] 对专业人员、患者和家庭护理人员“非工作时间”居家姑息治疗的优先事项:一项定性访谈研究”的勘误[j]。j .孕育。Stud. 171(2025) 105193]。
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-10-25 DOI: 10.1016/j.ijnurstu.2025.105254
Joanna Goodrich , Alice M. Firth , Inez Gaczkowska , Richard Harding , Fliss E.M. Murtagh , Catherine J. Evans
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引用次数: 0
Assistive technology products for toilet-use and continence containment problems in the home setting: A mapping review 家庭环境中厕所使用和控制问题的辅助技术产品:绘图审查
IF 7.1 1区 医学 Q1 NURSING Pub Date : 2025-10-24 DOI: 10.1016/j.ijnurstu.2025.105264
Marjolein Woodhouse , Miriam Avery , Lois Woods , David Alexander Scott , Mandy Fader , Margaret Macaulay , Karen Ashton , Catherine Murphy

Purpose

This study aimed to identify common toilet-use and continence containment problems among community-dwelling adults, explore the range of assistive products available for these issues, and map the products identified to the problems they address.

Design

A mapping review methodology was employed, modified to include grey literature, to identify the full range of toilet-use and continence containment assistive products that are designed for use in the home setting.

Methods

An initial inventory of toilet-use and continence containment problems was derived from toilet-use task sequence analysis and commonly occurring containment challenges. This was supplemented by scoping searches of grey literature and refined with feedback from partner representatives. Assistive products were identified through structured online searches and review of seminal texts. A nurse researcher with community health experience then mapped the categories of assistive products to the identified problems.

Results

Thirty-three toilet-use and containment problems were identified, stratified into 295 subproblems based on end-user characteristics, including physical and cognitive function, and urinary or faecal voiding needs. The search revealed 163 categories of assistive products and mapping these to the subproblems resulted in more than 1500 product-to-problem links. No suitable assistive product options were identified for six sub-problems.

Conclusion

Given the diversity of toilet-use and containment challenges faced by community-dwelling individuals and the array of available assistive products, this novel study highlights the complexity of matching products to individual needs. These findings emphasise the need for better resources to support individuals, caregivers and healthcare professionals in optimising decision-making on and selection of toilet-use and continence containment products.
目的:本研究旨在确定社区居民中常见的厕所使用和失禁问题,探索可用于这些问题的辅助产品的范围,并将已确定的产品与其所解决的问题进行映射。采用了DesignA绘图审查方法,并对其进行了修改,以纳入灰色文献,以确定设计用于家庭环境的厕所使用和失禁控制辅助产品的全系列。方法通过厕所使用任务序列分析和常见的控制挑战,对厕所使用和失禁控制问题进行初步调查。通过灰色文献的范围搜索和来自合作伙伴代表的反馈进行了补充。辅助产品是通过结构化的在线搜索和开创性文本的审查确定的。一名具有社区卫生经验的护士研究员随后将辅助产品的类别映射到已确定的问题。结果确定了33个厕所使用和控制问题,并根据最终用户特征(包括身体和认知功能以及排尿或排便需求)将其分为295个子问题。搜索显示了163个辅助产品类别,并将这些类别映射到子问题中,产生了超过1500个产品到问题的链接。六个子问题没有确定合适的辅助产品选择。鉴于社区居民的厕所使用和控制挑战的多样性以及可用辅助产品的多样性,这项新研究强调了将产品与个人需求相匹配的复杂性。这些发现强调需要更好的资源,以支持个人、护理人员和卫生保健专业人员优化厕所使用和失禁控制产品的决策和选择。
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引用次数: 0
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International Journal of Nursing Studies
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