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Parents' Experiences of Accessing Mental Health Services for Their Adolescents With Mental Health Challenges: A Scoping Review 父母为有心理健康问题的青少年提供心理健康服务的经历:范围研究》。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-15 DOI: 10.1111/jocn.17469
Seána Nic Dhonnacha, Lisa Kerr, Yvonne McCague, Des Cawley

Aim

To analyse the literature on parents' experiences of accessing mental health services with their adolescents for mental health challenges in Ireland.

Background

Health systems globally have inadequately addressed mental health service needs resulting in notable gaps between population needs and access to adolescent mental health services.

Methods

This scoping review followed Arksey and O'Malley's six-stage framework and PRISMA-ScR reporting guidelines. Five electronic databases SocINDEX, MEDLINE, CINHAL, Scopus and EBSCO were searched and reference lists screened 2015–2024.

Results

Twenty-three studies were included. Applying Braun and Clarke's thematic analysis identified three themes: adolescent community mental health services for adolescents with mental health challenges, accessing mental healthcare services via emergeny departments for adolescents with mental health challenges and parents' experiences of accessing mental health services for their adolescents with mental health challenges.

Conclusion

Parents' experiences of accessing mental health services for their adolescents are not fully understood, and further research is required to map key concepts to inform practice and policymaking.

Relevance to Clinical Practice

The findings from this scoping review highlight challenges for adolescent mental health services in Ireland and internationally. Heightening awareness of these issues is necessary to improve the clinical practice of nurses.

No Patient or Public Contribution

This was a scoping review study.

目的:分析有关爱尔兰父母与青少年一起接受心理健康服务以应对心理健康挑战的经验的文献:背景:全球卫生系统都没有充分满足心理健康服务的需求,导致人口需求与青少年心理健康服务之间存在明显差距:本范围界定综述遵循 Arksey 和 O'Malley 的六阶段框架和 PRISMA-ScR 报告指南。检索了 SocINDEX、MEDLINE、CINHAL、Scopus 和 EBSCO 五个电子数据库,并筛选了 2015-2024 年的参考文献列表:结果:共纳入 23 项研究。应用布劳恩和克拉克的主题分析法确定了三个主题:为有心理健康问题的青少年提供青少年社区心理健康服务、有心理健康问题的青少年通过急诊科获得心理保健服务以及家长为有心理健康问题的青少年获得心理健康服务的经历:结论:家长为青少年提供心理健康服务的经验尚未得到充分了解,需要进一步研究,以确定关键概念,为实践和政策制定提供依据:此次范围界定审查的结果凸显了爱尔兰及国际青少年心理健康服务所面临的挑战。提高对这些问题的认识对于改善护士的临床实践非常必要:这是一项范围界定研究。
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引用次数: 0
Family Resilience and Its Influencing Factors in Patients With Cancer and Their Family Members: A Systematic Review. 癌症患者及其家庭成员的家庭复原力及其影响因素:系统综述。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-15 DOI: 10.1111/jocn.17485
Xiaoke Qiu, Jiayu Mao, Can Wang, Xueli Yang, Qiuping Li

Aims: This review aims to explore factors influencing family resilience in families providing care for patients with cancer and to provide suggestions for future research directions.

Methods: Six electronic databases were searched including Web of Science, CINAHL, EMBASE, PsycINFO, PubMed and CNKI from their inception to December 2023. The article reference lists were also manually searched. The Mixed Method Appraisal Tool was used to assess the included studies in this review. The 27-item checklist Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement was followed to report this review.

Results: Twenty-one studies from six online databases reported that either individual or family factors have effects on family resilience and were described into five clusters on the basis of the Walsh model of family resilience, including demographic and clinical factors, personal strengths and resources, family stressors, family resilient coping processes and family resilient adaptation outcomes.

Conclusion: Family resilience in cancer families plays a pivotal role in coping with family stressors and facilitating positive outcomes through domains of coping. Future researches need to explore factors related to family resilience from dyadic perspectives and to establish multidisciplinary intervention strategies for developing levels of family resilience in cancer families.

Trial registration: PROSPERO: CRD42024535349.

目的:本综述旨在探讨影响癌症患者护理家庭复原力的因素,并为未来的研究方向提供建议:检索了六个电子数据库,包括 Web of Science、CINAHL、EMBASE、PsycINFO、PubMed 和 CNKI,检索时间从开始到 2023 年 12 月。文章的参考文献列表也进行了人工检索。本综述采用混合方法评估工具对纳入的研究进行评估。在报告本综述时,遵循了 27 项清单中的 "系统综述和元分析首选报告项目"(PRISMA)声明:来自六个在线数据库的 21 项研究报告了个人或家庭因素对家庭复原力的影响,并根据家庭复原力的沃尔什模型将其分为五组,包括人口和临床因素、个人力量和资源、家庭压力因素、家庭复原力应对过程和家庭复原力适应结果:癌症家庭的家庭复原力在应对家庭压力和通过应对领域促进积极结果方面发挥着关键作用。未来的研究需要从双亲的角度探索与家庭复原力相关的因素,并制定多学科干预策略,以提高癌症家庭的家庭复原力水平:试验注册:PROCROPERO:CRD42024535349。
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引用次数: 0
Experiences of Intensive Care Unit Patients as They Transition to the Ward: A Thematic Synthesis 重症监护室病人转入病房的经历:专题综述。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-15 DOI: 10.1111/jocn.17487
Li Yumei, Deping Zhang, Yu Xu

Background

During the transfer of intensive care unit (ICU) patients to general wards, patients often experience transfer anxiety due to changes in the healthcare environment, staff and unfamiliarity with the new ward. However, the experiences of ICU patients during this transition period have received less attention.

Aims

A systematic review and synthesis of the experiences of patients transitioning from the ICU to the ward.

Design

Thematic synthesis of qualitative studies.

Data Sources

We searched the PubMed, Embase, CINAHL and Web of Science databases for qualitative research on the transition-to-ward experience of patients in ICUs for the year 2023 February.

Review Methods

The quality of the literature was evaluated according to the qualitative research quality assessment criteria of the Joanna Briggs Institute, as outlined by the Australian Centre for Evidence-Based Healthcare. The data were then extracted from the studies, analysed and synthesised using a thematic synthesis approach.

Results

A total of 12 papers were included and the 32 findings were distilled and consolidated into three themes: emotional reactions; imperfections in the transition process; differences between wards and ICUs; and eight sub-themes: optimism; pessimism; emotionlessness; inadequate information; inadequate communication; physical condition; differences in care; differences in environment.

Conclusions

The transfer from an ICU to a general ward is a major change of environment for the patient and can trigger upset and anxiety. Planning for turn-out, meeting patients' information needs and easing patients' emotions are critical in this process.

背景:在重症监护病房(ICU)患者转入普通病房的过程中,由于医疗环境、工作人员的变化以及对新病房的不熟悉,患者往往会产生转院焦虑。目的:对重症监护室病人转入病房的经历进行系统回顾和综合:设计:对定性研究进行专题综合:数据来源:我们在PubMed、Embase、CINAHL和Web of Science数据库中搜索了2023年2月有关重症监护室患者过渡到病房经历的定性研究:根据澳大利亚循证医疗中心(Australian Centre for Evidence-Based Healthcare)制定的乔安娜-布里格斯研究所(Joanna Briggs Institute)定性研究质量评估标准对文献质量进行评估。然后从研究中提取数据,采用专题综合法对数据进行分析和综合:共收录了 12 篇论文,并将 32 项研究结果提炼和整合为三个主题:情绪反应;过渡过程中的不完善之处;病房与重症监护室之间的差异;以及八个次主题:乐观;悲观;无情感;信息不足;沟通不足;身体状况;护理差异;环境差异:从重症监护室转到普通病房对病人来说是环境的重大改变,可能会引发不安和焦虑。在这一过程中,制定转出计划、满足病人的信息需求和缓解病人的情绪至关重要。
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引用次数: 0
Analysis of Longitudinal Trajectory and Influencing Factors of Supportive Care Needs in Colorectal Cancer Patients With Enterostomy. 肠造口术结直肠癌患者支持性护理需求的纵向轨迹和影响因素分析
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17426
Lu Zhou, Hui Li, Zhengyang Zhang, Ling Wang

Aims: The aim of this study was to understand the dynamic changes in the needs of patients with enterostomy during the 3 months after discharge and its possible influencing factors.

Design: A prospective observational design.

Methods: This study investigated the supportive care needs of patients who underwent colorectal cancer surgery with colostomy in three Chinese hospitals from May 2023 to October 2023 during the 3 months following discharge from the hospital. The growth mix model was used to describe the needs trajectory and analyse the heterogeneity of the trajectory. Univariate analysis was used to find the factors that might affect the heterogeneity of needs trajectory of patients with enterostomy, and then logistic regression analysis was used to determine the influencing factors of the heterogeneity of needs trajectory of patients with enterostomy. The reporting of this study adhered to the STROBE checklist.

Results: A total of 232 patients with enterostomy completed follow-up. There was heterogeneity in the developmental trajectories of supportive care needs of enterostomy patients and the trajectories of the five dimensions of supportive care needs. The heterogeneity factors affecting the trajectory of supportive care needs included the enterostomy patient's psychosocial adjustment score, type of enterostomy, and educational background and the heterogeneity factors affecting the five dimensions trajectory of supportive care needs include psychosocial adjustment score, tumour staging, type of enterostomy, smoking, chemotherapy and enterostomy self-care knowledge score.

Conclusions: The needs of patients with enterostomy within 3 months after discharge were dynamic. Identifying and meeting the unmet needs of patients with enterostomy was crucial to improving the health-related quality of life of patients with enterostomy.

Patient or public contribution: None.

Relevance to clinical practice: The needs of patients with enterostomy were dynamic, with the needs of most patients with enterostomy decreasing within 3 months of discharge, but some patients with enterostomy continued to have high needs at 3 months after discharge, and clinical nurses were expected to pay special attention to these patients.

目的:本研究旨在了解肠造口患者出院后 3 个月内需求的动态变化及其可能的影响因素:设计:前瞻性观察设计:本研究调查了2023年5月至2023年10月在中国三家医院接受结直肠癌手术并行结肠造口术的患者在出院后3个月内的支持性护理需求。采用增长混合模型来描述需求轨迹,并分析轨迹的异质性。采用单变量分析找出可能影响肠造口术患者需求轨迹异质性的因素,然后采用逻辑回归分析确定肠造口术患者需求轨迹异质性的影响因素。本研究的报告遵循 STROBE 检查表:共有 232 名肠造口术患者完成了随访。肠造口患者支持性护理需求的发展轨迹和支持性护理需求五个维度的轨迹存在异质性。影响支持性护理需求轨迹的异质性因素包括肠造口患者的社会心理适应评分、肠造口类型和教育背景,影响支持性护理需求五个维度轨迹的异质性因素包括社会心理适应评分、肿瘤分期、肠造口类型、吸烟、化疗和肠造口自我护理知识评分:肠造口术患者出院后 3 个月内的需求是动态的。确定并满足肠造口术患者未得到满足的需求对于改善肠造口术患者与健康相关的生活质量至关重要:与临床实践的相关性肠造口术患者的需求是动态的,大多数肠造口术患者的需求在出院后 3 个月内有所下降,但部分肠造口术患者在出院后 3 个月仍有较高需求,临床护士应特别关注这些患者。
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引用次数: 0
Assessing the Risk of Delirium and Death in Sepsis Using the Braden Score: A Retrospective Study. 使用布莱登评分评估败血症患者谵妄和死亡风险:一项回顾性研究
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17476
Xinya Li, Yonglan Tang, Zihong Bai, Xin Liang, Xiaxuan Huang, Jianguang Chen, Hongtao Cheng, Jun Lyu, Yu Wang

Aims and objectives: To provide a viable tool for the early clinical identification of high-risk populations in patients with sepsis.

Background: Sepsis-associated delirium (SAD) has the potential to significantly impact the short- and long-term prognosis of patients. However, accurately predicting and effectively managing SAD remains a significant challenge.

Methods: This study employed a retrospective analysis of adult sepsis patients admitted to the intensive care unit (ICU) for the first time. Patients were divided into two groups based on their initial Braden score upon admission to the ICU: a high-risk group (≤ 15 points) and a low-risk group (> 15 points). The relationship between Braden score and delirium was assessed using logistic regression and restricted cubic splines, while restricted mean survival time was employed to analyse the relationship between Braden scores and patients' 90- and 180-day mortality.

Results: Of the 28,312 patients included in the study, those in the high-risk group exhibited a significantly elevated risk of delirium (44.8% vs. 29.7%) and higher 90-day (28.7% vs. 19.4%) and 180-day (33.2% vs. 24.1%) mortality rates (all p < 0.001). After adjusting for confounding variables, logistic regression demonstrated that the risk of delirium was 1.54 times higher in the high-risk group (95% CI = 1.45-1.64, p < 0.001). Following propensity score matching, the difference in survival was statistically significant at both time points, with the high-risk group having a reduced survival rate of 7.50 days (95% CI = -8.24, -6.75; p < 0.001) and 15.74 days (95% CI = -17.40, -14.08; p < 0.001) at 90 days and 180 days, respectively.

Conclusions: The Braden score is a simple and effective tool for the early identification of patients at increased risk of adverse outcomes in sepsis.

Design: Retrospective study.

Relevance to clinical practice: The Braden score can be employed by clinical nurses for the purpose of early identification of poor prognostic risk in patients with sepsis.

Reporting method: This study was conducted according to the Strengthening Research in Observational Studies in Epidemiology (STROBE) guidelines.

Patient or public contribution: Patients were involved in the sample of the study.

目的和目标背景:脓毒症相关谵妄(SAD)可能对患者的短期和长期预后产生重大影响:背景:脓毒症相关谵妄(SAD)可能对患者的短期和长期预后产生重大影响。然而,准确预测和有效管理 SAD 仍是一项重大挑战:本研究对首次入住重症监护室(ICU)的成人败血症患者进行了回顾性分析。根据患者进入重症监护室时的初始布莱登评分将其分为两组:高风险组(≤15分)和低风险组(>15分)。布莱登评分与谵妄之间的关系采用逻辑回归和限制性三次样条进行评估,而限制性平均生存时间则用于分析布莱登评分与患者90天和180天死亡率之间的关系:结果:在纳入研究的 28,312 名患者中,高危组患谵妄的风险显著升高(44.8% 对 29.7%),90 天(28.7% 对 19.4%)和 180 天(33.2% 对 24.1%)死亡率也较高(均为 p 结论:布莱登评分是一种简便易行的谵妄评分方法:布莱登评分是一种简单有效的工具,可用于早期识别脓毒症不良后果风险增加的患者:设计:回顾性研究:布莱登评分可用于临床护士早期识别脓毒症患者的不良预后风险:本研究根据加强流行病学观察性研究(STROBE)指南进行:患者参与了研究样本的采集。
{"title":"Assessing the Risk of Delirium and Death in Sepsis Using the Braden Score: A Retrospective Study.","authors":"Xinya Li, Yonglan Tang, Zihong Bai, Xin Liang, Xiaxuan Huang, Jianguang Chen, Hongtao Cheng, Jun Lyu, Yu Wang","doi":"10.1111/jocn.17476","DOIUrl":"https://doi.org/10.1111/jocn.17476","url":null,"abstract":"<p><strong>Aims and objectives: </strong>To provide a viable tool for the early clinical identification of high-risk populations in patients with sepsis.</p><p><strong>Background: </strong>Sepsis-associated delirium (SAD) has the potential to significantly impact the short- and long-term prognosis of patients. However, accurately predicting and effectively managing SAD remains a significant challenge.</p><p><strong>Methods: </strong>This study employed a retrospective analysis of adult sepsis patients admitted to the intensive care unit (ICU) for the first time. Patients were divided into two groups based on their initial Braden score upon admission to the ICU: a high-risk group (≤ 15 points) and a low-risk group (> 15 points). The relationship between Braden score and delirium was assessed using logistic regression and restricted cubic splines, while restricted mean survival time was employed to analyse the relationship between Braden scores and patients' 90- and 180-day mortality.</p><p><strong>Results: </strong>Of the 28,312 patients included in the study, those in the high-risk group exhibited a significantly elevated risk of delirium (44.8% vs. 29.7%) and higher 90-day (28.7% vs. 19.4%) and 180-day (33.2% vs. 24.1%) mortality rates (all p < 0.001). After adjusting for confounding variables, logistic regression demonstrated that the risk of delirium was 1.54 times higher in the high-risk group (95% CI = 1.45-1.64, p < 0.001). Following propensity score matching, the difference in survival was statistically significant at both time points, with the high-risk group having a reduced survival rate of 7.50 days (95% CI = -8.24, -6.75; p < 0.001) and 15.74 days (95% CI = -17.40, -14.08; p < 0.001) at 90 days and 180 days, respectively.</p><p><strong>Conclusions: </strong>The Braden score is a simple and effective tool for the early identification of patients at increased risk of adverse outcomes in sepsis.</p><p><strong>Design: </strong>Retrospective study.</p><p><strong>Relevance to clinical practice: </strong>The Braden score can be employed by clinical nurses for the purpose of early identification of poor prognostic risk in patients with sepsis.</p><p><strong>Reporting method: </strong>This study was conducted according to the Strengthening Research in Observational Studies in Epidemiology (STROBE) guidelines.</p><p><strong>Patient or public contribution: </strong>Patients were involved in the sample of the study.</p>","PeriodicalId":50236,"journal":{"name":"Journal of Clinical Nursing","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142407149","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Effectiveness of Integrated Care for Older Pepole (ICOPE) in Improving Intrinsic Capacity in Older Adults: A Systematic Review and Meta-Analysis. 老年人综合护理(ICOPE)在提高老年人内在能力方面的效果:系统回顾与元分析》。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17432
Wei Liu, Rixin Qin, Xueyan Zhang, Guichen Li, Yiming Qiu, Guangwei Zhang, Li Chen

Objective: Conduct a systematic review of existing studies on intrinsic capacity (IC) and a meta-analysis of studies to assess the overall effectiveness of ICOPE in improving IC in older adults.

Methods: Ten databases were systematically searched from inception to November 8, 2023, and the search was last updated on January 2, 2024. Randomised controlled trials (RCTs) were included. The main outcomes were IC (cognition, psychological, sensory, vitality and locomotion).

Results: The results showed ICOPE had a significant effect in improving cognitive function (SMD = 0.36; 95% CI, 0.17 to 0.56, p < 0.001, 12 RCTs, 7926 participants) and depressive symptoms (SMD = -0.70; 95% CI, -0.96 to -0.43, p < 0.001, 26 RCTs, 11,034 participants), but there was no statistically significant difference in improving locomotion (SMD = 0.16; 95% CI, -0.03 to 0.34, p = 0.098, 3 RCTs, 1580 participants). Meta-regression analysis shows that intervention duration should be paid attention to when the source of heterogeneity is discussed on the cognition.

Conclusion: The results suggest that ICOPE may be a potentially effective approach to help improve the IC in older adults, showing significant potential for improving cognitive function and reducing depressive symptoms in particular.

Implications for the profession and/or patient care: ICOPE is expected to provide effective strategies to enhance issues such as IC and may be an innovative way to improve the overall health of older adults. This result provides strong support for geriatric nursing practice and encourages the adoption of ICOPE as a viable nursing approach to promote healthy ageing.

目标: 对现有的有关内在能力(IC)的研究进行系统回顾,并对研究进行荟萃分析:对有关内在能力(IC)的现有研究进行系统回顾,并对研究进行荟萃分析,以评估 ICOPE 在改善老年人内在能力方面的总体效果:方法:从开始到 2023 年 11 月 8 日,对 10 个数据库进行了系统检索,最后一次更新是在 2024 年 1 月 2 日。研究纳入了随机对照试验(RCT)。主要结果为IC(认知、心理、感觉、活力和运动):结果表明,ICOPE 对改善认知功能有显著效果(SMD = 0.36;95% CI,0.17 至 0.56,P 结论:ICOPE 对改善认知功能有显著效果(SMD = 0.36;95% CI,0.17 至 0.56,P 结论):结果表明,ICOPE 可能是帮助改善老年人 IC 的一种潜在有效方法,在改善认知功能,特别是减少抑郁症状方面具有显著潜力:预计 ICOPE 将提供有效的策略来改善 IC 等问题,并可能成为改善老年人整体健康的创新方法。这一结果为老年护理实践提供了强有力的支持,并鼓励采用 ICOPE 作为促进健康老龄化的可行护理方法。
{"title":"Effectiveness of Integrated Care for Older Pepole (ICOPE) in Improving Intrinsic Capacity in Older Adults: A Systematic Review and Meta-Analysis.","authors":"Wei Liu, Rixin Qin, Xueyan Zhang, Guichen Li, Yiming Qiu, Guangwei Zhang, Li Chen","doi":"10.1111/jocn.17432","DOIUrl":"https://doi.org/10.1111/jocn.17432","url":null,"abstract":"<p><strong>Objective: </strong>Conduct a systematic review of existing studies on intrinsic capacity (IC) and a meta-analysis of studies to assess the overall effectiveness of ICOPE in improving IC in older adults.</p><p><strong>Methods: </strong>Ten databases were systematically searched from inception to November 8, 2023, and the search was last updated on January 2, 2024. Randomised controlled trials (RCTs) were included. The main outcomes were IC (cognition, psychological, sensory, vitality and locomotion).</p><p><strong>Results: </strong>The results showed ICOPE had a significant effect in improving cognitive function (SMD = 0.36; 95% CI, 0.17 to 0.56, p < 0.001, 12 RCTs, 7926 participants) and depressive symptoms (SMD = -0.70; 95% CI, -0.96 to -0.43, p < 0.001, 26 RCTs, 11,034 participants), but there was no statistically significant difference in improving locomotion (SMD = 0.16; 95% CI, -0.03 to 0.34, p = 0.098, 3 RCTs, 1580 participants). Meta-regression analysis shows that intervention duration should be paid attention to when the source of heterogeneity is discussed on the cognition.</p><p><strong>Conclusion: </strong>The results suggest that ICOPE may be a potentially effective approach to help improve the IC in older adults, showing significant potential for improving cognitive function and reducing depressive symptoms in particular.</p><p><strong>Implications for the profession and/or patient care: </strong>ICOPE is expected to provide effective strategies to enhance issues such as IC and may be an innovative way to improve the overall health of older adults. This result provides strong support for geriatric nursing practice and encourages the adoption of ICOPE as a viable nursing approach to promote healthy ageing.</p>","PeriodicalId":50236,"journal":{"name":"Journal of Clinical Nursing","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142407150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Power to the People: Contributions to the Involvement in Decision-Making About Nursing Care in Hospital Settings 人民的力量:对参与医院护理决策的贡献》(Power to the People: Contributions to the Involvement in Decision-Making about Nursing Care in Hospital Settings)。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17492
Diana Gabriela Simões Marques Dos Santos, António Fernando Salgueiro Amaral, Eduardo José Ferreira Dos Santos
<p>Involving the person throughout the nursing process, since the initial assessment to the diagnostic nursing activity, the care planning, the implementation of interventions and the final assessment, will allow them to become partners in the care, to explore their experiences in the transition process, and to respond to their needs, considering their preferences, values and culture. These statements are emphasised by the World Health Organization (<span>2015</span>), with the publication of the “WHO global strategy on integrated people-centred health services 2016–2026”, which advocates a future in which people have access to health care that meets their needs and preferences, in a secure, effective, timely, efficient and high-quality manner. In this sense, the World Health Organization (<span>2015</span>) establishes the involvement of people as strategic, with a view to improve health outcomes through the co-production of care, where shared decision-making and personalised care plans are described as potential policy options and interventions to support this strategy.</p><p>In order to discuss this issue, it is important to clarify: what is decision-making in nursing? Decision-making in nursing care is guided by the nursing process. This process is considered a systematised approach, based on critical thinking, the principle of person-centered care and evidence-based practice, being guided by five stages: initial assessment, diagnostic activity, care planning, implementation, and final assessment. Initial assessment involves the collection of subjective and objective data, through interviews and the collection of measurable data. Subsequently, the formulation of nursing diagnoses (clinical judgement about human responses to real or potential health problems of individuals, families, or communities) allows for the planning and implementation of nursing care. Care planning allows for the implementation of personalised, timely, and outcomes-oriented care. At this stage, objectives and outcomes to be achieved are formulated, based on the previously formulated nursing diagnoses. Implementation is the stage that involves delivering the nursing interventions outlined in the care plan. The final evaluation is crucial, highlighting the outcomes that are sensitive to nursing care. This evaluation requires adapting the care plan, which is a dynamic and continuous process (Toney-Butler and Thayer <span>2023</span>).</p><p>As a theoretical basis to understand the importance of people's involvement in decision-making about nursing care, several perspectives, theories and models can be adopted, of which the Transitions Theory can be highlighted for its comprehensiveness and commonalities with the Nursing Process. Changes in people's health can be the cause of transition processes, known as health-illness transitions. The theory also proposes developmental, situational, and organisational transitions. The nature of transitions is also characterised by patter
让患者参与整个护理过程,从初步评估到诊断性护理活动、护理计划、干预措施的实施和最终评估,将使他们成为护理工作的合作伙伴,探索他们在过渡过程中的经历,并考虑他们的偏好、价值观和文化,满足他们的需求。世界卫生组织(2015 年)在发布《2016-2026 年世界卫生组织以人为本的综合医疗服务全球战略》时强调了这些声明,该战略倡导人们在未来能够以安全、有效、及时、高效和高质量的方式获得满足其需求和偏好的医疗服务。从这个意义上讲,世界卫生组织(2015 年)将人的参与确立为战略,以期通过共同创造护理来改善健康结果,其中共同决策和个性化护理计划被描述为支持这一战略的潜在政策选择和干预措施。为了讨论这个问题,有必要澄清:什么是护理中的决策?护理决策以护理流程为指导。这一过程被认为是一种系统化的方法,以批判性思维、以人为本的护理原则和循证实践为基础,由五个阶段指导:初步评估、诊断活动、护理计划、实施和最终评估。初步评估包括通过访谈和收集可测量的数据来收集主观和客观数据。随后,制定护理诊断(对人类对个人、家庭或社区现实或潜在健康问题的反应的临床判断),以便规划和实施护理。护理规划有助于实施个性化、及时和以结果为导向的护理。在这一阶段,根据之前制定的护理诊断,制定要实现的目标和结果。实施阶段包括执行护理计划中概述的护理干预措施。最后的评估至关重要,要突出对护理敏感的结果。作为理解人们参与护理决策重要性的理论基础,可以采用多种观点、理论和模型,其中过渡理论因其全面性和与护理过程的共性而值得强调。人们健康状况的变化可能是过渡过程(即健康-疾病过渡)的原因。该理论还提出了发展过渡、情境过渡和组织过渡。过渡的性质还体现在模式和属性上。就模式而言,过渡可以是简单的(单次过渡),也可以是多次的(连续或同时),例如,一个人在被诊断出患有慢性疾病并为人父母后,就会经历健康-疾病过渡和情境过渡,在社会中扮演一个新的角色--为人父母(Meleis et al.2000)。意识是指对过渡的感知、了解和认识,以及对过渡过程的了解与经历过渡的人的反应和感知之间的一致程度。参与度是指人们对过渡相关过程的投入程度。参与度与认识水平有关,因为如果没有认识,人的参与度就会受到影响:如果没有认识到自己是如何经历转变过程的,就没有人会参与其中。因此,变化和差异被认为是过渡的属性,一旦所有的过渡都始于变化并产生变化,认 识并归因于它们的意义对于理解过渡过程至关重要。所有的过渡都需要时间,都会持续一段时间,尽管很难确定其起点和终点。最后,就临界点和临界事件而言,有些过渡与一个明显可识别的事件有关,如慢性病 的诊断,而有些则可能不那么具体(Meleis et al.
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引用次数: 0
Introduction and Systematic Review of the Good Nursing Care Scale. 良好护理量表简介和系统回顾。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17486
Tuula Mattila, Minna Stolt, Jouko Katajisto, Helena Leino-Kilpi

Aim(s): To provide an introduction to the Good Nursing Care Scale (GNCS) and systematically review the application of the scale in health research.

Design: Systematic review.

Methods: Empirical studies published in English or Finnish in peer-reviewed journals or as a summary of a PhD thesis where the scale was used for data collection amongst patients were included. Analysis was made by using descriptive statistics, narrative analysis, and evaluation of psychometric properties.

Data sources: PubMed, CINAHL, Cochrane, and Scopus in October 2023.

Results: A total of 26 full-text studies and summaries of PhD theses were included in the review. The GNCS has been developed systematically, and the theoretical structure has remained stable. The studies indicate a high level of patient-centered quality of nursing care. Validity and reliability evaluation and reporting were systematic in the studies and mainly indicate sufficient level. Variations between countries are not large, supporting the international use of the GNCS.

Conclusions: Patient-centered quality of nursing care is predominantly at high levels. However, systematic evaluation is needed to provide longitudinal data. For that purpose, the GNCS is one potential instrument.

Implications for the profession and patient care: Support for the use of existing, tested instruments is encouraged to provide critical ideas for the future needs of nurse practitioners, managers, teachers and researchers.

Impact: This paper impacts researchers interested in systematic evaluation of the patient-centered quality of nursing care and for practitioners taking care of patients. For researchers, it introduces a relevant instrument, the GNCS, for analysing the quality or for comparing the quality with other instruments. For practitioners, it produces evidence of the usability of the GNCS.

Reporting method: PRISMA guided the systematic review, and the COSMIN guideline was used for quality appraisal of included studies.

Patient or public contribution: No Patient or Public contribution.

目的:介绍良好护理量表(GNCS),并系统回顾该量表在健康研究中的应用:介绍良好护理量表(GNCS),系统回顾该量表在健康研究中的应用:系统回顾:方法:纳入以英语或芬兰语在同行评审期刊上发表的实证研究,或作为博士论文摘要在患者中使用该量表收集数据的研究。分析方法包括描述性统计、叙述性分析和心理测量学特性评估:数据来源:PubMed、CINAHL、Cochrane 和 Scopus(2023 年 10 月):综述共纳入 26 篇全文研究和博士论文摘要。GNCS 经过了系统化的发展,理论结构保持稳定。研究表明,以患者为中心的护理质量水平较高。研究中对有效性和可靠性的评估和报告都是系统性的,主要显示出足够的水平。各国之间的差异不大,支持在国际范围内使用 GNCS:结论:以患者为中心的护理质量主要处于较高水平。结论:以病人为中心的护理质量主要处于较高水平,但需要进行系统评估以提供纵向数据。为此,GNCS 是一个潜在的工具:鼓励支持使用现有的、经过测试的工具,为护士从业人员、管理人员、教师和研究人员的未来需求提供重要的思路:本文对有兴趣系统评估以患者为中心的护理质量的研究人员和护理患者的从业人员都有影响。对研究人员而言,本文介绍了一种相关工具--GNCS,用于分析护理质量或将护理质量与其他工具进行比较。对从业人员而言,它提供了 GNCS 可用性的证据:报告方法:PRISMA指导系统性综述,COSMIN指南用于纳入研究的质量评估:无患者或公众贡献。
{"title":"Introduction and Systematic Review of the Good Nursing Care Scale.","authors":"Tuula Mattila, Minna Stolt, Jouko Katajisto, Helena Leino-Kilpi","doi":"10.1111/jocn.17486","DOIUrl":"https://doi.org/10.1111/jocn.17486","url":null,"abstract":"<p><strong>Aim(s): </strong>To provide an introduction to the Good Nursing Care Scale (GNCS) and systematically review the application of the scale in health research.</p><p><strong>Design: </strong>Systematic review.</p><p><strong>Methods: </strong>Empirical studies published in English or Finnish in peer-reviewed journals or as a summary of a PhD thesis where the scale was used for data collection amongst patients were included. Analysis was made by using descriptive statistics, narrative analysis, and evaluation of psychometric properties.</p><p><strong>Data sources: </strong>PubMed, CINAHL, Cochrane, and Scopus in October 2023.</p><p><strong>Results: </strong>A total of 26 full-text studies and summaries of PhD theses were included in the review. The GNCS has been developed systematically, and the theoretical structure has remained stable. The studies indicate a high level of patient-centered quality of nursing care. Validity and reliability evaluation and reporting were systematic in the studies and mainly indicate sufficient level. Variations between countries are not large, supporting the international use of the GNCS.</p><p><strong>Conclusions: </strong>Patient-centered quality of nursing care is predominantly at high levels. However, systematic evaluation is needed to provide longitudinal data. For that purpose, the GNCS is one potential instrument.</p><p><strong>Implications for the profession and patient care: </strong>Support for the use of existing, tested instruments is encouraged to provide critical ideas for the future needs of nurse practitioners, managers, teachers and researchers.</p><p><strong>Impact: </strong>This paper impacts researchers interested in systematic evaluation of the patient-centered quality of nursing care and for practitioners taking care of patients. For researchers, it introduces a relevant instrument, the GNCS, for analysing the quality or for comparing the quality with other instruments. For practitioners, it produces evidence of the usability of the GNCS.</p><p><strong>Reporting method: </strong>PRISMA guided the systematic review, and the COSMIN guideline was used for quality appraisal of included studies.</p><p><strong>Patient or public contribution: </strong>No Patient or Public contribution.</p>","PeriodicalId":50236,"journal":{"name":"Journal of Clinical Nursing","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142407152","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Symptom Clusters in Breast Cancer Patients Receiving Adjuvant Chemotherapy: A Systematic Review 接受辅助化疗的乳腺癌患者的症状群:系统回顾。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17479
Yishu Qi, Huiyuan Li, Yao Guo, Ying Cao, Cho Lee Wong
<div> <section> <h3> Background</h3> <p>Breast cancer patients experience various adverse symptoms during adjuvant chemotherapy. These adverse symptoms often form symptom clusters and have a negative impact on patients.</p> </section> <section> <h3> Aims</h3> <p>To summarise common symptom clusters in different dimensions and their longitudinal changes among breast cancer patients receiving adjuvant chemotherapy.</p> </section> <section> <h3> Design</h3> <p>A systematic review.</p> </section> <section> <h3> Data Sources</h3> <p>Ten electronic databases were searched from 2001 to January 2024, and the search was last updated on 16 August 2024.</p> </section> <section> <h3> Methods</h3> <p>Two reviewers independently assessed the eligibility of each study and extracted data. The Standard Quality Assessment Criteria for Evaluating Primary Research Papers was used to evaluate the quality of included studies. The findings were synthesised narratively. This systematic review has been registered (CRD42022370210).</p> </section> <section> <h3> Results</h3> <p>Nine studies with a total of 1454 participants were included. The common symptom clusters in breast cancer patients receiving adjuvant chemotherapy were the gastrointestinal symptom cluster (nausea-lack of appetite), the fatigue-pain-sleep disturbance symptom cluster and the psychological symptom cluster (worry-sadness-nervousness-distress-feeling irritable-difficult concentrating). The severity dimension was the most frequently utilised in identifying symptom clusters, with the number and concurrence of symptom clusters showing variation over time.</p> </section> <section> <h3> Conclusions</h3> <p>This study summarised common symptom clusters in breast cancer patients receiving adjuvant chemotherapy and revealed their changes from symptom dimensions and the chemotherapy process. These findings support further exploration of symptom cluster changes and underlying mechanisms, facilitating the design of targeted management strategies, including appropriate interventions and measurement dimensions in clinical nursing, to ultimately reduce patients' symptom burden.</p> </section> <section> <h3> Impact</h3> <p>Common symptom clusters have been identified in breast cancer patients receiving adjuvant chemotherapy. Clinical nursing in oncology can prioritise these symptom c
背景:乳腺癌患者在辅助化疗期间会出现各种不良症状:乳腺癌患者在辅助化疗期间会出现各种不良症状。目的:总结接受辅助化疗的乳腺癌患者不同维度的常见症状群及其纵向变化:设计:系统回顾:数据来源:检索了2001年至2024年1月的10个电子数据库,最后一次更新时间为2024年8月16日:两名审稿人独立评估每项研究的资格并提取数据。采用《评估初级研究论文的标准质量评估标准》对纳入的研究进行质量评估。研究结果以叙述的方式进行综合。本系统综述已注册(CRD42022370210):结果:共纳入了 9 项研究,共有 1454 名参与者。接受辅助化疗的乳腺癌患者常见的症状群是胃肠道症状群(恶心-食欲不振)、疲劳-疼痛-睡眠障碍症状群和心理症状群(担心-悲伤-紧张-压力-感觉烦躁-难以集中注意力)。在确定症状群时,最常使用的是严重程度维度,而症状群的数量和并发程度则随时间而变化:本研究总结了接受辅助化疗的乳腺癌患者的常见症状群,并揭示了这些症状群在症状维度和化疗过程中的变化。这些发现支持进一步探索症状群的变化及其内在机制,有助于设计有针对性的管理策略,包括在临床护理中采取适当的干预措施和测量维度,最终减轻患者的症状负担:在接受辅助化疗的乳腺癌患者中发现了常见的症状群。肿瘤学临床护理可优先考虑这些症状群,并为患者提供有针对性的管理策略:报告方法:PRISMA指南和SWiM指南:无患者或公众贡献。
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引用次数: 0
Enhancing Clinical Relevance in the Management of Chronic Kidney Disease in Dialysis Patients. 提高透析患者慢性肾病管理的临床实用性。
IF 3.2 3区 医学 Q1 NURSING Pub Date : 2024-10-11 DOI: 10.1111/jocn.17491
Yuqian Zhang, Qianqian Chang
{"title":"Enhancing Clinical Relevance in the Management of Chronic Kidney Disease in Dialysis Patients.","authors":"Yuqian Zhang, Qianqian Chang","doi":"10.1111/jocn.17491","DOIUrl":"https://doi.org/10.1111/jocn.17491","url":null,"abstract":"","PeriodicalId":50236,"journal":{"name":"Journal of Clinical Nursing","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142407151","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
期刊
Journal of Clinical Nursing
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