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The effect of postpartum interventions on healing and pain in women with perineal trauma: A systematic review and meta-analysis 产后干预对会阴创伤妇女愈合和疼痛的影响:一项系统回顾和荟萃分析
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104976
Döndü Kurnaz, Gamze Fışkın Siyahtaş, Meltem Demirgöz Bal

Introduction

Interventions aimed at perineal healing and pain relief can have a positive impact on postpartum experiences in women who experience perineal trauma during childbirth.

Objective

The aim of this systematic review and meta-analysis was to compare various methods applied for healing and pain relief from perineal trauma based on primary studies.

Methods

The study protocol was developed following PRISMA guidelines, and Meta-Analyses guidelines. Searches were conducted between March and April 2024. Registration was completed using PROSPERO. Searches were performed using PubMed, the Cochrane Library, EBSCO, Embase, Web of Science, PsycINFO, Scopus, National Thesis Center, TR Dizin, Türkiye Klinikleri, and DergiPark Academic search engines. The methodological quality of the studies was assessed using the RoB-1 and RoB-2. Data were aggregated through meta-analysis, and a GRADE evidence profile was created.

Results

Nineteen studies involving 1899 participants were included in the meta-analysis. The results showed that interventions performed within the first 24 h after episiotomy did not reduce pain. However, the effects of the interventions were observed on the second day, with cold application identified as the most effective method. Additionally, interventions did not affect healing during the first three days, but a more pronounced improvement was noted in the intervention group by the fifth day. Healing began around the 7th–10th days even without intervention. The REEDA (redness, edema, ecchymosis, discharge, and approximation) score decreased most significantly in the group that received perineal education (diet, Kegel exercise, infection symptoms, and perineal hygiene).

Conclusion

Cold application is recommended on the second day to reduce pain following perineal trauma. Interventions were found to accelerate the healing process by initiating healing at least two days earlier, with perineal education being the most effective method. However, further research on topical herbal treatments and perineal hygiene education is needed to strengthen this evidence.
针对会阴愈合和疼痛缓解的干预措施可对分娩时经历会阴创伤的妇女的产后体验产生积极影响。
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引用次数: 0
Comparative effectiveness of delirium recognition with and without a clinical decision assessment system on outcomes of hospitalized older adults: Cluster randomized controlled trial 有和没有临床决策评估系统的谵妄识别对住院老年人结局的比较效果:整群随机对照试验。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104979
Jiamin Wang , Ying Wu , Yongjun Huang , Fangyu Yang

Background

Early recognition of delirium is essential for effective management, but it often goes unrecognized, resulting in adverse outcomes. Clinical decision support systems can enhance adherence to guidelines and improve patient outcomes. We developed a mobile-based clinical decision assessment tool (3D-DST) based on the 3-minute diagnostic interview for confusion assessment method-defined delirium (3D-CAM). Implementing the 3D-DST may enhance delirium recognition and adherence to interventions among healthcare professionals, potentially improving outcomes in older adults.

Objective

To test whether improved recognition of delirium could lead to better clinical outcomes in older adults.

Design

A cluster randomized controlled trial with pair-matching.

Setting

A tertiary geriatric hospital.

Participants

Patients aged ≥ 65 years.

Methods

Four general wards were paired and randomly assigned to the intervention group (two wards) or the control group (two wards). The intervention included routine delirium assessments by nurses using either the 3D-DST or the 3D-CAM, along with delirium prevention and intervention measures carried out by a multidisciplinary team. Outcomes measured included delirium incidence, duration, severity, length of stay, and adherence to the delirium assessment, prevention, and treatment protocol. A trained nursing researcher collected data on demographics, clinical characteristics, and primary and secondary outcomes.

Results

211 eligible patients participated (106 in the intervention group and 105 in the control group), with 21 identified as delirium-positive using the 3D-DST. The median Charlson comorbidity index score among older adults in the intervention group was 1 (1–2), compared to 2 (1–3) in the control group (P = 0.032). Nurses' adherence to delirium assessment was significantly higher in the intervention group than in the control group (73 % vs. 31 %). The recognition rate of delirium among nurses was 89 % in the intervention group and 42 % in the control group. There were no statistically significant differences in delirium duration (6 [3–9] vs. 7 [2–14], P = 0.967), incidence (8.5 % vs. 11.4 %, P = 0.500), severity (2 [1–3] vs. 2 [1–4], P = 0.891) or length of hospital stay (15 [14–18] vs. 18 [13–22], P = 0.568) between the intervention and control groups.

Conclusions

The 3D-DST enhanced adherence to routine delirium recognition by nurses. However, effective strategies are urgently needed to strengthen multidisciplinary collaboration and enhance adherence to delirium management among healthcare professionals.

Registration

Chinese Clinical Trial Registry, Identifier: ChiCTR1900028402.
背景:早期识别谵妄对有效治疗至关重要,但它经常被忽视,导致不良后果。临床决策支持系统可以加强对指南的遵守并改善患者的预后。我们开发了一种基于3分钟诊断访谈的移动临床决策评估工具(3D-DST),用于混乱评估方法定义的谵妄(3D-CAM)。实施3D-DST可以增强医疗保健专业人员对谵妄的识别和对干预措施的依从性,潜在地改善老年人的预后。目的:探讨提高对谵妄的认识是否能改善老年人的临床预后。设计:分组随机对照试验,配对。环境:三级老年医院。参与者:年龄≥65岁的患者。方法:将4个普通病房配对,随机分为干预组(2个病房)和对照组(2个病房)。干预包括由护士使用3D-DST或3D-CAM进行常规谵妄评估,以及由多学科团队进行谵妄预防和干预措施。测量的结果包括谵妄发生率、持续时间、严重程度、住院时间,以及对谵妄评估、预防和治疗方案的依从性。一位训练有素的护理研究员收集了人口统计学、临床特征和主要和次要结果的数据。结果:211例符合条件的患者(干预组106例,对照组105例),其中21例经3D-DST鉴定为谵妄阳性。干预组老年人Charlson合并症指数中位数为1(1-2),对照组为2(1-3),差异有统计学意义(P = 0.032)。干预组护士对谵妄评估的依从性明显高于对照组(73%对31%)。干预组护士谵妄的识别率为89%,对照组为42%。干预组与对照组谵妄持续时间(6例[3-9]比7例[2-14],P = 0.967)、发生率(8.5%比11.4%,P = 0.500)、严重程度(2例[1-3]比2例[1-4],P = 0.891)、住院时间(15例[14-18]比18例[13-22],P = 0.568)差异均无统计学意义。结论:3D-DST增强了护士对谵妄识别的依从性。然而,迫切需要有效的策略来加强多学科合作,提高医疗保健专业人员对谵妄管理的依从性。注册:中国临床试验注册中心,编号:ChiCTR1900028402。
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引用次数: 0
Efficacy of skin-to-skin contact between mother and infant on maternal outcomes during the third stage of labour: A systematic review and meta-analysis 母婴皮肤接触对分娩第三阶段产妇结局的影响:一项系统回顾和荟萃分析。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104981
Sandra Martínez-Rodríguez , Julián Rodríguez-Almagro , Alberto Bermejo-Cantarero , Estíbaliz Laderas-Díaz , Noelia Sanchez-Millan , Antonio Hernández-Martínez

Background

Postpartum haemorrhage is a preventable cause of maternal mortality that commonly occurs during the third stage of labour. Skin-to-skin contact is an intervention that can support the physiological processes of labour by increasing oxytocin levels, which can accelerate placental expulsion and enhance uterine contractions, thereby contributing to the prevention of postpartum haemorrhage.

Objective

This systematic review aims to evaluate the impact of skin-to-skin contact on key maternal variables during the third stage of labour, including the duration of this stage, placental integrity, the need for manual placental extraction, the administration of therapeutic uterotonics, and the position of the uterine fundus.

Methods

A systematic review with meta-analysis of randomised controlled trials and prospective quasi-experimental studies was conducted. Studies were searched in PubMed, Scopus, Cochrane, CINAHL, Google Scholar, and Web of Science. Statistical analysis was performed using STATA version 18. The results of the meta-analysis were reported using relative risk (RR) for dichotomous data and mean difference (MD) for continuous data, both with 95 % confidence intervals (CI). A random-effects model was employed due to the anticipated heterogeneity among the included studies. Sensitivity analyses were performed to assess the robustness of the findings, and a subgroup analysis was conducted based on the type of birth, study design, and country economic level.

Results

Twenty-five trials were included. Skin-to-skin contact significantly reduced the duration of the third stage of labour (MD: − 4.26; 95 %; CI: − 5.70, − 2.81), increased the likelihood of complete placental integrity (RR: 1.09; 95 % CI: 1.02, 1.16), and significantly reduced both the likelihood of a supraumbilical position of the uterine fundus (RR: 0.39; 95 % CI: 0.20, 0.76) and the need for uterotonic administration (RR: 0.24; 95 % CI: 0.12, 0.48).

Conclusions

Skin-to-skin contact is a simple practice that can favourably influence the physiological processes of labour and improve various maternal outcomes. These benefits include reducing the duration of the third stage of labour, ensuring complete birth of the placenta, decreasing the need for uterotonic administration, and increasing the likelihood of a proper uterine fundal position. Therefore, it is recommended to include this practice in labour care protocols.
背景:产后出血是一种可预防的产妇死亡原因,通常发生在分娩第三阶段。皮肤与皮肤接触是一种干预措施,可以通过增加催产素水平来支持分娩的生理过程,这可以加速胎盘排出并增强子宫收缩,从而有助于预防产后出血。目的:本系统综述旨在评估皮肤接触对分娩第三期母体关键变量的影响,包括该阶段的持续时间、胎盘完整性、人工胎盘提取的需要、治疗性子宫强张剂的使用以及子宫底的位置。方法:对随机对照试验和前瞻性准实验研究进行系统评价和荟萃分析。研究在PubMed, Scopus, Cochrane, CINAHL, b谷歌Scholar和Web of Science中进行了检索。使用STATA version 18进行统计分析。采用相对危险度(RR)对二分类数据和平均差异(MD)对连续数据进行meta分析,两者的置信区间(CI)均为95%。考虑到纳入研究的异质性,采用随机效应模型。进行敏感性分析以评估研究结果的稳健性,并根据出生类型、研究设计和国家经济水平进行亚组分析。结果:共纳入25项试验。皮肤接触显著缩短了分娩第三阶段的持续时间(MD: -4.26;95%;CI: -5.70, -2.81),胎盘完整可能性增加(RR: 1.09;95% CI: 1.02, 1.16),并显著降低子宫底位于脐上位置的可能性(RR: 0.39;95% CI: 0.20, 0.76)和需要子宫扩张给药(RR: 0.24;95% ci: 0.12, 0.48)。结论:皮肤与皮肤接触是一种简单的做法,可以有利地影响分娩的生理过程,改善产妇的各种结局。这些好处包括减少分娩第三阶段的持续时间,确保胎盘的完全出生,减少对子宫强直给药的需要,并增加适当的子宫底位置的可能性。因此,建议将这种做法纳入劳动护理协议。
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引用次数: 0
Family members' experiences of surrogate decision-making in hospice care: A systematic review of qualitative studies 安宁疗护中家属替代决策的经验:质性研究的系统回顾。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104987
Ting Yu , Yijing Li , Ziyi Hu , Shanshan Liu , Cong Wang , Qian Chen , Yan Jiang
<div><h3>Background</h3><div>Surrogate decision-makers play a key role in determining whether end-of-life patients receive hospice care. There is a need to better understand families' experiences of surrogate decision-making in hospice care for end-of-life patients to provide a basis for developing targeted interventions, such as decision support tools or counseling, to help family members navigate the decision-making process.</div></div><div><h3>Aim</h3><div>The aim was to analyze and synthesize global qualitative data on family members' experiences of surrogate decision-making regarding whether to receive hospice care for end-of-life patients.</div></div><div><h3>Design</h3><div>This was a systematic review of qualitative studies.</div></div><div><h3>Data sources</h3><div>The PubMed, Web of Science, Cochrane Library, Embase, Cumulated Index to Nursing and Allied Health Literature, Chinese Biomedical Literature Service System, China National Knowledge Infrastructure, WanFang and China Science and Technology Journal databases were searched from inception to September 2024. Studies related to family members making surrogate decisions about whether to receive hospice care for end-of-life patients were included.</div></div><div><h3>Review methods</h3><div>This review was guided by the Joanna Briggs Institute Manual for Systematic reviews of qualitative evidence. Two reviewers independently screened the studies and extracted the data. The eligible studies were assessed via the Joanna Briggs Institute critical appraisal instrument for qualitative research. Thematic synthesis was guided by the method developed by Thomas and Harden.</div></div><div><h3>Results</h3><div>A total of nine studies were included. The synthesis of qualitative data resulted in three themes: (1) Decision motivation between rationality and emotion. The reasons surrogate decision-makers considered hospice care for patients involved multiple aspects and were a result of both objective and subjective factors. (2) Decision preparation stemmed from knowledge and experience. A knowledge-based foundation and experiential grounding were needed to ensure that surrogate decision-makers make informed decision. (3) Decision reflection through looking back and forward. Surrogate decision-makers expressed satisfaction with the decision to choose hospice care for patients, coupled with serious consideration of personal future end-of-life decisions.</div></div><div><h3>Conclusion</h3><div>Determining whether patients receive hospice care at end of life is complex for family members. This process begins with the coexistence of rational and emotional motives for decision-making, involves preparation for decision-making through the acquisition of knowledge and experience about hospice care, and culminates in reflection on the entire decision-making process. These findings underscore the importance of providing sufficient informational and emotional support to family decision-makers, which can impro
背景:替代决策者在决定临终病人是否接受安宁疗护方面扮演关键角色。有必要更好地了解临终病人临终关怀中替代决策的家庭经验,为制定有针对性的干预措施提供基础,例如决策支持工具或咨询,以帮助家庭成员在决策过程中导航。目的:目的是分析和综合全球关于临终病人是否接受临终关怀的替代决策的家庭成员经验的定性数据。设计:这是一项定性研究的系统综述。数据来源:检索PubMed、Web of Science、Cochrane Library、Embase、护理与联合健康文献累积索引、中国生物医学文献服务系统、中国国家知识基础设施、万方、中国科技期刊数据库,检索时间为建库至2024年9月。研究包括家庭成员对是否接受临终关怀病人的替代决定。综述方法:本综述以乔安娜布里格斯研究所定性证据系统综述手册为指导。两名审稿人独立筛选研究并提取数据。合格的研究通过乔安娜布里格斯研究所的定性研究关键评估工具进行评估。主题合成以Thomas和Harden提出的方法为指导。结果:共纳入9项研究。综合定性数据得出三个主题:(1)理性与情感之间的决策动机。代理决策者考虑临终关怀的原因涉及多个方面,是客观和主观因素共同作用的结果。(2)决策准备源于知识和经验。需要以知识为基础和经验为基础,以确保代理决策者做出明智的决定。(3)回顾过去和展望未来的决策反思。代理决策者对病人选择临终关怀的决定表示满意,并认真考虑个人未来的临终决定。结论:决定临终病人是否接受安宁疗护对家属来说是件复杂的事。这个过程从理性与情感动机共存的决策开始,透过获取安宁疗护的知识与经验,为决策做准备,最后以反思整个决策过程而告终。这些发现强调了为家庭决策者提供足够的信息和情感支持的重要性,这可以改善决策并促进更富有同情心的临终关怀。未来的研究应侧重于制定有效的战略来加强这些支持系统。研究注册:在PROSPERO (CRD42024526197)上注册了一个协议。
{"title":"Family members' experiences of surrogate decision-making in hospice care: A systematic review of qualitative studies","authors":"Ting Yu ,&nbsp;Yijing Li ,&nbsp;Ziyi Hu ,&nbsp;Shanshan Liu ,&nbsp;Cong Wang ,&nbsp;Qian Chen ,&nbsp;Yan Jiang","doi":"10.1016/j.ijnurstu.2024.104987","DOIUrl":"10.1016/j.ijnurstu.2024.104987","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;div&gt;Surrogate decision-makers play a key role in determining whether end-of-life patients receive hospice care. There is a need to better understand families' experiences of surrogate decision-making in hospice care for end-of-life patients to provide a basis for developing targeted interventions, such as decision support tools or counseling, to help family members navigate the decision-making process.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Aim&lt;/h3&gt;&lt;div&gt;The aim was to analyze and synthesize global qualitative data on family members' experiences of surrogate decision-making regarding whether to receive hospice care for end-of-life patients.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Design&lt;/h3&gt;&lt;div&gt;This was a systematic review of qualitative studies.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Data sources&lt;/h3&gt;&lt;div&gt;The PubMed, Web of Science, Cochrane Library, Embase, Cumulated Index to Nursing and Allied Health Literature, Chinese Biomedical Literature Service System, China National Knowledge Infrastructure, WanFang and China Science and Technology Journal databases were searched from inception to September 2024. Studies related to family members making surrogate decisions about whether to receive hospice care for end-of-life patients were included.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Review methods&lt;/h3&gt;&lt;div&gt;This review was guided by the Joanna Briggs Institute Manual for Systematic reviews of qualitative evidence. Two reviewers independently screened the studies and extracted the data. The eligible studies were assessed via the Joanna Briggs Institute critical appraisal instrument for qualitative research. Thematic synthesis was guided by the method developed by Thomas and Harden.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;A total of nine studies were included. The synthesis of qualitative data resulted in three themes: (1) Decision motivation between rationality and emotion. The reasons surrogate decision-makers considered hospice care for patients involved multiple aspects and were a result of both objective and subjective factors. (2) Decision preparation stemmed from knowledge and experience. A knowledge-based foundation and experiential grounding were needed to ensure that surrogate decision-makers make informed decision. (3) Decision reflection through looking back and forward. Surrogate decision-makers expressed satisfaction with the decision to choose hospice care for patients, coupled with serious consideration of personal future end-of-life decisions.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;Determining whether patients receive hospice care at end of life is complex for family members. This process begins with the coexistence of rational and emotional motives for decision-making, involves preparation for decision-making through the acquisition of knowledge and experience about hospice care, and culminates in reflection on the entire decision-making process. These findings underscore the importance of providing sufficient informational and emotional support to family decision-makers, which can impro","PeriodicalId":50299,"journal":{"name":"International Journal of Nursing Studies","volume":"162 ","pages":"Article 104987"},"PeriodicalIF":7.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142899965","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
Corrigendum to “The effects of a facilitator-enabled online multicomponent iSupport for dementia programme: A multicentre randomised controlled trial” [Int. J. Nurs. Stud. 159 (2024) 104868] 一项多中心随机对照试验"[Int. J. Nurses Studios 159 (2024) 104868]的更正:多中心随机对照试验" [Int. J. Nurs. Stud. 159 (2024) 104868]。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104960
Lily Xiao , Shahid Ullah , Rujun Hu , Jing Wang , Huali Wang , Chia-Chi Chang , Timothy Kwok , Mingxia Zhu , Julie Ratcliffe , Henry Brodaty , Bianca Brijnath , Hui-Chen (Rita) Chang , Bel Wong , Yunrui Zhou , Jinjie He , Mengmeng Xia , Jhih-Yang Hong , Shirley Che , Rachel Milte
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引用次数: 0
Effectiveness of a nurse practitioner-led collaborative health care model on self-care, functional status, rehospitalization and medical costs in heart failure patients: A randomized controlled trial 执业护士主导的协同医疗模式对心力衰竭患者自我护理、功能状态、再住院和医疗费用的影响:一项随机对照试验
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104980
Chih-Wen Chen , Tsae-Jyy Wang , Chieh-Yu Liu , Yeu-Hui Chuang , Ching-Chuan Su , Shu-Fang Vivienne Wu
<div><h3>Background</h3><div>Heart failure is a serious and common condition that has garnered significant attention in the global public health domain. It often results in impaired function and reduced cardiac function status, leading to difficulties in self-care and diminished quality of life. To effectively address these complex challenges, the collaborative health care model has been proposed. This approach has proven effective in reducing rehospitalization and lowering medical costs.</div></div><div><h3>Objective</h3><div>To evaluate the effects of a nurse practitioner-led collaborative health care model on the self-care, functional status, rehospitalization and medical costs of patients with heart failure.</div></div><div><h3>Design</h3><div>A randomized controlled trial design.</div></div><div><h3>Setting</h3><div>Cardiology department of a regional teaching hospital in Southern Taiwan.</div></div><div><h3>Participants</h3><div>100 patients diagnosed with heart failure.</div></div><div><h3>Methods</h3><div>Patients diagnosed with heart failure were recruited through random allocation and.</div><div>randomly assigned to two groups. The control group included 50 patients who received routine nursing guidance; the experimental group also included 50 patients who participated in a 12-week collaborative health care program. Key outcomes, including self-care, functional status, rehospitalization, and medical costs, which were evaluated at 12, 16, and 20 weeks post-discharge.</div></div><div><h3>Results</h3><div>The intervention of the collaborative healthcare program significantly impacted self-care, functional status, rehospitalization, and medical costs. Significant improvements in self-care and functional status were observed at 20 weeks (Self-Care: β = 31.52, 95 % CI: 25.96 to 37.07, <em>p</em> < 0.001; Functional Status: χ<sup>2</sup> = 22.42, <em>p</em> < 0.001). Regarding rehospitalization, the average rehospitalization duration for the experimental group significantly increased compared to 1.45 months for the control group, with the experimental group averaging 3.00 months at the 20-week follow-up. Moreover, the experimental group also demonstrated a reduction in rehospitalization medical costs, particularly with significant effects observed in the early stages of intervention (β = −<!--> <!-->6147.94, 95 % CI: −<!--> <!-->10,763.99 to −<!--> <!-->1531.88, <em>p</em> = 0.009).</div></div><div><h3>Conclusion</h3><div>The use of a nurse practitioner-led collaborative health care model significantly improved self-care, function status and reduced rehospitalization while effectively lowering medical costs for patients with heart failure. Through professional team communication and collaboration, this approach provides more effective and comprehensive care, enhances patient self-management capabilities, and improves overall treatment outcomes. These results hold significant implications for clinical practice and provide empirical suppor
心力衰竭是一种严重和常见的疾病,在全球公共卫生领域引起了极大的关注。它通常导致功能受损和心功能状态降低,导致自我护理困难和生活质量下降。为了有效地应对这些复杂的挑战,协作式医疗保健模式被提出。事实证明,这种方法在减少再住院和降低医疗费用方面是有效的。
{"title":"Effectiveness of a nurse practitioner-led collaborative health care model on self-care, functional status, rehospitalization and medical costs in heart failure patients: A randomized controlled trial","authors":"Chih-Wen Chen ,&nbsp;Tsae-Jyy Wang ,&nbsp;Chieh-Yu Liu ,&nbsp;Yeu-Hui Chuang ,&nbsp;Ching-Chuan Su ,&nbsp;Shu-Fang Vivienne Wu","doi":"10.1016/j.ijnurstu.2024.104980","DOIUrl":"10.1016/j.ijnurstu.2024.104980","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;div&gt;Heart failure is a serious and common condition that has garnered significant attention in the global public health domain. It often results in impaired function and reduced cardiac function status, leading to difficulties in self-care and diminished quality of life. To effectively address these complex challenges, the collaborative health care model has been proposed. This approach has proven effective in reducing rehospitalization and lowering medical costs.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;div&gt;To evaluate the effects of a nurse practitioner-led collaborative health care model on the self-care, functional status, rehospitalization and medical costs of patients with heart failure.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Design&lt;/h3&gt;&lt;div&gt;A randomized controlled trial design.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Setting&lt;/h3&gt;&lt;div&gt;Cardiology department of a regional teaching hospital in Southern Taiwan.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Participants&lt;/h3&gt;&lt;div&gt;100 patients diagnosed with heart failure.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;Patients diagnosed with heart failure were recruited through random allocation and.&lt;/div&gt;&lt;div&gt;randomly assigned to two groups. The control group included 50 patients who received routine nursing guidance; the experimental group also included 50 patients who participated in a 12-week collaborative health care program. Key outcomes, including self-care, functional status, rehospitalization, and medical costs, which were evaluated at 12, 16, and 20 weeks post-discharge.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;The intervention of the collaborative healthcare program significantly impacted self-care, functional status, rehospitalization, and medical costs. Significant improvements in self-care and functional status were observed at 20 weeks (Self-Care: β = 31.52, 95 % CI: 25.96 to 37.07, &lt;em&gt;p&lt;/em&gt; &lt; 0.001; Functional Status: χ&lt;sup&gt;2&lt;/sup&gt; = 22.42, &lt;em&gt;p&lt;/em&gt; &lt; 0.001). Regarding rehospitalization, the average rehospitalization duration for the experimental group significantly increased compared to 1.45 months for the control group, with the experimental group averaging 3.00 months at the 20-week follow-up. Moreover, the experimental group also demonstrated a reduction in rehospitalization medical costs, particularly with significant effects observed in the early stages of intervention (β = −&lt;!--&gt; &lt;!--&gt;6147.94, 95 % CI: −&lt;!--&gt; &lt;!--&gt;10,763.99 to −&lt;!--&gt; &lt;!--&gt;1531.88, &lt;em&gt;p&lt;/em&gt; = 0.009).&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;The use of a nurse practitioner-led collaborative health care model significantly improved self-care, function status and reduced rehospitalization while effectively lowering medical costs for patients with heart failure. Through professional team communication and collaboration, this approach provides more effective and comprehensive care, enhances patient self-management capabilities, and improves overall treatment outcomes. These results hold significant implications for clinical practice and provide empirical suppor","PeriodicalId":50299,"journal":{"name":"International Journal of Nursing Studies","volume":"162 ","pages":"Article 104980"},"PeriodicalIF":7.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142874801","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
Factors influencing nurses and nursing students' attitudes towards vaccinations: A cross-sectional study 护士及护生对疫苗接种态度的影响因素:横断面研究。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104963
Jeremia Keisala , Erika Jarva , Dania Comparcini , Valentina Simonetti , Giancarlo Cicolini , John Unsworth , Marco Tomietto , Kristina Mikkonen
<div><h3>Background</h3><div>Vaccination hesitancy remains the main obstacle to improving vaccination coverage. Influenza and COVID-19 vaccination coverage among healthcare professionals is essential. It is crucial to study the vaccination attitudes of healthcare professionals as they significantly influence the vaccination attitudes and behaviour of the rest of the population.</div></div><div><h3>Objective</h3><div>The aim of this study was to describe the attitudes of Finnish nurses and nursing students towards COVID-19 and Influenza vaccination and explain what factors influence these attitudes.</div></div><div><h3>Design</h3><div>A cross-sectional study.</div></div><div><h3>Setting and participants</h3><div>A total of 1353 nurses from five hospital organisations and 580 nursing students from eight Universities of Applied Sciences participated in the survey. Participants were invited to complete the questionnaire through Webropol between March and September 2023.</div></div><div><h3>Methods</h3><div>To collect data anonymously, a self-reported web-based questionnaire combining the Vaccination Attitude Examination (VAX) scale and Bergen's Social Media Addiction (BSMA) scale was used. K-means cluster analysis was performed to describe vaccination attitude profiles.</div></div><div><h3>Results</h3><div>Four distinct vaccination attitude profiles were identified: Profile A - Confident Pro-Vaccine (n = 605) exhibited low hesitancy, with high confidence in vaccine safety and effectiveness; Profile B – Cautiously Pro-Vaccine (n = 764) showed moderate hesitancy, mainly concerned about unforeseen future effects; Profile C - Hesitant with Mistrust (n = 405) expressed high hesitancy, with significant worries about vaccine safety and mistrust in health authorities; and Profile D – Strongly Vaccine-Hesitant (n = 159) demonstrated very high hesitancy, marked by strong beliefs in potential long-term negative effects of vaccination. Significant differences in VAX-scale mean scores were found between the profiles, ranging from 1.27 for Profile A to 6.65 for Profile D. Overall, nursing students were more hesitant than practising nurses, with students being overrepresented in the more hesitant profiles. Clinical training in a COVID-19 unit was associated with more favourable vaccination attitudes among nursing students. The uptake of the full series of COVID-19 and annual Influenza vaccines was generally high in the sample (90.8 % and 87 %, respectively). However, a clear pattern between specific social media use and vaccination attitudes was not found. Major concerns related to vaccine hesitancy focused on the uncertainty of vaccines' long-term effects.</div></div><div><h3>Conclusion</h3><div>This study provides valuable insights into the complex nature of vaccination hesitancy among nurses and nursing students. These findings underscore the need for targeted interventions to address underlying concerns and promote vaccine acceptance within this demographic. In
背景:疫苗接种犹豫不决仍然是提高疫苗接种覆盖率的主要障碍。卫生保健专业人员的流感和COVID-19疫苗接种覆盖率至关重要。研究卫生保健专业人员的疫苗接种态度至关重要,因为他们对其他人口的疫苗接种态度和行为有重大影响。目的:本研究旨在描述芬兰护士和护生对COVID-19和流感疫苗接种的态度,并解释影响这些态度的因素。设计:横断面研究。调查地点及对象:共有来自五间医院机构的1353名护士及来自八所应用科技大学的580名护生参与调查。参与者被邀请在2023年3月至9月期间通过Webropol完成问卷调查。方法:采用基于网络的疫苗接种态度调查(VAX)量表和卑尔根社交媒体成瘾(BSMA)量表相结合的自述问卷,采用匿名方式收集数据。采用k -均值聚类分析描述疫苗接种态度概况。结果:确定了四种不同的疫苗接种态度:A型-自信的支持疫苗(n = 605)表现出低犹豫,对疫苗的安全性和有效性有很高的信心;谱B -谨慎支持疫苗(n = 764)表现出中度犹豫,主要担心不可预见的未来影响;特征C -犹豫与不信任(n = 405)表示高度犹豫,对疫苗安全和卫生当局的不信任有重大担忧;特征图D -强烈的疫苗犹豫(n = 159)表现出非常高的犹豫,表现为对疫苗接种潜在的长期负面影响的强烈信念。vax量表的平均得分在各概况之间存在显着差异,从概况A的1.27到概况d的6.65不等。总体而言,护生比执业护士更犹豫,学生在更犹豫的概况中被过度代表。在COVID-19单位的临床培训与护理学生中更有利的疫苗接种态度相关。样本中COVID-19全系列疫苗和年度流感疫苗的接种率普遍较高(分别为90.8%和87%)。然而,没有发现特定社交媒体使用与疫苗接种态度之间的明确模式。与疫苗犹豫有关的主要关切集中在疫苗长期效果的不确定性上。结论:本研究对护士和护生疫苗接种犹豫的复杂性提供了有价值的见解。这些发现强调有必要采取有针对性的干预措施,以解决潜在的问题并促进这一人群对疫苗的接受。在未来的研究中,有必要收集更深入的知识,特别是关于护生对疫苗接种的态度及其影响因素。
{"title":"Factors influencing nurses and nursing students' attitudes towards vaccinations: A cross-sectional study","authors":"Jeremia Keisala ,&nbsp;Erika Jarva ,&nbsp;Dania Comparcini ,&nbsp;Valentina Simonetti ,&nbsp;Giancarlo Cicolini ,&nbsp;John Unsworth ,&nbsp;Marco Tomietto ,&nbsp;Kristina Mikkonen","doi":"10.1016/j.ijnurstu.2024.104963","DOIUrl":"10.1016/j.ijnurstu.2024.104963","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;div&gt;Vaccination hesitancy remains the main obstacle to improving vaccination coverage. Influenza and COVID-19 vaccination coverage among healthcare professionals is essential. It is crucial to study the vaccination attitudes of healthcare professionals as they significantly influence the vaccination attitudes and behaviour of the rest of the population.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;div&gt;The aim of this study was to describe the attitudes of Finnish nurses and nursing students towards COVID-19 and Influenza vaccination and explain what factors influence these attitudes.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Design&lt;/h3&gt;&lt;div&gt;A cross-sectional study.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Setting and participants&lt;/h3&gt;&lt;div&gt;A total of 1353 nurses from five hospital organisations and 580 nursing students from eight Universities of Applied Sciences participated in the survey. Participants were invited to complete the questionnaire through Webropol between March and September 2023.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;To collect data anonymously, a self-reported web-based questionnaire combining the Vaccination Attitude Examination (VAX) scale and Bergen's Social Media Addiction (BSMA) scale was used. K-means cluster analysis was performed to describe vaccination attitude profiles.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;Four distinct vaccination attitude profiles were identified: Profile A - Confident Pro-Vaccine (n = 605) exhibited low hesitancy, with high confidence in vaccine safety and effectiveness; Profile B – Cautiously Pro-Vaccine (n = 764) showed moderate hesitancy, mainly concerned about unforeseen future effects; Profile C - Hesitant with Mistrust (n = 405) expressed high hesitancy, with significant worries about vaccine safety and mistrust in health authorities; and Profile D – Strongly Vaccine-Hesitant (n = 159) demonstrated very high hesitancy, marked by strong beliefs in potential long-term negative effects of vaccination. Significant differences in VAX-scale mean scores were found between the profiles, ranging from 1.27 for Profile A to 6.65 for Profile D. Overall, nursing students were more hesitant than practising nurses, with students being overrepresented in the more hesitant profiles. Clinical training in a COVID-19 unit was associated with more favourable vaccination attitudes among nursing students. The uptake of the full series of COVID-19 and annual Influenza vaccines was generally high in the sample (90.8 % and 87 %, respectively). However, a clear pattern between specific social media use and vaccination attitudes was not found. Major concerns related to vaccine hesitancy focused on the uncertainty of vaccines' long-term effects.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;This study provides valuable insights into the complex nature of vaccination hesitancy among nurses and nursing students. These findings underscore the need for targeted interventions to address underlying concerns and promote vaccine acceptance within this demographic. In","PeriodicalId":50299,"journal":{"name":"International Journal of Nursing Studies","volume":"162 ","pages":"Article 104963"},"PeriodicalIF":7.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142781711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Psychosocial effects of a humanoid robot on informal caregivers of people with dementia: A randomised controlled trial with nested interviews 类人机器人对痴呆症患者非正式照顾者的心理社会影响:一项嵌套访谈的随机对照试验。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104967
Julia Zuschnegg , Alfred Häussl , Gerald Lodron , Thomas Orgel , Silvia Russegger , Michael Schneeberger , Maria Fellner , Magdalena Holter , Dimitrios Prodromou , Anna Schultz , Regina Roller-Wirnsberger , Lucas Paletta , Marisa Koini , Sandra Schüssler
<div><h3>Background</h3><div>Dementia rates are rising globally, impacting healthcare systems and society. The care of people with dementia is largely provided by informal caregivers (e.g., family, friends), which can present significant challenges and increase caregivers' burden. New technologies, such as humanoid socially assistive robots, show promise in reducing this burden, as such robots were considered to be supportive devices for both informal caregivers and people with dementia.</div></div><div><h3>Objective</h3><div>To explore the psychosocial effects of the humanoid social assistive robot Coach Pepper (equipped with functions like tablet-based multimodal training for people with dementia) compared to exclusively tablet-based multimodal training for people with dementia on informal caregivers. Additionally, informal caregivers' attitudes and experiences with Coach Pepper were examined.</div></div><div><h3>Design</h3><div>A randomised controlled parallel two-arm trial with a nested qualitative study was conducted.</div></div><div><h3>Setting</h3><div>The study took place in the home setting (i.e. private households).</div></div><div><h3>Participants</h3><div>Thirty-two informal caregivers of people with dementia participated in the study.</div></div><div><h3>Methods</h3><div>Informal caregivers (and their loved one with dementia) were randomly assigned to Coach Pepper (n = 16) or a solely tablet-based multimodal training (n = 16) for a three-week period. Data for caregivers were collected at baseline and after the intervention by standardised questionnaires for caregiver burden (primary outcome), quality of life, depressive symptoms and affect. Additionally, acceptance was measured in both groups and semi-structured interviews were conducted in the Coach Pepper group post-interventionally.</div></div><div><h3>Results</h3><div>No significant differences in mean changes between groups were identified in the outcomes, except that two domains of acceptance (usefulness and accessibility) were rated significantly higher for the control group. Qualitative findings showed mostly positive attitudes towards Coach Pepper in dementia care and neutral feelings on caregiver burden. Caregivers reported usefulness of Coach Pepper on being assistive in six components of human needs: ‘learning ability’, ‘recreational activities’, ‘contact with others’, ‘mobility/body posture’, ‘communication’ and ‘avoiding danger’. However, they recommended further improvement in all fourteen components of human needs.</div></div><div><h3>Conclusions</h3><div>Coach Pepper had no significant psychosocial effects on informal caregivers of people with dementia. Qualitative findings demonstrated the participants' positive attitudes but highlighted a need for improvements regarding Coach Pepper's usability.</div></div><div><h3>Registration</h3><div><span><span>NCT03818217</span><svg><path></path></svg></span> (date of registration: 09.01.2019; date of first recruitment: 04.02.
背景:全球痴呆症发病率正在上升,影响着医疗保健系统和社会。痴呆症患者的照护主要由非正式照护者(例如家人、朋友)提供,这可能带来重大挑战并增加照护者的负担。类人社交辅助机器人等新技术有望减轻这一负担,因为这类机器人被认为是非正式护理人员和痴呆症患者的辅助设备。目的:探讨人形社会辅助机器人Pepper教练(配备了针对痴呆症患者的基于平板电脑的多模式培训等功能)与专门针对痴呆症患者的基于平板电脑的多模式培训对非正式护理人员的心理社会影响。此外,非正式护理人员的态度和经验的教练胡椒进行了检查。设计:采用嵌套定性研究的随机对照平行双臂试验。环境:研究在家庭环境中进行(即私人家庭)。参与者:32名痴呆症患者的非正式护理人员参与了这项研究。方法:非正式护理人员(及其所爱的痴呆症患者)被随机分配到Pepper教练组(n = 16)或完全基于平板电脑的多模式训练组(n = 16),为期三周。在基线和干预后,通过标准化问卷收集照顾者的数据,包括照顾者负担(主要结局)、生活质量、抑郁症状和影响。此外,对两组的接受度进行了测量,并在干预后对Coach Pepper组进行了半结构化访谈。结果:在结果中,各组之间的平均变化没有显著差异,除了对照组的接受度(有用性和可及性)两个领域的评分明显更高。质性调查结果显示,大多数人对佩珀教练的痴呆症护理持积极态度,对照顾者负担持中立态度。护理人员报告说,在人类需求的六个组成部分:“学习能力”、“娱乐活动”、“与他人接触”、“行动/身体姿势”、“沟通”和“避免危险”方面,Pepper教练是有用的。但是,他们建议进一步改善人类需要的所有14个组成部分。结论:佩珀教练对痴呆症患者的非正式照顾者没有显著的心理社会影响。定性调查结果显示了参与者的积极态度,但也强调了Coach Pepper的可用性需要改进。注册:NCT03818217(注册日期:09.01.2019;首次招聘日期:2019年2月4日)。
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引用次数: 0
Survivorship concerns among posttreatment cancer survivors in South Korea: A secondary analysis of a cross-sectional survey 韩国癌症治疗后幸存者的生存问题:一项横断面调查的二次分析。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104982
Soo Hyun Kim
<div><h3>Background</h3><div>Cancer survivors may have a variety of survivorship concerns despite their cancer treatment having ended, with some negatively affecting their health-related quality of life. An in-depth understanding of survivorship concerns is essential for the development of survivorship care programs. However, previous findings have been limited to Western countries, and evidence from Asian countries is lacking.</div></div><div><h3>Objective</h3><div>This study aimed to examine the prevalence of survivorship concerns among posttreatment cancer survivors in South Korea, identify factors associated with survivorship concerns, and explore their relationship with health-related quality of life.</div></div><div><h3>Design</h3><div>Secondary analysis of a cross-sectional survey.</div></div><div><h3>Setting</h3><div>Data were collected through an online survey of five online communities of cancer survivors in South Korea.</div></div><div><h3>Participants</h3><div>Overall, 1019 cancer survivors diagnosed with breast, colorectal, lung, stomach, and thyroid cancer (top five cancers in South Korea) who completed their cancer treatment.</div></div><div><h3>Methods</h3><div>The survey collected data on demographic, disease- and treatment-related characteristics, survivorship concerns, and health-related quality of life. Survivorship concerns were measured using the checklist for survivorship concerns from the National Comprehensive Cancer Network Guidelines for Cancer Survivorship, which includes 12 survivorship concerns (e.g. cardiac toxicity, distress, cognitive dysfunction, fatigue, lymphoedema). Health-related quality of life was assessed using the Korean version of the 30-item European Organisation for Research and Treatment of Cancer Quality of Life Core Questionnaire. Data were analysed using descriptive statistics, the Chi-square test, and multiple regression.</div></div><div><h3>Results</h3><div>The prevalence of survivorship concerns ranged from 34.7 % to 78.4 %. Fatigue (78.4 %), unhealthy lifestyle (74.8 %), cognitive dysfunction (60.5 %), insomnia (58.9 %), and distress (52.9 %) were the five most frequent concerns. Survivors aged in their 50s, those diagnosed with stomach cancer, those with an elapsed time of ≥<!--> <!-->2 years but <<!--> <!-->5 years since diagnosis, and those who had received chemotherapy and/or radiotherapy were significantly more likely to report survivorship concerns. Regression analyses revealed that all survivorship concerns were significant predictors of one or more subscales of health-related quality of life. Distress was found to be a significant predictor of all six subscales of the European Organisation for Research and Treatment of Cancer Quality of Life Core Questionnaire.</div></div><div><h3>Conclusions</h3><div>This study revealed that posttreatment cancer survivors in South Korea had various survivorship concerns that decreased their health-related quality of life. To improve their health-rel
背景:尽管癌症治疗已经结束,但癌症幸存者可能有各种各样的生存问题,其中一些对他们的健康相关生活质量产生了负面影响。对幸存者关怀的深入了解对于幸存者关怀项目的发展至关重要。然而,先前的研究结果仅限于西方国家,缺乏来自亚洲国家的证据。目的:本研究旨在研究韩国癌症治疗后幸存者中生存担忧的患病率,确定与生存担忧相关的因素,并探讨它们与健康相关生活质量的关系。设计:对横断面调查进行二次分析。背景:数据是通过对韩国五个癌症幸存者在线社区的在线调查收集的。参与者:总共有1019名被诊断患有乳腺癌、结肠直肠癌、肺癌、胃癌和甲状腺癌(韩国五大癌症)的癌症幸存者完成了癌症治疗。方法:调查收集了人口统计学、疾病和治疗相关特征、生存关注和健康相关生活质量的数据。使用《国家癌症综合网络癌症生存指南》中的生存问题清单来测量生存问题,其中包括12个生存问题(如心脏毒性、窘迫、认知功能障碍、疲劳、淋巴水肿)。与健康相关的生活质量是用韩国版的30项欧洲癌症研究和治疗组织生活质量核心问卷进行评估的。数据分析采用描述性统计、卡方检验和多元回归。结果:生存担忧的患病率从34.7%到78.4%不等。疲劳(78.4%)、不健康的生活方式(74.8%)、认知功能障碍(60.5%)、失眠(58.9%)和焦虑(52.9%)是五个最常见的问题。年龄在50岁以上的幸存者,被诊断为胃癌的幸存者,生存时间≥2年的幸存者,但结论:本研究显示,韩国治疗后的癌症幸存者存在各种生存担忧,这些担忧降低了他们与健康相关的生活质量。为了改善他们与健康相关的生活质量,系统地筛查生存问题和及时适当的干预措施至关重要。因此,我们的研究结果可以为亚洲有针对性的生存护理项目的发展做出贡献。研究注册:未注册。
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引用次数: 0
Job satisfaction among hospital nurses: An updated literature review 医院护士工作满意度:最新文献回顾
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.ijnurstu.2024.104964
Yang Zhao , Hong Lu , Xiu Zhu , Guihua Xiao

Background

Nurses' job satisfaction has long been a global concern because of the critical significance it holds on nurse turnover and the quality and safety of patient care.

Objectives

To perform an updated literature review of the newly emerging studies on job satisfaction among hospital nurses.

Design

Literature review.

Data sources

Ten electronic database (PubMed, Web of Science, Embase, CINAHL, PsycINFO, Applied Social Sciences Index, CNKI, SinoMed, CQVIP, WanFang) were searched for studies published between September 2018 and May 2024.

Review methods

Studies were included if they published in English or Chinese and focused on job satisfaction of qualified general nurses working in acute care hospitals. Data extraction, synthesis and content analysis were performed.

Results

Of the 28,584 studies originally identified, 52 studies were included in the final review. Thirty-eight influencing factors and twenty-nine predictors of nurses' job satisfaction across the domains of demographic characteristics, individual cognition and behaviors, and working environment and management were newly added in this updated review. Sixty-five factors, which were further grouped into eight subcategorizations: demographic characteristics, personality traits, emotion, behaviors, psychological and cognitive factors, organizational climate, leadership and management, were additionally identified as related factors of nurses' job satisfaction. Factors relating to nurses' individual cognition and behaviors mainly played mediating roles in the mediating pathways linking various factors with job satisfaction.

Conclusions

This review provides improved understanding of nurses' job satisfaction. Future studies could further explore the mechanisms by which factors relating to working environment and management predict or affect nurses' job satisfaction. The newly identified intrinsic factors from the mediating or moderating pathways offered valuable intervention insights for the improvement of nurses' job satisfaction.
护士的工作满意度长期以来一直是全球关注的问题,因为它对护士的流动和病人护理的质量和安全具有至关重要的意义。
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引用次数: 0
期刊
International Journal of Nursing Studies
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