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Predictors of recovery from dysphagia after stroke: A systematic review and meta-analysis 中风后吞咽困难恢复的预测因素:系统回顾和荟萃分析
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.002
Xiaoyan Jin , Shaomei Shang , HoiYee Tong , Ming Liu , Dan Li , Ying Xiao

Objective

This systematic review aimed to identify the predictors of recovery from dysphagia after stroke in the last ten years, thereby providing an evidence-based basis for nurses to identify high-risk patients and develop individualized rehabilitation plans to improve patient prognosis.

Methods

Databases including the China National Knowledge Infrastructure (CNKI), China Biology Medicine disc (CBMdisc), China Science and Technology Journal (VIP), WanFang, PubMed, Embase, CINAHL, Web of Science, the Cochrane Library, and Scopus were retrieved to search for literature on the predictors of recovery from dysphagia after stroke. The retrieval period was from January 2013 to December 2023. The quality of studies was assessed using the Newcastle-Ottawa Scale (NOS) and the Prediction model Risk of Bias Assessment Tool (PROBAST). Meta-analysis was performed using Revman5.3 and Stata15.1 software. The review protocol has been registered with PROSPERO (CRD42024605570).

Results

A total of 1,216 results were obtained, including 599 in English and 617 in Chinese. A total of 34 studies were included, involving 156,309 patients with post-stroke dysphagia, and the rate of dysphagia recovery increased from 13.53% at 1 week to 95% at 6 months after stroke. Meta-analysis results showed that older age [OR = 1.06, 95%CI (1.04, 1.08), P < 0.001], lower BMI [OR = 1.28, 95%CI (1.17, 1.40), P < 0.001], bilateral stroke [OR = 3.10, 95%CI (2.04, 4.72), P < 0.001], higher National Institutes of Health Stroke Scale (NIHSS) score [OR = 1.19, 95%CI (1.01, 1.39), P = 0.030], tracheal intubation [OR = 5.08, 95%CI (1.57, 16.39), P = 0.007] and aspiration [OR = 4.70, 95%CI (3.06, 7.20), P < 0.001] were unfavorable factors for the recovery of swallowing function in patients with post-stroke dysphagia.

Conclusions

The lack of standardized criteria for rehabilitation assessment of post-stroke dysphagia has resulted in reported recovery rates of swallowing function exhibiting wide variability. Nurses should take targeted preventive measures for patients aged ≥70 years, low BMI, bilateral stroke, high NIHSS score, tracheal intubation, and aspiration to promote the recovery of swallowing function in patients with post-stroke dysphagia.
目的探讨近十年脑卒中后吞咽困难患者康复的影响因素,为护士识别高危患者,制定个性化康复计划,改善患者预后提供循证依据。方法检索中国国家知识基础设施(CNKI)、中国生物医学磁盘(CBMdisc)、中国科学技术期刊(VIP)、万方、PubMed、Embase、CINAHL、Web of Science、Cochrane Library、Scopus等数据库,检索脑卒中后吞咽困难康复预测因素的相关文献。检索期为2013年1月至2023年12月。采用纽卡斯尔-渥太华量表(NOS)和预测模型偏倚风险评估工具(PROBAST)对研究质量进行评估。采用Revman5.3和Stata15.1软件进行meta分析。审查方案已在PROSPERO注册(CRD42024605570)。结果共获得1216条结果,其中英文599条,中文617条。共纳入34项研究,涉及156309例卒中后吞咽困难患者,卒中后1周吞咽困难恢复率从13.53%上升到6个月时的95%。meta分析结果显示,老年患者[OR = 1.06, 95%CI (1.04, 1.08), P <;0.001),低BMI (OR = 1.28, 95% ci (1.17, 1.40), P & lt;0.001),双边中风(OR = 3.10, 95% ci (2.04, 4.72), P & lt;0.001]、较高的美国国立卫生研究院卒中量表(NIHSS)评分[OR = 1.19, 95%CI (1.01, 1.39), P = 0.030]、气管插管[OR = 5.08, 95%CI (1.57, 16.39), P = 0.007]和误吸[OR = 4.70, 95%CI (3.06, 7.20), P <;0.001]是脑卒中后吞咽困难患者吞咽功能恢复的不利因素。结论卒中后吞咽困难的康复评估缺乏标准化的标准,导致吞咽功能的恢复率存在很大的差异。护理人员应对年龄≥70岁、BMI低、双侧卒中、NIHSS评分高的患者、气管插管、误吸等采取针对性预防措施,促进卒中后吞咽困难患者吞咽功能恢复。
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引用次数: 0
Psychological effects of virtual reality intervention on breast cancer patients with different personalities: A randomized controlled trial 虚拟现实干预对不同性格乳腺癌患者的心理影响:一项随机对照试验
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.008
Shanshan Wu , Guodu Liu , Jie Yang , Xinxin Xie , Mei-E Wu , Lili Wang , Yanhui Zhang , Jinmei Chen , Xiaowei Wang , Wanjiao Li , Yihong Qiu , Jie Chen

Objectives

To explore the efficacy and safety of virtual reality (VR) in relieving negative emotions in patients with breast cancer with different personalities.

Methods

A randomized controlled trial was conducted. Between April 2023 and October 2023, we enrolled patients with breast cancer treated in the Department of Breast Cancer and Oncology at Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangdong Province. The patients were randomly divided into an intervention group (n = 118) and a control group (n = 119) using block randomization. The intervention group received the VR intervention 3 – 5 times over 5 ± 2 weeks using natural landscapes with music or relaxation guidance, and the duration of each VR intervention was 15 ± 3 min. The control group received routine nursing care, including disease education and psychological counseling. Patients were assessed using the Type D Scale, Positive and Negative Affect Scale, and Distress Thermometer, and adverse events during the intervention were recorded.

Results

Overall, 85 patients completed the study (44 in the intervention group and 41 in the control group). Patients with Type D personalities showed more negative emotions [25.0 (21.5, 27.5) vs. 19.0 (16.0, 24.0), P = 0.001] and distressed attitudes [4.0 (2.0, 5.0) vs. 3.0 (1.0, 4.0), P = 0.020] with fewer positive emotions (27.2 ± 5.6 vs. 31.0 ± 5.9, P = 0.014) than those with non-Type D personalities. Total population analysis revealed no significant differences between the groups. However, in the subgroup analysis, patients with Type D personalities in the intervention group showed greater relief from negative emotions than those in the control group [median difference, −5.0 (−9.0, −2.5) vs. −2.0 (−4.0, 2.0), P = 0.046]. No significant differences were found between groups of patients with non-Type D personality traits. The proportion of adverse events was not significantly different between groups (P = 0.110).

Conclusions

Breast cancer patients with Type D personalities suffer more severe negative emotions and distress, and more attention should be paid to them. VR intervention significantly and safely reduced negative emotions in patients with Type D personalities.
目的探讨虚拟现实(VR)技术缓解不同性格乳腺癌患者负性情绪的有效性和安全性。方法采用随机对照试验。在2023年4月至2023年10月期间,我们招募了在广东省中山大学孙逸仙纪念医院乳腺癌肿瘤科接受治疗的乳腺癌患者。采用分组随机法将患者随机分为干预组(118例)和对照组(119例)。干预组采用自然景观、音乐或放松引导进行VR干预3 ~ 5次,每次干预时间15±3 min,共5±2周。对照组接受常规护理,包括疾病教育、心理疏导等。采用D型量表、积极和消极情绪量表、焦虑温度计对患者进行评估,并记录干预期间的不良事件。结果85例患者完成研究(干预组44例,对照组41例)。D型人格患者负性情绪较多[25.0(21.5,27.5)比19.0 (16.0,24.0),P = 0.001],苦恼态度较多[4.0(2.0,5.0)比3.0 (1.0,4.0),P = 0.020],积极情绪较少(27.2±5.6比31.0±5.9,P = 0.014)。总体分析显示各组之间没有显著差异。然而,在亚组分析中,干预组的D型人格患者比对照组的负性情绪得到了更大的缓解[中位差为- 5.0(- 9.0,- 2.5)比- 2.0 (- 4.0,2.0),P = 0.046]。非D型人格特征患者组间无显著差异。不良事件发生率组间比较差异无统计学意义(P = 0.110)。结论D型人格的乳腺癌患者负性情绪和痛苦更为严重,应引起重视。VR干预显著且安全地降低了D型人格患者的负性情绪。
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引用次数: 0
The development and application of the mobile frailty management platform for Chinese community-dwelling older adults 中国社区老年人移动衰弱管理平台的开发与应用
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.005
Jiayi Hou , Xinrui Wan , Mengjie Li , Guijuan He

Objectives

This study aimed to develop a mobile frailty management platform for Chinese community-dwelling older adults and evaluate its effectiveness, usability and safety.

Methods

Based on literature research, the research team combined the frailty cycle and integration models, self-determination theory, and technology acceptance models and determined the frailty interventions through expert discussion, then transformed it into multimedia resources, finally, engineers developed the mobile management platform. A cluster sampling, parallel, single-blind, controlled quasi-experimental trial was conducted. Sixty older adults from two community health service centers were recruited from March to August 2023. The control group received routine community care, while the intervention group used the mobile frailty management platform. The incidence of frailty, scores of quality of life, depression, sleep quality, and grip strength within 12 weeks were compared between the two groups, and the availability and safety of the platform were assessed.

Results

A total of 52 participants completed the study, 27 in the intervention group and 25 in the control group. At 12 weeks after the intervention, the frailty state of the intervention group was reversed to pre-frailty. There were no significant differences in the scores of quality of life, depression, sleep quality, and grip strength between the two groups before and 4 weeks after intervention. At 8 weeks and 12 weeks after the intervention, the quality of life, depression, and grip strength of the intervention group were improved with statistical significance (P < 0.05). Sleep quality was statistically significant only 12 weeks after the intervention (P < 0.05). System Usability Scale score for the platform was (87.96 ± 5.88), indicating a highly satisfactory user experience. Throughout the intervention, no adverse events were reported among the older adults.

Conclusions

The mobile frailty management platform effectively improved frailty status, depressive mood, sleep quality, grip strength, and quality of life for Chinese community-dwelling older adults. It holds clinical application value and is an effective tool for strengthening frailty management among Chinese community-dwelling older adults.
本研究旨在为中国社区老年人开发一个移动虚弱管理平台,并评估其有效性、可用性和安全性。方法研究团队在文献研究的基础上,结合脆弱性循环与集成模型、自我决定理论和技术接受模型,通过专家讨论确定脆弱性干预措施,并将其转化为多媒体资源,最后由工程师开发移动管理平台。采用整群抽样、平行、单盲、对照准实验方法进行研究。研究人员于2023年3月至8月从两个社区卫生服务中心招募了60名老年人。对照组采用常规社区护理,干预组采用移动衰弱管理平台。比较两组患者12周内的虚弱发生率、生活质量评分、抑郁评分、睡眠质量评分和握力评分,并评估平台的可用性和安全性。结果52人完成研究,干预组27人,对照组25人。干预12周后,干预组虚弱状态恢复到虚弱前状态。干预前和干预后4周,两组患者的生活质量、抑郁、睡眠质量、握力得分均无显著差异。干预后8周和12周,干预组患者的生活质量、抑郁情绪、握力均有改善,差异均有统计学意义(P <;0.05)。干预后仅12周睡眠质量有统计学意义(P <;0.05)。该平台的系统可用性量表得分为(87.96±5.88),用户体验非常满意。在整个干预过程中,老年人中没有报告不良事件。结论移动衰弱管理平台可有效改善中国社区老年人的衰弱状态、抑郁情绪、睡眠质量、握力和生活质量。具有临床应用价值,是加强我国社区老年人衰弱管理的有效工具。
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引用次数: 0
The relationship between proxy decision-making content and cues by families of patients with malignant brain tumor: A descriptive qualitative study 恶性脑肿瘤患者家属代理决策内容与提示的关系:一项描述性质的研究
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.001
Runa Tokunaga , Fumiyo Ishikawa

Objectives

This study aimed to clarify the relationship between the content of proxy decision-making made by families of patients with malignant brain tumors regarding treatment policies and daily care and the cues leading to those decisions.

Methods

Semi-structured personal interviews were used to collect data. Seven family members of patients with malignant brain tumors were selected to participate in the study by purposive sampling method from June to August 2022 in the Patient Family Association of Japan. Responses were content analyzed to explore the relationship between the content of decisions regarding “treatment policies” and “daily care” and the cues influencing those decisions. Semi-structured interviews were analyzed by using thematic analysis.

Results

The contents of proxy decisions regarding “treatment policies” included implementation, interruption, and termination of initial treatments, free medical treatments, use of respirators, and end-of-life sedation and included six cues: treatment policies suggested by the primary physician, information and knowledge about the disease and treatment obtained by the family from limited resources, perceived life threat from symptom worsening, words and reactions from the patient regarding treatment, patient’s personality and way of life inferred from their treatment preferences, family’s thoughts and values hoping for better treatment for the patient. Decisions for “daily care” included meal content and methods, excretion, mobility, maintaining cleanliness, rehabilitation, continuation or resignation from work, treatment settings (outpatient or inpatient), and ways to spend time outside and included seven cues: words and thoughts from the patient about their way of life, patient’s reactions and life history inferred from their preferred way of living, things the patient can do to maintain daily life and roles, awareness of the increasing inability to do things in daily life, family’s underlying thoughts and values about how to spend the remaining time, approval from family members regarding the care setting, advice from medical professionals on living at home.

Conclusions

For “treatment policies,” guidelines from medical professionals were a key cue, while for “daily care,” the small signs from the patients in their daily lives served as cues for proxy decision-making. This may be due to the lack of information available to families and the limited time available for discussion with the patient. Families of patients with malignant brain tumors repeatedly use multiple cues to make proxy decision-making under high uncertainty. Therefore, nurses supporting proxy decision-making should assess the family’s situation and provide cues that facilitate informed and confident decisions.
目的探讨恶性脑肿瘤患者家属在治疗政策、日常护理等方面的代理决策内容与决策线索之间的关系。方法采用半结构化个人访谈法收集资料。采用有目的抽样的方法,于2022年6月至8月在日本患者家庭协会中选取7名恶性脑肿瘤患者的家庭成员参与研究。对回应进行内容分析,以探索关于“治疗政策”和“日常护理”的决定内容与影响这些决定的线索之间的关系。采用主题分析法对半结构化访谈进行分析。结果“治疗政策”代理决策的内容包括初始治疗的实施、中断和终止、免费医疗、使用呼吸机和临终镇静,并包括6个线索:主治医生建议的治疗政策、家庭从有限资源中获得的疾病和治疗信息和知识、症状恶化所感知到的生命威胁、患者对治疗的言语和反应、患者从治疗偏好中推断出的个性和生活方式、家属希望患者得到更好治疗的想法和价值观。“日常护理”的决定包括膳食内容和方法、排泄、活动、保持清洁、康复、继续或放弃工作、治疗环境(门诊或住院)以及户外活动的方式,并包括七个线索:病人对自己生活方式的话语和想法,病人的反应和从他们喜欢的生活方式推断的生活史,病人可以做的事情来维持日常生活和角色,意识到越来越无法在日常生活中做事情,家人对如何度过剩余时间的潜在想法和价值观,家庭成员对护理环境的认可,医疗专业人员对在家生活的建议。结论对于“治疗政策”,医疗专业人员的指导方针是关键线索,而对于“日常护理”,患者日常生活中的小迹象是代理决策的线索。这可能是由于家庭缺乏可用的信息以及与患者讨论的时间有限。恶性脑肿瘤患者家属在高不确定性下反复使用多种线索进行代理决策。因此,支持代理决策的护士应评估家庭的情况,并提供线索,以促进知情和自信的决定。
{"title":"The relationship between proxy decision-making content and cues by families of patients with malignant brain tumor: A descriptive qualitative study","authors":"Runa Tokunaga ,&nbsp;Fumiyo Ishikawa","doi":"10.1016/j.ijnss.2025.02.001","DOIUrl":"10.1016/j.ijnss.2025.02.001","url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to clarify the relationship between the content of proxy decision-making made by families of patients with malignant brain tumors regarding treatment policies and daily care and the cues leading to those decisions.</div></div><div><h3>Methods</h3><div>Semi-structured personal interviews were used to collect data. Seven family members of patients with malignant brain tumors were selected to participate in the study by purposive sampling method from June to August 2022 in the Patient Family Association of Japan. Responses were content analyzed to explore the relationship between the content of decisions regarding “treatment policies” and “daily care” and the cues influencing those decisions. Semi-structured interviews were analyzed by using thematic analysis.</div></div><div><h3>Results</h3><div>The contents of proxy decisions regarding “treatment policies” included implementation, interruption, and termination of initial treatments, free medical treatments, use of respirators, and end-of-life sedation and included six cues: treatment policies suggested by the primary physician, information and knowledge about the disease and treatment obtained by the family from limited resources, perceived life threat from symptom worsening, words and reactions from the patient regarding treatment, patient’s personality and way of life inferred from their treatment preferences, family’s thoughts and values hoping for better treatment for the patient. Decisions for “daily care” included meal content and methods, excretion, mobility, maintaining cleanliness, rehabilitation, continuation or resignation from work, treatment settings (outpatient or inpatient), and ways to spend time outside and included seven cues: words and thoughts from the patient about their way of life, patient’s reactions and life history inferred from their preferred way of living, things the patient can do to maintain daily life and roles, awareness of the increasing inability to do things in daily life, family’s underlying thoughts and values about how to spend the remaining time, approval from family members regarding the care setting, advice from medical professionals on living at home.</div></div><div><h3>Conclusions</h3><div>For “treatment policies,” guidelines from medical professionals were a key cue, while for “daily care,” the small signs from the patients in their daily lives served as cues for proxy decision-making. This may be due to the lack of information available to families and the limited time available for discussion with the patient. Families of patients with malignant brain tumors repeatedly use multiple cues to make proxy decision-making under high uncertainty. Therefore, nurses supporting proxy decision-making should assess the family’s situation and provide cues that facilitate informed and confident decisions.</div></div>","PeriodicalId":37848,"journal":{"name":"International Journal of Nursing Sciences","volume":"12 2","pages":"Pages 169-175"},"PeriodicalIF":2.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143737795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Public participation willingness in out-of-hospital cardiopulmonary resuscitation: A systematic review and meta-analysis 院外心肺复苏公众参与意愿:系统回顾与荟萃分析
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.012
Yuqiu Cheng , Chunzhi Zhang , Li Chen , Hongjun Liu , Wanling He , Zeya Shi

Objective

This systematic review and meta-analysis aimed to identify the main factors influencing the public’s willingness to participate in out-of-hospital emergency care.

Methods

Studies were searched in online databases, including PubMed, Embase, Web of Science, and the Cochrane Library. The articles included in this review were published from inception to July 31, 2024. The Iain Crombie assessment tool was used to assess study quality. Meta-analysis was performed using RevMan (version 5.4) software. The review protocol has been registered with PROSPERO (CRD42024570491).

Results

A total of 1,434 research articles were initially identified, among which 18 were incorporated into this study, and all of the included studies were cross-sectional. Meta-analysis results demonstrated that gender (male; OR = 1.37, 95%CI: 1.28–1.47), profession (healthcare provider; OR = 0.17, 95%CI: 0.06–0.47), knowledge and skill level (OR = 1.63, 95%CI: 1.25–2.11), willingness to undergo training (OR = 2.68, 95%CI: 1.89–3.79), interest in first aid (OR = 2.08, 95%CI: 1.60–2.69), previous training (OR = 2.14, 95%CI: 1.49–3.08), and previous first-aid experience (OR = 1.70, 95%CI: 1.37–2.11) were the principal influencing factors of the public’s willingness to engage in out-of-hospital cardiopulmonary resuscitation.

Conclusion

Demographic factors, knowledge, belief, and behavior are crucial in influencing public emergency decision-making. Medical personnel could create specialized training programs based on relevant factors to enhance the public's willingness to engage in out-of-hospital CPR.
目的通过系统回顾和荟萃分析,探讨影响公众参与院外急救意愿的主要因素。方法在PubMed、Embase、Web of Science和Cochrane Library等在线数据库中检索研究。本综述纳入的文章发表时间为创刊至2024年7月31日。采用Iain Crombie评估工具评估研究质量。采用RevMan (version 5.4)软件进行meta分析。审查方案已在PROSPERO注册(CRD42024570491)。结果初步筛选出1434篇研究论文,其中18篇纳入本研究,纳入研究均为横断面研究。meta分析结果显示,性别(男性;OR = 1.37, 95%CI: 1.28-1.47),职业(医疗保健提供者;OR = 0.17, 95%CI: 0.06-0.47)、知识和技能水平(OR = 1.63, 95%CI: 1.25-2.11)、接受培训的意愿(OR = 2.68, 95%CI: 1.89-3.79)、对急救的兴趣(OR = 2.08, 95%CI: 1.60-2.69)、既往培训(OR = 2.14, 95%CI: 1.49-3.08)、既往急救经验(OR = 1.70, 95%CI: 1.37-2.11)是影响公众参与院外心肺复苏意愿的主要因素。结论人口因素、知识、信念和行为是影响突发公共事件决策的重要因素。医务人员可根据相关因素制定专门的培训方案,提高公众参与院外心肺复苏术的意愿。
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引用次数: 0
Digital components and interaction types in counseling interventions for childhood and adolescent obesity: A systematic review 儿童和青少年肥胖咨询干预的数字成分和互动类型:系统综述
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.014
Mari Virtanen , Heli Kerimaa , Niko Männikkö , Merja Männistö , Karoliina Paalimäki-Paakki , Minna Lahtinen , Miia Jansson , Kirsi Kivelä , Anne Oikarinen , Mira Rajala , Minna Vanhanen , Maria Kääriäinen , Pirjo Kaakinen

Objectives

Childhood and adolescent obesity are an increasing global health concern. This study aimed to evaluate the effectiveness of digital components and interaction types in counseling interventions for prevention and treatment.

Methods

All studies were searched in online databases and grey literature, including PubMed (Medline), Web of Science, CINAHL, Scopus, IEEE Xplore Digital Library, Journal of Medical Internet Research (JMIR), MedNar, EBSCO Open Dissertations. The search period is from inception to June 2023, and the languages are Finnish, English and Swedish. The research quality was evaluated using the web-based data management system Covidence for prevalence studies. The study protocol was registered with PROSPERO (registration number: CRD42021247595).

Results

In this review, 4,407 studies were screened, and 22 were included. These involved 3,433 participants and 264 child-parent pairs. The digital approaches included multicomponent elements like internet platforms, text messaging, video conferencing, online communities, wearable technology, and mobile apps, allowing one-way, two-way, and face-to-face interactions. Two studies showed statistically significant effects of treatment on BMI and waist-to-hip ratio. Most interventions reported positive outcomes, with no significant differences between groups, and none showed null effects during follow-up.

Conclusions

Digital multicomponents like mobile apps and wearables can help obese children and adolescents adopt healthier lifestyles. While these interventions show promise for obesity management, further research is needed to assess their effectiveness, particularly regarding nurses’ perspectives.
儿童和青少年肥胖是一个日益严重的全球健康问题。本研究旨在评估数字组件和交互类型在预防和治疗咨询干预中的有效性。方法检索PubMed (Medline)、Web of Science、CINAHL、Scopus、IEEE Xplore数字图书馆、Journal of Medical Internet Research (JMIR)、MedNar、EBSCO Open Dissertations等在线数据库和灰色文献。搜索期从开始到2023年6月,语言为芬兰语、英语和瑞典语。使用基于网络的流行病学研究数据管理系统covid - ence对研究质量进行评估。研究方案已在PROSPERO注册(注册号:CRD42021247595)。结果本综述共筛选4407项研究,纳入22项。这些研究涉及3,433名参与者和264对亲子对。数字方式包括多组件元素,如互联网平台、短信、视频会议、在线社区、可穿戴技术和移动应用程序,允许单向、双向和面对面的互动。两项研究显示,治疗对BMI和腰臀比有统计学意义上的显著影响。大多数干预措施报告了积极的结果,组间无显著差异,随访期间没有任何无效效果。结论移动应用和可穿戴设备等数字化多组件可以帮助肥胖儿童和青少年养成更健康的生活方式。虽然这些干预措施显示出肥胖管理的希望,但需要进一步的研究来评估其有效性,特别是从护士的角度来看。
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引用次数: 0
Associations between depression, resilience, and fatigue in patients with multivessel coronary disease: A cross-lag study 多支冠状动脉疾病患者抑郁、恢复力和疲劳之间的关系:一项交叉滞后研究
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.009
Binbin Sun , Jing Han , Beibei Tian , Yuexuan Xu , Jin Wang , Jianhui Wang

Objectives

This study aimed to examine the associations between depression, resilience, and fatigue in patients with multivessel coronary disease and verify their causal relationships.

Methods

Between October 2023 and June 2024, 316 patients with multivessel coronary disease were recruited from three tertiary hospitals in Tangshan, China. The Patient Health Questionnaire, Connor-Davidson Resilience Scale, and the Multidimensional Fatigue Inventory were administered to the patients on the third day of admission (T1), one month after discharge (T2), and three months after discharge (T3). Pearson correlation analysis was conducted to examine the relationships among depression, resilience, and fatigue in patients with multivessel coronary disease, and cross-lagged analysis to explore the temporal causal relationships.

Results

In patients with multivessel coronary disease, levels of depression and fatigue decreased from T1 to T3, while resilience scores increased during the same period. The correlation analysis revealed significant relationships among depression, resilience, and fatigue at T1, T2, and T3 (P < 0.01). The autoregressive paths indicated high stability over time for depression, medium stability for resilience, and low stability for fatigue. Cross-lagged paths demonstrated that depression at T1 significantly predicted fatigue at T2 (β = 0.461, P < 0.001), and depression at T2 significantly predicted fatigue at T3 (β = 0.957, P < 0.001). And resilience at T1 significantly predicted fatigue at T2 (β = −0.271, P < 0.001), and resilience at T2 significantly predicted fatigue at T3 (β = −0.176, P < 0.001). Additionally, resilience had a moderating effect on the relationship between depression and fatigue (β = −0.760, P < 0.001).

Conclusions

Our study confirmed that depression and resilience predicted fatigue in patients with multivessel coronary disease. To prevent and mitigate fatigue, alleviating depressive symptoms and enhancing resilience levels in patients at an early stage is essential.
目的本研究旨在探讨多支冠状动脉疾病患者抑郁、恢复力和疲劳之间的关系,并验证它们之间的因果关系。方法于2023年10月至2024年6月,从唐山市三所三级医院招募316例多支冠状动脉病患者。于入院第3天(T1)、出院后1个月(T2)和出院后3个月(T3)对患者进行患者健康问卷、Connor-Davidson弹性量表和多维疲劳量表。采用Pearson相关分析检验多支冠状动脉病患者抑郁、恢复力和疲劳之间的关系,并采用交叉滞后分析探讨时间因果关系。结果多支冠状动脉病变患者的抑郁和疲劳水平在T1 - T3期间呈下降趋势,而恢复力评分在同一时期呈上升趋势。相关分析显示,T1、T2和T3时抑郁、心理弹性和疲劳之间存在显著相关(P <;0.01)。自回归路径显示抑郁随时间的高稳定性,恢复力中等稳定性,疲劳低稳定性。交叉滞后路径显示,T1时的抑郁显著预测T2时的疲劳(β = 0.461, P <;T2时的抑郁显著预测T3时的疲劳(β = 0.957, P <;0.001)。T1时的弹性显著预测T2时的疲劳(β = - 0.271, P <;T2时的弹性显著预测T3时的疲劳(β = - 0.176, P <;0.001)。此外,心理弹性对抑郁和疲劳之间的关系有调节作用(β = - 0.760, P <;0.001)。结论我们的研究证实,抑郁和恢复力可预测多支冠状动脉疾病患者的疲劳。为了预防和减轻疲劳,在早期阶段减轻抑郁症状和提高患者的恢复能力水平至关重要。
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引用次数: 0
Evaluation of the measurement properties of online health information quality assessment tools: A systematic review 在线健康信息质量评估工具测量特性的评估:系统回顾
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-03-01 DOI: 10.1016/j.ijnss.2025.02.015
Yating Li , Hui Ouyang , Gan Lin , Yichao Peng , Jinghui Yao , Yun Chen

Objectives

This study aimed to evaluate the measurement properties and methodological quality of instruments developed to evaluate the quality of online health information.

Methods

In this study, a systematic search was conducted across a range of databases, including the China National Knowledge Infrastructure (CNKI), Wanfang, China Science and Technology Journal (VIP), SinoMed, PubMed, Web of Science, CINAHL, Embase, the Cochrane Library, PsycINFO, and Scopus. The search period spanned from the inception of the databases to October 2023. Two researchers independently conducted the literature screening and data extraction. The methodological quality of the included studies was assessed using the Consensus-based Standards for the Selection of Health Measurement Instruments (COSMIN) Risk of Bias checklist. The measurement properties were evaluated using the COSMIN criteria. The modified Grading, Recommendations, Assessment, Development, and Evaluation (GRADE) system was used to determine the quality grade.

Results

A total of 18 studies were included, and the measurement properties of 17 scales were assessed. Fifteen scales had content validity, three had structural validity, six had internal consistency, two had test-retest reliability, nine had interrater reliability, one had measurement error, six instruments had criterion validity, and three scales had hypotheses testing for construct validity; however, the evaluation of their methodological quality and measurement properties revealed deficiencies. Of these 17 scales, 15 were assigned a Level B recommendation, and two received a Level C recommendation.

Conclusions

The Health Information Website Evaluation Tool (HIWET) can be temporarily used to evaluate the quality of health information on websites. The Patient Education Materials Assessment Tool (PEMAT) can temporarily assess the quality of video-based health information. However, the effectiveness of both tools needs to be further verified.
目的评价在线健康信息质量评价工具的测量特性和方法学质量。方法系统检索中国知网(CNKI)、万方、中国科技期刊(VIP)、中国医学信息网(sinmed)、PubMed、Web of Science、CINAHL、Embase、Cochrane Library、PsycINFO和Scopus等数据库。搜索期从数据库建立到2023年10月。两位研究者独立进行文献筛选和数据提取。采用基于共识的健康测量工具选择标准(COSMIN)偏倚风险检查表对纳入研究的方法学质量进行评估。使用COSMIN标准评估测量性能。采用改进的分级、建议、评估、发展和评价(GRADE)系统来确定质量等级。结果共纳入18项研究,评估了17种量表的测量性质。15个量表具有内容效度,3个量表具有结构效度,6个量表具有内部一致性,2个量表具有重测信度,9个量表具有内部信度,1个量表具有测量误差,6个量表具有标准效度,3个量表具有结构效度的假设检验;然而,对其方法质量和测量特性的评估显示出不足之处。在这17个量表中,15个被定为B级建议,2个被定为C级建议。结论健康信息网站评价工具(HIWET)可临时用于评价网站健康信息的质量。患者教育材料评估工具(PEMAT)可以临时评估基于视频的健康信息的质量。然而,这两种工具的有效性需要进一步验证。
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引用次数: 0
Advance care planning readiness among older adults in aged service centers: A cross-sectional study 在老年服务中心的老年人中提前护理计划准备:一项横断面研究
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-01-01 DOI: 10.1016/j.ijnss.2024.12.005
Kalok Wong , Haobin Yuan , Stephen Tee , Sinkei Cheong

Objective

This study aimed to explore the readiness for advance care planning (ACP) among older adults in Macau’s day service centers and investigate the influencing factors.

Methods

A cross-sectional study was conducted from October to December 2022 using a convenience sampling method. A total of 312 older adults were selected from 13 day service centers for older adults in Macau, China. The Advance Care Planning Acceptance Questionnaire and the Family Adaptation, Partnership, Growth, Affection, Resolve (APGAR) Scale were used to survey the older adults.

Results

A total of 306 older adults completed the survey. The score for advance care planning readiness was 65.55 ± 10.69, and 59.5% of participants (n = 182) were willing to participate in ACP. The family function score was 7.24 ± 2.51, while 70.3% of participants were from a highly functional family. The higher family function indicating a higher readiness for advance care planning (r = 0.396, P < 0.001). The multiple linear regression analysis indicated that the variables “age,” “knowledge of ACP,” “experience with ACP,” and “received resuscitation of yourself, relatives or friends” combined with “family function” can influence advance care planning readiness among older adults (R2 = 0.317, F = 27.898, P < 0.001).

Conclusions

Older adults in Macau’s day service centers were willing to engage in ACP. The importance of family involvement is highlighted in the ACP readiness. Health education and improved family communication are vital for promoting ACP, which ensures individuals receive care when they lack the capacity to make that choice. Additionally, healthcare professionals should enhance communication and education with older adults during the medical care process.
目的探讨澳门日间服务中心老年人的提前照护计划准备情况及其影响因素。方法于2022年10月至12月采用方便抽样法进行横断面研究。在中国澳门的13个老年人日间服务中心共挑选了312名老年人。采用预先护理计划接受问卷和家庭适应、伙伴关系、成长、情感、决心(APGAR)量表对老年人进行调查。结果共有306名老年人完成了调查。提前护理计划准备得分为65.55±10.69,59.5% (n = 182)的参与者愿意参加ACP。家庭功能得分为7.24±2.51,70.3%的参与者来自高功能家庭。家庭函数越高,对提前护理计划的准备程度越高(r = 0.396, P <;0.001)。多元线性回归分析表明,“年龄”、“ACP知识”、“ACP经历”、“自己或亲友接受过复苏”等变量结合“家庭功能”对老年人的提前护理计划准备程度有影响(R2 = 0.317, F = 27.898, P <;0.001)。结论澳门日间服务中心的成年人有参与ACP的意愿。家庭参与的重要性在非加太计划的准备工作中得到强调。健康教育和改善家庭沟通对促进非加太至关重要,这确保个人在没有能力作出选择时得到照顾。此外,医疗保健专业人员应在医疗护理过程中加强与老年人的沟通和教育。
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引用次数: 0
Current situation and influencing factors of palliative care practice ability among oncology nurses: A multicenter cross-sectional study 肿瘤科护士姑息治疗实践能力现状及影响因素:一项多中心横断面研究
IF 2.9 3区 医学 Q1 NURSING Pub Date : 2025-01-01 DOI: 10.1016/j.ijnss.2024.12.006
Xiaofei Nie , Fanfan Lv , Longti Li , Jia Jia

Objectives

The study aimed to survey the current situation and explore the factors that influence the ability of palliative care practice among oncology nurses.

Methods

A multicenter cross-sectional study was conducted using stratified random sampling to select 26 tertiary hospitals’ oncology departments in Hubei Province, China. A total of 1,198 nurses were included and finished the questionnaire consisting of social demographic characteristics, Palliative Care Self-Report Practice Scale (PCPS), End-of-life Professional Caregiver Survey (EPCS), and Self-Perceived Pain Assessment Knowledge and Confidence Scale (Self-PAC) through the online platform. Data were analyzed using t-test, one-way ANOVA, Pearson correlation analysis, and multiple linear regression analysis in SPSS 26.0.

Results

The total score for PCPS was 67.17 ± 12.57, the three dimensions’ scores were: physical symptom care (32.50 ± 6.10), spiritual and psychological care (23.35 ± 4.97), communication (11.58 ± 2.48). There are significant positive correlations between the palliative care practice ability and core competence (r = 0.77, P < 0.01), as well as pain assessment ability (r = 0.56, P < 0.01). Multiple regression analysis identified female, with high education background (bachelor’s degree and master’s degree or above), interest in palliative care, pain assessment ability, and core competence were positive predictors of palliative care practice ability (Adjusted R2 = 0.668, P < 0.05).

Conclusions

The overall ability of the oncology nurses to practice palliative care was relatively high, but the palliative nurses reported suboptimal performance in the communication dimension of palliative nursing practice ability. To comprehensively improve oncology nurses’ palliative care practice ability, managers must consider the gender structure, educational background, enthusiasm for palliative care work, core competence, and pain assessment ability.
目的调查肿瘤科护士姑息治疗实践能力的现状,探讨影响姑息治疗实践能力的因素。方法采用分层随机抽样的方法,对湖北省26家三级医院肿瘤科进行多中心横断面研究。共纳入1198名护士,通过网络平台完成社会人口学特征问卷、姑息治疗自我报告实践量表(pps)、临终专业照护者调查问卷(EPCS)和自我感知疼痛评估知识与信心量表(Self-PAC)。采用SPSS 26.0软件进行t检验、单因素方差分析、Pearson相关分析和多元线性回归分析。结果ppps总分67.17±12.57分,三个维度得分分别为:躯体症状护理(32.50±6.10)分、精神与心理护理(23.35±4.97)分、沟通(11.58±2.48)分。姑息治疗实践能力与核心竞争力呈显著正相关(r = 0.77, P <;0.01)、疼痛评估能力(r = 0.56, P <;0.01)。多元回归分析发现,女性、高学历(本科及硕士以上学历)、对姑息治疗的兴趣、疼痛评估能力、核心能力是姑息治疗实践能力的正向预测因子(调整后R2 = 0.668, P <;0.05)。结论肿瘤科护士姑息治疗实践能力总体较高,但姑息治疗护士在姑息治疗实践能力沟通维度表现欠佳。要全面提高肿瘤科护士的姑息治疗实践能力,管理者必须考虑护士的性别结构、学历、对姑息治疗工作的热情、核心竞争力和疼痛评估能力。
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引用次数: 0
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International Journal of Nursing Sciences
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