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The impact of exercise during radiotherapy on treatment-related side effects in breast cancer patients: A systematic review and meta-analysis 乳腺癌患者放疗期间运动对治疗相关副作用的影响:系统回顾和荟萃分析。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-30 DOI: 10.1016/j.ijnurstu.2024.104990
XuFei Zheng , PeiQiang Peng , Yue Wang , LinFang Bian , KeXin Zhao , AoWen Shi , ZhongQi Jiang , LiJing Zhao , JunJie Jiang , Shuang Zhang

Purpose

Radiation therapy for breast cancer often causes side effects like cancer-related fatigue, depression, and sleep disorders, impacting health-related quality of life, psychosocial aspects, and physical function. Exercise therapy is commonly used to manage cancer-related fatigue, but its effectiveness remains uncertain due to varying patient conditions and adherence. This systematic review aims to assess exercise interventions during radiotherapy for their effects on physiological and psychological side effects in breast cancer patients, clarifying efficacy and exploring different intervention types.

Methods

Randomized controlled trials were searched in PubMed, EBSCO, Scopus, Web of Science, and the Cochrane Library up to April 24, 2024. Trials included breast cancer patients undergoing exercise therapy (e.g., running, yoga, Qi Gong, resistance training). Primary outcomes were cancer-related fatigue levels and quality of life; secondary outcomes included sleep quality and depressive symptoms.

Results

Sixteen trials with 1373 stage 0 to III breast cancer patients were analyzed. The results indicate that exercise during radiation therapy has a significant positive impact on reducing cancer-related fatigue compared to the control group (SMD = −0.29, 95% CL: −0.56 to −0.02, P = 0.032), subgroup analysis showed that compared to treadmill exercise, Tai Chi, and resistance training with equipment, yoga is more effective in improving cancer-related fatigue in breast cancer patients. Regarding improvement in quality of life (SMD = 0.29, 95 % CI: −0.08 to 0.66, P = 0.121), sleep quality (SMD: −0.27, 95 % CI: −0.62 to 0.07, P = 0.116), and depression (SMD: −0.01, 95 % CI: −0.35 to 0.34, P = 0.977), the three groups did not show significant statistical differences, but they demonstrated beneficial effects in alleviation, which require further studies for confirmation.

Conclusion

Exercise therapy can effectively alleviate cancer-related fatigue in breast cancer patients, with yoga being the most recommended form of exercise. Exercise therapy shows potential for improving quality of life, sleep, and depressive symptoms, necessitating more clinical studies for validation.
目的:乳腺癌放射治疗通常会导致癌症相关的疲劳、抑郁和睡眠障碍等副作用,影响与健康相关的生活质量、心理社会方面和身体功能。运动疗法通常用于治疗癌症相关的疲劳,但由于患者情况和依从性的不同,其有效性仍不确定。本系统综述旨在评估运动干预对乳腺癌放疗患者生理和心理副作用的影响,阐明其疗效,探索不同干预类型。方法:在PubMed、EBSCO、Scopus、Web of Science和Cochrane Library中检索截至2024年4月24日的随机对照试验。试验包括接受运动疗法(如跑步、瑜伽、气功、阻力训练)的乳腺癌患者。主要结局是癌症相关的疲劳水平和生活质量;次要结局包括睡眠质量和抑郁症状。结果:对16项试验1373例0至III期乳腺癌患者进行了分析。结果表明,与对照组相比,放射治疗期间的运动对减轻癌症相关疲劳有显著的积极影响(SMD = -0.29, 95% CL: -0.56至-0.02,P = 0.032),亚组分析显示,与跑步机运动、太极和器械阻力训练相比,瑜伽对改善乳腺癌患者癌症相关疲劳更有效。在生活质量(SMD = 0.29, 95% CI: -0.08 ~ 0.66, P = 0.121)、睡眠质量(SMD: -0.27, 95% CI: -0.62 ~ 0.07, P = 0.116)、抑郁(SMD: -0.01, 95% CI: -0.35 ~ 0.34, P = 0.977)改善方面,三组无显著统计学差异,但在缓解方面表现出有益效果,有待进一步研究证实。结论:运动疗法能有效缓解乳腺癌患者的癌症相关性疲劳,其中瑜伽是最受推荐的运动方式。运动疗法显示出改善生活质量、睡眠和抑郁症状的潜力,需要更多的临床研究来验证。
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引用次数: 0
Conversational agents in physical and psychological symptom management: A systematic review of randomized controlled trials 会话代理在生理和心理症状管理:随机对照试验的系统回顾。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-28 DOI: 10.1016/j.ijnurstu.2024.104991
Qingling Yang , Kin Cheung , Yan Zhang , Yazhou Zhang , Jing Qin , Yao Jie Xie
<div><h3>Background</h3><div>Effective management of physical and psychological symptoms is a critical component of comprehensive care for both chronic disease patients and apparently healthy individuals experiencing episodic symptoms. Conversational agents, which are dialog systems capable of understanding and generating human language, have emerged as a potential tool to enhance symptom management through interactive support.</div></div><div><h3>Objective</h3><div>To examine the characteristics and effectiveness of conversational agent-delivered interventions reported in randomized controlled trials (RCTs) in the management of both physical and psychological symptoms.</div></div><div><h3>Design</h3><div>A systematic review.</div></div><div><h3>Methods</h3><div>A comprehensive search was performed in Pubmed, ACM Digital Library, CINAHL, EMBASE, PyscInfo, Web of Science, Scopus and gray literature sources from their inception to Oct 2024. Search terms included “conversational agent”, “symptom”, “randomized controlled trial” and their synonyms and hyponyms. Duplicates were identified by EndNote, and titles, abstracts and full texts were independently screened according to predefined criteria. Data extraction focused on basic study characteristics and conversational agent details, with The Cochrane Risk of Bias 2.0 tool employed for bias assessment.</div></div><div><h3>Results</h3><div>The search yielded 2756 articles and 29 were finally included for review. The included studies predominantly came from developed countries (n = 23) and were conducted between 2020 and 2024 (n = 24). The studies frequently evaluated the feasibility and acceptability of conversational agent interventions (n = 14), with a predominantly focus on psychological symptoms (depression, anxiety, etc.) (n = 17). A few studies focused on physical symptoms (pain, etc.) (n = 4), while others addressed both symptoms (n = 8). Twenty-five distinct conversational agents (Woebot, Tess, etc.) were evaluated, utilizing platforms ranging from proprietary applications to common messaging channels like WeChat and Facebook Messenger. Cognitive Behavioral Therapy (CBT) was a commonly integrated approach (n = 22), with rule-based dialogs (n = 22) as the most commonly dialog system methods and Natural Language Processing (NLP) (n = 15) as the predominant AI techniques. The median recruitment and completion rates were 72 % and 79 %, respectively. The majority of studies reported positive user experiences and significant symptom management improvements (n = 22). However, risk of bias was high in seventeen studies and presented some concerns in nine others.</div></div><div><h3>Conclusions</h3><div>Conversational agents have shown promise in enhancing both physical and psychological symptom management through positive user experiences and effectiveness. However, the high risk of bias identified in many studies warrants caution in interpreting these findings. Future research should prioritize the me
背景:有效的生理和心理症状管理是慢性疾病患者和经历发作性症状的表面健康个体的综合护理的关键组成部分。会话代理是一种能够理解和生成人类语言的对话系统,已成为通过交互式支持加强症状管理的潜在工具。目的:研究随机对照试验(RCTs)中报告的会话代理提供的干预措施在治疗生理和心理症状方面的特点和有效性。设计:系统回顾。方法:综合检索Pubmed、ACM数字图书馆、CINAHL、EMBASE、PyscInfo、Web of Science、Scopus和灰色文献资源,检索时间自其成立至2024年10月。搜索词包括“会话代理”、“症状”、“随机对照试验”以及它们的同义词和下义词。通过EndNote识别重复,并根据预定义的标准独立筛选标题、摘要和全文。数据提取侧重于基本研究特征和会话代理细节,使用Cochrane Risk of Bias 2.0工具进行偏倚评估。结果:检索到2756篇文章,最终纳入综述29篇。纳入的研究主要来自发达国家(n = 23),在2020年至2024年间进行(n = 24)。这些研究经常评估会话代理干预的可行性和可接受性(n = 14),主要关注心理症状(抑郁、焦虑等)(n = 17)。少数研究关注身体症状(疼痛等)(n = 4),而其他研究关注两种症状(n = 8)。25种不同的会话代理(Woebot、Tess等)被评估,利用的平台从专有应用程序到微信和Facebook Messenger等常见消息传递渠道。认知行为疗法(CBT)是一种常见的综合方法(n = 22),其中基于规则的对话(n = 22)是最常见的对话系统方法,自然语言处理(NLP) (n = 15)是主要的人工智能技术。中位招募率和完成率分别为72%和79%。大多数研究报告了积极的用户体验和显著的症状管理改善(n = 22)。然而,17项研究的偏倚风险较高,另外9项研究存在一些问题。结论:会话代理通过积极的用户体验和有效性,在增强身体和心理症状管理方面显示出希望。然而,在许多研究中发现的高偏倚风险值得在解释这些发现时谨慎。未来的研究应优先考虑随机对照试验的方法学质量,以加强证据基础,支持使用会话代理作为症状管理的补充工具。
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引用次数: 0
Acknowledging: A classic grounded theory explaining how nurses' employ clinical judgement when complying with early warning system protocols 承认:一个经典的有根据的理论,解释护士在遵守早期预警系统协议时如何运用临床判断。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-25 DOI: 10.1016/j.ijnurstu.2024.104989
Justine Connor , Tracy Flenady , Trudy Dwyer , Deb Massey

Background

Recognition and response to clinical deterioration of hospitalised patients is a worldwide health priority area. In response to this concern, international bodies have implemented early warning systems to help clinicians keep people safe and prevent patient deterioration. Registered nurses hold a significant role in managing care provision and utilise early warning system tools to support their clinical judgement when making decisions about patient care.

Objective

To generate a theory explaining how registered nurses employ their clinical judgement when complying with an early warning system protocol.

Design

Classic grounded theory.

Participants

Participants included twenty registered nurses working with early warning systems who are currently employed in a state health care system within Australia. Data were collected via interviews generated from a grand tour question in line with classic grounded theory.

Methods

Classic grounded theory methodology and methods were used. This approach facilitated the identification of the participants main concern and supported the generation of a theory explaining how the participants resolved this issue.

Results

Analysis of data, including associated field notes and memos, identified participants often experienced unease when complying with an early warning system protocol and employing clinical judgement. The mental discomfort participants voiced in the interviews described internal conflicts that are reflective of the term ‘cognitive dissonance’. How the participants sought to resolve their cognitive dissonance, revealed participants' main concern as: Compliance with early warning systems is sometimes incongruent with nurses' use of clinical judgement. The outcome of this study is a grounded theory that explains how nurses resolve this concern through ‘Acknowledging’. Nurses acknowledge the efficacy of early warning systems, whilst valuing their clinical judgement and the importance of patient safety, through the subcategories of Acting and Pausing.

Conclusion

The Theory of Acknowledging explains how nurses overcome their main concern when employing clinical judgement and complying with early warning systems, whilst acknowledging the importance of ensuring patient safety. Reconciling the dissonance caused by trusting their clinical judgement and remaining compliant with early warning systems, enables nurse-led assessment of the patient, promoting patient safety.
Tweetable abstract: The theory of Acknowledging – How nurses employ clinical judgement when complying with early warning systems @Jusconnor25
背景:认识和应对住院患者的临床恶化是一个世界卫生优先领域。针对这一关切,国际机构实施了早期预警系统,以帮助临床医生保证人员安全并防止患者病情恶化。注册护士在管理护理提供方面发挥着重要作用,并利用预警系统工具来支持他们在做出患者护理决定时的临床判断。目的:产生一个理论解释注册护士如何运用他们的临床判断时,遵守预警系统协议。设计:经典接地理论。参与者:参与者包括20名在预警系统工作的注册护士,他们目前在澳大利亚的一个州卫生保健系统工作。数据是通过采访收集的,这些采访是根据经典的扎根理论从一个大旅行问题中产生的。方法:采用经典扎根理论的方法论和方法。这种方法有助于识别参与者的主要关注点,并支持生成一个理论来解释参与者如何解决这个问题。结果:数据分析,包括相关的现场记录和备忘录,确定参与者在遵守早期预警系统协议和采用临床判断时经常感到不安。参与者在访谈中表达的心理不适描述了反映“认知失调”一词的内部冲突。参与者如何寻求解决他们的认知失调,揭示了参与者的主要关注:对早期预警系统的遵守有时与护士使用临床判断不一致。这项研究的结果是一个有根据的理论,解释了护士如何通过“承认”来解决这种担忧。护士承认早期预警系统的有效性,同时重视他们的临床判断和患者安全的重要性,通过行动和暂停的子类别。结论:承认理论解释了护士在使用临床判断和遵守预警系统时如何克服他们的主要担忧,同时承认确保患者安全的重要性。由于信任他们的临床判断和保持对早期预警系统的依从性,调和造成的不和谐,使护士主导的患者评估,促进患者安全。承认理论——护士在遵守预警系统时如何运用临床判断@Jusconnor25。
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引用次数: 0
Understanding the experiences of people who have Postural Orthostatic Tachycardia Syndrome (POTS) and the health professionals who care for them: A grounded theory study
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-19 DOI: 10.1016/j.ijnurstu.2024.104986
H. Eftekhari , G. Pearce , S. Staniszewska , K. Seers
<div><div>Understanding the experiences of people who have postural orthostatic tachycardia syndrome (POTS) and the health professionals who care for them: a grounded theory study.</div></div><div><h3>Background</h3><div>Postural orthostatic tachycardia syndrome (POTS) is an under recognised, predominantly female condition. Awareness of this condition has increased due its association with Long-COVID. Understanding experiences informs areas for future study. Research into the experience of POTS is emerging, with no currently published studies including the experiences of health professionals.</div></div><div><h3>Aim</h3><div>This study aimed to understand experiences of POTS, its challenges, and aspects of care from the perspectives of people with the condition and health professionals who look after them.</div></div><div><h3>Design</h3><div>A grounded theory approach was taken to develop a conceptual framework of the experience of POTS conceptualised through a critical realist lens.</div></div><div><h3>Setting</h3><div>This United Kingdom based study included people with POTS from three national health care centres and a diverse range of health professionals.</div></div><div><h3>Participants</h3><div>Theoretical and purposive sampling recruited people with POTS, and snowball sampling recruited health professionals through a United Kingdom charity and arrhythmia nursing network. Health professionals were interviewed from a range of professions including nurses, secondary care consultants, primary care general practitioners, psychologists, physiotherapists, and an occupational therapist.</div></div><div><h3>Method</h3><div>Between September 2021 and September 2022 in-depth online semi-structured interviews were undertaken. Data were thematically analysed. Corbin and Strauss' Grounded Theory methods of constant comparison, memos, and a reflexive journal were used. Analysis moved from first open coding of health professional themes to more focused axial coding, data, and category linking. The study patient and public involvement group informed thematic development and theoretical sampling. The final themes were conceptualised through the critical realism's three layers of experience.</div></div><div><h3>Results</h3><div>Forty-four participants were included, 19 people with POTS and 25 health professionals. Three core themes were found: 1) A challenging condition, 2) POTS healthcare provision - services by accident not design, and 3) The need to validate experiences. Health professionals experienced challenges in their clinical self-efficacy. POTS care was driven by individual human agency and interpersonal relationships. People with POTS took individual responsibility for their self-management but were impacted by gender inequalities, a medical model prioritising guidelines, and a poor evidence-base.</div></div><div><h3>Conclusion</h3><div>This is the first qualitative study to explore both people with POTS and health professional experiences of loo
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引用次数: 0
Efficacy of a vein visualisation device for facilitating peripheral venous line placement in adult patients with sickle cell disease: A randomised clinical trial 静脉显像装置促进镰状细胞病患者外周静脉线放置的疗效:一项随机临床试验
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-19 DOI: 10.1016/j.ijnurstu.2024.104988
Anne Corbasson , Eric Fischer , Aurélie Vilfaillot , Ana Bento Da Costa , Marie Charmettan , Maria Ferreira , Carole Barthélémy , Walid Namaoui , Djamal Khimoud , Annabelle Beaudoin , Liliane Berkani , Constance Guillaud , Mehdi Khellaf , Edouard Flamarion , Adrien Michon , Emmanuel Lafont , Geoffrey Cheminet , Gilles Chatellier , Jacques Pouchot , Brigitte Ranque , Jean-Benoît Arlet

Background

Intravenous (IV) access is often required for the treatment of vaso-occlusive crises in patients with sickle cell disease, but can be particularly challenging due to recurrent venous damage. The AccuVein® device, uses near-infrared light technology to visualise veins for easier venepuncture.

Methods

A randomised, controlled trial of the efficacy of the AccuVeinAV400® device in the replacement of peripheral venous lines during a vaso-occlusive crisis was conducted at two centres in France. Adult patients with sickle cell disease were randomised to the AccuVein® or routine IV cannulation procedures. The primary outcome was the number of cannulation attempts needed for effective replacement of the peripheral IV line.

Results

Between April 10th, 2018, and March 22nd, 2022, 127 patients were randomised and 126 were analysed (median age: 27.5 years [interquartile range-IQR: 21.3–33.8]; homozygous genotype: 106 (84.1 %)). Although patients in the AccuVein® group reported lower levels of procedure-related pain, use of the device was not associated with a lower median number of venepuncture attempts (2 [1–3], vs. 2 [1–4] in the routine procedure group: p = 0.49). There were no statistically significant intergroup differences in the time to IV line replacement (9.6 [4.1–20.8] in the AccuVein® group vs. 11.7 [4.2–24.7] minutes in the routine procedure group), changes in patient and nurse anxiety and satisfaction levels, or the complication rate.

Conclusion

Use of the AccuVeinAV400® device was not associated with a significant decrease of the number of venepuncture attempts or of the time needed for IV line replacement during the management of vaso-occlusive crises. The study's results highlight the complexity of IV access in this clinical context.

Trial registration

ClinicalTrial.gov identifier: NCT03477552
背景:镰状细胞病患者的血管闭塞危象通常需要静脉注射,但由于静脉损伤复发,静脉注射尤其具有挑战性。AccuVein®设备使用近红外光技术来可视化静脉,以便于静脉穿刺。方法:在法国的两个中心进行了一项随机对照试验,研究了AccuVeinAV400®装置在血管闭塞危机期间替代外周静脉线的有效性。成年镰状细胞病患者被随机分配到AccuVein®或常规静脉插管组。主要结果是有效更换外周静脉管所需的插管次数。结果:2018年4月10日至2022年3月22日期间,127例患者被随机分组,126例患者被分析(中位年龄:27.5岁[四分位数间距- iqr: 21.3-33.8];纯合子基因型:106例(84.1%)。尽管AccuVein®组患者报告的手术相关疼痛水平较低,但使用该装置与静脉穿刺尝试次数中位数较低无关(2例[1-3],而常规手术组为2例[1-4]:p = 0.49)。在静脉滴注更换时间(AccuVein®组为9.6[4.1-20.8]分钟,常规操作组为11.7[4.2-24.7]分钟)、患者和护士焦虑和满意度水平的变化以及并发症发生率方面,组间差异无统计学意义。结论:在处理血管闭塞危机时,使用AccuVeinAV400®装置与静脉穿刺尝试次数或静脉换管所需时间的显著减少无关。这项研究的结果强调了在这种临床环境下静脉注射的复杂性。试验注册:ClinicalTrial.gov标识符:NCT03477552。
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引用次数: 0
Effects of behavioural activation on psychological distress among people with cancer: A systematic review and meta-analysis
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-18 DOI: 10.1016/j.ijnurstu.2024.104983
Meng Wei , Azlina Yusuf , Caryn Chan Mei Hsien , Maziah Ahmad Marzuki

Background

Cancer is a life-threatening disease that can have a significant impact on patients' psychological well-being. Behavioural activation is an emerging psychological therapy that has been suggested effective in improving depression and anxiety. However, no review has yet summarised its effects on psychological distress among people with cancer.

Objective

To identify studies of behavioural activation designed for people with cancer and examine the effects on psychological distress, including depression and anxiety.

Design

Systematic review and meta-analysis.

Methods

A systematic search of PubMed/MEDLINE, CINAHL, EMBASE, PsycINFO, and the Cochrane Library was performed from the inception to 6 April 2024. Randomised controlled trials reporting on the effects of behavioural activation on psychological distress among cancer patients were included. Two authors independently screened the eligible studies, assessed the quality of studies, and extracted data. The risk of bias was assessed using version 2 of the Cochrane risk-of-bias tool for randomised trials (RoB 2). The meta-analysis was performed by Review Manager 5.4, and narrative synthesis was employed when the meta-analysis was inappropriate. The Grading of Recommendations, Assessment, Development and Evaluation (GRADE) system was used to assess the certainty of the evidence.

Results

A total of nine studies were included in this systematic review, with 1811 participants. The pooled analysis showed that behavioural activation could improve depression (SMD = − 0.24, 95 % CI -0.44 - -0.03, p = 0.020; moderate quality of evidence), and anxiety (SMD = − 0.56, 95 % CI -1.01 - -0.10, p = 0.020; low quality of evidence) among people with cancer. The effects were robust in sensitivity analysis and yielded consistent results in studies that were not pooled due to insufficient data. Subgroup analyses suggested that face-to-face and group administration were more effective, whereas the effects of different dosages were uncertain. Besides, the effects of behavioural activation at different follow-up periods were not identified There was no consensus on the optimal components of intervention.

Conclusions

The evidence for behavioural activation as an effective treatment of psychological distress among people with cancer is promising. However, it should be noted that the quality of evidence was moderate and low, thus emphasising the need for caution when applying these findings. In order to explore which components may be most effective in improving psychological outcomes, more rigorous study designs and more detailed descriptions of interventions are necessary.

Registration

The protocol was registered on PROSPERO (Registration number: CRD42024533171).
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引用次数: 0
Comment on Miao et al. (2024) ‘A dynamic online nomogram for predicting the heterogeneity trajectories of frailty among elderly gastric cancer survivors’ 对 Miao 等人(2024 年)的评论《预测老年胃癌幸存者虚弱异质性轨迹的动态在线提名图》。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-01 DOI: 10.1016/j.ijnurstu.2024.104921
Yeping Zheng, Fengyan Pu
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引用次数: 0
Healthcare professionals' experience with nutritional care beyond formal quality systems — A qualitative study 医护人员在正规质量体系之外的营养护理经验 - 一项定性研究。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-01 DOI: 10.1016/j.ijnurstu.2024.104860
Randi Olsson Haave , Sigrid Nakrem , Line Melby
<div><h3>Background</h3><div>Numerous formal strategies, screening tools, and interventions have been used to prevent malnutrition in long-term care patients. Despite these efforts, the proportion of screened patients is low, and a large proportion are malnourished. Previous research has revealed that healthcare professionals use a broad approach in their nutritional care but has also emphasised the need for further investigation into these approaches.</div></div><div><h3>Objective</h3><div>To explore how healthcare professionals working in long-term care experience and apply nutritional care.</div></div><div><h3>Design</h3><div>A descriptive, exploratory, qualitative design containing 240 h of participant observation, 12 focus groups and 2 individual interviews.</div></div><div><h3>Setting(s)</h3><div>Twelve nursing homes and home care units in three Norwegian municipalities.</div></div><div><h3>Participants</h3><div>Participant observation of interactions between healthcare professionals and patients. Forty-three registered nurses participated in focus group or individual interviews.</div></div><div><h3>Methods</h3><div>The data were analysed using inductive thematic analysis.</div></div><div><h3>Results</h3><div>The analysis identified three themes: The first theme, limited significance of nutritional screening, showed that healthcare professionals experienced the limited value of nutritional screening, as it often did not capture patients' nutritional challenges. They also perceived nutritional screening as unsuitable for patients at the end of their lives, those with overweight-related complications, or undergoing rehabilitation. In addition, nutritional screening was perceived as something healthcare professionals did for their managers or administrators, not because it was crucial to providing good nutritional care. The second theme, provision of individualised food, captures the healthcare professionals' efforts in adapting and preparing food according to the patient's preferences. Facilitation to enable patients to make individual food choices and the use of food cards or lists were two approaches to individualising nutrition care. The third theme, making meals more than about food, elucidated how healthcare professionals used meals to help patients cope with their situations and experience social belonging. Conversations about or around meals were used to provide patients with a sense of belonging to their past or present situation. The meals were also used as a diversion strategy for patients with unrest, as arenas for daily activity training, and for meaningful social interactions between patients around the tables.</div></div><div><h3>Conclusions</h3><div>Nutritional screening and prevention of malnutrition are only one part of healthcare professionals' nutritional care. Individualised food and meals that create coping, a sense of belonging, and social experiences are equally important parts of their care. Emphasising healthcare prof
背景:许多正式的策略、筛查工具和干预措施都被用于预防长期护理患者营养不良。尽管做出了这些努力,但接受筛查的患者比例很低,而且很大一部分患者营养不良。以往的研究表明,医护人员在营养护理中采用了广泛的方法,但同时也强调了进一步调查这些方法的必要性:目的:探讨从事长期护理工作的医护人员如何体验和应用营养护理:设计:描述性、探索性、定性设计,包括 240 小时的参与观察、12 个焦点小组和 2 次个别访谈:地点: 挪威三个城市的 12 家养老院和家庭护理单位:对医护人员和病人之间的互动进行参与观察。43名注册护士参加了焦点小组或个别访谈:方法:采用归纳式主题分析法对数据进行分析:分析确定了三个主题:第一个主题 "营养筛查的意义有限 "表明,医护人员认为营养筛查的价值有限,因为它往往无法捕捉到患者的营养挑战。他们还认为营养筛查不适合生命垂危的患者、患有超重相关并发症的患者或正在接受康复治疗的患者。此外,营养筛查被认为是医护人员为其管理者或行政人员所做的事情,而不是因为它对提供良好的营养护理至关重要。第二个主题 "提供个性化食物 "反映了医护人员在根据病人的喜好调整和准备食物方面所做的努力。帮助病人做出个性化食物选择以及使用食物卡片或清单是个性化营养护理的两种方法。第三个主题 "让膳食不仅仅是食物 "阐明了医护人员如何利用膳食来帮助病人应对其处境并体验社会归属感。关于膳食的谈话或围绕膳食的谈话被用来为病人提供一种对其过去或现在处境的归属感。膳食还被用作一种转移病人不安情绪的策略、日常活动训练的场所以及病人在餐桌旁进行有意义的社交互动的场所:营养筛查和预防营养不良只是医护人员营养护理的一部分。个性化的食物和膳食能让医护人员产生应对能力、归属感和社交体验,这同样是医护人员护理工作的重要组成部分。强调医护人员以人为本的营养护理方法是有益的,因为这可以加强并进一步发展长期营养护理服务。
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引用次数: 0
Authors' response to “Comment on Miao et al. (2024) ‘A dynamic online nomogram for predicting the heterogeneity trajectories of frailty among elderly gastric cancer survivors’” 作者对 "Miao 等人(2024)'预测老年胃癌幸存者虚弱异质性轨迹的动态在线提名图'的评论 "的回应。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-01 DOI: 10.1016/j.ijnurstu.2024.104922
Yinning Guo, Xueyi Miao, Shuqin Zhu, Qin Xu
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引用次数: 0
Experiences and needs of family members following sudden cardiac death: A meta-synthesis 心脏性猝死后家庭成员的经历和需求:元综合。
IF 7.5 1区 医学 Q1 NURSING Pub Date : 2024-12-01 DOI: 10.1016/j.ijnurstu.2024.104872
Dan Zhang , Yiting Liu , Niu Chen , Yamin Li , Xiaofei Li

Objective

This meta-synthesis of qualitative studies aimed to explore the experiences and needs of family members of victims of sudden cardiac death.

Design

A meta-synthesis was conducted.

Data sources

Five databases (PubMed, CINAHL, EMBASE, Web of Science, and China National Knowledge Infrastructure) were searched from establishment to May 2024. From initial searches with essential keywords (sudden cardiac death, family members, and qualitative studies), 3021 articles were retrieved. There were eight studies in the meta-synthesis, selected on the basis of inclusion and exclusion criteria.

Review methods

We evaluated the quality of the included studies using the Critical Appraisal Skills Programme-Qualitative Research Checklist.

Results

Eight studies from six countries reported on the experiences and needs of family members who had lost someone to sudden cardiac death, and five analytical themes were synthesized: negative emotional reaction, finding cause of death, rebuilding life, meaning reconstruction and need for support. These experiences and needs fuse with each other and are relevant to the health and future of the family members.

Conclusion

Negative emotional reaction is a necessary process for family members dealing with sudden cardiac death, and rebuilding life is a challenge that family members must face. In the process of family members rebuilding normal life, finding the cause of death is the foundation, and meaning reconstruction is the core. Many of the needs faced by these family members are not well met, and policymakers and bereavement teams should provide comprehensive and personalized interventions for them.
目的这项定性研究的元综述旨在探讨心脏性猝死患者家属的经历和需求:数据来源:五个数据库(PubMed、CINAHL、EMBASE):数据来源:对五个数据库(PubMed、CINAHL、EMBASE、Web of Science 和中国国家知识基础设施)进行了检索,检索时间从建立到 2024 年 5 月。通过使用基本关键词(心脏性猝死、家庭成员和定性研究)进行初步检索,共检索到 3021 篇文章。根据纳入和排除标准,共有 8 项研究被纳入元综合:我们使用 "批判性评估技能计划-定性研究核对表 "对纳入研究的质量进行了评估:来自六个国家的八项研究报告了因心脏性猝死而丧生的家庭成员的经历和需求,并归纳出五个分析主题:负面情绪反应、寻找死因、重建生活、意义重建和支持需求。这些经历和需求相互融合,与家庭成员的健康和未来息息相关:负面情绪反应是家庭成员处理心脏性猝死的必要过程,而重建生活则是家庭成员必须面对的挑战。在家属重建正常生活的过程中,找到死因是基础,意义重建是核心。这些家庭成员所面临的许多需求都没有得到很好的满足,政策制定者和丧亲团队应该为他们提供全面和个性化的干预措施。
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引用次数: 0
期刊
International Journal of Nursing Studies
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