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Impact of Inequalities in Treatment for Prostate Cancer Affecting Demand for Secondary and Tertiary Services: Secondary Analysis of Linked National Datasets 前列腺癌治疗不平等对二级和三级服务需求的影响:相关国家数据集的二级分析。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151914
Ashleigh Lauren Ward , Susanne Cruickshank , Liz Forbat

Objectives

This study calculates the actual and weighted changes in population, incidence, and treatment use to better understand the inequities in use affecting the delivery of prostate cancer services.

Methods

Health data held by Scotland’s electronic Data Research and Innovation Service were linked with National Records of Scotland census data and Information Services Division health data to identify men aged ≥45 living in Scotland who had prostate cancer. Data were analyzed descriptively and weighted using National Records of Scotland census data.

Results

Demand for secondary and tertiary services nationally coincided with the implementation of new technologies and treatments in Scotland. Furthermore, differences in demand for treatment services were evident between regions that could not be explained by urban and rural factors.

Conclusion

These findings demonstrate the level of national variability that governments and health care administrations need to consider when distributing resources to services.

Implications for Nursing Practice

This report highlights the challenges for cancer nurses in maintaining skills and competencies in light of rapidly emerging technologies, and the unique demands on local and regional services, which will affect mentorship across regions.
目的:本研究计算人口、发病率和治疗使用的实际和加权变化,以更好地了解影响前列腺癌服务提供的使用不公平。方法:将苏格兰电子数据研究与创新服务中心持有的健康数据与苏格兰国家人口普查数据和信息服务部门的健康数据相关联,以确定居住在苏格兰的年龄≥45岁的前列腺癌男性。使用苏格兰国家记录人口普查数据对数据进行描述性分析和加权。结果:全国对二级和三级服务的需求与苏格兰新技术和治疗的实施相吻合。此外,治疗服务需求在区域之间的差异是明显的,不能用城乡因素来解释。结论:这些发现表明,各国政府和卫生保健管理部门在向服务部门分配资源时需要考虑国家差异的程度。对护理实践的影响:本报告强调了在快速发展的技术背景下,癌症护士在保持技能和能力方面面临的挑战,以及对地方和区域服务的独特需求,这将影响区域间的指导。
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引用次数: 0
What are the Key Components of an Advanced Nurse Practitioner (ANP) Led High-Risk Family History Breast Clinic? A Scoping Review. 高级执业护士(ANP)领导的高危家族史乳腺诊所的关键组成部分是什么?范围审查。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-09-25 DOI: 10.1016/j.soncn.2025.152018
Lisa Marie Cadden, Carla O'Neill, Mary Ryder

Objectives: To identify what is known in the existing literature about the key components of an advanced nurse practitioner led high-risk family history breast clinic.

Methods: This scoping review adheres the Joanna Briggs Institute scoping review framework and reported in line with the PRISMA Extension for Scoping Reviews (PRISMA-ScR) checklist. A systematic search of 4 databases including CINAHL, PubMed, Scopus and PsychINFO and sources of grey literature was conducted in October 2024 and December 2024. Data was extracted, synthesised and presented in narrative and table format.

Results: Seven papers met the inclusion criteria. Two themes emerged from the literature, risk assessment to determine breast cancer risk and the psychological impact of risk realisation on the patient and the nurse.

Conclusion: This scoping review aimed to identify the key components of an advanced nurse practitioner led high risk family history breast clinic. Two key components emerged from the literature namely risk assessment and the psychological impact of risk realisation. This review also identifies the recommended clinical outcomes following the identification of women at high risk for developing breast cancer. This review also aimed to identify the gaps in the literature regarding the role of the nurse within these clinics. The management of women identified to have psychological distress as a consequence of risk realisation.

Implications for nursing practice: Advanced nurse practitioners are well placed to lead the care of women at high-risk of developing breast cancer utilising a holistic approach, in conjunction with the multidisciplinary team.

目的:确定现有文献中已知的由高级执业护士领导的高危家族史乳腺诊所的关键组成部分。方法:该范围审查遵循乔安娜布里格斯研究所范围审查框架,并按照PRISMA范围审查扩展(PRISMA- scr)检查表进行报告。在2024年10月和2024年12月对CINAHL、PubMed、Scopus和PsychINFO 4个数据库和灰色文献来源进行了系统检索。数据被提取、合成并以叙述和表格的形式呈现。结果:7篇论文符合纳入标准。从文献中出现了两个主题,确定乳腺癌风险的风险评估和风险意识对患者和护士的心理影响。结论:本综述旨在确定高级执业护士领导的高危家族史乳腺诊所的关键组成部分。从文献中出现了两个关键组成部分,即风险评估和风险实现的心理影响。本综述还确定了在确定乳腺癌高危妇女后推荐的临床结果。本综述还旨在确定关于这些诊所中护士角色的文献差距。对因意识到风险而产生心理困扰的妇女的管理。对护理实践的影响:与多学科团队合作,高级护士从业人员可以很好地利用整体方法领导乳腺癌高危妇女的护理。
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引用次数: 0
Development and Validation of an Instrument to Measure Intention of Cancer Surveillance Among Patients With Hereditary Colorectal Cancer on the Basis of Theory of Planned Behavior. 基于计划行为理论的遗传性结直肠癌患者癌症监测意愿测量仪器的研制与验证。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-12 DOI: 10.1016/j.soncn.2025.151988
Qianqian Du, Lu Cui, Jingyue Xie, Xiaodan Wu, Xiaoxuan Wang, Chen Yuan, Meifen Zhang

Objective: Patients with hereditary colorectal cancer (HCRC) require consistent surveillance for both intestinal and extra-intestinal cancers. This study aims to develop a scale to measure variables associated with the intention of cancer surveillance behavior among patients with HCRC based on the Theory of Planned Behavior.

Methods: The preliminary scale was constructed using direct measures derived from a literature review, and belief-based indirect measures generated through a belief elicitation study involving 23 patients with HCRC. Then a sample of 134 patients was recruited to evaluated the validity and reliability of the scale.

Results: The finalized scale comprises 37 items with 4 subscales. The I-CVI ranged from 0.875 to 1.000, while the S-CVI/Ave for each subscale varied between 0.964 and 1.000. The Cronbach's α for the direct measures of each subscale ranged from 0.819 to 0.940. The intraclass correlation coefficient was between 0.609 and 0.893. Exploratory factor analysis revealed that the direct measures accounted for 80.133% of the variance. Convergent validity was established between the direct measures and the indirect measures (attitudes r = 0.469, P < .001; subjective norms r = 0.374, P < .001; perceived behavioral control r = 0.353, P < .001).

Conclusion: The scale demonstrates adequate construct validity, predictive validity, internal consistency reliability and test-retest reliability, making it a valuable tool for assessing beliefs regarding cancer surveillance in patients with HCRC.

Implications for nursing practice: This newly developed scale will provide critical insights into how intentions influence actual cancer surveillance behavior among patients with HCRC. This understanding will facilitate the design of nursing interventions aimed at enhancing surveillance behaviors and long-term health outcomes.

目的:遗传性结直肠癌(HCRC)患者需要对肠道和肠外肿瘤进行持续监测。本研究旨在以计划行为理论为基础,开发一种测量HCRC患者癌症监测行为意愿相关变量的量表。方法:初步量表采用文献综述的直接测量方法,以及23例HCRC患者的信念启发研究产生的基于信念的间接测量方法。然后招募134例患者进行量表的效度和信度评估。结果:定稿的量表包括37个条目,4个分量表。I-CVI在0.875 ~ 1.000之间,S-CVI/Ave在0.964 ~ 1.000之间。各分量表直接测量值的Cronbach’s α为0.819 ~ 0.940。类内相关系数在0.609 ~ 0.893之间。探索性因子分析显示,直接测量占方差的80.133%。直接测量法与间接测量法之间存在趋同效度(态度r = 0.469, P < 0.001;主观规范r = 0.374, P < 0.001;感知行为控制r = 0.353, P < 0.001)。结论:该量表具有较好的结构效度、预测效度、内部一致性信度和重测信度,是评估HCRC患者癌症监测信念的有效工具。对护理实践的启示:这个新开发的量表将提供关于意图如何影响HCRC患者实际癌症监测行为的关键见解。这种理解将有助于设计旨在加强监测行为和长期健康结果的护理干预措施。
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引用次数: 0
Lived Experiences of Iranian Oncology Nurses on Missed Nursing Care During a Public Health Crisis: Causes and Emotional Consequences 伊朗肿瘤护士在公共卫生危机期间错过护理的生活经历:原因和情感后果。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151947
Mahsa Pourshaban , Hadi Hasankhani , Atefeh Allahbakhshian , Sarieh Poortaghi
<div><h3>Objectives</h3><div><span>The COVID-19 pandemic posed unprecedented challenges for health care systems worldwide, particularly for oncology nurses in Iran, who grappled with significant issues related to missed </span>nursing care<span>. These challenges have raised critical concerns regarding their professional roles and emotional health. This study aims to investigate the lived experiences of Iranian oncology nurses, emphasizing the emotional ramifications of missed nursing care and the underlying factors that contributed to this phenomenon during the pandemic.</span></div></div><div><h3>Methods</h3><div>This research adopted a qualitative approach grounded in Heidegger’s hermeneutic phenomenology. The study involved 12 oncology nurses employed in various departments across five public hospitals in Tehran and Tabriz. Data collection spans from February 2023 to December 2024, utilizing in-depth, semi-structured interviews to garner rich, qualitative insights. Interviews were conducted until data saturation was reached, ensuring a comprehensive understanding of the participants’ experiences. The simultaneous analysis of the data follows the methodological framework established by Diekelmann et al. (1989).</div></div><div><h3>Results</h3><div>Through a detailed phenomenological analysis of the interviews, four primary themes emerged, accompanied by sixteen subthemes: “Existential Fatigue,” “Difficult Emotions,” “Nurse Assumptions,” and “Role Ambivalence.” The first two themes illuminate the emotional distress experienced by nurses as a direct outcome of the challenges posed by missed nursing care. Conversely, the latter themes shed light on the factors contributing to these instances of missed care amid the pandemic’s unique challenges.</div></div><div><h3>Conclusion</h3><div>Oncology nurses often grapple with intense emotional challenges as they strive to meet the demanding nature of their caregiving roles. This emotional strain can hinder their ability to fully connect with patients, leading to missed nursing opportunities that create a harmful cycle affecting both the well-being of the nurses and the outcomes for patients. This scenario highlights the deep link between emotional health and the quality of nursing practice. Additionally, biases and a sense of futility regarding certain interventions complicate their experiences, especially during crises, while the duality of their roles introduces conflicting expectations. This interplay underscores the complexities inherent in nursing, particularly in demanding situations.</div></div><div><h3>Implications for Nursing Practice</h3><div>These findings underscore the urgent necessity for comprehensive emotional health support and regular emotional assessments for oncology nurses to enhance their resilience. Creating a supportive and nurturing work environment<span>, coupled with targeted training to address common nurse assumptions and clarify role expectations, is essential. Such measures
2019冠状病毒病大流行给全球卫生保健系统带来了前所未有的挑战,特别是对伊朗的肿瘤科护士来说,她们面临着与错过护理相关的重大问题。这些挑战引起了人们对他们的职业角色和情感健康的严重关注。本研究旨在调查伊朗肿瘤科护士的生活经历,强调在大流行期间错过护理的情感后果和导致这种现象的潜在因素。方法:本研究采用以海德格尔的解释学现象学为基础的定性方法。这项研究涉及德黑兰和大不里士五家公立医院不同部门的12名肿瘤科护士。数据收集时间跨度为2023年2月至2024年12月,利用深入的半结构化访谈获得丰富的定性见解。访谈一直进行到数据饱和,以确保对参与者经历的全面理解。数据的同步分析遵循Diekelmann et al.(1989)建立的方法框架。结果:通过对访谈的详细现象学分析,出现了四个主要主题,伴随着16个次要主题:“存在疲劳”,“困难情绪”,“护士假设”和“角色矛盾”。前两个主题阐明了护士作为错过护理所带来的挑战的直接结果所经历的情绪困扰。相反,后一个主题揭示了在大流行面临独特挑战的情况下,导致这些错过护理的因素。结论:肿瘤护士在努力满足其护理角色的要求时,经常与强烈的情感挑战作斗争。这种情绪紧张会阻碍他们与患者充分沟通的能力,导致错过护理机会,从而形成一个有害的循环,影响护士的福祉和患者的结果。这一情景突出了情绪健康与护理实践质量之间的深刻联系。此外,对某些干预措施的偏见和徒劳感使他们的经历复杂化,特别是在危机期间,而他们角色的二元性引入了相互冲突的期望。这种相互作用强调了护理固有的复杂性,特别是在苛刻的情况下。对护理实践的启示:这些发现强调了对肿瘤护士进行全面的情绪健康支持和定期的情绪评估以增强其复原力的迫切必要性。创造一个支持性和养育性的工作环境,加上有针对性的培训,以解决常见的护士假设和明确角色期望,是至关重要的。这些措施对于提高护士保留率和确保高质量的病人护理至关重要。
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引用次数: 0
Oncology Advanced Practice Nurses’ Memorable Patient Care Experiences: A Qualitative Analysis 肿瘤高级执业护士令人难忘的病人护理经历:定性分析。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151910
Abigail G. Cohen , Vanessa Battista , Judith Paice , Betty R. Ferrell

Introduction

The purpose of this study was to describe oncology advanced practice nurses’ (APRNs) experiences caring for memorable patients, the meaning derived from patients’ experiences and the influence patients have had on their careers. This study builds on work describing the meaning of oncology nursing practice.

Methods/Results

Oncology APRNs (N=66) participating in an NCI funded ELNEC course responded to 3 open-ended prompts/questions: (1) Share a story about a memorable patient, (2) Why do you think the memory of this patient is meaningful to you? (3) How do you think caring for this patient has influenced your nursing career? A thematic, qualitative analysis of their responses identified several key themes including:
(1) Lessons learned: Usually profound, occasionally resulting in career altering impact.
(2) Admiration: Admiration for patients’ kindness, grace, strength, hope and courage through terminal illness.
(3) Delivery of high-quality palliative care: The foundation for deep connections and mutually beneficial relationships between APRNs and patients.
(4) Challenges: Clinical scenarios involving APRNs feeling like they failed; staff distress, trauma, or grief.

Conclusions

Oncology nurses described early nursing career experiences of patients as the greatest teachers and shared invaluable and transformative lessons learned about what it means to be human in the face of serious illness.
前言:本研究的目的是描述肿瘤高级执业护士(APRNs)护理难忘患者的经历,患者经历的意义以及患者对其职业生涯的影响。本研究建立在描述肿瘤护理实践意义的工作基础上。方法/结果:参加NCI资助的ELNEC课程的肿瘤学APRNs (N=66)回答了3个开放式提示/问题:(1)分享一个令人难忘的病人的故事;(2)为什么你认为对这个病人的记忆对你有意义?(3)您认为照顾这个病人对您的护理生涯有什么影响?对他们的回答进行专题定性分析,确定了几个关键主题,包括:(1)经验教训:通常是深刻的,偶尔会导致改变职业的影响。(2)钦佩:钦佩绝症患者的善良、优雅、力量、希望和勇气。(3)提供高质量的姑息治疗:APRNs与患者之间建立深度联系和互利关系的基础。(4)挑战:涉及APRNs感觉失败的临床场景;员工痛苦、创伤或悲伤。结论:肿瘤科护士将患者早期护理生涯的经历描述为最伟大的老师,并分享了宝贵的和变革性的经验教训,告诉他们面对严重疾病的人类意味着什么。
{"title":"Oncology Advanced Practice Nurses’ Memorable Patient Care Experiences: A Qualitative Analysis","authors":"Abigail G. Cohen ,&nbsp;Vanessa Battista ,&nbsp;Judith Paice ,&nbsp;Betty R. Ferrell","doi":"10.1016/j.soncn.2025.151910","DOIUrl":"10.1016/j.soncn.2025.151910","url":null,"abstract":"<div><h3>Introduction</h3><div>The purpose of this study was to describe oncology<span> advanced practice nurses’ (APRNs) experiences caring for memorable patients, the meaning derived from patients’ experiences and the influence patients have had on their careers. This study builds on work describing the meaning of oncology nursing practice.</span></div></div><div><h3>Methods/Results</h3><div>Oncology APRNs (N=66) participating in an NCI funded ELNEC course responded to 3 open-ended prompts/questions: (1) Share a story about a memorable patient, (2) Why do you think the memory of this patient is meaningful to you? (3) How do you think caring for this patient has influenced your nursing career? A thematic, qualitative analysis of their responses identified several key themes including:</div><div>(1) Lessons learned: Usually profound, occasionally resulting in career altering impact.</div><div>(2) Admiration: Admiration for patients’ kindness, grace, strength, hope and courage through terminal illness.</div><div>(3) Delivery of high-quality palliative care: The foundation for deep connections and mutually beneficial relationships between APRNs and patients.</div><div>(4) Challenges: Clinical scenarios involving APRNs feeling like they failed; staff distress, trauma, or grief.</div></div><div><h3>Conclusions</h3><div>Oncology nurses described early nursing career experiences of patients as the greatest teachers and shared invaluable and transformative lessons learned about what it means to be human in the face of serious illness.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 4","pages":"Article 151910"},"PeriodicalIF":2.3,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144188546","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Advancing Global Cancer Symptom Science: Insights and Strategies from the Inaugural Cancer Symptom Science Expert Meeting 推进全球癌症症状科学:来自首届癌症症状科学专家会议的见解和策略
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151905
Sara Colomer-Lahiguera , Rachel A. Pozzar , Carolyn S. Harris , Jeannine M. Brant , Yvette P. Conley , Mary E. Cooley , Manuela Eicher , Pamela S. Hinds , Doris Howell , Sandra A. Mitchell , Karin Ribi , Margaret Quinn Rosenzweig , Susan W. Wesmiller , Christine Miaskowski , Marilyn J. Hammer

Objectives

The inaugural “Cancer Symptom Science Expert Meeting,” held in Lausanne, Switzerland, on October 11 to 12, 2023, brought together 40 nurse scientists from seven countries. The event aimed to enhance collaboration across the global symptom science community; identify common research interests, gaps in knowledge, and opportunities for research; and develop strategies to address challenges and accelerate symptom science research internationally. This White Paper summarizes the discussions and recommendations deliberated during the meeting and introduces the Global Research Alliance in Symptom Science (GRASS).

Methods

This 2-day meeting featured presentations that highlighted critical issues and unanswered questions in cancer symptom science. Four core topic areas based on knowledge gaps were reflected throughout presentations. The co-occurrence of cancer with other chronic conditions (eg, cardiovascular disease, diabetes) that may share similar contributors and underlying mechanisms were included. Four working groups (WGs) were formed to identify gaps and opportunities associated with each topic and to outline strategic directions and essential actions to advance symptom science.

Results

WGs developed four recommendations. WG1 explored optimal approaches to collect, analyze, and use symptom data for research and clinical purposes. WG2 addressed the development of a minimum dataset or common data model for symptom science. WG3 focused on enhancement of best practices in implementation science strategies to improve uptake of evidence-based symptom management in routine care. WG4 addressed capacity building and infrastructure for the creation of a GRASS.

Conclusions

WGs’ recommendations underscore the commitment of an international coalition of scientists to advance symptom science. The symposium established the groundwork for the development of GRASS, dedicated to symptom science in cancer and other chronic conditions. Future directions include establishing regular scientific meetings, fostering interdisciplinary collaboration, and engaging with symptom scientists.

Implications for Nursing Practice

GRASS is an alliance for symptom science and its implementation into clinical practice. Nurses are at the forefront of this work.
首届“癌症症状科学专家会议”于2023年10月11日至12日在瑞士洛桑举行,来自7个国家的40名护士科学家齐聚一堂。该活动旨在加强全球症状科学界的合作;确定共同的研究兴趣、知识差距和研究机会;制定应对挑战的战略,加快国际症状科学研究。本白皮书总结了会议期间的讨论和建议,并介绍了全球症状科学研究联盟(GRASS)。方法:本次为期两天的会议重点介绍了癌症症状科学中的关键问题和未解决的问题。在整个报告中反映了基于知识差距的四个核心主题领域。癌症与其他慢性疾病(如心血管疾病、糖尿病)的共同发生可能具有相似的诱因和潜在机制。成立了四个工作组(wg),以确定与每个主题相关的差距和机会,并概述推进症状科学的战略方向和基本行动。结果工作组提出了四项建议。WG1探索了收集、分析和使用症状数据用于研究和临床目的的最佳方法。WG2讨论了症状科学的最小数据集或公共数据模型的开发。第三次工作组的重点是加强实施科学战略的最佳做法,以改善在常规护理中采用循证症状管理。第4届工作组讨论了创建GRASS的能力建设和基础设施问题。结论swgs的建议强调了国际科学家联盟推进症状科学的承诺。研讨会为GRASS的发展奠定了基础,致力于癌症和其他慢性疾病的症状科学。未来的发展方向包括建立定期的科学会议,促进跨学科合作,并与症状科学家接触。对护理实践的影响grass是症状科学及其在临床实践中的实施联盟。护士处于这项工作的最前线。
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引用次数: 0
Symptom Science in Pediatric Oncology 儿童肿瘤的症状科学。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151902
Sue Zupanec , Kathleen E. Montgomery , Pamela S. Hinds

Objectives

to describe the historical evolution of symptom science in pediatric oncology from single symptom measurement to standardizing patient- and caregiver-reported outcomes in clinical trials, including underlying theoretical guidance, contributions of advanced analytics, and the state of integration of the science into clinical practice. Developmental considerations are also described.

Methods

historical and current peer-reviewed literature including original research reports and reviews as well as clinical practice guidelines were reviewed and findings extracted.

Results

Standardized patient-, caregiver-, and clinician-reported symptom and treatment toxicity outcomes are now embedded in certain clinical trials of the largest pediatric oncology cooperative group. Though the 3 reports can be discordant, findings indicate the willingness of patients, caregivers and clinicians to report on symptoms and toxicities. Concurrently, advanced analytics have revealed the existence of patient subgroups in terms of symptom experiences. This latter finding combined with the use of estimated minimally important differences, makes possible the potential of tailoring symptom management. Embedding symptom reports in clinical practice in a standardized manner, including real time reports and care, is a future milestone in pediatric oncology symptom science.

Conclusions

Three symptom perspectives, the patient, family caregiver, and clinician, are essential to accurately measure and manage the impact of cancer therapies on patient symptoms, treatment tolerability, function, and quality of life.

Implications for Nursing Practice

Standardizing patient, family, and clinician reports will provide important research and clinical care advances. Embedding these 3 perspectives in nursing practice in a standardized approach is the next milestone for symptom science in pediatric oncology.
目的:描述儿童肿瘤学症状科学的历史演变,从单一症状测量到标准化临床试验中患者和护理人员报告的结果,包括潜在的理论指导,高级分析的贡献,以及将科学融入临床实践的状态。还描述了发展方面的考虑。方法:回顾历史和当前的同行评议文献,包括原始研究报告和综述以及临床实践指南,并提取研究结果。结果:标准化的患者、护理人员和临床医生报告的症状和治疗毒性结果现在被纳入了最大的儿科肿瘤合作小组的某些临床试验中。虽然这3份报告可能不一致,但研究结果表明,患者、护理人员和临床医生愿意报告症状和毒性。同时,先进的分析揭示了患者亚组在症状经历方面的存在。后一项发现与使用估计的最小重要差异相结合,使定制症状管理的潜力成为可能。将症状报告以标准化的方式嵌入临床实践,包括实时报告和护理,是未来儿科肿瘤症状科学的一个里程碑。结论:三个症状角度,患者、家庭照顾者和临床医生,对于准确测量和管理癌症治疗对患者症状、治疗耐受性、功能和生活质量的影响至关重要。对护理实践的影响:标准化患者、家属和临床医生报告将提供重要的研究和临床护理进展。将这三种观点以标准化的方式纳入护理实践是儿科肿瘤学症状科学的下一个里程碑。
{"title":"Symptom Science in Pediatric Oncology","authors":"Sue Zupanec ,&nbsp;Kathleen E. Montgomery ,&nbsp;Pamela S. Hinds","doi":"10.1016/j.soncn.2025.151902","DOIUrl":"10.1016/j.soncn.2025.151902","url":null,"abstract":"<div><h3>Objectives</h3><div>to describe the historical evolution of symptom science in pediatric oncology from single symptom measurement to standardizing patient- and caregiver-reported outcomes in clinical trials, including underlying theoretical guidance, contributions of advanced analytics, and the state of integration of the science into clinical practice. Developmental considerations are also described.</div></div><div><h3>Methods</h3><div>historical and current peer-reviewed literature including original research reports and reviews as well as clinical practice guidelines were reviewed and findings extracted.</div></div><div><h3>Results</h3><div>Standardized patient-, caregiver-, and clinician-reported symptom and treatment toxicity outcomes are now embedded in certain clinical trials of the largest pediatric oncology cooperative group. Though the 3 reports can be discordant, findings indicate the willingness of patients, caregivers and clinicians to report on symptoms and toxicities. Concurrently, advanced analytics have revealed the existence of patient subgroups in terms of symptom experiences. This latter finding combined with the use of estimated minimally important differences, makes possible the potential of tailoring symptom management. Embedding symptom reports in clinical practice in a standardized manner, including real time reports and care, is a future milestone in pediatric oncology symptom science.</div></div><div><h3>Conclusions</h3><div>Three symptom perspectives, the patient, family caregiver, and clinician, are essential to accurately measure and manage the impact of cancer therapies on patient symptoms, treatment tolerability, function, and quality of life.</div></div><div><h3>Implications for Nursing Practice</h3><div>Standardizing patient, family, and clinician reports will provide important research and clinical care advances. Embedding these 3 perspectives in nursing practice in a standardized approach is the next milestone for symptom science in pediatric oncology.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 4","pages":"Article 151902"},"PeriodicalIF":2.3,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144337260","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
State of the “Art” in Precision Health Symptom Science Research 精准健康症状科学研究的“新技术”
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151906
Christine Miaskowski , Sara Colomer-Lahiguera , Yvette P. Conley , Susan Dorsey , Marilyn J. Hammer , Carolyn Harris , Marques Shek Nam Ng , Michele Pelter , Nancy Redeker , Susan Wesmiller

Objectives

The purposes of this paper are to provide a historical perspective on precision health symptom science research; discuss current “conundrums” in precision health symptom science research, including gaps in knowledge and opportunities for growth; and highlight potential challenges that could impede the advancement of precision health symptom science research. The paper concludes with critical directions and recommendations for future research.

Methods

A narrative review of the literature on symptoms and symptom burden, across common medical conditions (ie, cancer, heart failure, chronic obstructive pulmonary disease, chronic kidney disease, human immunodeficiency virus, type 2 diabetes mellitus, was conducted to provide information on salient topics associated with precision health symptom science research.

Results

This paper provides an overview of the field of precision health symptom science research. Some of the conundrums discussed include measurement of single and multiple symptoms; interindividual variability in persons’ symptom experiences; the concept of “time” in the evaluation of symptoms; advantages and disadvantages of various analytic approaches; and the collection of “meaningful” data. Practical research examples and suggestions are included to guide the development and conduct of future studies.

Conclusions

The paper summarizes potential challenges and opportunities in precision health symptom science research. The final section of the paper provides a summary of critical directions and recommendations for future research.

Implications for Nursing Practice

Precision health symptom science is a relatively young field of scientific inquiry. However, the future of precision health symptom science research is both exciting and challenging. Knowledge gained in this field will result in the identification of risk factors for a higher symptom burden and the development and testing of personalized interventions to prevent and/or treat symptoms across one or more acute or chronic medical conditions.
目的:为精准健康症状科学研究提供一个历史视角;探讨当前精准健康症状科学研究的“难题”,包括知识缺口和发展机遇;并强调可能阻碍精准健康症状科学研究进展的潜在挑战。文章最后提出了未来研究的关键方向和建议。方法:对常见疾病(如癌症、心力衰竭、慢性阻塞性肺疾病、慢性肾脏疾病、人类免疫缺陷病毒、2型糖尿病)的症状和症状负担的文献进行叙述性回顾,以提供与精确健康症状科学研究相关的突出主题的信息。结果:综述了精准健康症状科学的研究领域。讨论的一些难题包括单一和多种症状的测量;个体间症状体验的差异;症状评价中的“时间”概念各种分析方法的优缺点;收集“有意义的”数据。本文还提供了实际研究实例和建议,以指导未来研究的发展和开展。结论:总结了精准健康症状科学研究面临的挑战和机遇。论文的最后一部分总结了未来研究的关键方向和建议。对护理实践的影响:精确健康症状科学是一个相对年轻的科学探究领域。然而,未来的精准健康症状科学研究既令人兴奋又充满挑战。在这一领域获得的知识将有助于确定导致更高症状负担的风险因素,并开发和测试个性化干预措施,以预防和/或治疗一种或多种急性或慢性疾病的症状。
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引用次数: 0
The Effect of a Musical Starry Sky Projector on Fatigue, Sleep, and Quality of Life in Pediatric Oncology Patients: A Randomized Controlled Trial 音乐星空投影仪对儿童肿瘤患者疲劳、睡眠和生活质量的影响:一项随机对照试验。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151911
Remziye Semerci Şahin , Tuba EREN , Aycan Kucukkaya , Polat Goktas , Gülcan AVCI , Filiz Savran

Objectives

This study aimed to evaluate the effect of an Ocean Wave and LED Starry Sky Projector on fatigue, sleep, and quality of life (QoL) in pediatric oncology patients.

Methods

This randomized controlled trial included 60 pediatric oncology patients aged 8 to 18 years who were newly diagnosed with cancer and undergoing chemotherapy. Participants were randomly allocated into two groups: intervention (n = 30) and control (n = 30). The intervention group received standard care plus nightly exposure to an Ocean Wave and LED Starry Sky Projector for 30 minutes before sleep, over a period of 1 week. The control group received standard care only. Data were collected using the Adolescent Information Form, Pediatric Quality of Life Scale, Visual Sleep Scale, and Fatigue Intensity Scale. Fatigue and sleep quality were assessed daily, while QoL was evaluated on the first and seventh days.

Results

The descriptive characteristics of children in the intervention and control groups were found to be homogeneously distributed. Although no statistically significant difference was observed in sleep quality between the groups on the first day (P > .05), significant differences favoring the intervention group were found from the second to the seventh day (P < .05). Similarly, no significant differences were found in fatigue levels between the two groups throughout the week (P > .05). There was no statistically significant difference in the mean scores of the “Pediatric Quality of Life Scale” between the groups (P > .05).

Conclusions

This study found that the ocean wave and LED starry sky projector significantly improved sleep quality over time in pediatric oncology patients but had no significant effect on fatigue or QoL.

Implications for Nursing Practice

Nurses can use musical projectors as a noninvasive, cost-effective tool to improve sleep quality in pediatric oncology patients during treatment.
目的:本研究旨在评估海浪和LED星空投影仪对儿科肿瘤患者疲劳、睡眠和生活质量的影响。方法:本随机对照试验纳入60例8 ~ 18岁新诊断为癌症并正在接受化疗的儿科肿瘤患者。参与者被随机分为两组:干预组(n = 30)和对照组(n = 30)。干预组接受标准护理,每晚睡前暴露在海浪和LED星空投影仪下30分钟,持续一周。对照组仅接受标准治疗。数据采用青少年信息表、儿童生活质量量表、视觉睡眠量表和疲劳强度量表收集。每天评估疲劳和睡眠质量,在第1天和第7天评估生活质量。结果:干预组和对照组患儿的描述性特征均呈均匀分布。第1天各组睡眠质量差异无统计学意义(P < 0.05),第2天至第7天干预组睡眠质量差异有统计学意义(P < 0.05)。同样,两组在一周内的疲劳程度也没有显著差异(P < 0.05)。两组患儿“儿童生活质量量表”平均得分比较,差异无统计学意义(P < 0.05)。结论:本研究发现,随着时间的推移,海浪和LED星空投影仪显著改善了儿科肿瘤患者的睡眠质量,但对疲劳和生活质量没有显著影响。对护理实践的启示:护士可以使用音乐投影仪作为一种无创的、经济有效的工具来改善儿科肿瘤患者治疗期间的睡眠质量。
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引用次数: 0
The Cost-Effectiveness of Nursing Interventions in Cancer Care: Systematic Review 癌症护理干预的成本-效果:系统回顾。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-08-01 DOI: 10.1016/j.soncn.2025.151907
İlknur Yazıcıoğlu , Gülcan Bağçivan , Anica Kolic

Objectives

This study aimed to comprehensively examine the studies evaluating the cost impact of nursing intervention in cancer care.

Methods

PubMed, Scopus, Web of Science, MEDLINE, Cochrane Library, and CINAHL were searched between 2001 and 2024 for randomized controlled trials examining the cost-effectiveness of nursing intervention in cancer care. The search strategy and selection process was done following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. Studies were included if they (1) involved nursing intervention (nurse-led or nurse involved), (2) were conducted with adult patients with cancer, (3) reported cost-effectiveness outcome, and (4) were randomized controlled trials. The study selection process was performed on the Rayyan program. The Consolidated Health Economic Evaluation Reporting Standards (CHEERS) checklist was used for quality assessment of included studies.

Results

Twenty-four studies met the criteria and were analyzed. More than half of the studies (18/24) were classified as moderate quality. The types of interventions were nursing care including follow-ups, home visits and needs assessment (n = 11, 46%), education program (n = 2, 8%), telephone follow-up (n = 6, 25%), psychosocial support (n = 1, 4%), group medical consultations (n = 1, 4%), and Geriatric Assessment Management (n = 1, 4%). Seventeen of the interventions were led by the nurse and five were performed by the health care team including a nurse.

Conclusions

In this systematic review, many of the included studies showed the cost-reducing effect of nurse care. Cost-effectiveness can be demonstrated as a way to convince health care system decision-makers to integrate an intervention into care services; in this respect, this result is significant.

Implications for Nursing Practice

Nurses are one of the key factors in the structure of health care delivery, including financing, cost-effectiveness, and resource management. In terms of cancer care, considering the high treatment costs in the world, there is a need to make the situation cost-effective. As providers of health care services, nurses should provide evidence of cost-reducing interventions.
目的:本研究旨在综合评估护理干预对癌症护理成本影响的研究。方法:检索2001年至2024年PubMed、Scopus、Web of Science、MEDLINE、Cochrane Library和CINAHL中有关癌症护理干预成本-效果的随机对照试验。搜索策略和选择过程遵循系统评价和荟萃分析(PRISMA)指南的首选报告项目。如果研究(1)涉及护理干预(护士主导或护士参与),(2)对成年癌症患者进行的研究,(3)报告的成本效益结果,以及(4)是随机对照试验,则纳入研究。研究选择过程是在Rayyan项目上进行的。采用综合卫生经济评价报告标准(CHEERS)检查表对纳入的研究进行质量评价。结果:24项研究符合标准并进行了分析。超过一半的研究(18/24)被归类为中等质量。干预护理的类型包括跟进、家访和需求评估(n = 11日46%),教育项目(n = 2 8%),电话随访(n = 6 25%),心理支持(n = 1,4%),组织医疗咨询(n = 1,4%)和老年评估管理(n = 1,4%)。其中17项干预由护士领导,5项干预由包括一名护士在内的卫生保健小组执行。结论:在本系统综述中,许多纳入的研究显示了护理降低成本的效果。成本效益可以证明是说服卫生保健系统决策者将干预措施纳入护理服务的一种方式;在这方面,这一结果意义重大。对护理实践的影响:护士是卫生保健服务结构的关键因素之一,包括融资、成本效益和资源管理。在癌症治疗方面,考虑到世界上高昂的治疗费用,有必要使这种情况具有成本效益。作为卫生保健服务的提供者,护士应提供降低成本的干预措施的证据。
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引用次数: 0
期刊
Seminars in Oncology Nursing
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