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Poorer Quality of Life Outcomes Are Associated with Higher Levels of Stress, Lower Levels of Resilience, and Poorer Adjustment to Cancer in Outpatients Receiving Chemotherapy 在接受化疗的门诊患者中,较差的生活质量与较高的压力水平、较低的恢复能力和较差的癌症适应能力有关。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.152015
Jung Ae Kim , Astrid Block , Sueann Mark , Bruce A. Cooper , Steven M. Paul , Frances Cartwright , Marilyn J. Hammer , Yvette P. Conley , Jon D. Levine , Christine Miaskowski

Objectives

The purposes were to identify subgroups of patients (n = 1324) with distinct quality of life (QOL) profiles and evaluate for differences among these subgroups in demographic and clinical characteristics, as well as levels of global, cancer-related, and cumulative life stress; resilience; and mental adjustment to cancer.

Methods

Prior to their second or third cycle of chemotherapy, patients completed a demographic questionnaire, measures of stress (Perceived Stress Scale, global stress), Impact of Event Scale-Revised (IES-R, cancer-related distress), Life Stressor Checklist-Revised (LSC-R, cumulative life stress); resilience (Connor-Davidson Resilience Scale [CDRS]), and mental adjustment (Mental Adjustment to Cancer Scale [MAC]). In addition, they completed the Multidimensional QOL Scale–Patient Version six times over two cycles of chemotherapy. Latent profile analysis was used to identify the distinct QOL profiles. Parametric and nonparametric tests were used to evaluate for differences in risk factors among the QOL profiles.

Results

Three distinct QOL profiles were identified (Low, 26.9%; Moderate, 44.7%; and High, 28.4%). Compared to the High QOL class, the other two classes were younger and more likely to be female and had a higher comorbidity burden and lower functional status. Differences among the QOL classes in PSS, IES-R, and LSC-R scores followed a similar pattern (Low > Moderate > High). Differences were found among the QOL classes in CDRS (Low < Moderate < High) and MAC (Low > Moderate > High) scores.

Conclusions

This study is the first to describe interindividual variability in QOL outcomes among patients receiving chemotherapy. Levels of cancer-related stress reported by Low and Moderate QOL classes suggest that these patients meet the diagnostic criteria for posttraumatic stress and have levels of resilience below the normative score for the general population.

Implications for Nursing Practice

Given that stress and resilience are modifiable risk factors, this information can be used by clinicians to design tailored interventions to improve patients’ QOL.
目的:目的是确定具有不同生活质量(QOL)概况的患者亚组(n = 1324),并评估这些亚组在人口统计学和临床特征以及总体,癌症相关和累积生活压力水平方面的差异;弹性;以及对癌症的心理调整。方法:在第二或第三个化疗周期之前,患者完成人口统计问卷,压力测量(感知压力量表,整体压力),事件影响量表-修订(IES-R,癌症相关压力),生活压力源清单-修订(LSC-R,累积生活压力);心理弹性(Connor-Davidson弹性量表[CDRS])和心理适应(心理癌症适应量表[MAC])。此外,他们在两个化疗周期内完成了六次多维生活质量量表-患者版本。潜在剖面分析用于识别不同的生活质量剖面。使用参数检验和非参数检验来评估生活质量档案中危险因素的差异。结果:确定了3种不同的生活质量谱(低,26.9%;中,44.7%;高,28.4%)。与高生活质量组相比,其他两组患者更年轻,女性居多,合并症负担较高,功能状态较低。PSS, IES-R和LSC-R评分在生活质量等级之间的差异遵循类似的模式(低>中>高)。CDRS评分(Low < Moderate < High)和MAC评分(Low > Moderate > High)存在差异。结论:本研究首次描述了化疗患者生活质量结果的个体差异。低度和中度生活质量分级报告的癌症相关压力水平表明,这些患者符合创伤后压力的诊断标准,其恢复能力水平低于一般人群的标准评分。对护理实践的启示:鉴于压力和恢复力是可改变的风险因素,临床医生可以使用这些信息来设计量身定制的干预措施,以改善患者的生活质量。
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引用次数: 0
The Experience of Patients with Cancer and Their Informal Caregivers Related to Adoptive Cell Therapy: A Qualitative Systematic Review 癌症患者及其非正式照顾者与过继细胞治疗相关的经验:一项质性系统回顾。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151912
Nina Canova , Kylie Teggart , Alexia Cavin-Trombert , Manuela Eicher , Francesca Bosisio , Sara Colomer-Lahiguera

Objectives

Adoptive cell therapy (ACT) is a growing personalized immuno-oncology approach, delivered both in standard of care (SOC) and clinical trial (CT) settings. Understanding patient and informal caregivers (ICs) experiences is crucial to optimizing care. This qualitative systematic review explores the ACT experience across three elements: actors (patients and ICs), settings (CT and SOC), and phases of the care continuum.

Methods

A systematic search was conducted across Medline, Embase, CINAHL, APA PsycInfo, Cochrane, Web of Science, ProQuest Dissertations & Theses, and Google Scholar up to May 8, 2024. Studies were appraised using the JBI Critical Appraisal Checklist for Qualitative Research, with data extracted and synthesized using a meta-aggregation approach. MAXQDA was used to generate co-occurrence networks between key elements and inductively derived codes. A comparative sentiment analysis highlighted emotional differences between CT and SOC settings.

Results

Nineteen qualitative studies were included, capturing experiences of patients (n = 19) and ICs (n = 7) receiving chimeric antigen receptor T cell (n = 17) and tumor-infiltrating lymphocyte (n = 2) therapy in CT (n = 13) and SOC (n = 9) settings. Findings revealed phase-specific challenges across physical, cognitive, psychological, emotional, social, financial, professional, communication, and informational domains. These challenges originate from ACT-related toxicities, care pathway complexity, and the novel nature of the therapy.

Conclusions

This review identifies the key challenges faced by patients and ICs throughout the ACT care pathway, emphasizing the need for tailored interventions based on the phase and setting, as well as improved support systems.

Implications for nursing practices

Recommended strategies include developing decision support tools, establishing caregiver support programs, and implementing navigation services to enhance patient and ICs experiences.
目的:过继细胞疗法(ACT)是一种不断发展的个性化免疫肿瘤学方法,可在标准治疗(SOC)和临床试验(CT)环境中进行。了解患者和非正式护理人员(ic)的经验对于优化护理至关重要。这篇定性系统综述探讨了ACT在三个方面的经验:参与者(患者和ic)、环境(CT和SOC)和护理连续体的各个阶段。方法:系统检索截至2024年5月8日的Medline、Embase、CINAHL、APA PsycInfo、Cochrane、Web of Science、ProQuest dissertis&thesis和谷歌Scholar。使用JBI定性研究关键评估清单对研究进行评估,并使用元聚合方法提取和合成数据。MAXQDA用于生成关键元件与归纳衍生代码之间的共现网络。对比情绪分析强调了CT和SOC设置之间的情绪差异。结果:19包括定性研究,获取患者的经验(n = 19)和ICs (n = 7)接收嵌合抗原受体T细胞(n = 17)和肿瘤浸润淋巴细胞(n = 2)治疗CT (n = 13)和SOC (n = 9)设置。研究结果揭示了生理、认知、心理、情感、社会、财务、专业、沟通和信息领域的阶段性挑战。这些挑战源于act相关的毒性、护理途径的复杂性和治疗的新颖性。结论:本综述确定了患者和ic在整个ACT治疗途径中面临的主要挑战,强调需要根据阶段和环境进行量身定制的干预措施,以及改进的支持系统。对护理实践的影响:建议的策略包括开发决策支持工具,建立护理人员支持计划,以及实施导航服务以提高患者和ic的体验。
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引用次数: 0
Development and Validation of a Patient-Reported Outcome Measure to Assess the Impact of Steroids in the Treatment of Myeloma: The Steroid Symptom Questionnaire–Multiple Myeloma 开发和验证患者报告的评估骨髓瘤治疗类固醇影响的结果测量:多发性骨髓瘤类固醇症状问卷。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151943
Tracy King , Louise Acret , Claudia Rutherford , Margaret-Ann Tait , Jacqueline Jagger , Julija Sipavicius , Georgia McCaughan , Douglas Joshua , Kate White

Objectives

Steroids routinely used in the treatment of multiple myeloma (MM) are associated with adverse effects affecting health-related quality of life (HRQoL). No assessment tool existed to measure the impact of steroids in this population. We developed and psychometrically evaluated the Steroid Symptom Questionnaire–Multiple Myeloma (SSQ-MM).

Methods

A conceptual framework for steroid-related PROs was developed through a systematic review and qualitative interviews. An existing tool was adapted and pretested with patients (n = 5), carers (n = 3), and clinicians (n = 9) for relevance and face validity. In field test 1, the draft-SSQ-MM was administered to 70 patients. Items were chosen based on item-level analysis for acceptability. In Field Test 2, the psychometric properties of the final SSQ-MM were assessed in 140 patients as part of a multicenter study. The SSQ-MM was administered alongside the EORTC QLQ-C30 and MY20, with the SSQ-MM administered again 1 week later.

Results

The SSQ-MM contains 20 items. Stability reliability was supported (ICC = 0.846), and item-total correlations ranged between 0.266 and 0.677, excluding hiccups and blood glucose, which were retained due to clinical relevance. Exploratory factor analysis supported a total score and four multi-item subscales with acceptable internal consistency (α = 0.64 to 0.82). We found evidence of convergent and divergent validity between scales measuring similar and dissimilar constructs on QLQ-C30. The SSQ-MM total score was able to differentiate between patient groups clinically known to differ.

Conclusions

The SSQ-MM provides a validated PROM for use in research and clinical settings to assess the impact of steroids and identify those who may benefit from dose reduction to improve PROs, including HRQoL.

Implications for Nursing Practice

Integrating assessment of steroid adverse effects using the SSQ-MM into routine nursing care can help direct timely interventions or referrals to assist patients better manage the emotional and behavioural effects of steroids. Dose optimisation may reduce steroid effects and improve HRQoL.
目的:用于治疗多发性骨髓瘤(MM)的常规类固醇与影响健康相关生活质量(HRQoL)的不良反应相关。没有评估工具来衡量类固醇对这一人群的影响。我们开发了类固醇症状问卷-多发性骨髓瘤(SSQ-MM)并进行了心理测量学评估。方法:通过系统回顾和定性访谈,建立类固醇相关PROs的概念框架。对现有工具进行调整,并对患者(n = 5)、护理人员(n = 3)和临床医生(n = 9)进行相关性和面部效度预测试。在现场试验1中,70例患者服用了draft-SSQ-MM。项目的选择是基于项目层面的可接受性分析。在现场测试2中,作为一项多中心研究的一部分,对140名患者进行了最终SSQ-MM的心理测量特性评估。SSQ-MM与EORTC QLQ-C30和MY20一起使用,SSQ-MM在1周后再次使用。结果:SSQ-MM量表共20个项目。稳定性可靠度得到支持(ICC = 0.846),项目-总相关性在0.266 ~ 0.677之间,不包括打嗝和血糖,由于临床相关性而保留。探索性因子分析支持总分和四个多条目子量表具有可接受的内部一致性(α = 0.64 ~ 0.82)。我们发现在QLQ-C30上测量相似和不同构式的量表之间存在趋同效度和发散效度的证据。SSQ-MM总分能够区分临床已知存在差异的患者组。结论:SSQ-MM提供了一个经过验证的PROM,可用于研究和临床环境,以评估类固醇的影响,并确定那些可能受益于减少剂量以改善PROs的患者,包括HRQoL。对护理实践的影响:使用SSQ-MM将类固醇不良反应评估整合到常规护理中,可以帮助直接及时干预或转诊,以帮助患者更好地管理类固醇的情绪和行为影响。剂量优化可减少类固醇效应,改善HRQoL。
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引用次数: 0
Finding the Right Time to Discuss Advance Care Planning with Myeloma Patients and Their Carers: An Opportunity for Nursing 寻找合适的时间与骨髓瘤患者和他们的护理人员讨论预先护理计划:护理的机会。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151913
Emma Matthews , Kate Montague-Hellen , Joanne Bird

Purpose

People with multiple myeloma are living longer with an incurable disease due to improved treatments. Despite advance care planning (ACP) and palliative care’s focus on improving symptom management and quality of life, there remains a perception among patients and clinicians that palliative care is only for end-of-life care, leading to uncertainty around when to introduce these conversations. This study examines the lived experiences of myeloma patients and their carers, exploring their views as to when and how they would like to commence meaningful conversations around palliative and end-of-life care.

Methods

Semistructured online interviews were conducted with multiple myeloma patients and their carers (N = 15). Verbatim transcriptions were analyzed using inductive thematic analysis.

Results

From 10 patient and 5 carer interviews, three themes were identified: responsibility, receptivity, and resources. ACP had either not been discussed or would not have been discussed had the patient or carer themself not initiated the discussion. Responsibility for initiating ACP conversations rested with both health care professionals and patients. There was no one, “right time” to do this, though diagnosis should be avoided. Conversations depended on resources, whether human, organizational, community, or charities, to facilitate effective ACP.

Conclusions

ACP conversations with myeloma patients are often delayed. Patients and carers believe it is the responsibility of health care professionals to initiate them at the right time. A period of adjustment is required after diagnosis, but there is no single “right time,” reflecting the heterogeneity of individual needs.

Implications for Nursing Practice

Nurses across all settings should be open and receptive to ACP conversations at all points along the myeloma trajectory. Nurses should normalize the initiation of ACP conversations early in the disease trajectory to promote, and remove barriers to, integrated palliative care. Hematology nurses should work collaboratively with palliative care nurses to support early symptom management for myeloma patients.
目的:由于治疗方法的改进,多发性骨髓瘤患者的寿命延长了。尽管预先护理计划(ACP)和姑息治疗的重点是改善症状管理和生活质量,但患者和临床医生仍然认为姑息治疗只适用于临终关怀,这导致了何时引入这些对话的不确定性。本研究考察了骨髓瘤患者及其护理人员的生活经历,探讨了他们对何时以及如何就姑息治疗和临终关怀展开有意义的对话的看法。方法:对多发性骨髓瘤患者及其护理人员进行半结构化在线访谈(N = 15)。逐字转录分析采用归纳主题性分析。结果:从10名患者和5名护理人员访谈中,确定了三个主题:责任,接受性和资源。ACP要么没有被讨论,要么如果不是病人或护理人员自己发起讨论,就不会被讨论。启动ACP对话的责任在于卫生保健专业人员和患者。没有一个“合适的时间”来做这个,尽管诊断应该避免。对话依赖于资源,无论是人力、组织、社区还是慈善机构,以促进有效的ACP。结论:ACP与骨髓瘤患者的对话经常延迟。患者和护理人员认为,医疗保健专业人员有责任在适当的时候启动它们。诊断后需要一段时间的调整,但没有单一的“正确时间”,这反映了个体需求的异质性。对护理实践的启示:所有环境下的护士都应该开放并接受骨髓瘤轨迹上所有点的ACP对话。护士应该在疾病早期规范ACP对话的启动,以促进和消除综合姑息治疗的障碍。血液科护士应与姑息护理护士协同工作,支持骨髓瘤患者的早期症状管理。
{"title":"Finding the Right Time to Discuss Advance Care Planning with Myeloma Patients and Their Carers: An Opportunity for Nursing","authors":"Emma Matthews ,&nbsp;Kate Montague-Hellen ,&nbsp;Joanne Bird","doi":"10.1016/j.soncn.2025.151913","DOIUrl":"10.1016/j.soncn.2025.151913","url":null,"abstract":"<div><h3>Purpose</h3><div>People with multiple myeloma are living longer with an incurable disease due to improved treatments. Despite advance care planning (ACP) and palliative care’s focus on improving symptom management and quality of life, there remains a perception among patients and clinicians that palliative care is only for end-of-life care, leading to uncertainty around when to introduce these conversations. This study examines the lived experiences of myeloma patients and their carers, exploring their views as to when and how they would like to commence meaningful conversations around palliative and end-of-life care.</div></div><div><h3>Methods</h3><div>Semistructured online interviews were conducted with multiple myeloma patients and their carers (N = 15). Verbatim transcriptions were analyzed using inductive thematic analysis.</div></div><div><h3>Results</h3><div>From 10 patient and 5 carer interviews, three themes were identified: responsibility, receptivity, and resources. ACP had either not been discussed or <em>would</em> not have been discussed had the patient or carer themself not initiated the discussion. Responsibility for initiating ACP conversations rested with both health care professionals and patients. There was no one, “right time” to do this, though diagnosis should be avoided. Conversations depended on resources, whether human, organizational, community, or charities, to facilitate effective ACP.</div></div><div><h3>Conclusions</h3><div>ACP conversations with myeloma patients are often delayed. Patients and carers believe it is the responsibility of health care professionals to initiate them at the right time. A period of adjustment is required after diagnosis, but there is no single “right time,” reflecting the heterogeneity of individual needs.</div></div><div><h3>Implications for Nursing Practice</h3><div>Nurses across all settings should be open and receptive to ACP conversations at all points along the myeloma trajectory. Nurses should normalize the initiation of ACP conversations early in the disease trajectory to promote, and remove barriers to, integrated palliative care. Hematology nurses should work collaboratively with palliative care nurses to support early symptom management for myeloma patients.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 5","pages":"Article 151913"},"PeriodicalIF":2.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144765788","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
Methods of Teaching Nurses Intravenous Systemic Anticancer Therapy Administration: A Scoping Review 对护士静脉全身抗癌治疗管理的教学方法进行综述。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151953
Michelle O’Dowd , Siobhan O’Dowd , Geraldine Austin , Orlaith Hernon , Caitríona Duggan , Peter J Carr

Objectives

The safe administration of intravenous (IV) systemic anticancer therapy (SACT) is a specialized and complex skill due to potential exposure to chemotoxic agents. Inadvertent exposure among millions receiving IV SACT annually may harm both patients and nurses. Identifying the literature's scope and gaps in teaching this clinical treatment is essential. The objective of this scoping review was to identify published literature on educational methods for teaching nurses the safe administration of IV SACT.

Methods

We conducted a JBI-guided scoping review. With a research librarian's assistance, we searched CINAHL, Embase (OVID), Medline (OVID), SCOPUS, and Google Scholar for grey literature. We included studies published between 2010-2023, in the English language, that examined or reported methods of teaching nurses to administer IV SACT safely. Extracted data was presented narratively using the patterns, advances, gaps, evidence for practice and research recommendations (PAGER) framework.

Results

Of 6,820 studies retrieved, 3,725 were screened, resulting in 222 full-text reviews with 20 included for data extraction. Four patterns emerged: education and training methods, interdisciplinary collaboration, global differences, and lack of long-term follow-up and re-validation of educational strategies employed. Teaching methods vary from traditional lectures and clinical practice to simulation, virtual reality, and smartphone applications. However, research, particularly in Europe, is limited, with no European studies cited in the literature.

Conclusions

The absence of randomized controlled trials on simulation-based IV SACT training presents an opportunity to improve oncology nursing education and inform evidence-based practice globally.

Implications for Nursing Practice

More interventional research is required, including meta-analyses and studies on emerging technologies such as simulation and artificial intelligence, to improve patient and provider safety. Such research could enhance patient safety by bridging the gap between clinical practice and skills training.
目的:静脉(IV)全身抗癌治疗(SACT)的安全管理是一项专业而复杂的技能,因为可能暴露于化学毒性药物。在每年接受SACT静脉注射的数百万人中,无意中暴露可能会对患者和护士造成伤害。确定文献的范围和差距,在教学这种临床治疗是必不可少的。本综述的目的是确定已发表的关于向护士传授静脉注射SACT安全管理的教育方法的文献。方法:我们进行了jbi指导的范围审查。在一位研究馆员的协助下,我们检索了CINAHL、Embase (OVID)、Medline (OVID)、SCOPUS和谷歌Scholar,寻找灰色文献。我们纳入了2010-2023年间发表的英语研究,这些研究检查或报道了教护士安全静脉注射SACT的方法。使用模式、进展、差距、实践证据和研究建议(PAGER)框架对提取的数据进行叙述。结果:在检索到的6820项研究中,筛选了3725项,得出222篇全文综述,其中20篇纳入数据提取。出现了四种模式:教育和培训方法、跨学科合作、全球差异以及缺乏长期跟踪和重新验证所采用的教育策略。教学方法多种多样,从传统的讲座和临床实践到模拟、虚拟现实和智能手机应用。然而,研究,特别是在欧洲,是有限的,没有在文献中引用欧洲的研究。结论:基于模拟的IV SACT培训缺乏随机对照试验,这为改善肿瘤护理教育和全球循证实践提供了机会。对护理实践的影响:需要更多的介入研究,包括元分析和新兴技术的研究,如模拟和人工智能,以提高患者和提供者的安全。这种研究可以通过弥合临床实践和技能培训之间的差距来加强患者安全。
{"title":"Methods of Teaching Nurses Intravenous Systemic Anticancer Therapy Administration: A Scoping Review","authors":"Michelle O’Dowd ,&nbsp;Siobhan O’Dowd ,&nbsp;Geraldine Austin ,&nbsp;Orlaith Hernon ,&nbsp;Caitríona Duggan ,&nbsp;Peter J Carr","doi":"10.1016/j.soncn.2025.151953","DOIUrl":"10.1016/j.soncn.2025.151953","url":null,"abstract":"<div><h3>Objectives</h3><div>The safe administration of intravenous (IV) systemic anticancer therapy (SACT) is a specialized and complex skill due to potential exposure to chemotoxic agents. Inadvertent exposure among millions receiving IV SACT annually may harm both patients and nurses. Identifying the literature's scope and gaps in teaching this clinical treatment is essential. The objective of this scoping review was to identify published literature on educational methods for teaching nurses the safe administration of IV SACT.</div></div><div><h3>Methods</h3><div>We conducted a JBI-guided scoping review. With a research librarian's assistance, we searched CINAHL, Embase (OVID), Medline (OVID), SCOPUS, and Google Scholar for grey literature. We included studies published between 2010-2023, in the English language, that examined or reported methods of teaching nurses to administer IV SACT safely. Extracted data was presented narratively using the patterns, advances, gaps, evidence for practice and research recommendations (PAGER) framework.</div></div><div><h3>Results</h3><div>Of 6,820 studies retrieved, 3,725 were screened, resulting in 222 full-text reviews with 20 included for data extraction. Four patterns emerged: education and training methods, interdisciplinary collaboration, global differences, and lack of long-term follow-up and re-validation of educational strategies employed. Teaching methods vary from traditional lectures and clinical practice to simulation, virtual reality, and smartphone applications. However, research, particularly in Europe, is limited, with no European studies cited in the literature.</div></div><div><h3>Conclusions</h3><div>The absence of randomized controlled trials on simulation-based IV SACT training presents an opportunity to improve oncology nursing education and inform evidence-based practice globally.</div></div><div><h3>Implications for Nursing Practice</h3><div>More interventional research is required, including meta-analyses and studies on emerging technologies such as simulation and artificial intelligence, to improve patient and provider safety. Such research could enhance patient safety by bridging the gap between clinical practice and skills training.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 5","pages":"Article 151953"},"PeriodicalIF":2.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144765789","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
Strength in shared experiences: A meta-synthesis of qualitative studies on peer support in haematologic cancer 分享经验的力量:血液学癌症同伴支持定性研究的综合。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151961
Merve Gozde Sezgin, Hicran Bektas

Objectives

Peer support can improve the disease and treatment processes of patients with haematologic cancer. This meta-synthesis aimed to systematically synthesize and interpret the qualitative evidence on how patients experience peer support throughout their illness trajectory.

Methods

This study employed a systematic qualitative meta-synthesis design, using the thematic synthesis approach described by Thomas and Harden. The databases Web of Science, EBSCOhost/CINAHL Complete, MEDLINE, Cochrane Library, ProQuest, PubMed, Scopus, ScienceDirect, and Springer Link were searched up to February 2025. Eligible studies were appraised using the Joanna Briggs Institute Critical Appraisal Checklist for Qualitative Research.

Results

Eight qualitative studies published between 2003 and 2024, with 129 participants across 4 countries, were included. The analysis yielded 4 analytical themes: psychological empowerment, emotional support, provision of information and guidance, and reconstruction of the recovery process.

Conclusion

This meta-synthesis suggests that peer support plays an important role in enhancing the emotional and psychological well-being of patients with haematologic cancer. Peer interactions help reduce fear, uncertainty, and loneliness while strengthening resilience, fostering practical coping strategies, and cultivating a sense of community and hope.

Implications for Nursing Practice

Peer support programs provide emotional resilience and practical guidance by alleviating fear, uncertainty, and loneliness among patients with haematologic cancer. The integration of structured peer support interventions into clinical practice may enhance the psychosocial outcomes of patients, promote empowerment, and support long-term survivorship.
目的:同伴支持可以改善血液学癌症患者的病情和治疗过程。本荟萃综合旨在系统地综合和解释关于患者在整个疾病轨迹中如何经历同伴支持的定性证据。方法:本研究采用Thomas和Harden的专题综合方法,采用系统的定性综合设计。检索截止到2025年2月的Web of Science、EBSCOhost/CINAHL Complete、MEDLINE、Cochrane Library、ProQuest、PubMed、Scopus、ScienceDirect和施普林格Link数据库。使用乔安娜布里格斯研究所定性研究关键评估清单对符合条件的研究进行评估。结果:2003年至2024年间发表的8项定性研究,包括来自4个国家的129名参与者。分析产生了4个分析主题:心理赋权、情感支持、提供信息和指导,以及重建恢复过程。结论:本综合研究提示同伴支持在提高血液病癌症患者的情绪和心理健康方面起着重要作用。同伴互动有助于减少恐惧、不确定性和孤独感,同时增强适应力,培养实用的应对策略,培养社区意识和希望。对护理实践的启示:同伴支持项目通过减轻血液学癌症患者的恐惧、不确定性和孤独感,提供情感弹性和实践指导。将结构化的同伴支持干预纳入临床实践可以提高患者的心理社会结果,促进赋权,并支持长期生存。
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引用次数: 0
Beyond the Pandemic: A Cross-Sectional Study of Hematology Cancer Patients’ Unmet Needs and Experiences of Cancer Care in Ireland and the UK 超越大流行:血液学癌症患者未满足的需求和癌症护理经验在爱尔兰和英国的横断面研究。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151957
Vanessa Boland , Liz O’Connell , Orlaith Cormican , Karen Campbell , Maura Dowling , Amanda Drury

Objectives

The rising incidence of hematological cancers, novel treatments, and increased survivorship highlight the need to understand patient needs postpandemic. This study explored the experiences of individuals affected by hematological cancers in Ireland and the UK as COVID-19 restrictions lifted.

Methods

A cross-sectional descriptive survey was conducted from March 2023 to March 2024 using validated measures of distress, resilience, and unmet needs. Adults with hematological cancers were recruited online through cancer organizations and networks across Ireland and the UK. Quantitative data were analyzed using descriptive and inferential statistics, and qualitative data through thematic analysis.

Results

Ninety-two individuals completed the survey. The top unmet needs were related to tiredness, concerns about appearance, and managing others’ expectations to return to “normal.” Many continued to feel the pandemic’s impact years later. Minimal differences in unmet needs were observed between countries, with participants reporting low distress and moderately high resilience. Thematic analysis of text responses identified three key themes: “psychological impact and self-care methods,” “navigating changing cancer care delivery,” and “sourcing social support,” reflecting the complexities of living with and beyond hematological cancers.

Conclusions

People with hematological cancers in Ireland and the UK continue to experience distress despite moderate resilience, indicating the lasting impact of the pandemic.

Implications for Nursing Practice

Persistent unmet needs around fatigue, appearance, and societal expectations remain. The identified themes underscore the need for supportive interventions focusing on psychological coping strategies, continuity in cancer care delivery, and social support to enhance the well-being of individuals living with and beyond hematological cancers.
目的:血液学癌症发病率的上升、新的治疗方法和生存率的提高突出了了解大流行后患者需求的必要性。这项研究探讨了随着COVID-19限制的解除,爱尔兰和英国受血液病癌症影响的个人的经历。方法:从2023年3月至2024年3月进行了一项横断面描述性调查,使用了痛苦、恢复力和未满足需求的有效测量。患有血液病的成年人是通过爱尔兰和英国的癌症组织和网络在线招募的。定量数据采用描述性和推断性统计进行分析,定性数据采用专题分析。结果:92人完成调查。排在前几位的未满足需求与疲劳、对外表的担忧以及管理他人对回归“正常”的期望有关。许多人在几年后仍然感受到大流行的影响。在未满足的需求方面,不同国家之间的差异很小,参与者报告的痛苦程度较低,适应力中等。对文本回复的主题分析确定了三个关键主题:“心理影响和自我护理方法”,“引导癌症护理服务的变化”和“寻求社会支持”,反映了血液病癌症患者和患者生活的复杂性。结论:爱尔兰和英国的血液癌患者尽管有适度的恢复能力,但仍继续经历痛苦,这表明大流行的持久影响。对护理实践的影响:围绕疲劳,外观和社会期望的持续未满足需求仍然存在。确定的主题强调了支持性干预的必要性,重点是心理应对策略、癌症护理提供的连续性和社会支持,以提高血液病患者和非血液病患者的福祉。
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引用次数: 0
Twenty Years of Nurse-Led Research in Hemato-Oncology: A Mapping Review 二十年来护士主导的血液肿瘤学研究:绘图回顾。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151958
Maura Dowling , Orlaith Hernon , Vanessa Boland , Ciara Nic Giolla Chomhaill , Teresa Meenaghan , Sarah Connolly , Fidelma Hackett , Caroline McCaughey , Barry Quinn , Tracy King , Bethany Maynard , Stavroula Chante , Geraldine Walpole , Orlaith Cormican , Karen Campbell

Objectives

Nurse-led research in hemato-oncology is diverse, but its nature and extent are unknown. This review aimed to identify and map nurse-led research in hemato-oncology over 20 years (2004-2024) to highlight under-researched gaps, describe methodological and topic trends, and allow comparison between geographical regions.

Methods

A mapping review was undertaken following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses, Scoping Review (PRISMA-ScR) checklist. Five databases were systematically searched: Medline (Ovid), CINAHL (EBSCOhost), Embase (Elsevier), ProQuest, and Scopus (Elsevier). Independent screening and data extraction were undertaken on the web-based platform Covidence.

Results

A total of 1,916 sources were included (n = 1,618 journal publications; n = 262 published conference abstracts; n = 36 doctoral dissertations). The most common methodology was non-experimental (60.5%), followed by qualitative (19.2%), experimental (12.5%), evidence syntheses (6.3%), and mixed methods (1.5%). Most of the studies were undertaken by nurses working in the USA, followed by nurses in China, Türkiye, Canada, Australia and Iran. Studies in pediatric, adolescent, and young adult settings represented 42.4% of the included studies. A high number of studies undertaken in hematopoietic stem cell transplant settings were found.

Conclusions

The number of research studies led by nurses in hemato-oncology settings, particularly in the USA, is upward. Most of the research undertaken has adopted a descriptive quantitative methodology. More interventional research is needed to contribute meaningfully to scientific knowledge that enhances the quality of care for individuals affected by blood cancer across the disease trajectory.

Implications for Nursing Practice

To support more nurse-led interventional research, strategic investment in mentorship, protected research time, interdisciplinary collaboration, structured clinical-academic posts, and funding pathways is needed.
目的:护士主导的血液肿瘤学研究是多种多样的,但其性质和程度是未知的。本综述旨在确定和绘制20年来(2004-2024年)护士主导的血液肿瘤学研究,以突出研究不足的差距,描述方法和主题趋势,并允许在地理区域之间进行比较。方法:根据系统评价和荟萃分析的首选报告项目,范围审查(PRISMA-ScR)清单进行制图审查。系统检索了5个数据库:Medline (Ovid)、CINAHL (EBSCOhost)、Embase (Elsevier)、ProQuest和Scopus (Elsevier)。在网络平台covid - ence上进行独立筛选和数据提取。结果:共纳入1,916个来源(n = 1,618篇期刊出版物;N = 262篇已发表的会议摘要;N = 36篇博士论文)。最常见的方法为非实验法(60.5%),其次为定性法(19.2%)、实验法(12.5%)、证据综合法(6.3%)和混合法(1.5%)。大多数研究是由在美国工作的护士进行的,其次是中国、土耳其、加拿大、澳大利亚和伊朗的护士。儿童、青少年和年轻人的研究占纳入研究的42.4%。在造血干细胞移植环境中进行了大量的研究。结论:由护士领导的血液肿瘤学研究的数量正在上升,尤其是在美国。所进行的大多数研究都采用了描述性定量方法。需要更多的介入性研究,为科学知识做出有意义的贡献,从而提高整个疾病轨迹中受血癌影响的个体的护理质量。对护理实践的影响:为了支持更多护士主导的介入研究,需要在指导、保护研究时间、跨学科合作、结构化临床学术职位和资助途径方面进行战略投资。
{"title":"Twenty Years of Nurse-Led Research in Hemato-Oncology: A Mapping Review","authors":"Maura Dowling ,&nbsp;Orlaith Hernon ,&nbsp;Vanessa Boland ,&nbsp;Ciara Nic Giolla Chomhaill ,&nbsp;Teresa Meenaghan ,&nbsp;Sarah Connolly ,&nbsp;Fidelma Hackett ,&nbsp;Caroline McCaughey ,&nbsp;Barry Quinn ,&nbsp;Tracy King ,&nbsp;Bethany Maynard ,&nbsp;Stavroula Chante ,&nbsp;Geraldine Walpole ,&nbsp;Orlaith Cormican ,&nbsp;Karen Campbell","doi":"10.1016/j.soncn.2025.151958","DOIUrl":"10.1016/j.soncn.2025.151958","url":null,"abstract":"<div><h3>Objectives</h3><div>Nurse-led research in hemato-oncology is diverse, but its nature and extent are unknown. This review aimed to identify and map nurse-led research in hemato-oncology over 20 years (2004-2024) to highlight under-researched gaps, describe methodological and topic trends, and allow comparison between geographical regions.</div></div><div><h3>Methods</h3><div>A mapping review was undertaken following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses, Scoping Review (PRISMA-ScR) checklist. Five databases were systematically searched: Medline (Ovid), CINAHL (EBSCOhost), Embase (Elsevier), ProQuest, and Scopus (Elsevier). Independent screening and data extraction were undertaken on the web-based platform Covidence.</div></div><div><h3>Results</h3><div>A total of 1,916 sources were included (n = 1,618 journal publications; n = 262 published conference abstracts; n = 36 doctoral dissertations). The most common methodology was non-experimental (60.5%), followed by qualitative (19.2%), experimental (12.5%), evidence syntheses (6.3%), and mixed methods (1.5%). Most of the studies were undertaken by nurses working in the USA, followed by nurses in China, Türkiye, Canada, Australia and Iran. Studies in pediatric, adolescent, and young adult settings represented 42.4% of the included studies. A high number of studies undertaken in hematopoietic stem cell transplant settings were found.</div></div><div><h3>Conclusions</h3><div>The number of research studies led by nurses in hemato-oncology settings, particularly in the USA, is upward. Most of the research undertaken has adopted a descriptive quantitative methodology. More interventional research is needed to contribute meaningfully to scientific knowledge that enhances the quality of care for individuals affected by blood cancer across the disease trajectory.</div></div><div><h3>Implications for Nursing Practice</h3><div>To support more nurse-led interventional research, strategic investment in mentorship, protected research time, interdisciplinary collaboration, structured clinical-academic posts, and funding pathways is needed.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 5","pages":"Article 151958"},"PeriodicalIF":2.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144859919","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
Psychosocial Distress Among Cancer Patients: A Concept Analysis 癌症患者的心理社会困扰:概念分析。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.152014
Jingyue Xie , Lu Cui , Qianqian Du , Ni Zhang , Xiaoxuan Wang , Chen Yuan , Xiaodan Wu , Meifen Zhang

Objective

To evaluate the literature to clarify the concept of psychosocial distress and to conceptualize it in cancer patients.

Methods

The Walker and Avant concept analysis approach was applied for this review. A comprehensive search of studies published from inception to March 2024 was searched in PubMed, EMBASE, Cochrane Library, Web of Science, and PsycINFO, utilizing the PRISMA 2020 reporting checklist. Additional studies were included by manually reviewing the reference lists from relevant research. A total of 5,941 studies were identified in the initial search, and 36 articles were ultimately included for further analysis and synthesis.

Results

Four attributes of psychosocial distress in terms of cancer were identified: role dysfunction, negative self-perception, disrupted daily life, and unpleasant emotion. Antecedents of psychosocial distress were cancer-related stress and the inability to cope. The consequences were identified as negative health-related behaviors and unhealthy outcomes.

Conclusions

The four identified attributes of psychosocial distress in cancer patients provide healthcare providers with a more comprehensive framework for assessment and recognition than existing instruments, which often focus only on anxiety and depression. It will aid researchers and healthcare providers in understanding the concept, guiding the development of suitable assessment instruments and the design of targeted psychosocial interventions.

Implications for Nursing Practice

Through clarifying the concept, this study may enhance health professional's understanding of the nature of psychosocial distress and improve their awareness of periodically assessing and managing individuals’ psychosocial distress.
目的:对文献进行评价,以澄清心理社会困扰的概念,并对癌症患者的心理社会困扰进行概念化。方法:采用Walker和Avant概念分析方法。利用PRISMA 2020报告清单,在PubMed、EMBASE、Cochrane Library、Web of Science和PsycINFO中检索了从成立到2024年3月发表的研究。通过手动审查相关研究的参考文献列表,纳入了其他研究。在最初的检索中,共有5941项研究被确定,36篇文章最终被纳入进一步的分析和综合。结果:确定了癌症患者心理社会困扰的四个特征:角色功能障碍、消极自我认知、日常生活中断和不愉快情绪。心理社会困扰的前因是癌症相关的压力和无法应对。其后果被确定为负面的健康相关行为和不健康的结果。结论:癌症患者心理社会困扰的四个特征为医疗保健提供者提供了一个比现有工具更全面的评估和识别框架,而现有工具通常只关注焦虑和抑郁。它将帮助研究人员和保健提供者理解这一概念,指导开发适当的评估工具和设计有针对性的心理社会干预措施。对护理实践的启示:透过厘清概念,本研究可增进卫生专业人员对心理社会困扰本质的了解,并提高他们定期评估和管理个体心理社会困扰的意识。
{"title":"Psychosocial Distress Among Cancer Patients: A Concept Analysis","authors":"Jingyue Xie ,&nbsp;Lu Cui ,&nbsp;Qianqian Du ,&nbsp;Ni Zhang ,&nbsp;Xiaoxuan Wang ,&nbsp;Chen Yuan ,&nbsp;Xiaodan Wu ,&nbsp;Meifen Zhang","doi":"10.1016/j.soncn.2025.152014","DOIUrl":"10.1016/j.soncn.2025.152014","url":null,"abstract":"<div><h3>Objective</h3><div>To evaluate the literature to clarify the concept of psychosocial distress and to conceptualize it in cancer patients.</div></div><div><h3>Methods</h3><div>The Walker and Avant concept analysis approach was applied for this review. A comprehensive search of studies published from inception to March 2024 was searched in PubMed, EMBASE, Cochrane Library, Web of Science, and PsycINFO, utilizing the PRISMA 2020 reporting checklist. Additional studies were included by manually reviewing the reference lists from relevant research. A total of 5,941 studies were identified in the initial search, and 36 articles were ultimately included for further analysis and synthesis.</div></div><div><h3>Results</h3><div>Four attributes of psychosocial distress in terms of cancer were identified: role dysfunction, negative self-perception, disrupted daily life, and unpleasant emotion. Antecedents of psychosocial distress were cancer-related stress and the inability to cope. The consequences were identified as negative health-related behaviors and unhealthy outcomes.</div></div><div><h3>Conclusions</h3><div>The four identified attributes of psychosocial distress in cancer patients provide healthcare providers with a more comprehensive framework for assessment and recognition than existing instruments, which often focus only on anxiety and depression. It will aid researchers and healthcare providers in understanding the concept, guiding the development of suitable assessment instruments and the design of targeted psychosocial interventions.</div></div><div><h3>Implications for Nursing Practice</h3><div>Through clarifying the concept, this study may enhance health professional's understanding of the nature of psychosocial distress and improve their awareness of periodically assessing and managing individuals’ psychosocial distress.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 5","pages":"Article 152014"},"PeriodicalIF":2.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144994095","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
Effectiveness of Physical Exercise on Hematopoietic Stem Cell Transplantation: An Umbrella Review 体育锻炼对造血干细胞移植的有效性:综述。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2025-10-01 DOI: 10.1016/j.soncn.2025.151956
Menghua Ye , Yan Xu , Ting Liu , Yang Qiu , Xiaopei Mao , Xiaolan Zhang , Binlian Yao , Min Xu

Objectives

To systematically evaluate and synthesize the available evidence regarding whether physical exercise is effective on improving outcomes in patients undergoing hematopoietic stem cell transplantation (HSCT).

Study Design

There were altogether 10 databases adopted for retrieving systematic reviews till March 2024. The Measurement Tool to Assess Systematic Reviews II (AMSTAR-II) statement and the Grading of Recommendations Assessment, Development and Evaluation system were employed for assessing, summarizing, and grading the evidence. Study duplication was measured by the corrected covered area.

Results

There were 10 studies enrolled, and they had poor level of evidence and overall methodological quality, among which, eight had extremely low methodological quality, whereas two reviews had low methodological quality. We then assessed the evidence quality of 41 primary outcome measures; as a result, 17, 14, and 10 pieces of evidence were rated as moderate, low, and critically low quality separately.

Conclusions

Physical exercise benefits HSCT patients by improving quality of life and reducing fatigue. Evidence quality is moderate to critically low, requiring cautious interpretation.

Implications for Nursing Practice

Physical exercise helps to reduce fatigue, improving quality of life, and should be included in the standard of care for patients undergoing HSCT.
目的:系统评价和综合现有的关于体育锻炼是否能有效改善造血干细胞移植(HSCT)患者预后的证据。研究设计:截至2024年3月,共采用10个数据库进行系统综述检索。采用评估系统评价的测量工具II (AMSTAR-II)声明和建议分级评估、发展和评价系统对证据进行评估、总结和分级。研究重复是通过校正覆盖面积来测量的。结果:纳入10篇文献,证据水平和整体方法学质量较差,其中8篇文献方法学质量极低,2篇文献方法学质量较低。然后,我们评估了41个主要结局指标的证据质量;结果,17、14和10个证据分别被评为中度、低质量和极低质量。结论:体育锻炼可以改善HSCT患者的生活质量和减轻疲劳。证据质量为中等至极低,需要谨慎解释。对护理实践的启示:体育锻炼有助于减轻疲劳,提高生活质量,应纳入HSCT患者的护理标准。
{"title":"Effectiveness of Physical Exercise on Hematopoietic Stem Cell Transplantation: An Umbrella Review","authors":"Menghua Ye ,&nbsp;Yan Xu ,&nbsp;Ting Liu ,&nbsp;Yang Qiu ,&nbsp;Xiaopei Mao ,&nbsp;Xiaolan Zhang ,&nbsp;Binlian Yao ,&nbsp;Min Xu","doi":"10.1016/j.soncn.2025.151956","DOIUrl":"10.1016/j.soncn.2025.151956","url":null,"abstract":"<div><h3>Objectives</h3><div>To systematically evaluate and synthesize the available evidence regarding whether physical exercise is effective on improving outcomes in patients undergoing hematopoietic stem cell transplantation (HSCT).</div></div><div><h3>Study Design</h3><div>There were altogether 10 databases adopted for retrieving systematic reviews till March 2024. The Measurement Tool to Assess Systematic Reviews II (AMSTAR-II) statement and the Grading of Recommendations Assessment, Development and Evaluation system were employed for assessing, summarizing, and grading the evidence. Study duplication was measured by the corrected covered area.</div></div><div><h3>Results</h3><div>There were 10 studies enrolled, and they had poor level of evidence and overall methodological quality, among which, eight had extremely low methodological quality, whereas two reviews had low methodological quality. We then assessed the evidence quality of 41 primary outcome measures; as a result, 17, 14, and 10 pieces of evidence were rated as moderate, low, and critically low quality separately.</div></div><div><h3>Conclusions</h3><div>Physical exercise benefits HSCT patients by improving quality of life and reducing fatigue. Evidence quality is moderate to critically low, requiring cautious interpretation.</div></div><div><h3>Implications for Nursing Practice</h3><div>Physical exercise helps to reduce fatigue, improving quality of life, and should be included in the standard of care for patients undergoing HSCT.</div></div>","PeriodicalId":54253,"journal":{"name":"Seminars in Oncology Nursing","volume":"41 5","pages":"Article 151956"},"PeriodicalIF":2.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144796059","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
期刊
Seminars in Oncology Nursing
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