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Implementation of a lisocabtagene maraleucel chimeric antigen receptor T-cell therapy outpatient monitoring program: Multicenter nursing/advanced practice provider perspectives. lisocabtagene maraleucel嵌合抗原受体T细胞疗法门诊监测计划的实施:多中心护理/高级医疗服务提供者的观点。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-11-22 DOI: 10.1016/j.soncn.2024.151758
Nicole McEntee, Jacqueline Manago, ChiaChun Lu, Lucy Holmes

Objectives: Lisocabtagene maraleucel (liso-cel; Breyanzi), an autologous chimeric antigen receptor T-cell therapy, has demonstrated efficacy and safety in relapsed/refractory large B-cell lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma, follicular lymphoma, and mantle cell lymphoma. Outpatient monitoring after liso-cel administration has shown lower health care resource utilization and cost and high patient satisfaction. However, outpatient monitoring programs require well-designed processes with collaborations from multiple stakeholders across several facilities. The study objective is to provide learnings and key considerations from nurses and advanced practice providers (APP) with experience setting up and managing liso-cel outpatient monitoring programs.

Data source: Author experience gathered from 3 institutions at 2 workshops.

Results: In the reviewed programs, patients are discharged on the same day after liso-cel infusion and observation. They are required to remain within a short distance of the facility for ≥4 weeks with admission to treatment facilities upon experiencing adverse events (AE). Nurses/APPs report several key features of successful programs: flexibility to carry out essential roles/functions based on institution's resources and staff structure, a phased or hybrid (hospital/clinic) approach to program launch, a core team to run and guide the program, robust training for staff, options to tailor AE monitoring based on institution guidelines, and coordinated transitions between multiple stakeholders and facilities.

Conclusions: Nurses/APPs are critical contributors to liso-cel outpatient monitoring programs. Success in providing appropriate, complex individualized care in these programs can be achieved by using a multistakeholder approach with appropriate staff and patient/caregiver training and careful coordination across multiple functions and facilities.

Implications for nursing practice: The learnings and resources presented may provide insight to considerations around the development of a cell therapy outpatient monitoring program. However, the information provided here should be taken together with other relevant resources and guidelines and should be adapted to align with the institution's own guidelines.

研究目的Lisocabtagene maraleucel(liso-cel;Breyanzi)是一种自体嵌合抗原受体T细胞疗法,对复发/难治性大B细胞淋巴瘤、慢性淋巴细胞白血病/小淋巴细胞淋巴瘤、滤泡淋巴瘤和套细胞淋巴瘤具有疗效和安全性。使用 liso-cel 后的门诊监测显示,医疗资源使用率和成本较低,患者满意度较高。然而,门诊监测计划需要多个机构的多方利益相关者通力合作,精心设计流程。本研究旨在提供护士和高级医疗服务提供者(APP)在建立和管理利索塞尔门诊监测项目方面的经验和主要注意事项:数据来源:作者在 2 次研讨会上从 3 家机构收集的经验:在所审查的项目中,患者在输注和观察利索凝胶后当天即可出院。他们需要在医疗机构附近逗留≥4周的时间,一旦出现不良反应(AE),则需转入治疗机构。护士/APPs 报告了成功项目的几个关键特征:根据机构的资源和人员结构灵活履行基本角色/职能、分阶段或混合(医院/诊所)方式启动项目、核心团队运行和指导项目、对员工进行强有力的培训、根据机构指南定制 AE 监测选项,以及在多个利益相关者和机构之间协调过渡:结论:护士/APP 是 liso-cel 门诊监测项目的重要贡献者。通过采用多方参与的方法,对员工和患者/护理人员进行适当的培训,并在多个职能部门和机构之间进行细致的协调,可以成功地在这些项目中提供适当、复杂的个性化护理:本文介绍的知识和资源可为制定细胞治疗门诊病人监测计划提供参考。然而,此处提供的信息应与其他相关资源和指南一并考虑,并应根据机构自身的指南进行调整。
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引用次数: 0
Effectiveness of Exercise-Based Interventions on Fatigue among Head and Neck Cancer Patients on Radiotherapy: Systematic Review with Meta-Analysis. 以运动为基础的干预措施对头颈癌放疗患者疲劳的效果:系统回顾与元分析》。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-11-20 DOI: 10.1016/j.soncn.2024.151755
Shalini Ganesh Nayak, Krishna Sharan, Ravishankar Nagaraja, Anice George

Objectives: Fatigue is a significant challenge among head and neck cancer patients undergoing radiotherapy, impacting their well-being and daily functioning. Exercise-based interventions hold promise in alleviating this fatigue burden. This systematic review aims to evaluate the effectiveness of exercise-based interventions on fatigue among patients with head and neck cancer receiving radiotherapy.

Methods: We systematically searched for the studies in Cumulative Index to Nursing and Allied Health Literature, PubMed, Cochrane Library Database, MEDLINE, and Google Scholar in the English language from 2000 to 2023. Two reviewers independently identified the articles using key thesaurus and free text terms based on the inclusion criteria. The review was guided by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Statement. Meta-analysis was done by using RevMan 5.3 software.

Results: The systematic review included nine trials encompassing 647 participants, out of which five were randomized control trials and were selected for meta-analysis. Pooled data from randomized control trials showed that exercise-based interventions were effective in reducing few dimensions of fatigue such as general fatigue, physical fatigue, emotional fatigue significantly (P < .001) among Head and Neck Cancer patients receiving radiotherapy.

Conclusion: Preliminary evidence from the review suggests that engaging in exercise-based interventions may reduce fatigue among patients with head and neck cancer receiving radiotherapy. However, future research is necessary, as most of the articles in current review were either pilot studies or feasibility trials.

Implications for nursing practice: This systematic review and meta-analysis protocol was registered in PROSPERO with the register number CRD42023428284.

目的:疲劳是接受放疗的头颈部癌症患者面临的一项重大挑战,影响着他们的身心健康和日常功能。运动干预有望减轻这种疲劳负担。本系统性综述旨在评估运动干预对接受放疗的头颈部癌症患者疲劳的有效性:我们系统地检索了 2000 年至 2023 年期间在 Cumulative Index to Nursing and Allied Health Literature、PubMed、Cochrane Library Database、MEDLINE 和 Google Scholar 中的英文研究。两名审稿人根据纳入标准,使用关键词库和自由文本术语对文章进行了独立鉴定。综述以《系统综述和元分析首选报告项目声明》为指导。使用 RevMan 5.3 软件进行了元分析:系统综述包括九项试验,共有 647 人参加,其中五项是随机对照试验,并被选中进行荟萃分析。来自随机对照试验的汇总数据显示,在接受放疗的头颈部癌症患者中,以运动为基础的干预措施能有效减少疲劳的几个维度,如一般疲劳、身体疲劳和情绪疲劳(P < .001):综述的初步证据表明,参与运动干预可减轻接受放疗的头颈癌患者的疲劳感。然而,由于本次综述中的大多数文章都是试点研究或可行性试验,因此未来的研究还很有必要:本系统综述和荟萃分析方案已在 PROSPERO 注册,注册号为 CRD42023428284。
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引用次数: 0
Adaptation of the Shirom-Melamed Burnout Measure in Parents of Turkish Pediatric Oncology Patients. 土耳其儿科肿瘤患者家长对 Shirom-Melamed 职业倦怠测量法的适应性研究。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-11-20 DOI: 10.1016/j.soncn.2024.151759
Ayşe Ay, Remziye Semerci, Pınar Taşpınar, Gülşah Tanyildiz, Serap Karaman

Objectives: This study was conducted to adapt the Shirom-Melamed Burnout Measure (SMBM) in parents of Turkish pediatric oncology patients.

Methods: This methodological and descriptive study was conducted with 184 parents of pediatric oncology patients from December 2023 to July 2024. Data was collected face to face interviews via an information form and the SMBM. Translation processes, expert opinions, and content validity were meticulously addressed. Data analysis was utilized by IBM SPSS Statistics and AMOS 25.

Results: The mean age of parents was 37.02 ± 8.20, and 94.6% of the parents were mothers. The scale demonstrated high validity (content validity index = 0.97) and excellent internal consistency (Cronbach's alpha = 0.91). The Exploratory Factor Analysis revealed a 4-factor structure, explaining 67.60% of the variance. A modified 4-factor 19-item model of the provided excellent model fit (chi-square/df = 1.946, RMSEA = 0.072, GFI = 0.861, CFI = 0.932, IFI = 0.933, RFI = 0.849, NFI = 0.871, TLI = 0.920).

Conclusions: The Turkish scale with 4-factor 19-item is a valid and reliable tool can be used to determine the burnout level of parents of pediatric oncology patients.

Implications for nursing practice: Healthcare providers should use the SMBM to assess parental burnout, develop targeted support programs, and evaluate the impact of caregiving on parents' well-being.

研究目的本研究旨在调整土耳其儿科肿瘤患者家长的希罗姆-梅拉梅德职业倦怠测量法(SMBM):这项方法学和描述性研究于 2023 年 12 月至 2024 年 7 月对 184 名儿科肿瘤患者的父母进行了调查。通过信息表和 SMBM 面对面访谈收集数据。对翻译过程、专家意见和内容效度进行了细致的处理。数据分析采用 IBM SPSS 统计软件和 AMOS 25:父母的平均年龄为 37.02±8.20 岁,94.6% 的父母为母亲。量表具有较高的有效性(内容效度指数=0.97)和良好的内部一致性(克朗巴赫α=0.91)。探索性因子分析显示了一个 4 因子结构,解释了 67.60% 的方差。修改后的 4 因子 19 项模型具有极佳的模型拟合度(chi-square/df = 1.946,RMSEA = 0.072,GFI = 0.861,CFI = 0.932,IFI = 0.933,RFI = 0.849,NFI = 0.871,TLI = 0.920):土耳其量表包含 4 个因子 19 个项目,是一种有效且可靠的工具,可用于确定儿科肿瘤患者家长的职业倦怠水平:医疗服务提供者应使用SMBM评估父母的职业倦怠,制定有针对性的支持计划,并评估护理工作对父母福祉的影响。
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引用次数: 0
Experiences in Recruitment for Hispanic, Non-Hispanic Black, and Other Non-White Cancer Survivors Through Community Outreach and Other Targeted Approaches. 通过社区宣传和其他有针对性的方法招募西班牙裔、非西班牙裔黑人和其他非白人癌症幸存者的经验。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-30 DOI: 10.1016/j.soncn.2024.151719
Memnun Seven, Emefa Awo Adawudu, Ann Marie Moraitis, Brenda D Evans, Susan Sturgeon, Jennifer Wenzel, Marilyn J Hammer

Objectives: Recruitment of racial/ethnic underserved populations in oncology research is essential to address health disparities. This article presents strategies and lessons learned from community outreach and other approaches for recruiting non-Hispanic Black, Hispanic, and other non-White survivors of cancer into a pilot study that investigated biopsychosocial determinants of health behaviors.

Methods: We critically examined the participant recruitment approaches to explore challenges and successful strategies and develop recommendations for future studies. Direct recruitment strategies included engaging with research staff members' personal community contacts/liaisons and participating in community outreach events (eg, farmers' markets, block parties, library events, cancer awareness events). Indirect recruitment strategies included posting and distribution of study flyers in community centers (eg, LIVESTRONG® at the YMCA, churches, libraries), online platforms (eg, FORCE, Survivor Journey website), and invitation letters sent to individuals identified as eligible through a single state cancer registry.

Results: Between April 2022 and May 2023, among the 64 individuals recruited, 36 were non-Hispanic Black, 25 were Hispanic, and three were American Indian/Alaska Native people. The use of a state cancer registry (64.1%), snowballing/word of mouth (7.8%), and advertisement through an established cancer support organization (ie, FORCE) website (7.8%) were the most effective strategies in this study.

Conclusion: Recruitment of non-Hispanic Black, Hispanic, and other non-White people into biobehavioral studies through community-engaged research is challenging and requires long-term commitment and engagement with partners from target communities and affiliated organizations.

Implication for nursing practice: Registries and community outreach events can build trust for successful enrollment. Using multiple strategies can provide the best opportunities to reach diverse populations and enroll them in cancer-related research studies.

目标:在肿瘤学研究中招募未得到充分服务的种族/族裔人群对于解决健康差异问题至关重要。本文介绍了在一项调查健康行为的生物心理社会决定因素的试点研究中招募非西班牙裔黑人、西班牙裔和其他非白人癌症幸存者的社区外展和其他方法的策略和经验教训:我们对参与者招募方法进行了严格审查,以探索挑战和成功策略,并为未来研究提出建议。直接招募策略包括与研究人员的个人社区联系人/联络人接触,以及参加社区外展活动(如农贸市场、街区聚会、图书馆活动、癌症宣传活动)。间接招募策略包括在社区中心(如基督教青年会、教堂、图书馆的 LIVESTRONG®)、在线平台(如 FORCE、Survivor Journey 网站)张贴和分发研究传单,以及向通过单一州癌症登记处确定为符合条件的个人发送邀请信:2022 年 4 月至 2023 年 5 月间,在招募的 64 人中,36 人为非西班牙裔黑人,25 人为西班牙裔,3 人为美国印第安人/阿拉斯加原住民。在这项研究中,最有效的策略是使用州癌症登记处(64.1%)、滚雪球/口口相传(7.8%)以及通过已有的癌症支持组织(即 FORCE)网站发布广告(7.8%):结论:通过社区参与式研究招募非西班牙裔黑人、西班牙裔和其他非白人参与生物行为研究具有挑战性,需要目标社区和附属组织的长期承诺和合作伙伴的参与:对护理实践的启示:登记处和社区外联活动可以为成功注册建立信任。采用多种策略可为接触不同人群并让他们参与癌症相关研究提供最佳机会。
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引用次数: 0
“Pioneers, yes. We all should think that way” Improving Papua New Guinea Cancer Nurses Education through an International Partnership "先锋,是的。我们都应该这样想",通过国际合作改善巴布亚新几内亚癌症护士教育。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-30 DOI: 10.1016/j.soncn.2024.151723
Catherine Paterson , Merilyn Nicholas , Peter Fore , Delosi Eawetau , Hazel Agudiyosi , Esther Paul Pakau , Standa Norbert , Sheryl Wala , Jasmine Bujalski , Peter Olali , Meredith Leonard , Delilah Shelley , Cathy Young , Jodi Rawlinson , Desmond Yip , Melissa O'Brien , Wendy Spencer , Pauline Rose

Objectives

First, to understand Papua New Guinea (PNG) oncology nursing issues perceived through the nurses’ lens of unmet supportive care needs of people affected by cancer and to identify nurses’ self-perceived educational priorities in cancer care. Second, to evaluate the tailored bidirectional learning and knowledge transfer among the participants of the Australia Capital Territory Health and PNG Oncology Nursing Development Program hosted in Australia in June 2023.

Methods

A qualitative descriptive study was conducted. Two focus groups were audio-recorded, transcribed, and analyzed using inductive thematic analysis. Based on PNG oncology nurses’ experiences and self-assessed educational needs, the findings were analyzed and presented separately for Time 1 before the PNG Oncology Nursing Development program and Time 2 following the completion of the program.

Results

The findings from the Time 1 focus group identified four themes: (1) educational priorities, (2) system-wide challenges, (3) patient unmet care needs, and (4) cultural beliefs. After the completion of the educational program, there were four emergent themes: (1) new educational experiences, (2) learnings into practice, (3) culturally sensitive nursing, and (4) leadership (PNG nursing trailblazers). This study, for the first time, provided the PNG RNs with a “voice,” to empower them to take more leading roles in important decision-making regarding care structures and management.

Conclusion

Policymakers, government officials, and international cancer organizations must continue to work together to support cancer control in PNG in light of the current and projected limited resources and barriers to timely cancer diagnosis and treatment in PNG.

Implications for Nursing Practice

Through observing and learning from a modern cancer department, PNG oncology nurses have gained insight into what is needed for a safe cancer service for both patients and nurses. Oncology nursing education in PNG needs to be further developed, enhanced, and supported for sustainability of cancer nurses in the long term.

目标:首先,从护士的视角了解巴布亚新几内亚(PNG)的肿瘤护理问题,即癌症患者未得到满足的支持性护理需求,并确定护士在癌症护理方面自我感觉的教育重点。其次,评估 2023 年 6 月在澳大利亚举办的澳大利亚首都直辖区卫生和巴布亚新几内亚肿瘤护理发展计划参与者之间量身定制的双向学习和知识转移:进行了一项定性描述性研究。对两个焦点小组进行了录音、转录,并使用归纳式主题分析法进行了分析。根据巴布亚新几内亚肿瘤科护士的经验和自我评估的教育需求,分别对巴布亚新几内亚肿瘤科护理发展计划之前的第一阶段和计划完成之后的第二阶段的研究结果进行了分析和阐述:第一阶段焦点小组的研究结果确定了四个主题:(1) 教育优先事项;(2) 整个系统面临的挑战;(3) 患者未得到满足的护理需求;(4) 文化信仰。教育项目结束后,出现了四个新的主题:(1)新的教育经验;(2)将所学应用于实践;(3)对文化敏感的护理;(4)领导力(巴布亚新几内亚护理开拓者)。这项研究首次为巴布亚新几内亚注册护士提供了 "发言权",使她们有能力在有关护理结构和管理的重要决策中发挥更大的领导作用:政策制定者、政府官员和国际癌症组织必须继续合作,支持巴布亚新几内亚的癌症控制工作,因为巴布亚新几内亚目前和预计的资源有限,而且在及时诊断和治疗癌症方面存在障碍:通过观察和学习现代化的癌症科室,巴新的肿瘤科护士深入了解了为患者和护士提供安全的癌症服务所需的条件。巴布亚新几内亚的肿瘤护理教育需要进一步发展、加强和支持,以实现癌症护士的长期可持续发展。
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引用次数: 0
The Congruence and Interrelationship: A Dyadic Perspective on the Subjective Cognitive Impairment in the Patients with Colorectal Cancer and Their Spousal Caregivers 一致性与相互关系:大肠癌患者及其配偶照顾者主观认知障碍的二元视角。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-28 DOI: 10.1016/j.soncn.2024.151717
Ye Wang , Xiaoke Qiu , Yi Zhang , Rongyu Li , Zheng Sun , Qiuping Li

Objectives

Patients with colorectal cancer (CRC) reported experiencing subjective cognitive impairment (SCI), and their spousal caregivers perceived the patients’ SCI. This cross-sectional study assessed the congruence of SCI between the patients’ self-reports and the spousal caregivers’ perceptions and examined the factors affecting SCI from the dyadic perspective.

Methods

A total of 200 dyads of patients with CRC and their spousal caregivers were invited to complete the survey, which evaluated the SCI, dyadic coping (DC), quality of life, anxiety, and depression for the dyads. Congruence was analyzed using the intraclass correlation coefficient (ICC) and paired-sample t test. Impacting factors analysis was conducted using Pearson correlations, hierarchical multiple regression, and actor–partner interdependence mediation model.

Results

The congruency of SCI between the patient-reported and the spouse-perceived ranged from moderate to good (ICC = 0.75 to 0.86). After controlling demographic variables (the patients’ gender and spouses’ work status), the DC of both patients and spousal caregivers, and the emotional health of patients were significant predictors for patients’ SCI (all P < .05). In the actor–partner interdependence mediation model, there was an actor effect between DC and SCI for both patients and spousal caregivers and a partner effect between DC and SCI for patients. Moreover, patients’ emotional health (anxiety and depression) had the mediating effect between DC and SCI for both patients and spousal caregivers.

Conclusion

Spousal caregivers played a vital role in assessment and management in the SCI of patients. The DC of patients and spousal caregivers and the emotional health of patients (eg, anxiety and depression) were major predictors for the SCI of patients.

Implications for Nursing

Nursing providers should consider the importance of patients’ and spousal caregivers’ perspectives in assessing and managing SCI. This study supports nurses focusing on the congruence and interrelationship of SCI to enhance DC for CRC patients and their spousal caregivers. This approach aims to reduce emotional distress and develop cognitive interventions from a dyadic perspective.

研究目的结肠直肠癌(CRC)患者自述有主观认知障碍(SCI),而其配偶护理人员则认为患者有主观认知障碍。这项横断面研究评估了患者自我报告与配偶照顾者感知的 SCI 之间的一致性,并从夫妇的角度研究了影响 SCI 的因素:共邀请了 200 对 CRC 患者及其配偶照顾者完成调查,评估了他们的 SCI、伴侣应对(DC)、生活质量、焦虑和抑郁情况。采用类内相关系数(ICC)和配对样本 t 检验分析一致性。影响因素分析采用了皮尔逊相关、分层多元回归和行为者-伴侣相互依赖中介模型:患者报告的 SCI 与配偶感知的 SCI 之间的一致性从中等到良好不等(ICC = 0.75 至 0.86)。在控制了人口统计学变量(患者的性别和配偶的工作状况)后,患者和配偶照顾者的直流电以及患者的情绪健康对患者的 SCI 有显著的预测作用(所有 P < .05)。在行为者-伙伴相互依赖中介模型中,患者和配偶照顾者的 DC 与 SCI 之间存在行为者效应,而患者的 DC 与 SCI 之间存在伙伴效应。此外,患者和配偶照顾者的情绪健康(焦虑和抑郁)在DC和SCI之间具有中介效应:结论:配偶照顾者在患者 SCI 的评估和管理中发挥着重要作用。患者和配偶照顾者的 DC 以及患者的情绪健康(如焦虑和抑郁)是预测患者 SCI 的主要因素:对护理工作的启示:护理人员在评估和管理 SCI 时应考虑患者和配偶护理者观点的重要性。本研究支持护士关注 SCI 的一致性和相互关系,以加强 CRC 患者及其配偶护理者的 DC。这种方法旨在减少情绪困扰,并从患者双方的角度制定认知干预措施。
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引用次数: 0
Cancer-Related Cognitive Impairment Associated with APOE rs7412 and BDNF rs6265 in Breast Cancer Survivors 与乳腺癌幸存者 APOE rs7412 和 BDNF rs6265 相关的癌症相关认知障碍
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-28 DOI: 10.1016/j.soncn.2024.151721
Chao-Pin Hsiao , Taichi Goto , Diane Von Ah , Leorey N. Saligan

Objectives

Cancer-related cognitive impairment (CRCI) is a highly prevalent and debilitating symptom reported by breast cancer survivors (BCS). The etiology of CRCI remains unclear, leading to poor symptom management. Building from prior studies, BCS with the C/C genotype of apolipoprotein E (APOE) rs7412 and the T/T genotype of brain-derived neurotrophic factor (BDNF) rs6265 were hypothesized to experience more severe CRCI. Therefore, we investigated the relationships between the severity of CRCI and polymorphisms of APOE and BDNF among BCS.

Methods

This was a subanalysis of data from a larger descriptive, correlational, and cross-sectional study. Subjective and objective CRCI were measured using the Patient-Reported Outcomes Measurement Information System and CANTAB Cambridge Cognitive assessment, respectively. Buccal swab samples were collected to evaluate the single nucleotide polymorphisms. Multivariable generalized linear regression models were used to analyze data.

Results

APOE rs7412 and BDNF rs6265 were significantly associated with lower self-reported cognitive abilities in a total of 353 BCS. Age was positively associated with self-reported cognitive scores, indicating that younger BCS perceived lower cognitive abilities. Individuals carrying genotype of C/T for APOE with the C/C or C/T for BDNF showed positive associations with cognitive abilities.

Conclusions

Younger BCS with the C/C genotype for APOE rs7412 and the T/T genotype for BDNF rs6265 may be at risk for CRCI. Knowledge regarding predictive markers for CRCI symptoms is essential for precision symptom management. Further investigation with a longitudinal and translational design is necessary to explore the etiologies for CRCI.

Implications for Nursing Practice

Integrating genetic phenotyping into routine clinical practice will provide nurses with unique opportunities to understand individual susceptibilities, and how symptoms may trigger other symptoms. Further, findings from these innovative investigations will provide symptom interventionists and implementation scientists with critical data to optimize individualized strategies for symptom prevention, detection, and management.

目的:与癌症相关的认知障碍(CRCI)是乳腺癌幸存者(BCS)报告的一种高发且使人衰弱的症状。CRCI 的病因仍不清楚,导致症状管理不善。在先前研究的基础上,我们假设具有脂蛋白 E(APOE)rs7412 的 C/C 基因型和脑源性神经营养因子(BDNF)rs6265 的 T/T 基因型的乳腺癌幸存者会经历更严重的 CRCI。因此,我们研究了 BCS 中 CRCI 严重程度与 APOE 和 BDNF 多态性之间的关系:这是一项大型描述性、相关性和横断面研究数据的子分析。主观和客观 CRCI 分别采用患者报告结果测量信息系统和 CANTAB 剑桥认知评估进行测量。收集颊拭子样本以评估单核苷酸多态性。采用多变量广义线性回归模型分析数据:结果:在总共 353 名 BCS 患者中,APOE rs7412 和 BDNF rs6265 与自我报告的认知能力较低显著相关。年龄与自我报告的认知能力得分呈正相关,表明较年轻的 BCS 认知能力较低。APOE基因型为C/T、BDNF基因型为C/C或C/T的个体与认知能力呈正相关:结论:具有 APOE rs7412 的 C/C 基因型和 BDNF rs6265 的 T/T 基因型的年轻 BCS 可能有患上 CRCI 的风险。了解 CRCI 症状的预测标志物对于精确的症状管理至关重要。有必要采用纵向和转化设计进行进一步调查,以探索 CRCI 的病因:将基因表型整合到常规临床实践中将为护士提供独特的机会来了解个体易感性,以及症状是如何引发其他症状的。此外,这些创新调查的结果将为症状干预专家和实施科学家提供重要数据,以优化症状预防、检测和管理的个性化策略。
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引用次数: 0
Neurotoxicity in Cancer Survivorship: The Significance of Cancer-Related Cognitive Impairment and Chemotherapy-Induced Peripheral Neuropathy 癌症幸存者的神经毒性:与癌症相关的认知障碍和化疗引起的周围神经病变的重要性》(The Significance of Cancer-Related Cognitive Impairment and Chemotherapy-Induced Peripheral Neuropathy.
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-24 DOI: 10.1016/j.soncn.2024.151724
Ellen M. Lavoie Smith, Diane Von Ah
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引用次数: 0
Understanding Nurses' Role in Systemic Anti-cancer Therapy Day Unit: A Qualitative Study. 了解护士在系统性抗癌治疗日间病房中的角色:定性研究。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-24 DOI: 10.1016/j.soncn.2024.151720
Zhuming Bao, Jenny Harris, Verna Lavender, Anne Marie Rafferty, Jo Armes
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引用次数: 0
Worse Morning Energy Profiles Are Associated with Significant Levels of Stress and Decrements in Resilience in Patients Receiving Chemotherapy 化疗患者晨间精力状况不佳与压力水平和恢复力下降有关。
IF 2.3 4区 医学 Q1 NURSING Pub Date : 2024-08-20 DOI: 10.1016/j.soncn.2024.151718
Alexandra Shelley , Sueann Mark , Astrid Block , Steven M. Paul , Bruce A. Cooper , Marilyn J. Hammer , Yvette P. Conley , Jon Levine , Christine Miaskowski

Objectives

Evidence suggests that lower levels of morning energy are associated with higher levels of stress and lower levels of resilience in patients receiving chemotherapy. Study purposes were to identify subgroups of patients with distinct morning energy profiles; evaluate for differences among the profiles in demographic and clinical characteristics, as well as measures of stress, resilience, and coping.

Methods

A total of 1,343 outpatients receiving chemotherapy completed a demographic questionnaire and measures of global, cancer-related, and cumulative life stress, and resilience at study enrollment. Morning energy was assessed using the Lee Fatigue Scale at six time points over two cycles of chemotherapy. Latent profile analysis was used to identify subgroups of patients with distinct morning energy profiles. Differences among the subgroups were evaluated using parametric and nonparametric tests.

Results

Three morning energy profiles were identified (i.e., High (17.3%), Low (60.3%), Very Low (22.4%)). Compared to High class, the other two morning energy classes were less likely to be employed; had a lower functional status and a higher comorbidity burden; and were more likely to self-report depression and back pain. For all three types of stress, significant differences were found among the three classes with scores that demonstrated a dose response effect (i.e., High < Low < Very Low; as decrements in morning energy increased, stress scores increased). Compared to High class, Very Low class reported higher rates of physical and sexual abuse. The resilience scores exhibited a dose response effect as well (i.e., High > Low > Very Low). Patients with the two worst energy profiles reported a higher use of disengagement coping strategies.

Conclusions

Findings highlight the complex relationships among decrements in morning energy, various types of stress, resilience, and coping in patients undergoing chemotherapy.

Implications for Nursing Practice

Clinicians need to assess for stress and adverse childhood experiences to develop individualized management plans to increase patients’ energy levels.

研究目的有证据表明,接受化疗的患者晨间能量水平较低与压力水平较高和复原力水平较低有关。研究目的是确定具有不同晨间能量特征的患者亚群;评估不同特征的患者在人口统计学和临床特征以及压力、复原力和应对措施方面的差异:共有 1,343 名接受化疗的门诊患者填写了一份人口统计学问卷,并在入组时测量了整体、癌症相关、累积性生活压力和复原力。在两个化疗周期的六个时间点,使用李氏疲劳量表对患者的晨间精力进行评估。通过潜伏特征分析,确定了具有不同晨间能量特征的患者亚组。使用参数和非参数检验对亚组之间的差异进行评估:确定了三种晨间能量特征(即高(17.3%)、低(60.3%)和极低(22.4%))。与 "精力充沛 "组相比,其他两个 "精力充沛 "组受雇的可能性较低;功能状况较差,合并症负担较重;自我报告抑郁和背痛的可能性较大。在所有三种压力类型中,三个等级的得分都存在显著差异,并表现出剂量反应效应(即高 < 低 < 非常低;随着晨间能量下降幅度的增加,压力得分也随之增加)。与 "高 "组相比,"极低 "组报告的身体虐待和性虐待的比例更高。复原力得分也表现出剂量反应效应(即高 > 低 > 非常低)。能量状况最差的两个等级的患者使用脱离应对策略的比例较高:研究结果凸显了化疗患者晨间能量下降、各种类型的压力、复原力和应对策略之间的复杂关系:护理实践的启示:临床医生需要评估压力和不良童年经历,以制定个性化的管理计划,提高患者的精力水平。
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Seminars in Oncology Nursing
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