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Association between postoperative urinary incontinence severity and anxiety in patients with prostate cancer: A chain mediation analysis of ehealth literacy and pelvic floor muscle training adherence 前列腺癌患者术后尿失禁严重程度与焦虑之间的关系:电子健康素养和骨盆底肌肉训练依从性的连锁中介分析
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-23 DOI: 10.1016/j.apjon.2025.100842
Qiuxia Qin, Juan Liu, Duo Zhang, Yuming Zhang, Xiaoqin Xie, Fan Yang, Lihong Huang, Xiaoqin Chen

Objective

This study aimed to examine the chain mediating roles of eHealth literacy and pelvic floor muscle training (PFMT) adherence in the association between urinary incontinence (UI) severity and anxiety.

Methods

A cross-sectional study was conducted using convenience sampling to recruit 240 patients with prostate cancer one month after surgery. Validated instruments were used to assess PFMT adherence (PFMT Adherence Scale), eHealth literacy (eHEALS), UI severity (International Consultation on Incontinence Questionnaire-Short Form), and anxiety (Generalized Anxiety Disorder-7). Structural equation modeling (SEM) was performed using AMOS 24.0 to evaluate direct and indirect effects. Mediation effects were tested using bias-corrected bootstrap analyses with 5000 resamples and 95% CI.

Results

At one month postoperatively, 45.05% of patients experienced anxiety, 60.40% reported moderate-to-severe urinary incontinence, and 71.78% demonstrated low eHealth literacy. High adherence to PFMT was observed in only 36.63% of participants. UI severity was indirectly associated with anxiety through three pathways: eHealth literacy (β = 0.154, P < 0.01), PFMT adherence (β = −0.047, P < 0.05), and a sequential pathway involving both eHealth literacy and PFMT adherence (β = 0.038, P < 0.01). eHealth literacy accounted for 22.3% of the total effect, PFMT adherence for 6.8%, and their combined chain mediation effect for 5.5%.

Conclusions

Urinary incontinence severity one month after prostate cancer surgery is a significant predictor of anxiety, exerting both direct and indirect effects. eHealth literacy and PFMT adherence function as important psychological and behavioral mediators, together explaining 34.6% of the total effect. Interventions aimed at enhancing eHealth literacy and promoting structured pelvic floor muscle training may help reduce postoperative anxiety and support recovery in this population.
目的本研究旨在探讨电子健康素养和骨盆底肌肉训练(PFMT)依从性在尿失禁(UI)严重程度与焦虑之间的连锁中介作用。方法采用方便抽样方法,对240例前列腺癌术后1个月患者进行横断面研究。使用经过验证的工具来评估PFMT依从性(PFMT依从性量表)、电子健康素养(eHEALS)、尿失禁严重程度(国际失禁咨询问卷-短表)和焦虑(广泛性焦虑症-7)。采用AMOS 24.0进行结构方程建模(SEM),评价直接和间接影响。采用偏差校正的自举分析对5000个样本和95% CI进行了中介效应检验。结果术后1个月,45.05%的患者出现焦虑,60.40%的患者出现中重度尿失禁,71.78%的患者出现低电子健康素养。只有36.63%的参与者观察到PFMT的高依从性。UI严重程度通过三条途径与焦虑间接相关:电子健康素养(β = 0.154, P < 0.01), PFMT依从性(β = - 0.047, P < 0.05),以及涉及电子健康素养和PFMT依从性的顺序途径(β = 0.038, P < 0.01)。电子健康素养占总效应的22.3%,PFMT依从性占6.8%,其联合连锁中介效应占5.5%。结论前列腺癌术后1个月尿失禁严重程度是焦虑的重要预测因子,有直接和间接影响。电子健康素养和PFMT依从性是重要的心理和行为中介,共同解释了34.6%的总效应。旨在提高电子健康素养和促进结构化盆底肌肉训练的干预措施可能有助于减少这一人群的术后焦虑和支持康复。
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引用次数: 0
Adaptation and psychometric validation of the Turkish version of the motivation for healing scale in patients with cancer 土耳其版癌症患者治疗动机量表的适应和心理计量学验证
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-23 DOI: 10.1016/j.apjon.2025.100841
Özkan Uğuz , Gülseren Keskin

Objective

The Motivation for Healing Scale (MHS) is a valid and reliable instrument for assessing the motivation for healing in patients with cancer. This methodological study aimed to translate the MHS into Turkish and evaluate the validity and reliability of the Turkish version (T-MHS).

Methods

The study sample consisted of 320 oncology patients selected using convenience sampling method. The T-MHS was assessed for face, content, construct, and convergent validity, as well as internal consistency and test-retest reliability. Face validity was evaluated by patients, content validity was evaluated using the Content Validity Index (CVI), and construct validity was evaluated using Confirmatory Factor Analysis (CFA). Convergent validity was examined by correlating the T-MHS scores with illness uncertainty and hope. Reliability was determined using Cronbach's alpha and test-retest method. Statistical analyses were performed using IBM SPSS Statistics (version 30.0) and AMOS (version 26.0).

Results

The mean patient age was 52.99 ± 13.50 years. The T-MHS demonstrated strong content validity (CVI = 0.98) and high internal consistency (Cronbach's α = 0.87). Test-retest analysis confirmed good stability over time. CFA supported the original five-factor structure and showed excellent model fit. Convergent validity was confirmed by a positive correlation with hope (r = 0.57, P < 0.001) and a negative correlation with illness uncertainty (r = −0.62, P < 0.001).

Conclusions

The T-MHS is a reliable and valid instrument for the clinical assessment of patients with cancer and for research aimed at interventions that enhance motivation for healing in this population.
目的采用愈合动机量表(MHS)评估癌症患者的愈合动机,是一种有效、可靠的工具。本方法学研究旨在将MHS翻译成土耳其语,并评估土耳其语版本(T-MHS)的效度和信度。方法采用方便抽样法抽取320例肿瘤患者作为研究样本。评估T-MHS的面效度、内容效度、结构效度和收敛效度,以及内部一致性和重测信度。面部效度由患者评估,内容效度采用内容效度指数(CVI)评估,结构效度采用验证性因子分析(CFA)评估。通过将T-MHS得分与疾病不确定性和希望相关联来检验收敛效度。信度采用Cronbach’s alpha法和重测法测定。采用IBM SPSS Statistics(30.0版本)和AMOS(26.0版本)进行统计分析。结果患者平均年龄为52.99±13.50岁。T-MHS具有较强的内容效度(CVI = 0.98)和较高的内部一致性(Cronbach’s α = 0.87)。反复测试分析证实了良好的稳定性。CFA支持原始的五因子结构,模型拟合良好。收敛效度与希望呈正相关(r = 0.57, P < 0.001),与疾病不确定性负相关(r = - 0.62, P < 0.001)。结论T-MHS是一种可靠和有效的癌症患者临床评估和研究干预措施的工具,旨在提高这一人群的治疗动机。
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引用次数: 0
Improvements of an oral anti-cancer drug safety management program for patients with cancer 癌症患者口服抗癌药物安全管理方案的改进
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-23 DOI: 10.1016/j.apjon.2025.100833
Hong Yang , Hong Zhang , Jingjuan Zhou , Hongli Li , Renxiu Guo , Hong Zhang , Miaoning You , Liyan Zhang , Wanrong Liu , Yuhan Lu

Objective

To evaluate the impact of an oral anti - cancer drug safety management program on nurses and patients.

Methods

This study was a hospital-level quality-improvement evaluation (pre–post, quasi-experimental design) and was not registered as a clinical trial. It was conducted from August 2024 to December 2024 in a tertiary hospital in Beijing. The program comprised three stages: preparation, training, implementation and supervision. It included tiered training for nurses based on established nursing standards, standardized health education checklists for patients, and continuous support through virtual and in-person clinic visit. Associated improvements were evaluated using self-designed questionnaires. Data were collected from nurses before training and 2 months after program implementation, and from patients before and 1 month after education. Descriptive statistics and non-parametric paired sample tests were used for analysis.

Results

A total of 632 nurses participated in the program, of which 381 nurses completed both evaluations. The knowledge and behavior scores of nurses regarding on correct medication administration, protection against drug exposure, and early management of adverse reactions improved significantly (P < 0.001). The full-score rates for knowledge and behavior increased from 71.82% and 71.55% to92.65% and 94.49%, respectively (Z = −11.462, −13.104, respectively; both P < 0.001). A total of 643 patients received guidance, of which 384 patients completed both evaluations. The knowledge and behavior scores of patients also improved significantly (P < 0.001), with the full-score rates increasing from 59.46% and 68.29% to78.62% and 85.11%, respectively (Z = −11.473, −12.415, respectively; both P < 0.001).

Conclusions

Meaningful improvements were achieved through enhancements to the oral anti-cancer drug safety management program. Standardized training and structured implementation enabled nurses to provide evidence-based patient guidance, thereby enhancing patients' knowledge and skills in safe medication management.
目的评价口服抗癌药物安全管理方案对护士和患者的影响。方法本研究为医院级质量改进评价(前后准实验设计),未注册为临床试验。研究于2024年8月至2024年12月在北京某三级医院进行。该计划包括三个阶段:准备、培训、实施和监督。它包括根据已建立的护理标准对护士进行分层培训,为患者提供标准化的健康教育清单,并通过虚拟和面对面的诊所访问提供持续支持。使用自行设计的问卷评估相关的改善。数据收集于培训前和项目实施后2个月的护士,以及培训前和培训后1个月的患者。采用描述性统计和非参数配对样本检验进行分析。结果共有632名护士参与该项目,其中381名护士完成了两项评估。护士在正确用药、预防药物暴露、不良反应早期处理方面的知识和行为得分显著提高(P < 0.001)。知识和行为的满分率分别从71.82%和71.55%上升到92.65%和94.49% (Z = - 11.462, - 13.104, P均为0.001)。共有643例患者接受了指导,其中384例患者完成了两项评估。患者的知识和行为评分也有明显改善(P < 0.001),满分率分别从59.46%和68.29%提高到78.62%和85.11% (Z = - 11.473, - 12.415, P均为0.001)。结论通过加强口服抗癌药物安全管理,取得了显著的改善效果。规范化培训和结构化实施使护士能够提供循证患者指导,从而提高患者在安全用药管理方面的知识和技能。
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引用次数: 0
Bridging symptoms linking postoperative symptom clusters seven days after esophagectomy: A multicenter network analysis of 418 patients with esophageal cancer 食管切除术后7天的桥接症状:418例食管癌患者的多中心网络分析
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-09 DOI: 10.1016/j.apjon.2025.100830
Yanni Qin , Jing Chen , Ying Li , Ranran Qin , Shuwen Li

Objective

To identify symptom clusters and key bridging symptoms among patients with esophageal cancer on postoperative day 7 after esophagectomy, and to examine sociodemographic correlates of these bridging symptoms.

Methods

This multicenter, cross-sectional study was conducted in three tertiary hospitals in Hefei, Anhui Province, China, between January 2024 and January 2025. A total of 418 patients with esophageal cancer completed the 28-item Convalescent Symptom Assessment Scale for Esophagectomy Patients (CSAS-EC) on postoperative day 7. Exploratory factor analysis (EFA) was used to identify symptom clusters. Symptom networks were estimated using the EBICglasso model (qgraph/bootnet), and bridge centrality indices (bridge strength and bridge expected influence) were calculated using the networktools package to identify bridging symptoms. Network stability was assessed using 1000 bootstrap samples. Independent-samples t-tests and one-way ANOVA were applied to explore associations between bridging symptom severity and sociodemographic characteristics.

Results

Four distinct symptom clusters were identified: psychological, surgery-related, life-disturbance, and local symptoms. Network analysis revealed that disturbed sleep (bridge strength = 0.690), incisional pain (0.587), and limited mobility (0.537) were the top three bridging symptoms linking different clusters. The stability of bridge centrality indices was robust (CS-cor = 0.672 for both bridge strength and bridge expected influence). The severity of these key symptoms differed significantly according to age, sex, place of residence, and caregiver status (all P < 0.05).

Conclusions

Disturbed sleep, incisional pain and limited mobility act as key bridging symptoms linking distinct symptom clusters in patients with Esophageal cancer seven days after esophagectomy. Prioritizing interventions that address these symptoms may interrupt inter-cluster symptom propagation and improve efficiency of postoperative symptom management.
目的探讨食管癌患者食管切除术后第7天的症状群和关键桥接症状,并探讨这些桥接症状的社会人口学相关性。方法于2024年1月至2025年1月在安徽省合肥市三所三级医院进行多中心横断面研究。418例食管癌患者于术后第7天完成28项食管切除术患者恢复期症状评估量表(CSAS-EC)。探索性因素分析(EFA)用于识别症状聚类。使用EBICglasso模型(qgraph/bootnet)估计症状网络,并使用networktools软件包计算桥梁中心性指数(桥梁强度和桥梁预期影响)以识别桥接症状。使用1000个bootstrap样本评估网络稳定性。应用独立样本t检验和单因素方差分析探讨桥接症状严重程度与社会人口学特征之间的关系。结果确定了四种不同的症状群:心理、手术相关、生活干扰和局部症状。网络分析显示,睡眠障碍(桥强度= 0.690)、切口疼痛(0.587)和行动受限(0.537)是连接不同聚类的前三大桥接症状。桥梁中心性指标稳定性较好(桥梁强度和桥梁预期影响CS-cor = 0.672)。这些关键症状的严重程度因年龄、性别、居住地和照顾者状况而有显著差异(均P <; 0.05)。结论食管癌患者食管癌切除术后7天,睡眠障碍、切口疼痛和活动受限是连接不同症状群的关键桥接症状。优先处理这些症状的干预措施可能会中断群集间症状的传播,并提高术后症状管理的效率。
{"title":"Bridging symptoms linking postoperative symptom clusters seven days after esophagectomy: A multicenter network analysis of 418 patients with esophageal cancer","authors":"Yanni Qin ,&nbsp;Jing Chen ,&nbsp;Ying Li ,&nbsp;Ranran Qin ,&nbsp;Shuwen Li","doi":"10.1016/j.apjon.2025.100830","DOIUrl":"10.1016/j.apjon.2025.100830","url":null,"abstract":"<div><h3>Objective</h3><div>To identify symptom clusters and key bridging symptoms among patients with esophageal cancer on postoperative day 7 after esophagectomy, and to examine sociodemographic correlates of these bridging symptoms.</div></div><div><h3>Methods</h3><div>This multicenter, cross-sectional study was conducted in three tertiary hospitals in Hefei, Anhui Province, China, between January 2024 and January 2025. A total of 418 patients with esophageal cancer completed the 28-item Convalescent Symptom Assessment Scale for Esophagectomy Patients (CSAS-EC) on postoperative day 7. Exploratory factor analysis (EFA) was used to identify symptom clusters. Symptom networks were estimated using the EBICglasso model (qgraph/bootnet), and bridge centrality indices (bridge strength and bridge expected influence) were calculated using the networktools package to identify bridging symptoms. Network stability was assessed using 1000 bootstrap samples. Independent-samples t-tests and one-way ANOVA were applied to explore associations between bridging symptom severity and sociodemographic characteristics.</div></div><div><h3>Results</h3><div>Four distinct symptom clusters were identified: psychological, surgery-related, life-disturbance, and local symptoms. Network analysis revealed that disturbed sleep (bridge strength = 0.690), incisional pain (0.587), and limited mobility (0.537) were the top three bridging symptoms linking different clusters. The stability of bridge centrality indices was robust (CS-cor = 0.672 for both bridge strength and bridge expected influence). The severity of these key symptoms differed significantly according to age, sex, place of residence, and caregiver status (all <em>P</em> &lt; 0.05).</div></div><div><h3>Conclusions</h3><div>Disturbed sleep, incisional pain and limited mobility act as key bridging symptoms linking distinct symptom clusters in patients with Esophageal cancer seven days after esophagectomy. Prioritizing interventions that address these symptoms may interrupt inter-cluster symptom propagation and improve efficiency of postoperative symptom management.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100830"},"PeriodicalIF":2.8,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145838852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Empowering oncology nurses: The transformative power of mentorship in cancer care 赋予肿瘤护士权力:癌症护理指导的变革力量
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-08 DOI: 10.1016/j.apjon.2025.100831
Sultan Kav
{"title":"Empowering oncology nurses: The transformative power of mentorship in cancer care","authors":"Sultan Kav","doi":"10.1016/j.apjon.2025.100831","DOIUrl":"10.1016/j.apjon.2025.100831","url":null,"abstract":"","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100831"},"PeriodicalIF":2.8,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145838855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Disease-related communication difficulties and dyadic coping among patients with breast cancer and their spouses: An actor–partner interdependence model 乳腺癌患者及其配偶的疾病相关沟通困难和二元应对:一个行动者-伴侣相互依赖模型
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-08 DOI: 10.1016/j.apjon.2025.100829
Lingling Yang , Xi Zhang , Meina Yang , Liping Zhang , Rong Wang , Ting Wang

Objective

To examine the association between disease communication problems and dyadic coping in patients with breast cancer and their spouses.

Methods

Dyadic coping and disease communication problems were assessed using the General Data Questionnaire, Chinese version of the Dyadic Coping Inventory, and the Cancer-Related Communication Problems within Couples Scale. Actor–partner interaction between dyadic coping and disease communication problems was modeled.

Results

The mean disease communication problems scores were 7.08 ± 2.86 for patients and 7.07 ± 2.87 for spouses. Significant differences were observed between patients and spouses in the emotional support, treatment-specific issues, and protective buffering dimensions of disease communication problems (P < 0.05). The mean dyadic coping scores were 118.67 ± 13.16 for patients and 117.82 ± 12.86 for spouses. Patients reported significantly higher negative coping scores than their spouses (P < 0.01). Disease communication problems in patients and spouses were significantly negatively correlated with self- and partner-dyadic coping scores (r = −0.360 to −0.433, P < 0.01). Disease communication problems of patients and spouses were negatively affected by self and partner positive dyadic coping, while positively influencing negative dyadic coping.

Conclusions

Dyadic coping levels in couples are interactively influenced by their own communication problems and their partner's communication problems. A couple-centered disease communication strategy should be established to improve psychological and social adaptation among spouses. Such an approach may strengthen collaborative coping, deepen relational intimacy, enhance support efficacy, and provide a stronger psychosocial foundation for disease management.
目的探讨乳腺癌患者及其配偶疾病沟通问题与二元应对的关系。方法采用《一般资料问卷》、中文版《双重应对量表》和《夫妻癌症相关沟通问题量表》对夫妻的双重应对和疾病沟通问题进行评估。对二元应对和疾病沟通问题之间的行为者-伴侣互动进行了建模。结果患者平均疾病沟通问题得分为7.08±2.86分,配偶平均疾病沟通问题得分为7.07±2.87分。患者和配偶在情感支持、治疗特异性问题和疾病沟通问题的保护性缓冲维度上存在显著差异(P < 0.05)。患者的平均二元应对得分为118.67±13.16,配偶的平均二元应对得分为117.82±12.86。患者的负性应对得分明显高于配偶(P < 0.01)。患者和配偶的疾病沟通问题与自我和伴侣双元应对得分呈显著负相关(r = - 0.360 ~ - 0.433, P < 0.01)。患者和配偶的疾病沟通问题受自我和伴侣积极应对的负向影响,而对消极应对的正向影响。结论夫妻双向应对水平受自身沟通问题和伴侣沟通问题的交互影响。建立以夫妻为中心的疾病沟通策略,提高夫妻之间的心理和社会适应能力。这种方法可以加强协作应对,加深关系亲密,提高支持效能,并为疾病管理提供更强大的社会心理基础。
{"title":"Disease-related communication difficulties and dyadic coping among patients with breast cancer and their spouses: An actor–partner interdependence model","authors":"Lingling Yang ,&nbsp;Xi Zhang ,&nbsp;Meina Yang ,&nbsp;Liping Zhang ,&nbsp;Rong Wang ,&nbsp;Ting Wang","doi":"10.1016/j.apjon.2025.100829","DOIUrl":"10.1016/j.apjon.2025.100829","url":null,"abstract":"<div><h3>Objective</h3><div>To examine the association between disease communication problems and dyadic coping in patients with breast cancer and their spouses.</div></div><div><h3>Methods</h3><div>Dyadic coping and disease communication problems were assessed using the General Data Questionnaire, Chinese version of the Dyadic Coping Inventory, and the Cancer-Related Communication Problems within Couples Scale. Actor–partner interaction between dyadic coping and disease communication problems was modeled.</div></div><div><h3>Results</h3><div>The mean disease communication problems scores were 7.08 ± 2.86 for patients and 7.07 ± 2.87 for spouses. Significant differences were observed between patients and spouses in the emotional support, treatment-specific issues, and protective buffering dimensions of disease communication problems (<em>P</em> &lt; 0.05). The mean dyadic coping scores were 118.67 ± 13.16 for patients and 117.82 ± 12.86 for spouses. Patients reported significantly higher negative coping scores than their spouses (<em>P</em> &lt; 0.01). Disease communication problems in patients and spouses were significantly negatively correlated with self- and partner-dyadic coping scores (<em>r</em> = −0.360 to −0.433, <em>P</em> &lt; 0.01). Disease communication problems of patients and spouses were negatively affected by self and partner positive dyadic coping, while positively influencing negative dyadic coping.</div></div><div><h3>Conclusions</h3><div>Dyadic coping levels in couples are interactively influenced by their own communication problems and their partner's communication problems. A couple-centered disease communication strategy should be established to improve psychological and social adaptation among spouses. Such an approach may strengthen collaborative coping, deepen relational intimacy, enhance support efficacy, and provide a stronger psychosocial foundation for disease management.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100829"},"PeriodicalIF":2.8,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145882134","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Development and implementation of a supportive care model for cancer patients in the last days of life: A hospital-based program 癌症患者生命最后几天支持性护理模式的发展和实施:基于医院的项目
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-04 DOI: 10.1016/j.apjon.2025.100828
Xiaoting Hou , Renxiu Guo , Wenhua Yu , Ling Yuan , Guoxia Chen , Xiaoxiao Ma , Yujie Zhou , Xue Zhang , Li Liu , Yunhua Wang , Yuhan Lu

Objective

The quality of end-of-life care for cancer patients in China remains unsatisfactory, particularly during their last days and hours, highlighting an urgent need for improvement. This study is aimed to develop and implement a hospital-based quality improvement (QI) program to provide supportive care for terminally ill cancer patients, with the goal of improving the quality of death of cancer patients and family satisfaction.

Methods

This QI program primarily included three phases: developing evidence-based practice standards and related materials; conducting stratified training and providing the bundled supportive care strategies; and implementing quality supervision. The supportive care provided to terminally ill cancer patients and their families consists 30 bundled strategies divided into 5 parts: recognition and confirmation that the person may enter the last few days of life, end-of-life communication, patient-centered supportive care, family-centered supportive care and bereavement support for the family. The quality of death of cancer patients was assessed from the perspective of charge nurses and family members using the Good Death Inventory (GDI), and family satisfaction was evaluated using the Family Satisfaction with Advanced Cancer Care-2 (FAMCARE-2) scale.

Results

One hundred and fourteen patients from five hospitals located in Beijing, Nanjing, and Kunming were provided the supportive care between May 2023 to August 2024, and 112 (98.2%) nurses and 103 (90.4%) families completed the follow-up evaluation. The total GDI score, which ranges from 54 to 378 with higher score indicating a better quality of death, was recorded as 299.81 ± 53.70 from the perspectives of nurses and 310.76 ± 49.55 from family members. The FAMCARE-2 score ranging from 17 to 85 with higher scores indicating greater satisfaction was 80.52 ± 8.75, with scores for symptom control, information support, family support, and patient psychological support at 23.73 ± 2.80, 18.87 ± 2.25, 18.94 ± 2.35, and 18.98 ± 1.95, respectively.

Conclusions

This study systematically implemented supportive care strategies tailored to the needs of patients and their families at the end of life through a hospital-based program and achieving satisfactory outcomes. The systematic approach and innovation of the program are worthy of further promotion.
目的中国癌症患者临终关怀的质量仍然不理想,特别是在他们生命的最后几天和几个小时,迫切需要改善。本研究旨在制定并实施以医院为基础的质量改善(QI)计划,为晚期癌症患者提供支持性护理,以提高癌症患者的死亡质量和家属满意度。方法本项目主要包括三个阶段:制定循证实践标准和相关材料;开展分层培训并提供捆绑的支持性护理策略;实施质量监督。为癌症晚期患者及其家属提供的支持性护理包括30个捆绑策略,分为5个部分:识别和确认患者可能进入生命的最后几天,临终沟通,以患者为中心的支持性护理,以家庭为中心的支持性护理和对家庭的丧亲支持。采用“好死量表”(GDI)从主管护士和家属角度评估癌症患者的死亡质量,采用“晚期癌症护理家庭满意度-2”(FAMCARE-2)量表评估家庭满意度。结果在2023年5月至2024年8月期间,来自北京、南京和昆明5家医院的114例患者接受了支持性护理,112名护士(98.2%)和103名家庭(90.4%)完成了随访评价。总GDI评分范围为54 ~ 378分,评分越高死亡质量越好,护士角度为299.81±53.70分,家属角度为310.76±49.55分。FAMCARE-2评分(17 ~ 85分)为80.52±8.75分,得分越高满意度越高,其中症状控制、信息支持、家庭支持和患者心理支持得分分别为23.73±2.80分、18.87±2.25分、18.94±2.35分和18.98±1.95分。结论本研究通过医院为基础的项目,系统地实施了针对患者及其家属临终需求的支持性护理策略,并取得了满意的结果。方案的系统性和创新性值得进一步推广。
{"title":"Development and implementation of a supportive care model for cancer patients in the last days of life: A hospital-based program","authors":"Xiaoting Hou ,&nbsp;Renxiu Guo ,&nbsp;Wenhua Yu ,&nbsp;Ling Yuan ,&nbsp;Guoxia Chen ,&nbsp;Xiaoxiao Ma ,&nbsp;Yujie Zhou ,&nbsp;Xue Zhang ,&nbsp;Li Liu ,&nbsp;Yunhua Wang ,&nbsp;Yuhan Lu","doi":"10.1016/j.apjon.2025.100828","DOIUrl":"10.1016/j.apjon.2025.100828","url":null,"abstract":"<div><h3>Objective</h3><div>The quality of end-of-life care for cancer patients in China remains unsatisfactory, particularly during their last days and hours, highlighting an urgent need for improvement. This study is aimed to develop and implement a hospital-based quality improvement (QI) program to provide supportive care for terminally ill cancer patients, with the goal of improving the quality of death of cancer patients and family satisfaction.</div></div><div><h3>Methods</h3><div>This QI program primarily included three phases: developing evidence-based practice standards and related materials; conducting stratified training and providing the bundled supportive care strategies; and implementing quality supervision. The supportive care provided to terminally ill cancer patients and their families consists 30 bundled strategies divided into 5 parts: recognition and confirmation that the person may enter the last few days of life, end-of-life communication, patient-centered supportive care, family-centered supportive care and bereavement support for the family. The quality of death of cancer patients was assessed from the perspective of charge nurses and family members using the Good Death Inventory (GDI), and family satisfaction was evaluated using the Family Satisfaction with Advanced Cancer Care-2 (FAMCARE-2) scale.</div></div><div><h3>Results</h3><div>One hundred and fourteen patients from five hospitals located in Beijing, Nanjing, and Kunming were provided the supportive care between May 2023 to August 2024, and 112 (98.2%) nurses and 103 (90.4%) families completed the follow-up evaluation. The total GDI score, which ranges from 54 to 378 with higher score indicating a better quality of death, was recorded as 299.81 ± 53.70 from the perspectives of nurses and 310.76 ± 49.55 from family members. The FAMCARE-2 score ranging from 17 to 85 with higher scores indicating greater satisfaction was 80.52 ± 8.75, with scores for symptom control, information support, family support, and patient psychological support at 23.73 ± 2.80, 18.87 ± 2.25, 18.94 ± 2.35, and 18.98 ± 1.95, respectively.</div></div><div><h3>Conclusions</h3><div>This study systematically implemented supportive care strategies tailored to the needs of patients and their families at the end of life through a hospital-based program and achieving satisfactory outcomes. The systematic approach and innovation of the program are worthy of further promotion.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100828"},"PeriodicalIF":2.8,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145882133","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
A longitudinal study of supportive care needs among Chinese parents of children with acute lymphoblastic leukemia 中国急性淋巴细胞白血病患儿家长支持性护理需求的纵向研究
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-04 DOI: 10.1016/j.apjon.2025.100827
Jingting Wang , Zhuting Zheng , Tian Jin , Yingwen Wang , Huifang Wu , Qi Yang , Linyu Ma , Wen Zhang , Changrong Yuan

Objective

To determine parents' supportive care needs trajectories over the first 8 months following their children's diagnosis and identify the predictors of these trajectories.

Methods

Overall, 100/112 Chinese parents of children newly diagnosed with ALL were recruited. The parents' supportive care needs were tracked at four key time points when the needs were most likely to change: post-diagnosis, induction remission phase, consolidation therapy phase, and post-acute treatment. Latent class growth modeling (LCGM) or growth mixture model (GMM) was used to identify trajectories within each of six needs domains of supportive care needs. Logistic regression was used to identify factors predicting trajectory patterns.

Results

Overall, parents' supportive care needs peaked immediately after diagnosis, declined throughout treatment, and stabilized between the consolidation and post-acute stages. Notably, the trajectories of each domain varied across parent subgroups. Three health care and informational needs trajectories, two daily care and communication needs trajectories, two psychological and spiritual needs trajectories, two medical service needs trajectories, three economic needs trajectories, and two emotional needs trajectories were identified. The class membership was significantly associated with parents' education level, employment status, the family's residency area, average monthly household income, type of medical payment, daily caregiving time, age of child, single child, parents' self-efficacy, and caregiving ability (P < 0.05).

Conclusions

This study identified the dynamic evolution and distinct trajectories of parents’ supportive care needs, along with their key predictors. The findings provide a solid foundation for developing stage- and population-specific interventions, offering practical guidance for optimizing family-centered care and informing supportive policy formulation in pediatric oncology settings.
目的确定儿童确诊后前8个月父母的支持性护理需求轨迹,并确定这些轨迹的预测因子。方法共招募100/112名新诊断为ALL患儿的中国父母。在诊断后、诱导缓解期、巩固治疗期和急性治疗后四个最可能改变的关键时间点对父母的支持性护理需求进行跟踪。使用潜在类别生长模型(LCGM)或生长混合模型(GMM)来确定支持护理需求的六个需求域内的轨迹。采用逻辑回归来确定预测轨迹模式的因素。结果总体而言,父母的支持护理需求在诊断后立即达到高峰,在整个治疗过程中下降,并在巩固期和急性期后保持稳定。值得注意的是,每个域的轨迹在父亚群之间是不同的。确定了3条卫生保健和信息需求轨迹、2条日常护理和交流需求轨迹、2条心理和精神需求轨迹、2条医疗服务需求轨迹、3条经济需求轨迹和2条情感需求轨迹。班级成员与父母受教育程度、就业状况、家庭居住地区、家庭月平均收入、医疗支付方式、每日照顾时间、子女年龄、独生子女、父母自我效能感、照顾能力显著相关(P < 0.05)。结论本研究确定了父母支持护理需求的动态演变和独特的轨迹,以及他们的关键预测因素。研究结果为制定针对阶段和人群的干预措施提供了坚实的基础,为优化以家庭为中心的护理提供了实用指导,并为儿科肿瘤学环境中的支持性政策制定提供了信息。
{"title":"A longitudinal study of supportive care needs among Chinese parents of children with acute lymphoblastic leukemia","authors":"Jingting Wang ,&nbsp;Zhuting Zheng ,&nbsp;Tian Jin ,&nbsp;Yingwen Wang ,&nbsp;Huifang Wu ,&nbsp;Qi Yang ,&nbsp;Linyu Ma ,&nbsp;Wen Zhang ,&nbsp;Changrong Yuan","doi":"10.1016/j.apjon.2025.100827","DOIUrl":"10.1016/j.apjon.2025.100827","url":null,"abstract":"<div><h3>Objective</h3><div>To determine parents' supportive care needs trajectories over the first 8 months following their children's diagnosis and identify the predictors of these trajectories.</div></div><div><h3>Methods</h3><div>Overall, 100/112 Chinese parents of children newly diagnosed with ALL were recruited. The parents' supportive care needs were tracked at four key time points when the needs were most likely to change: post-diagnosis, induction remission phase, consolidation therapy phase, and post-acute treatment. Latent class growth modeling (LCGM) or growth mixture model (GMM) was used to identify trajectories within each of six needs domains of supportive care needs. Logistic regression was used to identify factors predicting trajectory patterns.</div></div><div><h3>Results</h3><div>Overall, parents' supportive care needs peaked immediately after diagnosis, declined throughout treatment, and stabilized between the consolidation and post-acute stages. Notably, the trajectories of each domain varied across parent subgroups. Three health care and informational needs trajectories, two daily care and communication needs trajectories, two psychological and spiritual needs trajectories, two medical service needs trajectories, three economic needs trajectories, and two emotional needs trajectories were identified. The class membership was significantly associated with parents' education level, employment status, the family's residency area, average monthly household income, type of medical payment, daily caregiving time, age of child, single child, parents' self-efficacy, and caregiving ability (<em>P</em> &lt; 0.05).</div></div><div><h3>Conclusions</h3><div>This study identified the dynamic evolution and distinct trajectories of parents’ supportive care needs, along with their key predictors. The findings provide a solid foundation for developing stage- and population-specific interventions, offering practical guidance for optimizing family-centered care and informing supportive policy formulation in pediatric oncology settings.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100827"},"PeriodicalIF":2.8,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145838853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Managing psychological distress in women with breast cancer: A systematic review of intervention trends in the past decade 管理女性乳腺癌患者的心理困扰:过去十年干预趋势的系统回顾
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-02 DOI: 10.1016/j.apjon.2025.100826
Haejeong An , Yoonjung Kim

Objective

The rising incidence and survival rates of breast cancer have increased the number of breast cancer survivors (BCSs) experiencing psychological distress that often overlaps with anxiety, depression, and fear of recurrence. Many existing interventions neglect the unique psychosocial contexts of BCSs, and unclear definitions of distress hinder consistent assessment and management. This systematic review evaluated recent interventions targeting psychological distress in BCSs and offers evidence-based insights.

Methods

Following PRISMA guidelines, six databases were searched for randomized controlled trials on distress interventions for BCSs published between 2014 and July 2025. Study quality was evaluated using Cochrane's RoB 2 tool, and data on intervention characteristics, outcomes, and measurement instruments were extracted.

Results

Fourteen randomized control trials involving 2447 BCSs were included. Among them, 8 (57%) report significant reductions, with six showing immediate post-intervention effects and two demonstrating effects only at follow-up (effect sizes ranged from small to large, Cohen's d = 0.44–1.54). Effective interventions included mindfulness-based approaches, virtual reality-integrated psychotherapy, and cognitive-behavioral therapy combined with hypnosis. In contrast, cognitive-focused interventions lacking experiential components and minimally structured digital programs showed non-significant results.

Conclusions

Effective distress management requires multimodal, theory-based interventions delivered by trained professionals, rather than cognitive-focused or minimally structured approaches. Future interventions should incorporate standardized distress assessment tools and clearly articulated theoretical frameworks, focusing on younger survivors, who remain significantly underrepresented. Although digital platforms enhance accessibility, their effectiveness depends on evidence-based content and structured implementation. Strengthening these elements will improve both the comparability and overall effectiveness of interventions for BCSs.
目的随着乳腺癌发病率和生存率的上升,越来越多的乳腺癌幸存者(BCSs)经历着焦虑、抑郁和害怕复发的心理困扰。许多现有的干预措施忽视了bcs独特的社会心理环境,并且不明确的痛苦定义阻碍了一致的评估和管理。本系统综述评估了最近针对bcs心理困扰的干预措施,并提供了基于证据的见解。方法根据PRISMA指南,检索2014年至2025年7月间发表的6个数据库中关于BCSs窘迫干预的随机对照试验。使用Cochrane的RoB 2工具评估研究质量,并提取有关干预特征、结果和测量工具的数据。结果纳入14项随机对照试验,共纳入2447例bcs。其中8例(57%)报告显著降低,6例显示干预后即刻效果,2例仅在随访中显示效果(效应大小从小到大,Cohen’s d = 0.44-1.54)。有效的干预包括基于正念的方法、虚拟现实综合心理治疗和认知行为疗法结合催眠。相比之下,缺乏经验成分的以认知为中心的干预和最低结构的数字程序显示出不显著的结果。结论有效的痛苦管理需要由训练有素的专业人员提供多模式、基于理论的干预,而不是以认知为中心或最低结构的方法。未来的干预措施应纳入标准化的痛苦评估工具和明确阐述的理论框架,重点关注仍然严重不足的年轻幸存者。尽管数字平台提高了可访问性,但其有效性取决于基于证据的内容和结构化的实施。加强这些要素将提高bcs干预措施的可比性和总体有效性。
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引用次数: 0
Stigma experiences among young and middle-aged testicular cancer survivors in China: A phenomenological study 中国中青年睾丸癌幸存者的耻辱感经历:现象学研究
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2025-12-02 DOI: 10.1016/j.apjon.2025.100825
Yu Zhao , Dan Li , Meng Zhang , Wei Yan , Hong Shen , Miaomiao Xu , Yuxin Liu

Objective

To explore the lived experiences and core structures of stigma among young and middle-aged Chinese testicular cancer (TC) survivors using a phenomenological approach.

Methods

A qualitative phenomenological study was conducted with 15 TC survivors aged 18–45 years, purposively recruited from a tertiary hospital in Beijing. In-depth semi-structured interviews were conducted, with data collection continuing until thematic saturation was reached. All interviews were audio-recorded, transcribed verbatim, and analyzed using Colaizzi's seven-step method to extract significant statements, formulate meanings, and generate themes.

Results

Four overarching themes and 11 subthemes emerged, situated within a social–ecological framework. (1) Internalized and Embodied Stigma (Individual Level): Shame-driven self-blame, hypervigilance toward bodily changes, and intergenerational transmission of stigma. (2) Relational Diplomacy and “Face” Management (Interpersonal Level): The ambivalence of family secrecy, strategic management of social capital, and contraction of social networks. (3) System-Driven Stigma (Community/Institutional Level): Cultural moralization of illness, clinical interactions inadvertently reinforcing stigma, and structural discrimination or neglect. (4) Confucian Ideology of the Body (Societal/Cultural Level): Moral weight of perceived lineage disruption and cultural expectations of bodily integrity.

Conclusions

Stigma among young and middle-aged Chinese TC survivors is pervasive and shaped by the interplay of biological vulnerability, Confucian moral values, and institutional structures. A comprehensive, culturally grounded, multi-level stigma-reduction strategy—spanning the individual, family, community, and health care system—is urgently needed to support psychosocial adaptation and improve survivorship outcomes.
目的用现象学方法探讨中国中青年睾丸癌(TC)幸存者的生活经历和耻辱感的核心结构。方法从北京某三级医院择取15例年龄在18 ~ 45岁的TC幸存者进行定性现象学研究。进行了深入的半结构化访谈,继续收集数据,直到达到主题饱和。所有的访谈都被录音,逐字抄写,并使用Colaizzi的七步法进行分析,以提取重要的陈述,形成意义,并产生主题。结果:在社会生态框架内,出现了4个总体主题和11个副主题。(1)内化与具身污耻感(个体层面):羞耻感驱动的自责、对身体变化的过度警惕和污耻感的代际传递。(2)关系外交与“面子”管理(人际层面):家庭保密的矛盾心理、社会资本的战略管理和社会网络的收缩。(3)系统驱动的病耻感(社区/机构层面):疾病的文化道德化、无意中强化病耻感的临床互动以及结构性歧视或忽视。(4)儒家的身体意识形态(社会/文化层面):对世系断裂的认知和对身体完整性的文化期望的道德权重。结论:在中国中青年TC幸存者中,耻辱感普遍存在,并受到生物脆弱性、儒家道德价值观和制度结构的相互影响。迫切需要一个全面的、以文化为基础的、多层次的减少耻辱感的策略——跨越个人、家庭、社区和卫生保健系统——以支持社会心理适应和改善生存结果。
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引用次数: 0
期刊
Asia-Pacific Journal of Oncology Nursing
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