Depression and anxiety among patients treated for bladder cancer: examining clinical, demographic, and psychosocial predictors.

IF 1.5 Q3 UROLOGY & NEPHROLOGY
American journal of clinical and experimental urology Pub Date : 2023-10-15 eCollection Date: 2023-01-01
Nihal E Mohamed, Tung-Ming Leung, Emma Kt Benn, Talia G Korn, Imran Ali, Dhruti Patel, Adam Gonzalez, Diane Z Quale
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Abstract

Introduction and objective: The significant impact of bladder cancer and treatment on patient health related quality of life (HRQoL) and emotional wellbeing has been documented. Increasing evidence from cancer research emphasizes the importance of examining patients supportive care needs and received social support as factors that could influence their emotional adjustment. The purpose of the study was to assess the demographic and clinical predictors of depression and anxiety among bladder cancer patients and its associations with patient reported supportive care needs and perceived availability of social support.

Methods: A cross-sectional design was used to investigate the study questions. Bladder cancer patients were recruited from the Bladder Cancer Advocacy Network (BCAN) to complete a questionnaire that included the Hospital Anxiety and Depression Scale (HADS), bladder cancer patient need survey (BCNAS-32), and the social provisions scale (SPS). The inclusion criteria restricted our sample to include bladder cancer patients who were English speakers, aged 18-85 years, and were able and willing to provide informed consent. Patients who had metastatic disease, cancer recurrence, or other primary cancers at the time of assessment were excluded from the study.

Results: Participants included 159 bladder cancer patients. The mean age was 62±9.4 years and 51% were male. Almost two-thirds (62%) of patients reported a diagnosis of muscle invasive bladder cancer (MIBC), 25% patient reported clinically significant levels of anxiety, 17% reported clinically significant levels of depression, and 13% and 17% reported abnormal borderline abnormal levels for anxiety and depression, respectively. Univariate regression analyses revealed significant associations between HADS total score, HADS depression and anxiety subscales, patient age, physical functioning/daily living needs, sexuality needs, and perceived social support with higher total scores, anxiety, and depression scores associated with younger age, higher unmet needs, and lower levels of social support. Multivariate regression analyses, showed similar findings confirming the associations depicted by the univariate regression analyses.

Conclusions: Bladder cancer patients experience significant levels of depression and anxiety and these levels are associated with patient age, supportive care unmet needs and lack of social support. Patient focused interventions could be tailored to address these issues with the goal to improve patient HRQoL and emotional adjustment.

癌症患者的抑郁和焦虑:检查临床、人口统计学和心理社会预测因素。
引言和目的:癌症和治疗对患者健康相关生活质量(HRQoL)和情绪健康的重大影响已被记录在案。来自癌症研究的越来越多的证据强调了检查患者支持性护理需求和获得社会支持的重要性,这些因素可能会影响他们的情绪调整。本研究的目的是评估癌症患者抑郁和焦虑的人口统计学和临床预测因素及其与患者报告的支持性护理需求和感知的社会支持可用性的关系。方法:采用横断面设计对研究问题进行调查。从癌症倡导网络(BCAN)招募癌症膀胱患者,以完成包括医院焦虑和抑郁量表(HADS)、癌症膀胱患者需求调查(BCNAS-32)和社会保障量表(SPS)的问卷调查。纳入标准限制我们的样本包括膀胱癌症患者,这些患者年龄18-85岁,会说英语,能够并愿意提供知情同意书。在评估时患有转移性疾病、癌症复发或其他原发性癌症的患者被排除在研究之外。结果:参与者包括159名癌症患者。平均年龄62±9.4岁,51%为男性。近三分之二(62%)的患者报告诊断为肌肉浸润性膀胱癌症(MIBC),25%的患者报告临床显著水平的焦虑,17%报告临床显著程度的抑郁,13%和17%报告焦虑和抑郁的异常临界异常水平。单变量回归分析显示,HADS总分、HADS抑郁和焦虑分量表、患者年龄、身体功能/日常生活需求、性需求和感知社会支持之间存在显著相关性,总分、焦虑和抑郁得分较高与年龄较小、未满足需求较高和社会支持水平较低有关。多变量回归分析显示了类似的结果,证实了单变量回归分析所描述的相关性。结论:癌症患者经历了显著水平的抑郁和焦虑,这些水平与患者年龄、未满足的支持性护理需求和缺乏社会支持有关。以患者为中心的干预措施可以针对这些问题进行定制,目的是提高患者的HRQoL和情绪调整。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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