Cheng Huilin, Leung Carmen Wai Lim, Ng Jeffrey Sheung Ching, Wong Kam Hung, Natarajan Deepa, Chan Lut Ming, Ng Nancy Hiu Yim, Tsang Tsz Wai, Leung Wai Ming, Lo Raymond See Kit
School of Nursing, The Hong Kong Polytechnic University, Hong Kong, China.
Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, China.
BMC Palliat Care. 2025 May 4;24(1):127. doi: 10.1186/s12904-025-01689-3.
Cancer cachexia (CC) is a fatal syndrome most prevalent in palliative care patients and is typically characterized by a progressive increase in weight loss and anorexia. The inability to detect and accurately appraise CC symptoms early can lead to a delayed diagnosis of CC and late initiation of symptom management, subsequently resulting in shorter survival. Research has shown that both patients and primary family caregivers are burdened by worsening CC symptoms, making them susceptible to reduced quality of life (QOL) and increased psychological distress in particular, and necessitating an exploration of ways to improve their well-being. Guided by the Theory of Dyadic Illness Management supplemented by the Symptom Appraisal Pathway Model, the study will be the first to provide a comprehensive understanding of the role of dyadic appraisal of patients' CC symptoms on psychological distress and QOL of palliative care patients and their primary family caregivers over an eight-week follow-up period.
This study will adopt a longitudinal mixed-methods design, combining both quantitative and qualitative data collection at baseline and eight weeks after baseline. 281 dyads of patients with CC and caregivers will be recruited from palliative care units of three hospitals in Hong Kong. Both patients and caregivers will complete a set of questionnaires measuring appraisal of patients' CC symptoms and own psychological distress, and QOL, separately. Semi-structured joint interviews will also be conducted with the same dyads. Quantitative data will be analyzed using the actor-partner interdependence model and the polynomial regression with response surface analysis, while qualitative data will be subjected to qualitative content analysis and trajectory analysis. The findings of the two datasets will be integrated via joint displays.
Findings of this study are expected to advance the emerging science on dyadic symptom management by testing the utility of the theory of Dyadic Illness Management and the Symptom Appraisal Pathway Model, but also to inform the design and content of a theory- and evidence-based CC management intervention to reduce psychological distress and to achieve optimal QOL in CC dyads.
癌症恶病质(CC)是一种在姑息治疗患者中最常见的致命综合征,其典型特征是体重减轻和厌食症逐渐加重。早期无法检测和准确评估CC症状会导致CC诊断延迟和症状管理的延迟启动,进而导致生存期缩短。研究表明,CC症状的恶化给患者及其主要家庭照顾者都带来了负担,尤其使他们容易出现生活质量(QOL)下降和心理困扰增加的情况,因此有必要探索改善他们幸福感的方法。本研究以二元疾病管理理论为指导,并辅以症状评估途径模型,将首次全面了解患者CC症状的二元评估对姑息治疗患者及其主要家庭照顾者在八周随访期内的心理困扰和生活质量的作用。
本研究将采用纵向混合方法设计,在基线和基线后八周收集定量和定性数据。将从香港三家医院的姑息治疗病房招募281对CC患者及其照顾者。患者和照顾者都将分别完成一套问卷,测量对患者CC症状的评估、自身的心理困扰和生活质量。还将对同一对患者和照顾者进行半结构化联合访谈。定量数据将使用actor-partner相互依赖模型和响应面分析的多项式回归进行分析,而定性数据将进行定性内容分析和轨迹分析。两个数据集的结果将通过联合展示进行整合。
本研究的结果预计将通过测试二元疾病管理理论和症状评估途径模型的效用,推进关于二元症状管理的新兴科学,同时为基于理论和证据的CC管理干预措施的设计和内容提供信息,以减少心理困扰并在CC患者-照顾者二元组中实现最佳生活质量。