School of Nursing, University of Wisconsin - Madison, Madison, WI, USA.
University of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Support Care Cancer. 2024 Aug 21;32(9):604. doi: 10.1007/s00520-024-08818-3.
Symptom clusters have important health implications in the context of cancer, but the symptom cluster experiences of cancer caregivers and patient-caregiver dyads are not well studied. To date, most studies report statistically derived symptom clusters among patients and fail to consider the caregivers' experience. This study aimed to assess and characterize self-reported symptom cluster experiences in cancer patient-caregiver dyads.
We recruited 30 patient-caregiver dyads from the outpatient oncology clinics at a Comprehensive Cancer Center in the Midwestern U.S. Participants completed web-based surveys reporting their symptom clusters at weekly intervals over 8 weeks of cancer treatment.
Among 48 eligible dyads, 30 (63%) agreed to participate, 29 provided data, and ≥ 80% (24 patients, 26 caregivers) completed the study. Twenty-eight patients (97%) and twenty-two caregivers (76%) reported experiencing symptoms in clusters. There was substantial variability in the symptoms reported, perceived causality, and directional relationships among symptoms, however both patients' and caregivers' frequently described symptom clusters with psychoneurologic components (co-occurring pain, fatigue, sleep disturbance, anxiety, depression, lack of appetite and/or cognitive disturbance). Symptom clusters were perceived to have a moderate impact on patients' daily lives and a mild-to-moderate impact on caregivers' daily lives.
Dyad members experienced and successfully self-reported symptom clusters, with psychoneurologic symptom clusters prevalent among both patients and their caregivers. Self-report of symptom cluster experiences provides unique insight relevant to clinical management. Findings provide foundational support for development and testing of dyad-based interventions to mitigate symptom clusters and their negative impact on daily life among cancer-patient caregiver dyads.
在癌症背景下,症状群对健康具有重要影响,但癌症护理者和患者-护理者二人组的症状群体验尚未得到充分研究。迄今为止,大多数研究报告的是患者中基于统计学的症状群,而没有考虑护理者的体验。本研究旨在评估和描述癌症患者-护理者二人组中自我报告的症状群体验。
我们从美国中西部综合癌症中心的门诊肿瘤诊所招募了 30 对患者-护理者二人组。参与者每周填写一次网络调查,报告他们在癌症治疗 8 周期间的症状群。
在 48 对符合条件的二人组中,有 30 对(63%)同意参与,有 29 对提供了数据,有≥80%(24 名患者,26 名护理者)完成了研究。28 名患者(97%)和 22 名护理者(76%)报告了症状群。报告的症状、感知的因果关系和症状之间的方向关系存在很大差异,但患者和护理者经常描述了具有心理神经学成分的症状群(同时出现疼痛、疲劳、睡眠障碍、焦虑、抑郁、缺乏食欲和/或认知障碍)。症状群被认为对患者的日常生活有中度影响,对护理者的日常生活有轻度至中度影响。
二人组的成员经历并成功地自我报告了症状群,患者和他们的护理者都普遍存在心理神经学症状群。对症状群体验的自我报告提供了与临床管理相关的独特见解。研究结果为开发和测试基于二人组的干预措施提供了基础支持,以减轻癌症患者-护理者二人组的症状群及其对日常生活的负面影响。