Ostan Rita, Gambino Giuseppe, Franchini Luca, Neri Gianpaolo, Malavasi Italo, Roganti Daniele, Pannuti Raffaella, Veronese Simone, Biasco Guido, Varani Silvia
National Tumor Assistance (ANT) Foundation, Via Jacopo di Paolo, 36, 40128, Bologna, Italy.
FARO Foundation, Turin, Italy.
Support Care Cancer. 2025 Mar 19;33(4):301. doi: 10.1007/s00520-025-09363-3.
Integrated Palliative care Outcome Scale (IPOS) is a specific tool for assessing needs in palliative care, recording and monitoring physical symptoms, emotional concerns, and communication and practical issues. This study aimed to evaluate if the IPOS tool was able to assess the impact of at-home palliative care program on physical symptoms and psychosocial problems in advanced cancer patients.
This observational prospective longitudinal mixed-method study included advanced cancer patients assisted at home. IPOS questionnaire (patient version-7-day recall) was administered at the entry, after 2 and 4 weeks. A qualitative thematic analysis (TA) of the first open-ended question was performed. Change over time in IPOS scores was analyzed by Friedman's test for repeated measures.
Among the 60 patients included (29 men, 31 women; 68.2 ± 14.0 years), 47 completed the 4-week observation period. TA indicated that the 3 main themes running through the three surveys (at the entry, day 14, and day 28) relate patients' concerns about symptoms and side effects of treatments, family members, the evolution of the disease, and the daily issues. Repeated measures test demonstrated that patients entering with medium-high IPOS total score (n = 27) showed a significant decrease in IPOS total score (p = 0.003), physical symptoms (p = 0.002), and communication and practice (p = 0.028) subscales after 2 and 4 weeks.
Patients entering in home care with higher burden of symptoms and psychosocial problems reported significant decrease in IPOS scores. In these patients, IPOS was responsive to change showing substantial clinical improvements after the activation of home assistance.
综合姑息治疗结果量表(IPOS)是一种用于评估姑息治疗需求、记录和监测身体症状、情感问题以及沟通和实际问题的特定工具。本研究旨在评估IPOS工具是否能够评估居家姑息治疗项目对晚期癌症患者身体症状和心理社会问题的影响。
这项观察性前瞻性纵向混合方法研究纳入了接受居家护理的晚期癌症患者。在入组时、2周和4周后发放IPOS问卷(患者版-7天回顾)。对第一个开放式问题进行了定性主题分析(TA)。通过Friedman重复测量检验分析IPOS评分随时间的变化。
纳入的60例患者中(29例男性,31例女性;68.2±14.0岁),47例完成了4周的观察期。主题分析表明,贯穿三次调查(入组时、第14天和第28天)的三个主要主题涉及患者对治疗症状和副作用、家庭成员、疾病进展以及日常问题的担忧。重复测量检验表明,入组时IPOS总分中等偏高的患者(n = 27)在2周和4周后IPOS总分(p = 0.003)、身体症状(p = 0.002)以及沟通和实践(p = 0.028)子量表均显著下降。
症状和心理社会问题负担较重的居家护理患者报告IPOS评分显著下降。在这些患者中,IPOS对变化有反应,在启动居家护理后显示出显著的临床改善。