Driessen Helen P A, Busschbach Jan J V, van der Rijt Carin C D, Elfrink Erna J, Raijmakers Natasja J H, van Roij Janneke, Rietjens Judith, Kranenburg Leonieke W
Department of Psychiatry, Section Medical Psychology and Psychotherapy, Erasmus Medical Center, Rotterdam, The Netherlands
Department of Psychiatry, Section Medical Psychology and Psychotherapy, Erasmus Medical Center, Rotterdam, The Netherlands.
BMJ Support Palliat Care. 2023 Jul 25. doi: 10.1136/spcare-2023-004242.
The care needs of patients with advanced cancer and their relatives change throughout the disease trajectory. This study focused on the care-related problems and needs of patients with advanced cancer and their relatives. This was done from the perspective of centres for information and support.
This cross-sectional study used data from the eQuiPe study: an observational cohort study in which 40 Dutch hospitals participated. All adult patients with a diagnosis of a metastasised tumour and their relatives were eligible. Measures included information on the patients' and relatives' care problems and needs, assessed by the short version of the Problems and Needs in Palliative Care questionnaire. Socioeconomic demographics were also collected.
1103 patients with advanced cancer and 831 relatives were included. Both patients (M=60.3, SD=29.0) and relatives (M=59.2, SD=26.6) experienced most problems in the domain of 'psychological issues'. Both patients (M=14.0, SD=24.2) and relatives (M=17.7, SD=25.7) most frequently reported unmet needs within this domain. The most often reported unmet need by patients was 'worrying about the future of my loved ones' (22.0%); for relatives this was 'fear for physical suffering of the patient' (32.8%). There was no clear relationship between socioeconomic demographics and the experienced unmet needs.
The most often mentioned unmet needs consisted of fears and worries, followed by a broad range of topics within multiple domains. Centres for information and support may play a role in reducing the unmet needs of (potential) visitors as these centres provide support on a broad range of topics.
晚期癌症患者及其亲属的护理需求在疾病发展过程中会发生变化。本研究聚焦于晚期癌症患者及其亲属与护理相关的问题和需求。该研究是从信息与支持中心的角度进行的。
这项横断面研究使用了来自eQuiPe研究的数据:一项观察性队列研究,有40家荷兰医院参与。所有诊断为转移性肿瘤的成年患者及其亲属均符合条件。测量指标包括通过姑息治疗问题与需求问卷简版评估的患者及亲属的护理问题和需求信息。还收集了社会经济人口统计学数据。
纳入了1103例晚期癌症患者和831名亲属。患者(M = 60.3,标准差 = 29.0)和亲属(M = 59.2,标准差 = 26.6)在“心理问题”领域遇到的问题最多。患者(M = 14.0,标准差 = 24.2)和亲属(M = 17.7,标准差 = 25.7)在该领域最常报告未满足的需求。患者最常报告的未满足需求是“担心我所爱的人的未来”(22.0%);亲属则是“担心患者身体遭受痛苦”(32.8%)。社会经济人口统计学与未满足的需求之间没有明确的关系。
最常提到的未满足需求包括恐惧和担忧,其次是多个领域的广泛主题。信息与支持中心可能在减少(潜在)来访者未满足的需求方面发挥作用,因为这些中心在广泛的主题上提供支持。