Beraldi Anna, Kukk Ene, Nest Alexandra, Schubert-Fritschle Gabriele, Engel Jutta, Heußner Pia, Herschbach Peter
Medical Clinic and Policlinic III, Psycho-Oncology, University Hospital Grosshadern, Ludwig-Maximilians-Universität München, Marchioninistr. 15, 81377, Munich, Germany,
Support Care Cancer. 2015 May;23(5):1285-94. doi: 10.1007/s00520-014-2467-x. Epub 2014 Oct 17.
The purpose of this study is to establish whether mental health (MH) outcomes, attitudes towards cancer-specific MH (CSMH) resources, and the availability of such resources differ between rural and urban cancer patients.
Three months after surgery for colorectal cancer, patients received a questionnaire for completion at home assessing distress, depression, anxiety, acceptance, knowledge and use of CSMH resources and the doctor-patient relationship. We adjusted our sample to reference data of the Munich Cancer Registry and documented CSMH resources (e.g. cancer-specific information centres and cancer support groups) using a systematic Internet search.
Five hundred thirty-four patients participated with a mean age of 68.9 years; 44.5 % were female. Urban patients talked less with their doctor about their emotional state (65 %, p < 0.01) and showed poorer knowledge of CSMH resources (60 %, p < 0.002). A good doctor-patient relationship was associated with a better MH outcome. A significant predictor for acceptance was distress. Ninety-four percent of patients without a nearby support facility lived in rural areas (p < 0.001). There were no group differences concerning distress, MH outcomes, or acceptance of CSMH resources.
Despite a higher availability of CSMH resources, urban patients showed poorer doctor-patient relationships and less knowledge of such resources than rural patients. Overall, knowledge and use of these resources were poor. The amount of support facilities available therefore appears to be less important than establishing an efficient communication network between patients, doctors and providers of CSMH resources to achieve satisfaction with treatment of urban and rural cancer patients.
本研究旨在确定农村和城市癌症患者在心理健康(MH)结果、对癌症特异性心理健康(CSMH)资源的态度以及此类资源的可获得性方面是否存在差异。
结直肠癌手术后三个月,患者收到一份问卷,在家中完成,评估痛苦、抑郁、焦虑、接受程度、对CSMH资源的了解和使用情况以及医患关系。我们将样本与慕尼黑癌症登记处的参考数据进行了调整,并通过系统的互联网搜索记录了CSMH资源(如癌症特异性信息中心和癌症支持小组)。
534名患者参与,平均年龄68.9岁;44.5%为女性。城市患者与医生谈论自己情绪状态的次数较少(65%,p<0.01),对CSMH资源的了解较差(60%,p<0.002)。良好的医患关系与更好的MH结果相关。接受程度的一个重要预测因素是痛苦。94%没有附近支持设施的患者居住在农村地区(p<0.001)。在痛苦、MH结果或对CSMH资源的接受程度方面没有组间差异。
尽管CSMH资源的可获得性较高,但城市患者的医患关系比农村患者差,对这些资源的了解也较少。总体而言,这些资源的了解和使用情况较差。因此,可用支持设施的数量似乎不如在患者、医生和CSMH资源提供者之间建立高效的沟通网络重要,以实现城乡癌症患者对治疗的满意度。