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丹麦癌症康复研究:FOCARE研究项目参与者的社会特征与癌症晚期效应

Research in Danish cancer rehabilitation: social characteristics and late effects of cancer among participants in the FOCARE research project.

作者信息

Høybye Mette Terp, Dalton Susanne Oksbjerg, Christensen Jane, Larsen Lone Ross, Kuhn Katrin Gaardbo, Jensen Jette Nygaard, Carlsen Kathrine, Johansen Christoffer

机构信息

Department of Psychosocial Cancer Research, Institute of Cancer Epidemiology, Danish Cancer Society, Copenhagen, Denmark.

出版信息

Acta Oncol. 2008;47(1):47-55. doi: 10.1080/02841860701418846.

Abstract

Worldwide, the number of cancer survivors is increasing, owing to improvements in cancer therapy, resulting in an increased need to address the physical and mental sequelae of cancer. This paper introduces a Danish psychosocial cancer intervention and presents the baseline characteristics of the cancer survivors with respect to cancer site, sociodemographic variables, social network, lifestyle, self-rated health and the prevalence of cancer-related late effects. The study is part of the FOCARE research project, in which the long-term effects of the rehabilitation programme are evaluated systematically. The study is based on data from a self-administered baseline questionnaire filled in by 2 174 cancer survivors who registered for a 1-week, publicly paid rehabilitation retreat and were invited to participate in the FOCARE study in the period 25 November 2002 to 31 December 2005. The response rate at baseline was 86% (n = 1876). Most participants were younger women with breast cancer. They were generally well educated and working. The cancer survivors reported having comprehensive social networks and being physically active. Several cancer-related symptoms were reported by women with cancers at selected sites, of which fatigue was the most prevalent. More than half reported good-to-excellent self-rated health, while fair-to-poor health was reported by 40%, most of whom were survivors of lung (56%) and haematological (48%) cancers. The results indicate that Danish cancer survivors experience considerably reduced physical health, possibly as late physical effects of treatment. The problems reported by the cancer survivors suggest that cancer rehabilitation should include these aspects of living after cancer and take account of differences among cancer survivors with regard to cancer site, sex, age, family, working status and social position. These challenges might be addressed optimally in multi-dimensional rehabilitation programmes.

摘要

在全球范围内,由于癌症治疗水平的提高,癌症幸存者的数量正在增加,这导致应对癌症身心后遗症的需求也日益增长。本文介绍了丹麦的一项癌症心理社会干预措施,并呈现了癌症幸存者在癌症部位、社会人口统计学变量、社会网络、生活方式、自评健康状况以及癌症相关迟发效应患病率方面的基线特征。该研究是FOCARE研究项目的一部分,在该项目中,对康复计划的长期效果进行了系统评估。本研究基于2174名癌症幸存者自行填写的基线调查问卷数据,这些幸存者报名参加了为期1周的公费康复疗养,并受邀在2002年11月25日至2005年12月31日期间参与FOCARE研究。基线时的回复率为86%(n = 1876)。大多数参与者是患有乳腺癌的年轻女性。她们普遍受过良好教育且有工作。癌症幸存者报告称拥有广泛的社会网络且身体活跃。患有特定部位癌症的女性报告了几种与癌症相关的症状,其中疲劳最为普遍。超过一半的人报告自评健康状况良好至极佳,而40%的人报告健康状况一般至较差,其中大多数是肺癌(56%)和血液系统癌症(48%)的幸存者。结果表明,丹麦癌症幸存者的身体健康状况明显下降,这可能是治疗的晚期身体影响。癌症幸存者报告的问题表明,癌症康复应涵盖癌症后生活的这些方面,并考虑到癌症幸存者在癌症部位、性别、年龄、家庭、工作状况和社会地位方面的差异。这些挑战可能在多维度康复计划中得到最佳解决。

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