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癌症幸存者的后续护理:年轻成年人的观点

Follow-up care for cancer survivors: views of the younger adult.

作者信息

Absolom K, Eiser C, Michel G, Walters S J, Hancock B W, Coleman R E, Snowden J A, Greenfield D M

机构信息

Department of Psychology, University of Sheffield, Sheffield S10 2SJ, UK.

出版信息

Br J Cancer. 2009 Aug 18;101(4):561-7. doi: 10.1038/sj.bjc.6605213. Epub 2009 Jul 28.

DOI:10.1038/sj.bjc.6605213
PMID:19638979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2736810/
Abstract

BACKGROUND

Since the launch of the National Cancer Survivorship Initiative, there has been a surge of interest surrounding the value and organisation of long-term follow-up care after cancer treatment. We report the views of 309 adult cancer survivors (aged 18-45 years) on provision of follow-up and preferences for care.

METHODS

A total of 207 survivors completed questionnaires before and after routine consultant-led follow-up appointments and 102 were recruited by post. Measures of health status (including late effects, perceived vulnerability to late effects and quality of life), reasons for attending follow-up (clinical and supportive), issues to be discussed at follow-up and preferences for different models of care were assessed.

RESULTS

In all, 59% of the survivors reported experiencing one or more cancer-related health problems. Survivors rated clinical reasons for attending follow-up more highly than supportive reasons (P<0.001), although nutritional advice and counselling were considered useful (60 and 47%, respectively). Those still receiving scheduled follow-up appointments did not discuss the range of issues intended with 'late effects' and 'fertility', which were particularly under-discussed. Hospital rather than GP follow-up was more highly rated.

CONCLUSION

Survivors value the clinical reassurance currently provided by consultant-led care. However, supportive needs are not systematically addressed. Multi-disciplinary services are recommended to meet supportive needs in addition to clinical care.

摘要

背景

自国家癌症幸存者倡议启动以来,围绕癌症治疗后长期随访护理的价值和组织,人们的兴趣激增。我们报告了309名成年癌症幸存者(年龄在18 - 45岁之间)对随访服务提供情况及护理偏好的看法。

方法

共有207名幸存者在常规由顾问主导的随访预约前后完成了问卷调查,102名通过邮寄方式招募。评估了健康状况指标(包括远期效应、对远期效应的感知易感性和生活质量)、参加随访的原因(临床和支持性)、随访中要讨论的问题以及对不同护理模式的偏好。

结果

总体而言,59%的幸存者报告经历了一种或多种与癌症相关的健康问题。幸存者对参加随访的临床原因的评分高于支持性原因(P<0.001),尽管营养建议和咨询被认为是有用的(分别为60%和47%)。那些仍在接受定期随访预约的人没有讨论“远期效应”和“生育能力”等一系列预期问题,这些问题尤其未得到充分讨论。医院随访而非全科医生随访的评分更高。

结论

幸存者重视目前由顾问主导的护理所提供的临床安心感。然而,支持性需求未得到系统解决。除临床护理外,建议提供多学科服务以满足支持性需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac6b/2736810/0d6e4cc9a0b0/6605213f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac6b/2736810/0d6e4cc9a0b0/6605213f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac6b/2736810/0d6e4cc9a0b0/6605213f1.jpg

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