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因罕见遗传性癌症综合征而被诊断或有发展为肿瘤风险的个体的伴侣的困扰。

Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes.

机构信息

The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Division of Psychosocial Research and Epidemiology, Amsterdam, The Netherlands.

出版信息

Psychooncology. 2011 Jun;20(6):631-8. doi: 10.1002/pon.1951. Epub 2011 Mar 7.

Abstract

OBJECTIVE

Li Fraumeni syndrome (LFS) and Von Hippel-Lindau disease (VHL) are two rare hereditary tumor syndromes, characterized by a high risk of developing multiple tumors at various sites and ages for which preventive and treatment options are limited. For partners, it may be difficult to deal with the on-going threat of tumors in both their spouse and children. Therefore, this study aims to evaluate the prevalence of and factors associated with psychological distress among partners of individuals with or at high risk of LFS or VHL.

METHODS

As part of a nationwide, cross-sectional study, partners of individuals diagnosed with or at high risk of LFS or VHL were invited to complete a self-report questionnaire assessing distress, worries, and health-related quality of life.

RESULTS

Fifty-five (58%) of those high-risk individuals with a partner consented to having their partner approached for the study. In total, 50 partners (91%) completed the questionnaire, of whom 28% reported clinically relevant levels of syndrome-related distress. Levels of distress and worries of the partners and their high-risk spouse were significantly correlated. Younger age and a lack of social support were also associated significantly with heightened levels of distress and worries. The majority of partners (76%) believed that professional psychosocial support should be routinely offered to them.

CONCLUSIONS

Approximately one-quarter of the partners exhibit clinically relevant levels of distress that warrant psychological support. The distress levels of the 'patient' could potentially be used to identify partners at risk of developing clinically relevant levels of distress.

摘要

目的

李-佛美尼综合征(LFS)和冯·希佩尔-林道病(VHL)是两种罕见的遗传性肿瘤综合征,其特征是在不同部位和年龄发生多种肿瘤的风险很高,预防和治疗选择有限。对于伴侣来说,可能很难应对配偶和孩子身上持续存在的肿瘤威胁。因此,本研究旨在评估 LFS 或 VHL 患者或高危人群的伴侣中心理困扰的患病率和相关因素。

方法

作为一项全国性的横断面研究的一部分,邀请 LFS 或 VHL 确诊或高危患者的伴侣填写一份自我报告问卷,评估其困扰、担忧和与健康相关的生活质量。

结果

55 名(58%)高危个体的伴侣同意让其伴侣参与该研究。共有 50 名伴侣(91%)完成了问卷,其中 28%报告存在与综合征相关的临床显著困扰水平。伴侣和其高危配偶的困扰和担忧水平显著相关。年龄较小和缺乏社会支持也与较高水平的困扰和担忧显著相关。大多数伴侣(76%)认为应该向他们提供常规的专业心理社会支持。

结论

大约四分之一的伴侣表现出临床显著的困扰水平,需要心理支持。“患者”的困扰水平可能被用来识别可能出现临床显著困扰水平的伴侣。

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