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遗传性癌症遗传咨询和基因检测受检者的入侵和回避行为

Intrusion and avoidance in subjects undergoing genetic investigation and counseling for hereditary cancer.

机构信息

Department of Public Health and Primary Health Care, University of Bergen, 5018 Bergen, Norway.

出版信息

Support Care Cancer. 2009 Nov;17(11):1371-81. doi: 10.1007/s00520-009-0594-6. Epub 2009 Feb 18.

DOI:10.1007/s00520-009-0594-6
PMID:19224252
Abstract

GOALS OF WORK

Genetic counseling for hereditary cancer is expected to involve a growing number of individuals in the near future since an increasing number of genetic tests are offered. This study was designed to identify psychosocial variables predicting distress after genetic investigation and genetic counseling (GC) in order to develop new counseling strategies.

MATERIALS AND METHODS

A prospective multi-site study was undertaken on 214 patients undergoing GC for hereditary cancer to explore the relationships between socio-demographic variables, medical variables, social support, self-efficacy, physical functioning, satisfaction with GC, the level of worry after GC, results of genetic testing, and the course and outcomes of distress. Distress was measured with the Impact of Event Scale, which includes subscales of intrusion and avoidance. Patients completed questionnaires mailed to them before and after GC.

MAIN RESULTS

The mean level of intrusion and avoidance was moderate, even though one quarter of participants reported a severe level of intrusion at baseline. Subjects with a low level of self-efficacy at baseline and high level of worry immediately after GC seemed to be vulnerable to both intrusion and avoidance. Lower level of intrusion was also associated with having a first-degree relative with cancer, while a lower avoidance level was associated with a higher level of education, having cancer, more social support, and higher satisfaction with GC.

CONCLUSIONS

In this study, subjects who had lower level of self-efficacy at baseline and a high level of worry immediately after GC seemed to be vulnerable to both intrusion and avoidance in this study.

摘要

工作目标

由于遗传性癌症的基因检测数量不断增加,预计在不久的将来,遗传性癌症的基因咨询将涉及越来越多的人。本研究旨在确定遗传检测和遗传咨询(GC)后预测困扰的心理社会变量,以便制定新的咨询策略。

材料和方法

对 214 名接受遗传性癌症 GC 的患者进行了前瞻性多地点研究,以探讨社会人口统计学变量、医学变量、社会支持、自我效能、身体功能、对 GC 的满意度、GC 后担忧水平、遗传检测结果以及困扰的过程和结果之间的关系。使用包括侵入和回避两个分量表的事件影响量表来衡量困扰程度。患者在 GC 前后填写邮寄给他们的问卷。

主要结果

尽管四分之一的参与者在基线时有严重的侵入性,但侵入和回避的平均水平是中度的。基线自我效能水平低、GC 后立即担心水平高的受试者似乎容易受到侵入和回避的影响。较低的侵入水平也与一级亲属患有癌症有关,而较低的回避水平与较高的教育水平、患有癌症、更多的社会支持和对 GC 的更高满意度有关。

结论

在这项研究中,基线自我效能水平较低且 GC 后立即担心水平较高的受试者似乎容易受到侵入和回避的影响。

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Unmet needs in cancer patients: development of a supportive needs screening tool (SNST).癌症患者未满足的需求:一种支持性需求筛查工具(SNST)的开发。
Support Care Cancer. 2009 Jan;17(1):33-45. doi: 10.1007/s00520-008-0448-7. Epub 2008 May 16.
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