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探索携带BRCA致病变异的女性生殖决策的情感影响。

Exploring the Emotional Effects of Reproductive Decision-Making in Women With a BRCA Pathogenic Variant.

作者信息

Skrovanek Elizabeth, Bender Catherine M, Dunbar-Jacob Jacqueline, Mai Phuong L, Sereika Susan M, Wesmiller Susan W

机构信息

Elizabeth Skrovanek.

Catherine M. Bender.

出版信息

Oncol Nurs Forum. 2025 Jun 12;52(4):302-312. doi: 10.1188/25.ONF.302-312.

Abstract

OBJECTIVES

To evaluate how reproductive decision-making in women with a known BRCA pathogenic variant is influenced by emotional states and individual factors.

SAMPLE & SETTING: 85 women with a BRCA pathogenic variant from a familial cancer registry at a local university hospital system in Pennsylvania.

METHODS & VARIABLES: This exploratory, descriptive study used the validated Appraisal of Life Events Scale to measure emotional states. Binary logistic regression was used to analyze the relationships among emotional states, BRCA pathogenic variant status, and individual factors in reproductive decision-making.

RESULTS

Age at genetic testing and number of children significantly predicted decisions about having more children. Among women with family history of ovarian cancer, perceived loss/benefit was significantly associated with reproductive decision-making. Loss/benefit was significantly related to reproductive decision-making among women with family history of ovarian cancer.

IMPLICATIONS FOR NURSING

Recognizing the emotional impact of reproductive decision-making in women at risk for hereditary cancer could aid in improving their overall health and psychosocial outcomes.

摘要

目的

评估已知携带BRCA致病变异的女性的生殖决策是如何受到情绪状态和个体因素影响的。

样本与研究背景

来自宾夕法尼亚州当地大学医院系统家族癌症登记处的85名携带BRCA致病变异的女性。

方法与变量

这项探索性描述性研究使用经过验证的生活事件评估量表来测量情绪状态。二元逻辑回归用于分析情绪状态、BRCA致病变异状态和生殖决策中的个体因素之间的关系。

结果

基因检测时的年龄和子女数量显著预测了关于生育更多子女的决策。在有卵巢癌家族史的女性中,感知到的损失/益处与生殖决策显著相关。在有卵巢癌家族史的女性中,损失/益处与生殖决策显著相关。

对护理的启示

认识到遗传性癌症风险女性生殖决策中的情绪影响,有助于改善她们的整体健康和心理社会结局。

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本文引用的文献

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NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024.
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