早发性乳腺癌患者遗传咨询转诊模式的变化:瑞典南部一项基于人群的研究。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Public Health Genomics Pub Date : 2020-01-01 Epub Date: 2020-07-08 DOI:10.1159/000508684
Annelie Augustinsson, Carolina Ellberg, Ulf Kristoffersson, Håkan Olsson, Hans Ehrencrona
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引用次数: 1

摘要

瑞典国家乳腺癌指南建议,所有年龄在35岁或35岁以下被诊断为乳腺癌的女性,无论是否有癌症家族史,都应到当地的肿瘤遗传诊所进行遗传咨询和检测。本研究的主要目的是评估居住在BC诊断和治疗医院的地点是否与并非所有在瑞典南部诊断为≤35岁的BC患者都参加了遗传咨询和检测的事实有关。2000年至2013年期间,瑞典南部保健区的279名妇女在≤35岁时被诊断患有BC。收集了患者在BC诊断时的居住地、治疗医院、在隆德肿瘤遗传诊所登记和第一次会面的时间以及基因检测等信息。在2018年8月之前的随访期间,64%的人在诊所登记(60%的人接受了基因检测),36%的人没有。来自2个县和农村地区的BC患者
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer: A Population-Based Study in Southern Sweden.

Swedish national breast cancer guidelines recommend that all women diagnosed with breast cancer (BC) at the age of 35 years or younger should be referred to their regional oncogenetic clinic for genetic counseling and testing, regardless of family history of cancer. The main objective of this study was to evaluate whether place of residence at BC diagnosis and treating hospital were associated with the fact that not all BC patients diagnosed at ≤35 years in the southern part of Sweden have attended genetic counseling and testing. Between 2000 and 2013, 279 women in the South Swedish Health Care Region were diagnosed with BC at ≤35 years. Information regarding place of residence at BC diagnosis, treating hospital, time of registration and first meeting at the Oncogenetic Clinic in Lund, and genetic testing was collected. With a follow-up period until August 2018, 64% were registered at the clinic (60% underwent genetic testing) and 36% were not. BC patients from 2 counties and from rural settings with a population of <10,000 inhabitants were significantly less likely to be registered at the clinic. Our results suggest that place of residence at BC diagnosis and treating hospital were associated with the probability of referral for genetic counseling and testing for women diagnosed with BC at ≤35 years in the South Swedish Health Care Region. We propose, as a generalizable finding, that further educational and outreach activities within the health care system and the community may be needed to ensure that all women diagnosed with early-onset BC receive proper genetic counseling.

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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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