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将有遗传性乳腺癌和卵巢癌风险的低收入女性有效转诊至遗传咨询:一项随机延迟干预对照试验。

Effective Referral of Low-Income Women at Risk for Hereditary Breast and Ovarian Cancer to Genetic Counseling: A Randomized Delayed Intervention Control Trial.

作者信息

Pasick Rena J, Joseph Galen, Stewart Susan, Kaplan Celia, Lee Robin, Luce Judith, Davis Sharon, Marquez Titas, Nguyen Tung, Guerra Claudia

机构信息

Rena J. Pasick, Celia Kaplan, Tung Nguyen, and Claudia Guerra are with the Department of Medicine, Division of General Internal Medicine, University of California, San Francisco. Galen Joseph is with the Department of Anthropology, History, and Social Medicine, University of California, San Francisco. Susan Stewart is with the Division of Biostatistics, University of California, Davis. Robin Lee is with the Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco. Judith Luce is with the Department of Medicine, Division of Hematology and Oncology, San Francisco General Hospital, University of California, San Francisco. Sharon Davis and Titas Marquez are with the Cancer Prevention Institute of California, Fremont.

出版信息

Am J Public Health. 2016 Oct;106(10):1842-8. doi: 10.2105/AJPH.2016.303312. Epub 2016 Aug 23.

Abstract

OBJECTIVES

To determine the effectiveness of a statewide telephone service in identifying low-income women at risk for hereditary breast and ovarian cancer and referring them to free genetic counseling.

METHODS

From June 2010 through August 2011, eligible callers to California's toll-free breast and cervical cancer telephone service were screened for their family histories of breast and ovarian cancer. High-risk women were identified and called for a baseline survey and randomization to an immediate offer of genetic counseling or a mailed brochure on how to obtain counseling. Clinic records were used to assess receipt of genetic counseling after 2 months.

RESULTS

Among 1212 eligible callers, 709 (58.5%) agreed to answer family history questions; 102 (14%) were at high risk (25% Hispanic, 46% White, 10% Black, 16% Asian, 3% of other racial/ethnic backgrounds). Of the high-risk women offered an immediate appointment, 39% received counseling during the intervention period, as compared with 4.5% of those receiving the brochure.

CONCLUSIONS

A public health approach to the rare but serious risk of hereditary breast and ovarian cancer can be successful when integrated into the efforts of existing safety net organizations.

摘要

目的

确定一项全州范围的电话服务在识别有遗传性乳腺癌和卵巢癌风险的低收入女性并将她们转介至免费基因咨询方面的有效性。

方法

2010年6月至2011年8月,对拨打加利福尼亚州免费乳腺癌和宫颈癌电话服务的符合条件的来电者进行乳腺癌和卵巢癌家族史筛查。识别出高危女性并致电她们进行基线调查,然后随机分为立即提供基因咨询或邮寄一份关于如何获得咨询的宣传册两组。利用诊所记录评估2个月后基因咨询的接受情况。

结果

在1212名符合条件的来电者中,709名(58.5%)同意回答家族史问题;102名(14%)为高危人群(25%为西班牙裔,46%为白人,10%为黑人,16%为亚洲人,3%为其他种族/族裔背景)。在被提供立即预约的高危女性中,39%在干预期间接受了咨询,而接受宣传册的女性这一比例为4.5%。

结论

当将针对遗传性乳腺癌和卵巢癌这种罕见但严重风险的公共卫生方法纳入现有安全网组织的工作中时,可能会取得成功。

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本文引用的文献

1
Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.
J Natl Cancer Inst. 2014 Nov 5;106(12). doi: 10.1093/jnci/dju328. Print 2014 Dec.
3
Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.
J Clin Oncol. 2014 Mar 1;32(7):618-26. doi: 10.1200/JCO.2013.51.3226. Epub 2014 Jan 21.
4
What hinders minority ethnic access to cancer genetics services and what may help?
Eur J Hum Genet. 2014 Jul;22(7):866-74. doi: 10.1038/ejhg.2013.257. Epub 2013 Nov 20.
5
Practical aspects of genetic counseling in breast cancer: lights and shadows.
Breast. 2013 Aug;22(4):375-82. doi: 10.1016/j.breast.2013.04.006. Epub 2013 May 11.
9
An evidence integration triangle for aligning science with policy and practice.
Am J Prev Med. 2012 Jun;42(6):646-54. doi: 10.1016/j.amepre.2012.02.016.
10
Efficient identification and referral of low-income women at high risk for hereditary breast cancer: a practice-based approach.
Public Health Genomics. 2012;15(3-4):172-80. doi: 10.1159/000336419. Epub 2012 Apr 4.

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