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社区医疗保健系统中家族病史风险评估工具的使用:初级保健提供者的观点

The use of a family history risk assessment tool within a community health care system: views of primary care providers.

作者信息

Christianson Carol A, Powell Karen Potter, Hahn Susan Estabrooks, Blanton Susan H, Bogacik Jessica, Henrich Vincent C

机构信息

The Center for Biotechnology, Genomics and Health Research, The University of North Carolina at Greensboro, USA.

出版信息

J Genet Couns. 2012 Oct;21(5):652-61. doi: 10.1007/s10897-011-9479-1. Epub 2012 Jan 21.

DOI:10.1007/s10897-011-9479-1
PMID:22271379
Abstract

Primary care providers (PCPs) offered input regarding the incorporation of a family health history (FHH) risk assessment tool into a community health care system (CHCS). Sixteen PCPs participated in one of three focus groups. Perceived impediments included the lack of standard screening guidelines, effective screening tests, genetic counseling resources, and services for high-risk patients. The PCPs were concerned about their level of expertise, the cost of preventive health care, and genetic discrimination. They also were concerned about the use of a FHH tool by oncologists within the CHCS because of communication gaps between oncologists and PCPs, lack of clarity regarding follow-up and legal liability, and reimbursement issues. To integrate a FHH tool into a CHCS, PCPs will need consultation and referral services, evidence-based recommendations, and "just-in-time" educational resources. Oncologists who use the tool will need to develop a streamlined communication system with PCPs, establish clearly defined roles, and ensure patient follow-up.

摘要

初级保健提供者(PCP)就将家族健康史(FHH)风险评估工具纳入社区医疗系统(CHCS)提供了相关意见。16名初级保健提供者参加了三个焦点小组中的一个。他们意识到的障碍包括缺乏标准筛查指南、有效的筛查测试、遗传咨询资源以及针对高危患者的服务。初级保健提供者担心自己的专业水平、预防性医疗保健的成本以及基因歧视问题。他们还担心社区医疗系统中的肿瘤学家使用家族健康史工具,因为肿瘤学家和初级保健提供者之间存在沟通差距、后续跟进和法律责任不明确以及报销问题。为了将家族健康史工具整合到社区医疗系统中,初级保健提供者将需要咨询和转诊服务、基于证据的建议以及“及时”的教育资源。使用该工具的肿瘤学家需要与初级保健提供者建立简化的沟通系统,明确各自的角色,并确保对患者进行后续跟进。

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1
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Genet Med. 2010 Sep;12(9):587-93. doi: 10.1097/GIM.0b013e3181ed3f97.
2
Health Heritage© a web-based tool for the collection and assessment of family health history: initial user experience and analytic validity.健康传承©:一款用于收集和评估家族健康史的网络工具——初步用户体验与分析效度
Public Health Genomics. 2010;13(7-8):477-91. doi: 10.1159/000294415. Epub 2010 Apr 29.
3
A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: recommendations of the United States secretary for health and human services advisory committee on heritable disorders in newborns and children.
Updates in gynecologic care for individuals with lynch syndrome.
林奇综合征患者妇科护理的最新进展。
Front Oncol. 2023 Mar 1;13:1127683. doi: 10.3389/fonc.2023.1127683. eCollection 2023.
4
Pilot study of an online training program to increase genetic literacy and communication skills in oncology healthcare professionals discussing BRCA1/2 genetic testing with breast and ovarian cancer patients.一项在线培训计划的初步研究,旨在提高肿瘤医疗保健专业人员在与乳腺癌和卵巢癌患者讨论 BRCA1/2 基因检测时的基因知识和沟通技巧。
Fam Cancer. 2022 Apr;21(2):157-166. doi: 10.1007/s10689-021-00261-1. Epub 2021 May 10.
5
How do non-geneticist physicians deal with genetic tests? A qualitative analysis.非遗传学家的医生如何处理基因检测?定性分析。
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6
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J Community Genet. 2019 Apr;10(2):237-247. doi: 10.1007/s12687-018-0381-5. Epub 2018 Sep 12.
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4
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Annu Rev Public Health. 2010;31:69-87 1 p following 87. doi: 10.1146/annurev.publhealth.012809.103621.
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Can Fam Physician. 2009 Dec;55(12):e92-9.
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7
Long-term outcomes of the "Genetics in Primary Care" faculty development initiative.“初级保健遗传学”师资发展计划的长期成果。
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8
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9
Educational needs in genetic medicine: primary care perspectives.遗传医学中的教育需求:初级保健视角
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10
Genetics in clinical practice: general practitioners' educational priorities in European countries.临床实践中的遗传学:欧洲国家全科医生的教育重点
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