Reconsidering the family history in primary care

被引:242
作者
Rich, EC
Burke, W
Heaton, CJ
Haga, S
Pinsky, L
Short, MP
Acheson, L
机构
[1] Creighton Univ, Dept Med, Omaha, NE 68131 USA
[2] Univ Washington, Dept Med Hist & Eth, Seattle, WA 98195 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Family Med, New Brunswick, NJ USA
[4] Ctr Advancement Gen, Rockville, MD USA
[5] Univ Washington, Dept Med, Seattle, WA USA
[6] Amer Med Assoc, Off Biomed Sci & Clin Res, Chicago, IL 60610 USA
[7] Case Western Reserve Univ, Dept Family Med, Cleveland, OH 44106 USA
基金
美国国家卫生研究院; 美国医疗保健研究与质量局;
关键词
genetics; primary care; family history; genetic testing; medical history taking; pedigree;
D O I
10.1111/j.1525-1497.2004.30401.x
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
OBJECTIVE: The purpose of this paper is to review the role of the family history in predictive genetic testing, describe how family history taking is practiced in adult primary care, identify the current barriers to appropriate application of the family history, and outline the requirements for a new family history tool for primary care. DESIGN: We reviewed current perspectives on the family history, identifying key references in the medical literature and web-based family history tools through discussions with multiple content experts in clinical genetics, family medicine, and internal medicine. We conducted a Medline query using the search terms family history and primary care to identify references from the past 10 years. To illustrate the usefulness of family history information, we calculated the predictive value of family history and genetic information for familial adenomatous polyposis using current references and standard formulas. We identified paper and web-based family history tools through discussions with content experts. We also conducted a search on the World Wide Web to identify resources for electronic medical record and family history. RESULTS: The family history is the most important tool for diagnosis and risk assessment in medical genetics, and promises to serve as a critical element in the use of predictive genetic testing in primary care. Traditional medical education about family history has often been unsophisticated and use of family history in adult primary care has been limited, compounded by multiple substantive barriers. Although there are numerous paper and computer-based aides for taking the family history, none currently meets all the needs of adult primary care. CONCLUSIONS: The patient's family history remains a critical element in risk assessment for many conditions, but substantive barriers impede application in primary care practice, and evidence for its contribution to improved health outcomes is limited in this setting. Short of radical changes in reimbursement, new tools will be required to aid primary care physicians in the efficient collection and application of patient family history in the era of genetic testing.
引用
收藏
页码:273 / 280
页数:8
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