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Family history-taking in community family practice: Implications for genetic screening
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  • Published: 01 May 2000

Family history-taking in community family practice: Implications for genetic screening

  • Louise S Acheson1,
  • Georgia L Wiesner1,
  • Stephen J Zyzanski1,
  • Meredith A Goodwin1 &
  • …
  • Kurt C Stange1 

Genetics in Medicine volume 2, pages 180–185 (2000)Cite this article

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Abstract

Purpose: To identify characteristics of physicians, patients, and visits associated with obtaining family history information in community family practice.

Methods: Research nurses directly observed 4454 patient visits to 138 family physicians and reviewed office medical records.

Results: Family history was discussed during 51% of visits by new patients and 22% of visits by established patients. Physicians' rates of family history-taking varied from 0% to 81% of visits. Family history was more often discussed at well care rather than illness visits. The average duration of family history discussions was <2.5 minutes.

Conclusions: These data can form the basis for realistic interventions to increase the use of family history in primary care.

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Authors and Affiliations

  1. Case Western Reserve University and University Hospitals of Cleveland, Cleveland, Ohio

    Louise S Acheson, Georgia L Wiesner, Stephen J Zyzanski, Meredith A Goodwin & Kurt C Stange

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  1. Louise S Acheson
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  2. Georgia L Wiesner
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  3. Stephen J Zyzanski
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  4. Meredith A Goodwin
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Acheson, L., Wiesner, G., Zyzanski, S. et al. Family history-taking in community family practice: Implications for genetic screening. Genet Med 2, 180–185 (2000). https://doi.org/10.1097/00125817-200005000-00004

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  • Received: 07 February 2000

  • Accepted: 24 March 2000

  • Issue date: 01 May 2000

  • DOI: https://doi.org/10.1097/00125817-200005000-00004

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Keywords

  • Family history
  • primary care
  • family practice
  • genetic services

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Genetics in Medicine (Genet Med)

ISSN 1530-0366 (online)

ISSN 1098-3600 (print)

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