Literature DB >> 24044145

Development and validation of a primary care-based family health history and decision support program (MeTree).

Lori A Orlando1, Adam H Buchanan, Susan E Hahn, Carol A Christianson, Karen P Powell, Celette Sugg Skinner, Blair Chesnut, Colette Blach, Barbara Due, Geoffrey S Ginsburg, Vincent C Henrich.   

Abstract

INTRODUCTION: Family health history is a strong predictor of disease risk. To reduce the morbidity and mortality of many chronic diseases, risk-stratified evidence-based guidelines strongly encourage the collection and synthesis of family health history to guide selection of primary prevention strategies. However, the collection and synthesis of such information is not well integrated into clinical practice. To address barriers to collection and use of family health histories, the Genomedical Connection developed and validated MeTree, a Web-based, patient-facing family health history collection and clinical decision support tool. MeTree is designed for integration into primary care practices as part of the genomic medicine model for primary care.
METHODS: We describe the guiding principles, operational characteristics, algorithm development, and coding used to develop MeTree. Validation was performed through stakeholder cognitive interviewing, a genetic counseling pilot program, and clinical practice pilot programs in 2 community-based primary care clinics.
RESULTS: Stakeholder feedback resulted in changes to MeTree's interface and changes to the phrasing of clinical decision support documents. The pilot studies resulted in the identification and correction of coding errors and the reformatting of clinical decision support documents. MeTree's strengths in comparison with other tools are its seamless integration into clinical practice and its provision of action-oriented recommendations guided by providers' needs. LIMITATIONS: The tool was validated in a small cohort.
CONCLUSION: MeTree can be integrated into primary care practices to help providers collect and synthesize family health history information from patients with the goal of improving adherence to risk-stratified evidence-based guidelines.

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Mesh:

Year:  2013        PMID: 24044145      PMCID: PMC5215064     

Source DB:  PubMed          Journal:  N C Med J        ISSN: 0029-2559


  36 in total

1.  The 'new genetics' and primary care: GPs' views on their role and their educational needs.

Authors:  E K Watson; D Shickle; N Qureshi; J Emery; J Austoker
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Review 2.  The challenge of integrating genetic medicine into primary care.

Authors:  J Emery; S Hayflick
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3.  GPs' views on their role in cancer genetics services and current practice.

Authors:  A Fry; H Campbell; H Gudmunsdottir; R Rush; M Porteous; D Gorman; A Cull
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4.  Racial and ethnic differences in parents' assessments of pediatric care in Medicaid managed care.

Authors:  R Weech-Maldonado; L S Morales; K Spritzer; M Elliott; R D Hays
Journal:  Health Serv Res       Date:  2001-07       Impact factor: 3.402

5.  New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

Authors:  H F Vasen; P Watson; J P Mecklin; H T Lynch
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6.  BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes.

Authors:  Donald A Berry; Edwin S Iversen; Daniel F Gudbjartsson; Elaine H Hiller; Judy E Garber; Beth N Peshkin; Caryn Lerman; Patrice Watson; Henry T Lynch; Susan G Hilsenbeck; Wendy S Rubinstein; Kevin S Hughes; Giovanni Parmigiani
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7.  Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics.

Authors:  R T Acton; N M Burst; L Casebeer; S M Ferguson; P Greene; B L Laird; L Leviton
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8.  The genetic family history as a risk assessment tool in internal medicine.

Authors:  Theresa M Frezzo; Wendy S Rubinstein; Daniel Dunham; Kelly E Ormond
Journal:  Genet Med       Date:  2003 Mar-Apr       Impact factor: 8.822

9.  Colorectal cancer screening and surveillance: clinical guidelines and rationale-Update based on new evidence.

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10.  Family history-taking in community family practice: implications for genetic screening.

Authors:  L S Acheson; G L Wiesner; S J Zyzanski; M A Goodwin; K C Stange
Journal:  Genet Med       Date:  2000 May-Jun       Impact factor: 8.822

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  38 in total

1.  Multi-source development of an integrated model for family health history.

Authors:  Elizabeth S Chen; Elizabeth W Carter; Tamara J Winden; Indra Neil Sarkar; Yan Wang; Genevieve B Melton
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2.  Are Australasian Genetic Counselors Interested in Private Practice at the Primary Care Level of Health Service?

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Review 3.  What characterizes cancer family history collection tools? A critical literature review.

Authors:  J E Cleophat; H Nabi; S Pelletier; K Bouchard; M Dorval
Journal:  Curr Oncol       Date:  2018-08-14       Impact factor: 3.677

4.  Use of a patient-entered family health history tool with decision support in primary care: impact of identification of increased risk patients on genetic counseling attendance.

Authors:  Adam H Buchanan; Carol A Christianson; Tiffany Himmel; Karen P Powell; Astrid Agbaje; Geoffrey S Ginsburg; Vincent C Henrich; Lori A Orlando
Journal:  J Genet Couns       Date:  2014-08-15       Impact factor: 2.537

Review 5.  Review and Comparison of Electronic Patient-Facing Family Health History Tools.

Authors:  Brandon M Welch; Kevin Wiley; Lance Pflieger; Rosaline Achiangia; Karen Baker; Chanita Hughes-Halbert; Heath Morrison; Joshua Schiffman; Megan Doerr
Journal:  J Genet Couns       Date:  2018-03-06       Impact factor: 2.537

6.  Genetics in primary health care and the National Policy on Comprehensive Care for People with Rare Diseases in Brazil: opportunities and challenges for professional education.

Authors:  Débora Gusmão Melo; Pamela Karen de Paula; Stephania de Araujo Rodrigues; Lucimar Retto da Silva de Avó; Carla Maria Ramos Germano; Marcelo Marcos Piva Demarzo
Journal:  J Community Genet       Date:  2015-04-18

7.  Results and Lessons of a Pilot Study of Cascade Screening for Familial Hypercholesterolemia in US Primary Care Practices.

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8.  Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment.

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Review 9.  Family health history: underused for actionable risk assessment.

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Review 10.  Implementing genomics and pharmacogenomics in the clinic: The National Human Genome Research Institute's genomic medicine portfolio.

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Journal:  Atherosclerosis       Date:  2016-08-26       Impact factor: 5.162

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