Literature DB >> 24254914

Genetic services and attitudes in primary care pediatrics.

Michael L Rinke1, Natalie Mikat-Stevens, Robert Saul, Amy Driscoll, Jill Healy, Beth A Tarini.   

Abstract

Given the integral role primary care pediatricians (PCPs) play in caring for children with genetic conditions, we aimed to identify current practices of PCPs regarding genetic patients, their attitudes toward genetic medical care and their choices regarding family history taking. We conducted an on-line survey of a national convenience sample of PCPs associated with the American Academy of Pediatrics' Quality Improvement Innovation Networks. Eighty-eight respondents (29% response rate) were included in the analysis. Seventy-four (86%) reported ordering genetic based tests three or less times annually. Eleven (13%) strongly agreed that they discuss with patients the potential risks, benefits, and limitations of genetic tests. Forty-three (49%) agreed or strongly agreed that they feel competent in providing healthcare to patients related to genetics and genomics. Perceived competence was not associated with more recent training (P = 0.29), number of genetic tests ordered annually (P = 0.84) or mean number of weekly patient encounters (P = 0.15). 100% of participants stated that taking a family history is important. 27 (31%) agreed or strongly agreed that they gather a minimum of a three-generation family history. Forty-one of the 63 participants with an electronic health record (65%) reported their system was fair or poor in its ability to easily capture a three-generation family history. PCPs interested in quality improvement reported variation in care practices for children with genetic diseases and a majority did not feel competent to provide genetic related healthcare. Research should focus on improving the care and diagnosis of children with genetic disorders and enhanced integration of genetic medicine into routine primary preventative care.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  electronic health record; family history; genetics; pediatrics; primary care

Mesh:

Year:  2013        PMID: 24254914     DOI: 10.1002/ajmg.a.36339

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  11 in total

1.  Survey of family history taking and genetic testing in pediatric practice.

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Journal:  Per Med       Date:  2018-05-30       Impact factor: 2.512

Review 3.  Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States.

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Journal:  Hum Mol Genet       Date:  2018-08-01       Impact factor: 6.150

4.  Potential Role of Genomic Sequencing in the Early Diagnosis of Treatable Genetic Conditions.

Authors:  Hengameh Zahed; Teresa N Sparks; Ben Li; Adnan Alsadah; Joseph T C Shieh
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5.  Lessons from Freelancing, Lighting Design to Genetic Counseling.

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6.  Paediatricians underuse recommended genetic tests in children with global developmental delay.

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Journal:  Paediatr Child Health       Date:  2018-04-05       Impact factor: 2.253

7.  A systematic approach to the reporting of medically relevant findings from whole genome sequencing.

Authors:  Heather M McLaughlin; Ozge Ceyhan-Birsoy; Kurt D Christensen; Isaac S Kohane; Joel Krier; William J Lane; Denise Lautenbach; Matthew S Lebo; Kalotina Machini; Calum A MacRae; Danielle R Azzariti; Michael F Murray; Christine E Seidman; Jason L Vassy; Robert C Green; Heidi L Rehm
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Review 9.  A systematic review of interventions to provide genetics education for primary care.

Authors:  Milena Paneque; Daniela Turchetti; Leigh Jackson; Peter Lunt; Elisa Houwink; Heather Skirton
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10.  Increasing confidence and changing behaviors in primary care providers engaged in genetic counselling.

Authors:  Michael S Wilkes; Frank C Day; Tonya L Fancher; Haley McDermott; Erik Lehman; Robert A Bell; Michael J Green
Journal:  BMC Med Educ       Date:  2017-09-13       Impact factor: 2.463

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