Literature DB >> 29733703

Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.

Diane Hauser1, Aniwaa Owusu Obeng2, Kezhen Fei3, Michelle A Ramos4, Carol R Horowitz5.   

Abstract

We surveyed 488 primary care providers in community and academic practices in New York City in the period 2014-16 about their views on genetic testing for chronic diseases. The majority of the providers, most of whom were current or recent physicians in training, had had formal genetics education and had positive views of the utility of genetic testing. However, they felt unprepared to work with patients at high risk for genetic conditions and were not confident about interpreting test results. Many were concerned that genetic testing might lead to insurance discrimination and lacked trust in companies that offer genetic tests. These findings point to some of the attitudes and knowledge gaps among the providers that should be considered in the clinical implementation of genomic medicine for chronic conditions. Enhanced training, guidelines, clinical tools, and awareness of patient protections might support the effective adoption of genomic medicine by primary care providers.

Entities:  

Keywords:  Chronic Disease; Disparities; Genomics; Physicians; Primary Care

Mesh:

Year:  2018        PMID: 29733703      PMCID: PMC6503526          DOI: 10.1377/hlthaff.2017.1548

Source DB:  PubMed          Journal:  Health Aff (Millwood)        ISSN: 0278-2715            Impact factor:   6.301


  20 in total

1.  The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.

Authors:  Carol R Horowitz; Lori A Orlando; Anne M Slavotinek; Josh Peterson; Frank Angelo; Barbara Biesecker; Vence L Bonham; Linda D Cameron; Stephanie M Fullerton; Bruce D Gelb; Katrina A B Goddard; Benyam Hailu; Ragan Hart; Lucia A Hindorff; Gail P Jarvik; Dave Kaufman; Eimear E Kenny; Sara J Knight; Barbara A Koenig; Bruce R Korf; Ebony Madden; Amy L McGuire; Jeffrey Ou; Melissa P Wasserstein; Mimsie Robinson; Howard Leventhal; Saskia C Sanderson
Journal:  Am J Hum Genet       Date:  2019-05-16       Impact factor: 11.025

2.  Perspectives on Precision Health Among Racial/Ethnic Minority Communities and the Physicians That Serve Them.

Authors:  Lisa G Rosas; Catherine Nasrallah; Van Ta Park; Jan J Vasquez; Ysabel Duron; Owen Garrick; Riccesha Hattin; Mildred Cho; Sean P David; Jill Evans; Rhonda McClinton-Brown; Christopher Martin
Journal:  Ethn Dis       Date:  2020-04-02       Impact factor: 1.847

3.  Barriers and Facilitators for Population Genetic Screening in Healthy Populations: A Systematic Review.

Authors:  Emily C Shen; Swetha Srinivasan; Lauren E Passero; Caitlin G Allen; Madison Dixon; Kimberly Foss; Brianna Halliburton; Laura V Milko; Amelia K Smit; Rebecca Carlson; Megan C Roberts
Journal:  Front Genet       Date:  2022-07-04       Impact factor: 4.772

4.  Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record.

Authors:  Gai Elhanan; Daniel Kiser; Iva Neveux; Shaun Dabe; Alexandre Bolze; William J Metcalf; James T Lu; Joseph J Grzymski
Journal:  Front Genet       Date:  2022-04-27       Impact factor: 4.772

5.  Understanding What Information Is Valued By Research Participants, And Why.

Authors:  Consuelo H Wilkins; Brandy M Mapes; Rebecca N Jerome; Victoria Villalta-Gil; Jill M Pulley; Paul A Harris
Journal:  Health Aff (Millwood)       Date:  2019-03       Impact factor: 6.301

6.  A stepwise approach to implementing pharmacogenetic testing in the primary care setting.

Authors:  Kristin Wiisanen Weitzel; Benjamin Q Duong; Meghan J Arwood; Aniwaa Owusu-Obeng; Noura S Abul-Husn; Barbara A Bernhardt; Brian Decker; Joshua C Denny; Eric Dietrich; John Gums; Ebony B Madden; Toni I Pollin; Rebekah Ryanne Wu; Susanne B Haga; Carol R Horowitz
Journal:  Pharmacogenomics       Date:  2019-10       Impact factor: 2.533

7.  State of recent literature on communication about cancer genetic testing among Latinx populations.

Authors:  Daniel Chavez-Yenter; Wen-Ying Sylvia Chou; Kimberly A Kaphingst
Journal:  J Genet Couns       Date:  2020-11-03       Impact factor: 2.717

8.  Pilot Study of Return of Genetic Results to Patients in Adult Nephrology.

Authors:  Jordan G Nestor; Maddalena Marasa; Hila Milo-Rasouly; Emily E Groopman; S Ali Husain; Sumit Mohan; Hilda Fernandez; Vimla S Aggarwal; Dina F Ahram; Natalie Vena; Kelsie Bogyo; Andrew S Bomback; Jai Radhakrishnan; Gerald B Appel; Wooin Ahn; David J Cohen; Pietro A Canetta; Geoffrey K Dube; Maya K Rao; Heather K Morris; Russell J Crew; Simone Sanna-Cherchi; Krzysztof Kiryluk; Ali G Gharavi
Journal:  Clin J Am Soc Nephrol       Date:  2020-04-16       Impact factor: 10.614

9.  Development of Customizable Implementation Guides to Support Clinical Adoption of Pharmacogenomics: Experiences of the Implementing GeNomics In pracTicE (IGNITE) Network.

Authors:  Benjamin Q Duong; Meghan J Arwood; J Kevin Hicks; Amber L Beitelshees; Francesco Franchi; John T Houder; Nita A Limdi; Kelsey J Cook; Aniwaa Owusu Obeng; Natasha Petry; Sony Tuteja; Amanda R Elsey; Larisa H Cavallari; Kristin Wiisanen
Journal:  Pharmgenomics Pers Med       Date:  2020-07-17

10.  Pharmacogenetics to Avoid Loss of Hearing (PALOH) trial: a protocol for a prospective observational implementation trial.

Authors:  John Henry McDermott; Rachel Mahood; Duncan Stoddard; Ajit Mahaveer; Mark A Turner; Rachel Corry; Julia Garlick; Gino Miele; Shaun Ainsworth; Laura Kemp; Iain Bruce; Richard Body; Fiona Ulph; Rhona Macleod; Karen Harvey; Nicola Booth; Peter Roberts; Paul Wilson; William G Newman
Journal:  BMJ Open       Date:  2021-06-16       Impact factor: 2.692

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