Literature DB >> 33629958

Barriers and Facilitators to Genetic Service Delivery Models: Scoping Review.

Melissa Raspa1, Rebecca Moultrie1, Danielle Toth1, Saira Naim Haque1.   

Abstract

BACKGROUND: Advances in diagnostics testing and treatment of genetic conditions have led to increased demand for genetic services in the United States. At the same time, there is a shortage of genetic services professionals. Thus, understanding the models of service delivery currently in use can help increase access and improve outcomes for individuals identified with genetic conditions.
OBJECTIVE: This review aims to provide an overview of barriers and facilitators to genetic service delivery models to inform future service delivery.
METHODS: We conducted a scoping literature review of the evidence to more fully understand barriers and facilitators around the provision of genetic services.
RESULTS: There were a number of challenges identified, including the limited number of genetics specialists, wait time for appointments, delivery of services by nongenetics providers, reimbursement, and licensure. The ways to address these challenges include the use of health information technology such as telehealth, group genetic counseling, provider-to-provider education, partnership models, and training; expanding genetic provider types; and embedding genetic counselors in clinical settings.
CONCLUSIONS: The literature review highlighted the need to expand access to genetic services. Ways to expand services include telehealth, technical assistance, and changing staffing models. In addition, using technology to improve knowledge among related professionals can help expand access. ©Melissa Raspa, Rebecca Moultrie, Danielle Toth, Saira Naim Haque. Originally published in the Interactive Journal of Medical Research (http://www.i-jmr.org/), 25.02.2021.

Entities:  

Keywords:  genetic services; genetics; rare diseases; telehealth

Year:  2021        PMID: 33629958     DOI: 10.2196/23523

Source DB:  PubMed          Journal:  Interact J Med Res        ISSN: 1929-073X


  5 in total

1.  Adapting a Theoretically-Based intervention for underserved clinical populations at increased risk for hereditary Cancer: Lessons learned from the BRCA-Gist experience.

Authors:  Alejandra Hurtado-de-Mendoza; Valerie F Reyna; Christopher R Wolfe; Sara Gómez-Trillos; Arnethea L Sutton; Ashleigh Brennan; Vanessa B Sheppard
Journal:  Prev Med Rep       Date:  2022-07-05

2.  Demographic Differences Among US Department of Veterans Affairs Patients Referred for Genetic Consultation to a Centralized VA Telehealth Program, VA Medical Centers, or the Community.

Authors:  Maren T Scheuner; Alexis K Huynh; Catherine Chanfreau-Coffinier; Barbara Lerner; Alicia R Gable; Martin Lee; Alissa Simon; Randall Coeshott; Alison B Hamilton; Olga V Patterson; Scott DuVall; Marcia M Russell
Journal:  JAMA Netw Open       Date:  2022-04-01

Review 3.  Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies.

Authors:  Priyalakshmi Panikker; Shomereeta Roy; Anuprita Ghosh; B Poornachandra; Arkasubhra Ghosh
Journal:  Front Med (Lausanne)       Date:  2022-07-15

4.  Real-World Evaluation of a Population Germline Genetic Screening Initiative for Family Medicine Patients.

Authors:  Megan Leigh Hutchcraft; Shulin Zhang; Nan Lin; Ginny Lee Gottschalk; James W Keck; Elizabeth A Belcher; Catherine Sears; Chi Wang; Kun Liu; Lauren E Dietz; Justine C Pickarski; Sainan Wei; Roberto Cardarelli; Robert S DiPaola; Jill M Kolesar
Journal:  J Pers Med       Date:  2022-08-08

Review 5.  Current Status of Genetic Counselling for Rare Diseases in Spain.

Authors:  Sara Álvaro-Sánchez; Irene Abreu-Rodríguez; Anna Abulí; Clara Serra-Juhe; Maria Del Carmen Garrido-Navas
Journal:  Diagnostics (Basel)       Date:  2021-12-09
  5 in total

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