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E-raamat: Understanding Disparities in Access to Genomic Medicine: Proceedings of a Workshop

  • Formaat: 126 pages
  • Ilmumisaeg: 28-Dec-2018
  • Kirjastus: National Academies Press
  • Keel: eng
  • ISBN-13: 9780309485265
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  • Formaat: 126 pages
  • Ilmumisaeg: 28-Dec-2018
  • Kirjastus: National Academies Press
  • Keel: eng
  • ISBN-13: 9780309485265
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Genomic medicine is defined as the routine use of genomic information about an individual as part of his or her clinical care as well as the health outcomes and policy implications of that clinical use. It is one approach that has the potential to improve the quality of health care by allowing practitioners to tailor prevention, diagnostic, and treatment strategies to individual patients. In recent years, research breakthroughs, technological advances, and the decreasing cost of DNA sequencing have led to the wider adoption of genomic medicine. However, as with the introduction of new technologies into health care, there are concerns that genetic and genomic testing and services will not reach all segments of the population both now and in the near future, and there remains a gap in knowledge regarding potential health care disparities in genomic medicine and precision health approaches.





On June 27, 2018, the National Academies of Sciences, Engineering, and Medicine hosted a public workshop to examine the gaps in knowledge related to access to genomic medicine and to discuss health care disparities and possible approaches to overcoming the disparate use of genomic medicine among populations. Workshop participants discussed research on access to genetics and genomics services in medically underserved areas, model programs of care for diverse patient populations, and current challenges and possible best practices for alleviating health care disparities as they relate to genomics-based approaches. This publication summarizes the presentations and discussions from the workshop.

Table of Contents



Front Matter 1 Introduction and Overview 2 Exploring the Barriers to Accessing Genomic and Genetic Services 3 The Role of Health Systems in Delivering Equitable Access 4 How Can Providers and Payers Make Genomic Medicine More Accessible? 5 Exploring Innovative Solutions and Models of Success 6 Considering Unmet Needs to Alleviate Disparities in Genomic Medicine References Appendix A: Summary of the Pre-Workshop Twitter Chat Appendix B: Workshop Agenda Appendix C: Speaker Biographical Sketches Appendix D: Statement of Task Appendix E: Registered Attendees
Acronyms And Abbreviations xix
1 Introduction And Overview
1(10)
Overview of the Workshop
3(1)
Organization of the Workshop and Proceedings
4(1)
Setting the Stage: An Introduction to Genomic Medicine and Disparities
5(6)
2 Exploring The Barriers To Accessing Genomic And Genetic Services
11(12)
Family Secrets Kill Families: A Personal Story About Genetic Testing and Communication
13(1)
Examining Potential Drivers of Health Care Disparities
14(2)
Patient-Reported Barriers to Genomic Testing
16(3)
Challenges Facing Rural Communities
19(1)
Reaction and Commentary: The Value of a Patient-Centered Health Care System
20(3)
3 The Role Of Health Systems In Delivering Equitable Access
23(12)
Veterans Health Administration Genomic Care
24(2)
Providing Genomic Medicine in a Resource-Constrained System
26(3)
A Population Health Approach to Cancer Genetic Risk Assessment and Health Disparities
29(3)
Discussion
32(3)
4 How Can Providers And Payers Make Genomic Medicine More Accessible?
35(12)
Finding Ways for Genomic Medicine to Reduce Existing Health Care Disparities
36(1)
Disparities in Access to Precision Medicine: A View from Psychiatry
37(3)
Ensuring That Genomic Medicine Is Provided Equitably
40(2)
The Role of Large Employers in Addressing Disparities and Improving Access to Care
42(1)
Discussion
43(4)
5 Exploring Innovative Solutions And Models Of Success
47(14)
Alternative Models of Clinical Service Delivery and the Impact of Disparities in BRCA Testing
49(2)
Access and Communication: The Bridge Connecting Genetic Discoveries with Minority Patients
51(3)
Recruiting Minority Populations in Genomic Studies Through Community-Based Outreach
54(2)
Indiana Genomics Implementation Opportunity for the Underserved
56(2)
Discussion
58(3)
6 Considering Unmet Needs To Alleviate Disparities In Genomic Medicine
61(10)
Overcoming Challenges to Increase Access to Genetics and Genomics
61(3)
Possible Ways to Improve Diversity and Reduce Health Care Disparities in Genomic Medicine
64(6)
Final Thoughts
70(5)
References 71(4)
Appendixes
A Summary Of The Pre-Workshop Twitter Chat
75(4)
B Workshop Agenda
79(6)
C Speaker Biographical Sketches
85(12)
D Statement Of Task
97(2)
E Registered Attendees
99