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A01=and Medicine
A01=Board on Health Sciences Policy
A01=Engineering
A01=Health and Medicine Division
A01=National Academies of Sciences
A01=Roundtable on Genomics and Precision Health
Age Group_Uncategorized
Age Group_Uncategorized
Author_and Medicine
Author_Board on Health Sciences Policy
Author_Engineering
Author_Health and Medicine Division
Author_National Academies of Sciences
Author_Roundtable on Genomics and Precision Health
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B01=Meredith Hackmann
B01=Sarah Beachy
B01=Siobhan Addie
B01=Theresa Wizemann
Category1=Non-Fiction
Category=MFN
COP=United States
Delivery_Delivery within 10-20 working days
Language_English
PA=Available
Price_€20 to €50
PS=Active
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Implementing and Evaluating Genomic Screening Programs in Health Care Systems: Proceedings of a Workshop

Genomic applications are being integrated into a broad range of clinical and research activities at health care systems across the United States. This trend can be attributed to a variety of factors, including the declining cost of genome sequencing and the potential for improving health outcomes and cutting the costs of care. The goals of these genomics-based programs may be to identify individuals with clinically actionable variants as a way of preventing disease, providing diagnoses for patients with rare diseases, and advancing research on genetic contributions to health and disease. Of particular interest are genomics- based screening programs, which will, in this publication, be clinical screening programs that examine genes or variants in unselected populations in order to identify individuals who are at an increased risk for a particular health concern (e.g., diseases, adverse drug outcomes) and who might benefit from clinical interventions.

On November 1, 2017, the National Academies of Sciences, Engineering, and Medicine hosted a public workshop to explore the challenges and opportunities associated with integrating genomics-based screening programs into health care systems. This workshop was developed as a way to explore the challenges and opportunities associated with integrating genomics-based programs in health care systems in the areas of evidence collection, sustainability, data sharing, infrastructure, and equity of access. This publication summarizes the presentations and discussions from the workshop.

Table of Contents
  • Front Matter
  • 1 Introduction
  • 2 Evidence Considerations for Integrating Genomics-Based Programs into Health Care Systems
  • 3 Financial Considerations for Implementing Genomics-Based Screening Programs
  • 4 Exploring Approaches to Optimize Data Sharing Among Early Implementers of Genomics-Based Programs
  • 5 Understanding Participant Needs and Preferences and Improving Diversity and Equity
  • 6 Improving Health Through the Integration of Genomics-Based Programs: Potential Next Steps
  • References
  • Appendix A: Workshop Agenda
  • Appendix B: Speaker Biographies
  • Appendix C: Statement of Task
  • Appendix D: Registered Attendees
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A01=and MedicineA01=Board on Health Sciences PolicyA01=EngineeringA01=Health and Medicine DivisionA01=National Academies of SciencesA01=Roundtable on Genomics and Precision HealthAge Group_UncategorizedAuthor_and MedicineAuthor_Board on Health Sciences PolicyAuthor_EngineeringAuthor_Health and Medicine DivisionAuthor_National Academies of SciencesAuthor_Roundtable on Genomics and Precision Healthautomatic-updateB01=Meredith HackmannB01=Sarah BeachyB01=Siobhan AddieB01=Theresa WizemannCategory1=Non-FictionCategory=MFNCOP=United StatesDelivery_Delivery within 10-20 working daysLanguage_EnglishPA=AvailablePrice_€20 to €50PS=Activesoftlaunch
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Product Details
  • Dimensions: 152 x 229mm
  • Publication Date: 16 Jun 2018
  • Publisher: National Academies Press
  • Publication City/Country: United States
  • Language: English
  • ISBN13: 9780309473415

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