자료유형 | E-Book |
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개인저자 | Beachy, Sarah H., rapporteur. Alper, Joe, rapporteur. Addie, Siobhan, rapporteur. |
단체저자명 | National Academies of Sciences, Engineering, and Medicine (U.S.). Roundtable on Genomics and Precision Health,issuing body. |
서명/저자사항 | Understanding disparities in access to genomic medicine :proceedings of a workshop /Siobhan Addie, Joe Alper, and Sarah H. Beachy, rapporteurs ; Roundtable on Genomics and Precision Health, Board on Health Sciences Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine.[electronic resource] |
발행사항 | Washington, D.C. : National Academies Press, [2018] |
형태사항 | 1 online resource (xx, 105 pages) : 1 color illustration |
소장본 주기 | Master record variable field(s) change: 050, 072, 082, 650 - OCLC control number change |
ISBN | 9780309485265 0309485266 9780309485289 0309485282 |
기타표준부호 | 10.17226/25277doi |
서지주기 | Includes bibliographical references. |
내용주기 | Introduction and overview -- Exploring the barriers to accessing genomic and genetic services -- The role of health systems in delivering equitable access -- How can providers and payers make genomic medicine more accessible? -- Exploring innovative solutions and models of success -- Considering unmet needs to alleviate disparities in genomic medicine. |
요약 | "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"--Publisher's description. |
회의명 | Understanding Disparities in Access to Genomic Medicine (Workshop)(2018 :Washington, D.C.), |
일반주제명 | Genomics. Genetics, Medical. Healthcare Disparities. Health Services Accessibility. Medical genetics -- Congresses. Genomes -- Medical care -- Congresses. HEALTH & FITNESS / Diseases / General. MEDICAL / Clinical Medicine. MEDICAL / Diseases. MEDICAL / Evidence-Based Medicine. MEDICAL / Internal Medicine. |
주제명(지명) | United States. |
언어 | 영어 |
기타형태 저록 | Print version:Understanding Disparities in Access to Genomic Medicine : Proceedings of a Workshop.Washington, D.C. : National Academies Press, [2018]9780309485258 |
대출바로가기 | http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=2014963 |
인쇄
No. | 등록번호 | 청구기호 | 소장처 | 도서상태 | 반납예정일 | 예약 | 서비스 | 매체정보 |
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1 | WE00015396 | 616.042 | 가야대학교/전자책서버(컴퓨터서버)/ | 대출가능 |