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Assessing genomic sequencing information for health care decision making : workshop summary
Assessing genomic sequencing information for health care decision making : workshop summary
- 자료유형
- 단행본
- Control Number
- n888201733
- International Standard Book Number
- 9780309304955 electronic bk.
- International Standard Book Number
- 0309304954 electronic bk.
- International Standard Book Number
- 9780309304948 (paperback)
- International Standard Book Number
- 0309304946 (paperback)
- Library of Congress Call Number
- RB155
- Dewey Decimal Classification Number
- 616/.042-23
- Main Entry-Meeting Name
- Assessing Genomic Sequencing Information for Health Care Decision Making (Workshop), (2014. Washington, D.C.) author.
- Physical Description
- 1 online resource (xx, 105 pages) : illustrations
- Summary, Etc.
- 요약"Rapid advances in technology have lowered the cost of sequencing an individual's genome from the several billion dollars that it cost a decade ago to just a few thousand dollars today and have correspondingly greatly expanded the use of genomic information in medicine. Because of the lack of evidence available for assessing variants, evaluation bodies have made only a few recommendations for the use of genetic tests in health care. For example, organizations, such as the Evaluation of Genomic Applications in Practice and Prevention working group, have sought to set standards for the kinds of evaluations needed to make population-level health decisions. However, due to insufficient evidence, it has been challenging to recommend the use of a genetic test. An additional challenge to using large-scale sequencing in the clinic is that it may uncover "secondary," or "incidental," findings - genetic variants that have been associated with a disease but that are not necessarily related to the conditions that led to the decision to use genomic testing. Furthermore, as more genetic variants are associated with diseases, new information becomes available about genomic tests performed previously, which raises issues about how and whether to return this information to physicians and patients and also about who is responsible for the information. To help develop a better understanding of how genomic information is used for healthcare decision making, the Roundtable on Translating Genomic-Based Research for Health of the Institute of Medicine held a workshop in Washington, DC in February 2014. Stakeholders, including clinicians, researchers, patients, and government officials, discussed the issues related to the use of genomic information in medical practice. Assessing Genomic Sequencing Information for Health Care Decision Making is the summary of that workshop. This report compares and contrasts evidence evaluation processes for different clinical indications and discusses key challenges in the evidence evaluation process"--Publisher's description.
- Bibliography, Etc. Note
- Includes bibliographical references.
- Formatted Contents Note
- 완전내용Introduction -- How evidence is gathered and evaluated -- Patient care and health decisions -- The development of practice guidelines -- How insurers decide whether to pay for testing -- Addressing challenges.
- Subject Added Entry-Topical Term
- Medical genetics Social aspects Congresses
- Subject Added Entry-Topical Term
- Genomics Congresses
- Subject Added Entry-Topical Term
- Genetic epidemiology Congresses
- Subject Added Entry-Topical Term
- Genetic Testing Congresses
- Subject Added Entry-Topical Term
- Genomics Congresses
- Subject Added Entry-Topical Term
- Individualized Medicine Congresses
- Subject Added Entry-Topical Term
- Decision Making Congresses
- Subject Added Entry-Topical Term
- Delivery of Health Care Congresses
- Subject Added Entry-Topical Term
- Genetics, Medical Congresses
- Subject Added Entry-Topical Term
- HEALTH & FITNESS / Diseases / General
- Subject Added Entry-Topical Term
- MEDICAL / Clinical Medicine
- Subject Added Entry-Topical Term
- MEDICAL / Diseases
- Subject Added Entry-Topical Term
- MEDICAL / Evidence-Based Medicine
- Subject Added Entry-Topical Term
- MEDICAL / Internal Medicine
- Subject Added Entry-Topical Term
- Genetic epidemiology.
- Subject Added Entry-Topical Term
- Genomics.
- Subject Added Entry-Topical Term
- Medical genetics Social aspects.
- Added Entry-Personal Name
- Beachy, Sarah H.
- Added Entry-Personal Name
- Johnson, Samuel G.
- Added Entry-Personal Name
- Olson, Steve , 1956-
- Added Entry-Personal Name
- Berger, Adam C.
- Added Entry-Corporate Name
- Institute of Medicine (U.S.) Roundtable on Translating Genomic-Based Research for Health
- Additional Physical Form Entry
- Print versionAssessing Genomic Sequencing Information for Health Care Decision Making (Workshop) (2014 : Washington, D.C.). Assessing genomic sequencing information for health care decision making Washington, D.C. : National Academies Press, 2014. 9780309304948 0309304946
- Electronic Location and Access
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:441919