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Assessing genomic sequencing information for health care decision making : workshop summary
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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  
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Control Number  
joongbu:441919
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