Assessing genomic sequencing information for health care decision making : workshop summary /
"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...
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| Format: | Electronic Conference Proceeding eBook |
| Language: | English |
| Published: |
Washington, D.C. :
National Academies Press,
2014
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| Series: | Online access: NCBI NCBI Bookshelf.
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| Subjects: | |
| Local Note: | ProQuest Ebook Central |
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| 111 | 2 | |a Assessing Genomic Sequencing Information for Health Care Decision Making (Workshop) |d (2014 : |c Washington, D.C.). |e author. | |
| 245 | 1 | 0 | |a Assessing genomic sequencing information for health care decision making : |b workshop summary / |c Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy ; Sarah H. Beachy, Samuel G. Johnson, Adam C. Berger, and Steve Olson, rapporteurs ; Institute of Medicine of the National Academies. |
| 264 | 1 | |a Washington, D.C. : |b National Academies Press, |c [2014] | |
| 264 | 4 | |c ©2014 | |
| 300 | |a 1 online resource (xx, 105 pages) : |b illustrations | ||
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| 504 | |a Includes bibliographical references. | ||
| 505 | 0 | |a Introduction -- 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. | |
| 520 | |a "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 | ||
| 588 | 0 | |a Online resource; title from resource home page (National Academies Press, viewed August 21, 2014). | |
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Medical genetics |x Social aspects |v Congresses. | |
| 650 | 0 | |a Genomics |v Congresses. | |
| 650 | 0 | |a Genetic epidemiology |v Congresses. | |
| 650 | 0 | |a Genetic screening. | |
| 650 | 0 | |a Genomics. | |
| 650 | 0 | |a Decision making. | |
| 650 | 0 | |a Medical care. | |
| 650 | 0 | |a Medical genetics. | |
| 650 | 0 | |a Precision medicine. | |
| 650 | 1 | 2 | |a Genetic Testing |
| 650 | 1 | 2 | |a Genomics |
| 650 | 2 | 2 | |a Decision Making |
| 650 | 2 | 2 | |a Delivery of Health Care |
| 650 | 2 | 2 | |a Genetics, Medical |
| 650 | 2 | 2 | |a Precision Medicine |
| 650 | 2 | |a Patient Care | |
| 650 | 7 | |a decision making. |2 aat | |
| 655 | 2 | |a Congress | |
| 655 | 7 | |a proceedings (reports) |2 aat | |
| 655 | 7 | |a Conference papers and proceedings. |2 lcgft | |
| 700 | 1 | |a Beachy, Sarah H., |e rapporteur. | |
| 700 | 1 | |a Johnson, Samuel G., |e rapporteur. | |
| 700 | 1 | |a Olson, Steve, |d 1956- |e rapporteur. |1 https://id.oclc.org/worldcat/entity/E39PBJpV6yX9jFKMQMYFvVkhpP | |
| 700 | 1 | |a Berger, Adam C., |e rapporteur. | |
| 710 | 2 | |a Institute of Medicine (U.S.). |b Roundtable on Translating Genomic-Based Research for Health, |e issuing body. | |
| 758 | |i has work: |a Assessing genomic sequencing information for health care decision making (Text) |1 https://id.oclc.org/worldcat/entity/E39PCH7bg6B6HMWck4Pp7fx343 |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
| 776 | 0 | 8 | |i Print version: |a Assessing Genomic Sequencing Information for Health Care Decision Making (Workshop) (2014 : Washington, D.C.). |t Assessing genomic sequencing information for health care decision making. |d Washington, D.C. : National Academies Press, 2014 |z 9780309304948 |z 0309304946 |
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