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Journal ArticleDOI

Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey.

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TLDR
An anonymous, cross‐sectional, fax‐based, national survey of US physicians' level of knowledge and extent of use of pharmacogenomic testing highlights the need for more effective physician education on the clinical value, availability, and interpretation of Pharmacogenomic tests.
Abstract
To develop a benchmark measure of US physicians' level of knowledge and extent of use of pharmacogenomic testing, we conducted an anonymous, cross-sectional, fax-based, national survey. Of 397,832 physicians receiving the survey questionnaire, 10,303 (3%) completed and returned it; the respondents were representative of the overall US physician population. The factors associated with the decision to test were evaluated using χ(2) and multivariate logistic regression. Overall, 97.6% of responding physicians agreed that genetic variations may influence drug response, but only 10.3% felt adequately informed about pharmacogenomic testing. Only 12.9% of physicians had ordered a test in the previous 6 months, and 26.4% anticipated ordering a test in the next 6 months. Early and future adopters of testing were more likely to have received training in pharmacogenomics, but only 29.0% of physicians overall had received any education in the field. Our findings highlight the need for more effective physician education on the clinical value, availability, and interpretation of pharmacogenomic tests.

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Pharmacogenomics in the clinic

TL;DR: Current efforts that focus on the processes required to appropriately act on pharmacogenomic variability in the clinic are moving away from discovery and towards implementation of an evidenced-based strategy for improving the use of medications, thereby providing a cornerstone for precision medicine.
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Preemptive Clinical Pharmacogenetics Implementation: Current Programs in Five US Medical Centers

TL;DR: Current programs that use preemptive genotyping to optimize the pharmacotherapy of patients are discussed and key processes for implementation are highlighted, including clinical decision support.
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Pharmacogenomics and individualized medicine: translating science into practice.

TL;DR: Key components to successful clinical implementation of pharmacogenomics will include consistent interpretation of Pharmacogenomics test results, availability of clinical guidelines for prescribing on the basis of testresults, and knowledge‐based decision support systems.
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Primary care physicians' knowledge of and experience with pharmacogenetic testing

TL;DR: Primary care practitioners envision a major role for themselves in the delivery of PGx testing but recognize their lack of adequate knowledge and experience about these tests, and development of effective tools for guiding PCPs in the use ofPGx tests should be a high priority.
References
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Journal ArticleDOI

Inheritance and Drug Response

TL;DR: The underlying message is that inherited variations in drug effect are common and that some tests that incorporate pharmacogenetics into clinical practice are now available, with many more to follow.
Journal ArticleDOI

Genomic Medicine — An Updated Primer

TL;DR: The fundamental bases of genetic and genomic discovery are described and a new series: Genomic Medicine is launched, describing the practice of medicine is increasingly informed by genomic discovery.
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Physician Use of Genetic Testing for Cancer Susceptibility

TL;DR: In this article, a nationally representative survey was conducted to estimate prevalence of cancer susceptibility tests (CST) use by United States physicians and assess demographic, training, practice setting, and practice patterns associated with use.
Journal Article

Physician use of genetic testing for cancer susceptibility: results of a national survey.

TL;DR: It is found that lower CST use was associated with not knowing if there were local testing and counseling facilities and the importance of establishing effective clinical approaches to test use and promoting physician education to facilitate communication with patients about cancer genetics.
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