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Clinical Integration of Next Generation Sequencing: Coverage and Reimbursement Challenges

Overview of attention for article published in The Journal of Law, Medicine & Ethics, January 2021
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4 news outlets
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1 policy source
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2 X users
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Citations

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Title
Clinical Integration of Next Generation Sequencing: Coverage and Reimbursement Challenges
Published in
The Journal of Law, Medicine & Ethics, January 2021
DOI 10.1111/jlme.12160
Pubmed ID
Authors

Patricia A. Deverka, Jennifer C. Dreyfus

Abstract

Public and private payers face complex decisions regarding whether, when, and how to cover and reimburse for next generation sequencing (NGS)-based tests. Yet a predictable reimbursement pathway is critical both for patient access and incentives to provide the market with better clinical evidence. While preliminary data suggests that payers will use similar evidentiary standards as those used to evaluate established molecular diagnostic tests, the volume and complexity of information generated by NGS raises a host of additional considerations for payers that are specific to this technology.

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X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 75 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 3%
Belgium 1 1%
Unknown 72 96%

Demographic breakdown

Readers by professional status Count As %
Other 15 20%
Student > Ph. D. Student 12 16%
Researcher 10 13%
Student > Master 10 13%
Student > Postgraduate 4 5%
Other 11 15%
Unknown 13 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 15 20%
Medicine and Dentistry 14 19%
Biochemistry, Genetics and Molecular Biology 10 13%
Economics, Econometrics and Finance 4 5%
Social Sciences 4 5%
Other 10 13%
Unknown 18 24%