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1.
Pharmacogenomics ; 21(11): 785-796, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32748688

RESUMO

Pharmacogenomics test coverage and reimbursement are major obstacles to clinical uptake. Several early adopter programs have been successfully initiated through dedicated investments by federal and institutional research funding. As a result of research endeavors, evidence has grown sufficiently to support development of pharmacogenomics guidelines. However, clinical uptake is still limited. Third-party payer support plays an important role in increasing adoption, which to date has been limited to reactive single-gene testing. Access to and interest in direct-to-consumer genetic testing are driving demand for increasing healthcare providers and third-party awareness of this burgeoning field. Pharmacogenomics implementation models developed by early adopters promise to expand patient access and options, as testing continues to increase due to growing consumer interest and falling test prices.


Assuntos
Planejamento em Saúde Comunitária/economia , Acessibilidade aos Serviços de Saúde/economia , Reembolso de Seguro de Saúde/economia , Testes Farmacogenômicos/economia , Planejamento em Saúde Comunitária/tendências , Pessoal de Saúde/economia , Pessoal de Saúde/educação , Pessoal de Saúde/tendências , Acessibilidade aos Serviços de Saúde/tendências , Humanos , Reembolso de Seguro de Saúde/tendências , Assistência Médica/economia , Assistência Médica/tendências , Testes Farmacogenômicos/tendências , Medicina de Precisão/economia , Medicina de Precisão/tendências
2.
Pharmacogenomics ; 21(11): 809-820, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32635876

RESUMO

In this Perspective, the authors discuss the state of pharmacogenomics testing addressing a number of advances, challenges and barriers, including legal ramifications, changes to the regulatory landscape, coverage of testing and the implications of direct-to-consumer genetic testing on the provision of care to patients. Patient attitudes toward pharmacogenomics testing and associated costs will play an increasingly important role in test acquisition and subsequent utilization in a clinical setting. Additional key steps needed include: further research trials demonstrating clinical utility and cost-effectiveness of pharmacogenetic testing, evidence review to better integrate genomic information into clinical practice guidelines in target therapeutic areas to help providers identify patients that may benefit from pharmacogenetic testing and engagement with payers to create a path to reimbursement for pharmacogenetic tests that currently have sufficient evidence of clinical utility. Increased adoption of testing by payers and improved reimbursement practices will be needed to overcome barriers, especially as the healthcare landscape continues to shift toward a system of value-based care.


Assuntos
Triagem e Testes Direto ao Consumidor/economia , Triagem e Testes Direto ao Consumidor/legislação & jurisprudência , Testes Farmacogenômicos/economia , Testes Farmacogenômicos/legislação & jurisprudência , Medicina de Precisão/economia , Análise Custo-Benefício/economia , Análise Custo-Benefício/legislação & jurisprudência , Rotulagem de Medicamentos/economia , Rotulagem de Medicamentos/legislação & jurisprudência , Humanos , Imperícia/economia , Imperícia/legislação & jurisprudência
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