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research:pgx_drug_exposure [2015/02/18 11:17] rkboyce |
research:pgx_drug_exposure [2017/01/15 00:04] (current) rkboyce |
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- | **Objective:** Derive data that large healthcare organizations can combine data on risks of adverse events and cost data to conduct cost-effectiveness / cost-benefit analyses for pre-emptive pharmacogenomics testing | + | **Objective:** Derive data that large healthcare organizations can combine with data on risks of adverse events and cost data to conduct cost-effectiveness / cost-benefit analyses for pre-emptive pharmacogenomics testing |
**Rationale:** Very few studies have been conducted that report on the potential return on investment for pre-emptive pharmacogenomics testing. The studies that have been published suggest that pre-emptive pharmacogenomics testing may produce a return on investment but much depends on if a sufficient number of drugs with pharmacogenes are covered by a single test. Since the current data are limited to relatively localized settings and might not be of generalizable use to other health organizations, it's of interest to implement a new study using the OHDSI research network. | **Rationale:** Very few studies have been conducted that report on the potential return on investment for pre-emptive pharmacogenomics testing. The studies that have been published suggest that pre-emptive pharmacogenomics testing may produce a return on investment but much depends on if a sufficient number of drugs with pharmacogenes are covered by a single test. Since the current data are limited to relatively localized settings and might not be of generalizable use to other health organizations, it's of interest to implement a new study using the OHDSI research network. | ||
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**Coordinating Institution(s):** University of Pittsburgh, Medical University of Vienna, Columbia University, Regenstrief Institute, Janssen R&D, AstraZeneca | **Coordinating Institution(s):** University of Pittsburgh, Medical University of Vienna, Columbia University, Regenstrief Institute, Janssen R&D, AstraZeneca | ||
- | ** Additional Participants (currently seeking other collaborators):** Patrick Ryan, Jon Duke, George Hripcsak, Abraham G. Hartzema, Christian Reich | + | ** Additional Participants (currently seeking other collaborators):** Patrick Ryan, Jon Duke, George Hripcsak, Abraham G. Hartzema, Christian Reich, Dan Malone |
- | **Full Protocol:** //<if available, a link to protocol. not necessary for initial planning>// | + | **Full Protocol:** [[https://docs.google.com/document/d/1u3AE5DtkEp3m8OcbwkGHtXBVefYGGJ_1RMO3OnqpXiY/edit|Google doc for the protocol]] |
**Initial Proposal Date:** 2/16/2015 | **Initial Proposal Date:** 2/16/2015 | ||
- | **Launch Date:** //<fill out once finalized>// | + | **Launch Date:** This was a test research network study and has met its objectives as of 12/1/2016. |
**Study Closure Date: //<fill out once finalized>//** | **Study Closure Date: //<fill out once finalized>//** | ||
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===== Discussion ===== | ===== Discussion ===== | ||
- | //Post a thread letting everyone know about this new proposed study at [[http://forums.ohdsi.org/c/researchers]]// | + | [[http://forums.ohdsi.org/t/ohdsi-study-3-incidence-of-exposure-to-drugs-for-which-pre-emptive-pharmacogenomic-testing-is-available/387]] |
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===== Datasets Run ===== | ===== Datasets Run ===== |