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HID Provides Concurrent Drug Review to Ensure in Real Time that
Drugs Are Prescribed Appropriately.
Utilizing Concurrent Review
The objective of a Concurrent Drug Review Program (CDRP) is to identify
drugs or classes of drugs that should require a Prior Authorization
(PA) before dispensing. This ensures that the drugs are being prescribed
appropriately and in accordance with the FDA approved product labeling.
This program can also ascertain that the patient for whom the drugs
are being prescribed has tried and failed other alternative therapies
that can be used first according to evidence based rules.
Some potential target drugs or drugs classes for the CDRP
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Proton Pump Inhibitors |
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COX II Inhibitors |
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2nd generation Non-Sedating Antihistamines |
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Other |
Concurrent review is based on specific criteria developed for
each drug or drug class in accordance with the FDA approved indications
for that drug or drug class. The Medicaid P&T committee approves
all criteria.
Drugs considered for the CDRP are usually those drugs which have
a potential for abuse, misuse, or inappropriate use in prescribing
and/or dispensing patterns. Whole classes of drugs are on PA list
rather than only one or two drugs of a class, as may be the case
in a Preferred Drug List.
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| Mr. Steve Espy, R.Ph., (left)
explaining the CDRP operation to Congressman Mike Rogers, R-Alabama. |
Health Information Designs has active, efficient, Concurrent Drug
Review Programs in Alabama and Mississippi. The Relational Claims
Database allows HID to perform sophisticated analysis that identify
the drug classes that would be most beneficial to place in the program.
This program has saved our clients over $20,000,000 per year in
the PPI drug class alone, with no discernible increase or shift
in related medical costs.
Requiring Mandatory Use
of Generics >
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