Prescription Drug Monitoring Programs (CRS Report for Congress)
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Release Date |
Revised May 24, 2018 |
Report Number |
R42593 |
Report Type |
Report |
Authors |
Kristin M. Finklea, Specialist in Domestic Security; Erin Bagalman, Analyst in Health Policy; Lisa N. Sacco, Analyst in Illicit Drugs and Crime Policy |
Source Agency |
Congressional Research Service |
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Summary:
In the midst of national concern over the opioid epidemic, federal and state officials are paying
greater attention to the manner in which opioids are prescribed. Nearly all prescription drugs
involved in overdoses are originally prescribed by a physician (rather than, for example, being
stolen from pharmacies). Thus, attention has been directed toward better understanding how
opioids are being prescribed and preventing the diversion of prescription drugs after the
prescriptions are dispensed.
Prescription drug monitoring programs (PDMPs) maintain statewide electronic databases of
prescriptions dispensed for controlled substances (i.e., prescription drugs with a potential for
abuse that are subject to stricter government regulation). Information collected by PDMPs may be
used to educate and inform prescribers, pharmacists, and the public; identify or prevent drug
abuse and diversion; facilitate the identification of prescription drug-addicted individuals and
enable intervention and treatment; outline drug use and abuse trends to inform public health
initiatives; or educate individuals about prescription drug use, abuse, diversion, and PDMPs
themselves.
As of February 2018, 50 states, the District of Columbia, and two territories (Guam and Puerto
Rico) had operational PDMPs within their borders.
How PDMPs are organized and operated varies among states. Each state determines which
agency houses the PDMP; which controlled substances must be reported; which types of
dispensers (e.g., pharmacies) are required to submit data; how often data are collected; who may
access information in the PDMP database (e.g., prescribers, dispensers, or law enforcement); the
circumstances under which the information may (or must) be accessed; and what enforcement
mechanisms are in place for noncompliance.
PDMP costs may vary widely, with startup costs that can range as high as $450,000 to over $1.5
million and annual operating costs ranging from $125,000 to nearly $1.0 million. States finance
PDMPs using monies from a variety of sources including the state general fund, prescriber and
pharmacy licensing fees, state controlled substance registration fees, health insurers’ fees, directsupport
organizations, state grants, and/or federal grants.
The federal government supports state PDMPs through programs at the Departments of Justice
(DOJ) and Health and Human Services (HHS). Since FY2002, DOJ has administered the Harold
Rogers Prescription Drug Monitoring Program, and in FY2017, DOJ incorporated this grant
program into the new Comprehensive Opioid Abuse Program. HHS programs include National
All Schedules Prescription Electronic Reporting (NASPER), State Demonstration Grants for
Comprehensive Opioid Abuse Response, Opioid Prevention in States grants, State Targeted
Response to the Opioid Crisis Grants, and various pilots and initiatives under the Office of the
National Coordinator for Health Information Technology (ONC). Of note, NASPER last received
appropriations (of $2.0 million) in FY2010.
State PDMPs vary with respect to whether or how information contained in the database is shared
with other states. Federal policymakers have repeatedly emphasized the importance of enhancing
interstate information sharing and the interoperability of state PDMPs. In 2011, the Obama
Administration included efforts to increase interstate data sharing in its action plan to counter
prescription drug abuse. In 2017, a presidential commission recommended, among other things,
that the Trump Administration support legislation to require DOJ to fund a “data-sharing hub”
and require states receiving federal grant funds to share PDMP data.
The available evidence suggests that PDMPs can be effective in reducing the time required for
drug diversion investigations, changing prescribing behavior, reducing “doctor shopping,” and
reducing prescription drug abuse. Assessments of effectiveness should also take into
consideration potential unintended consequences of PDMPs, such as limiting access to
medications for legitimate use or pushing drug diversion activities over the border into a
neighboring state. Experts suggest that PDMP effectiveness might be improved by increasing the
timeliness, completeness, consistency, and accessibility of the data.
Policy issues that might come before Congress include the role of state PDMPs in federal efforts
to combat prescription drug abuse, the role of the federal government in interstate data-sharing
and interoperability, and the possible link between the crackdown on prescription drug abuse and
the uptick in illicit opioid (e.g., heroin and illicit fentanyl) abuse. While establishment and
enhancement of PDMPs enjoy relatively broad support, stakeholders express concerns about
health care versus law enforcement uses of PDMP data (particularly with regard to protection of
personally identifiable health information).