News Release

About 12 percent of patients who receive common cardiac device implants develop persistent opioid use

Penn Medicine study shows that higher initial prescriptions can lead to longer-term opioid use

Peer-Reviewed Publication

University of Pennsylvania School of Medicine

PHILADELPHIA — About 12 percent of patients who receive implantable cardiac devices such as a pacemaker or defibrillator and fill an opioid prescription after surgery will consistently use the pain medication in the months afterward, raising the potential for addiction following these common procedures and identifying another pathway that could contribute to the national opioid crisis, according to a new study by researchers at the Perelman School of Medicine at the University of Pennsylvania. The findings are published in Circulation.

Using data from a national insurance-claims database of adult patients undergoing cardiac implantable electronic device procedures from 2004 to 2018, the Penn researchers found that, of their sample of 143,400 patients, 15,316 patients filled an opioid prescription within two weeks of surgery. Of those patients, persistent opioid use—defined as filling another opioid prescription between one and six months after the procedure—occurred in 1,901 patients (who did not have a history of opioid use), or 12.4 percent, compared to 5.4 percent of patients without an initial opioid prescription.

“Even a small number of oxycodones can start the addiction process,” said senior author David S. Frankel, MD, an associate professor of Cardiovascular Medicine and director of the Cardiac Electrophysiology Fellowship Program at Penn. “The significance of this study is to make other electrophysiologists aware that even a low-risk procedure like a pacemaker or a defibrillator can lead to chronic opioid use and that physicians may want to be more conservative in prescribing opioids after surgery.”

Because opioids include a variety of medications containing oral hydrocodone, oxycodone, hydromorphone, tramadol, codeine and other drug types, the researchers converted the initial post-procedure opioid script—the prescribed dose multiplied by the total number of pills—into oral morphine equivalents to have a standardized measurement. They found that patients who received an initial dose of postoperative opioids exceeding 135 oral morphine equivalents—or 18 tablets of five-milligram oxycodone—were at higher risk for persistent opioid use.

With this prescription amount generally being lower than more invasive cardiac procedures, such as open-heart surgery, Frankel said it’s important for physicians to understand the risk of opioid dependence even with more minor procedures and that excessive opioid prescriptions increase the risk of subsequent dependence. The study, he said, supports lower opioid doses at discharge and using alternative pain management strategies, such as longer-lasting regional anesthesia during procedures, known as peripheral nerve blocks, or nonopioid medications like Tylenol and Advil after surgery. Patients should also receive clear counsel, Frankel said, to expect a few days of pain and to emphasize that experiencing this pain is normal and that it should get better.

In addition to these interventions by care teams, lawmakers and health care systems, including Penn Medicine, are taking various steps to reduce opioid prescriptions, such as limiting prescription supplies to a certain number of days or using automated text messaging systems to check in with patients on their post-surgery pain and opioid use.

“We’re still in the midst of a very lethal health crisis with opioid overdoses, and prescription opioids are often the initial exposure,” Frankel said. “Opioid dependence isn’t something that you as the provider can predict; it’s better to assume that anyone could be susceptible.”

The study was supported by the Mark Marchlinski EP Research and Education Fund.

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Penn Medicine is one of the world’s leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation’s first medical school) and the University of Pennsylvania Health System, which together form a $8.9 billion enterprise.

The Perelman School of Medicine has been ranked among the top medical schools in the United States for more than 20 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $496 million awarded in the 2020 fiscal year.

The University of Pennsylvania Health System’s patient care facilities include: the Hospital of the University of Pennsylvania and Penn Presbyterian Medical Center—which are recognized as one of the nation’s top “Honor Roll” hospitals by U.S. News & World Report—Chester County Hospital; Lancaster General Health; Penn Medicine Princeton Health; and Pennsylvania Hospital, the nation’s first hospital, founded in 1751. Additional facilities and enterprises include Good Shepherd Penn Partners, Penn Medicine at Home, Lancaster Behavioral Health Hospital, and Princeton House Behavioral Health, among others.

Penn Medicine is powered by a talented and dedicated workforce of more than 44,000 people. The organization also has alliances with top community health systems across both Southeastern Pennsylvania and Southern New Jersey, creating more options for patients no matter where they live.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2020, Penn Medicine provided more than $563 million to benefit our community.


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