News | Remote Monitoring | July 21, 2023

AliveCor and Thomas Jefferson University Hospital Partner to Evaluate KardiaMobile 6L for QT Prolongation Screening in Patients Treated for Opioid Use Disorder

Pilot study will assess positive impacts of real-time safety monitoring on patient outcomes and treatment experience 

Pilot study will assess positive impacts of real-time safety monitoring on patient outcomes and treatment experience

July 21, 2023 — AliveCor, a leading innovator in FDA-cleared personal electrocardiogram (ECG) technology, today announced a partnership with the Jefferson Narcotic Addiction Rehabilitation Program (NARP) and Thomas Jefferson University Hospital in Philadelphia to evaluate the benefits of QTc monitoring with KardiaMobile 6L for patients receiving methadone maintenance therapy for opioid use disorder.  

In the six-month pilot study, healthcare professionals will use KardiaMobile 6L, the only medical-grade, six-lead personal ECG device that is FDA-cleared to measure QTc intervals, to detect QT prolongation, a potentially dangerous side effect associated with certain medications like methadone. 

“We are excited to partner with Thomas Jefferson University Hospital on this important study that will illuminate the benefits of real-time QTc interval monitoring with KardiaMobile 6L on patients’ outcomes and their treatment experience,” said Patricia Baran, Senior Vice President, Enterprise North America & Biopharma Worldwide. “By enabling clinicians to efficiently detect cardiac side effects, they can better counsel patients about taking the appropriate steps to mitigate risks to their heart health.” 

“Rapid, point-of-care devices can have an important role in streamlining the cardiac safety monitoring required by many behavioral disorder medicines, which are a critical part of comprehensive treatment strategies for people with substance use disorders,” said William Jangro, DO, Medical Director, Jefferson NARP.  

“We look forward to assessing how efficient QTc monitoring with KardiaMobile 6L increases compliance with guideline recommendations, improves the patient experience, enhances treatment, and allows for interdepartmental collaboration,” said Daniel Frisch, MD, Associate Professor of Medicine Electrophysiology Section, Thomas Jefferson University Hospital. 

KardiaMobile 6L was cleared by the FDA in July 2021 for use by healthcare professionals to calculate patients’ QTc interval. 

 

About the Pilot Study:  

During the six-month pilot, each new patient and each patient undergoing an annual physical at Jefferson NARP will have their ECG recorded with KardiaMobile 6L to detect potential QT prolongation. Recordings will be automatically uploaded to the clinic’s KardiaStation, AliveCor’s workflow solution for in-person instant ECG analysis. 

For more information: www.alivecor.com 

 

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