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
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
"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
"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
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,
About
About Jefferson:
Jefferson, which is principally located in the greater
View original content to download multimedia:https://www.prnewswire.com/news-releases/alivecor-and-thomas-jefferson-university-hospital-partner-to-evaluate-kardiamobile-6l-for-qt-prolongation-screening-in-patients-treated-for-opioid-use-disorder-301881575.html
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