News Release
howard herrmann
Howard C. Herrmann, MD

PHILADELPHIA— Physicians at Penn Medicine have completed the first procedure in the Small Annuli Randomized to Evolut or Sapien (SMART) post-market trial, a randomized, head-to-head study comparing two transcatheter aortic valve replacement (TAVR) systems in patients with severe symptomatic aortic stenosis (AS).

The SMART trial compares valve safety and performance of the self-expanding Medtronic Evolut™ PRO and PRO+TAVR Systems with the balloon-expandable SAPIEN 3 and SAPIEN 3 Ultra Transcatheter Heart Valves manufactured by Edwards Lifesciences. The study will enroll approximately 700 patients at more than 90 international sites, and is being led by Howard C. Herrmann, MD, the John Winthrop Bryfogle Professor of Cardiovascular Diseases at the Perelman School of Medicine at the University of Pennsylvania and Health System Director for Interventional Cardiology. Herrmann and Pavan Atluri, MD, an associate professor of Surgery, recently completed treatment of the first patient in the study.

The study evaluates valve performance in patients with small annuli, a small aortic valve, which represents about 30% of the global TAVR market. Due to its focus on small annulus patients, the SMART Trial will enroll predominantly women, which will provide important clinical insight into a currently underrepresented patient population in the TAVR literature.

“Penn Medicine has been in on the ground floor of many of the early and landmark trials in TAVR research since performing one of the first investigational procedures in 2007, and, since then, we have completed thousands of these procedures,” Herrmann said. “Subsequently, multiple devices have been FDA-approved, and the procedure has grown to become the predominant one for all patients with aortic stenosis. The outcome of this study will help cardiac teams to make more tailored decisions about which kind of valve to use on which patients.”

The TAVR procedure uses a catheter — inserted through a small incision in the groin or in the left side of the chest — to place a new aortic valve where the patient’s native valve was, pushing the faulty valve aside. Today, Penn Medicine performs more than 500 TAVR procedures each year, improving quality of life for patients suffering from severe aortic stenosis symptoms like chest pain, shortness of breath, fainting and fatigue. Without treatment, more than half of severe aortic stenosis patients die within two years.

The start of the new trial marks another “first” in Penn’s history of innovation in this space, which includes nearly 15 years of TAVR expertise and collaboration between interventional cardiology and cardiac surgery. Researchers at the Perelman School of Medicine at the University of Pennsylvania were among the leaders of early TAVR trials and remain on the cutting edge of TAVR technology, which now allows a broader range of patients to undergo the procedure. TAVR was approved by the U.S. Food and Drug Administration in 2011, following trials among patients initially who would not have been eligible for traditional open-heart surgery due to their age or other medical conditions.

“Valve design (hemodynamics) are important in order to provide patients with the most optimal valve function in the short term, as well as to contribute to long term valve performance and durability,” Herrmann said.

The SMART Trial includes pre-specified endpoints of hemodynamic (blood flow) superiority and clinical non-inferiority with the Evolut platform compared to Sapien for mortality, stroke, or rehospitalization at 12 months. The results from the head-to-head study will provide evidence to help heart teams more selectively tailor valve selection.

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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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