Henry Ford Hospital patient is first in the US to receive angina device

Cardiologists at Henry Ford Hospital performed the first implantation in the United States of a device approved for use in Europe for hard-to-treat angina.

The Neovasc Reducer was successfully implanted in a middle-aged, Detroit-area man on June 19. Henry Ford Health System cardiologist Gerald Koenig led the procedure, with support from cardiologists Ryan Gindi and Janakkumar Kansagra, and cardiac electrophysiologist Claudio Schuger.

“Angina affects millions of people in the United States,” said Dr. Koenig, research director for the Cardiac Catheterization Laboratory at Henry Ford Hospital and catheterization lab medical director at Henry Ford West Bloomfield Hospital. “Unfortunately, bypass and medical intervention provides little relief to some. So we are hopeful that this procedure can be of some benefit.”

Angina—slight to debilitating chest pain—is thought to be caused by a lack of blood flow to certain areas of the heart. Bypass, stenting and certain medicines help many by improving blood flow to affected areas. But those options have little or short-lived effects for others.

The “reducer” is a stainless steel, hourglass-shaped mesh that is 3 millimeters in diameter at its smallest point. Through a catheter inserted in the patient’s groin area, the reducer is placed inside the heart in a minimally invasive procedure similar to implanting a coronary stent. The procedure typically takes about 20 minutes. Within six to eight weeks, tissue then grows over the mesh, narrowing the passageway.

The procedure attempts to address angina by creating a backflow pressure into the heart by narrowing the area of the heart where blood flows out, the coronary sinus. That backflow pressure pushes blood into areas that need additional oxygenation.

The idea originated in the 1950s with Dr. Claude S. Beck, prior to the development of heart bypass surgery or the use of stents, Dr. Koenig said. In an open heart surgery, Dr. Beck stitched the coronary sinus to a narrower 3 mm.

“They saw a dramatic improvement in a vast majority of patients,” Dr. Koenig said. “Seventy percent of patients had some relief of their angina.”

Prior to the Henry Ford patient’s procedure in June, he told his doctors he could walk about two blocks before experiencing angina, which he rated a 7-8/10 on a pain scale. He also used nitroglycerin two to three times per week to alleviate symptoms. At an Aug. 12 follow-up appointment 12 weeks after the procedure, he reported walking several miles without any symptoms and taking nitroglycerin one or two times per month. He said he was rarely experiencing chest discomfort, and any chest pain was rated at a 3/4.

Doctors had stopped using the procedure with the development of heart bypass in the 1960s and coronary stenting in the 1980s. But it drew interest again as a non-invasive approach in the early 2000s. The device has been commercially available in Europe since 2015, according to the Canadian manufacturer, Neovasc Inc. The product is still in development in the United States, and U.S. trials are pending.

In the case of the Henry Ford Hospital patient, Henry Ford administration and the U.S. Food & Drug Administration (FDA) permitted the device to be used as a “compassionate use” case. In those situations, there are no other medically viable, commercially approved options available for the patient.

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