FDA approved an implantable device sold by Impulse Dynamics to treat patients with Class III moderate to severe heart failure who are not suitable for cardiac resynchronization therapy (CRT).

‘Heart failure patients have limited treatment alternatives. But, a new device approved by the FDA can help treat heart failure patients who have no alternative treatment options.’
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After the device is implanted, a physician tests and programmes the device, which delivers electrical impulses to the heart during regular heartbeats to help improve the heart's squeezing capability. Read More..





The device would be beneficial for patients not suited to treatment with other heart failure devices such as cardiac resynchronization therapy to restore a normal timing pattern of the heartbeat, the US FDA noted in a statement.
"Patients with moderate-to-severe chronic heart failure have limited treatment options. And for those who are unable to be treated due to underlying conditions or who have not responded to available treatments, their quality of life may be impacted, with limits on the types of physical activities they can do," said Bram Zuckerman, Director at FDA's Centre for Devices and Radiological Health.
"The FDA recognized the unmet need for these patients and worked with the manufacturer...to efficiently bring this product to market while ensuring it meets our regulatory requirements for safety and effectiveness," Zuckerman added.
For the study, the US FDA evaluated data from two clinical trials with a total of 389 patients with moderate-to-severe heart failure.
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The Optimizer Smart system improves the quality of life and functional status of certain heart failure patients.
Source-IANS