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News You Need to Know Today
How to prevent AFib after cardiac surgery | 2 new recalls for Medtronic | CABG device a 'breakthrough' | Surgeon makes history
Wednesday, July 29, 2026
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Editor's Choice: Cardiac Surgery

New STS guideline tackles the prevention of AFib after cardiac surgery

Among the guideline's most significant changes is a Class I recommendation for prophylactic amiodarone.

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Subhasis Chatterjee, MD, FACS, FACC, FCCP, Associate Professor of Surgery, Director Thoracic Surgical ICU and ECMO Program, Baylor St. Lukes, explains the new 2026 guidelines for management of new onset post-operative atrial fibrillation (AFib), which he spoke about at the American Association for Thoracic Surgery (AATS) 2026 annual meeting.
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New STS guideline tackles the prevention of AFib after cardiac surgery

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Subhasis Chatterjee, MD, FACS, FACC, FCCP, Associate Professor of Surgery, Director Thoracic Surgical ICU and ECMO Program, Baylor St. Lukes, explains the new 2026 guidelines for management of new onset post-operative atrial fibrillation (AFib), which he spoke about at the American Association for Thoracic Surgery (AATS) 2026 annual meeting.
Among the guideline's most significant changes is a Class I recommendation for prophylactic amiodarone.
READ MORE >

Medtronic recalls thousands of cannulae due to risk of leaks

More than 50,000 devices are being recalled due to pinhole leaks associated with multiple risks. Customers should return any unused cannulae to Medtronic.

READ MORE >
fda medical device recall
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Medtronic recalls thousands of cannulae due to risk of leaks

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fda medical device recall
More than 50,000 devices are being recalled due to pinhole leaks associated with multiple risks. Customers should return any unused cannulae to Medtronic.
READ MORE >

Surgeon hails new CABG technology as a 'technical breakthrough'

The new-look ELANA device from AMT Medical could simplify CABG procedures and help improve patient access to minimally invasive and robotic surgical techniques.

READ MORE >
Distal anastomoses are almost exclusively hand-sewn as a current standard of care, which limits the widespread implementation of less-invasive approaches. This trial looked at the ability of the ELANA device to more easily construct distal anastomoses in CABG.
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Surgeon hails new CABG technology as a 'technical breakthrough'

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Distal anastomoses are almost exclusively hand-sewn as a current standard of care, which limits the widespread implementation of less-invasive approaches. This trial looked at the ability of the ELANA device to more easily construct distal anastomoses in CABG.
The new-look ELANA device from AMT Medical could simplify CABG procedures and help improve patient access to minimally invasive and robotic surgical techniques.
READ MORE >

Heart surgeon makes history, performs first robotic procedure of its kind

A surgeon in Michigan has performed the world’s first single-port robotic mitral valve repair.

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Rakesh M. Suri, MD, DPhil, Corewell Health William Beaumont University Hospital
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Heart surgeon makes history, performs first robotic procedure of its kind

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Rakesh M. Suri, MD, DPhil, Corewell Health William Beaumont University Hospital
A surgeon in Michigan has performed the world’s first single-port robotic mitral valve repair.
READ MORE >

CMS proposes Medicare payment cuts in 2027—physician groups pledge to bring about change

Cardiologists received a nice bump in pay in 2026 thanks to a one-time 2.5% conversion factor increase. That expires at the end of the year, however, and physicians will see their payments decrease as a result.

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Medicare money bills dollars
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CMS proposes Medicare payment cuts in 2027—physician groups pledge to bring about change

Share on Twitter Share on Facebook Share on Linkedin
Medicare money bills dollars
Cardiologists received a nice bump in pay in 2026 thanks to a one-time 2.5% conversion factor increase. That expires at the end of the year, however, and physicians will see their payments decrease as a result.
READ MORE >

Swallowed needle leads to serious heart damage—persistent care saves the day

The patient had a habit of holding sewing needles in his mouth while he worked as a tailor. He did not mention this at first, however, creating a challenge for his care team.

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Accidentally swallowing a sewing needle could have cost one 54-year-old patient his life. His care team was persistent, however, exploring his unexplained symptoms until they identified the problem.
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Swallowed needle leads to serious heart damage—persistent care saves the day

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Accidentally swallowing a sewing needle could have cost one 54-year-old patient his life. His care team was persistent, however, exploring his unexplained symptoms until they identified the problem.
The patient had a habit of holding sewing needles in his mouth while he worked as a tailor. He did not mention this at first, however, creating a challenge for his care team.
READ MORE >

Medtronic recalls surgical devices due to risk of blood contamination

Trace amounts of blood were identified within the sealed packaging of these devices. No patients were exposed to the foreign material, and no adverse events were reported, but Medtronic is recalling the devices as a precaution.

READ MORE >
Recall | Product recall
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Medtronic recalls surgical devices due to risk of blood contamination

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Recall | Product recall
Trace amounts of blood were identified within the sealed packaging of these devices. No patients were exposed to the foreign material, and no adverse events were reported, but Medtronic is recalling the devices as a precaution.
READ MORE >

FDA approves surgical device for high-risk aortic procedures

The AMDS Hybrid Prosthesis was designed to help clinicians treat DeBakey Type 1 dissections complicated by malperfusion. It works as a complement to hemiarch replacement, preserving the native arch and making reinterventions possible if needed. 

READ MORE >
Artivion, an Atlanta-based medical device company, has received a Humanitarian Device Exemption (HDE) from the U.S. Food and Drug Administration (FDA) for its AMDS Hybrid Prosthesis designed to treat DeBakey Type 1 dissections when malperfusion occurs. This HDE ensures select patients can be treated with the device before the FDA makes its final approval decision.
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FDA approves surgical device for high-risk aortic procedures

Share on Twitter Share on Facebook Share on Linkedin
Artivion, an Atlanta-based medical device company, has received a Humanitarian Device Exemption (HDE) from the U.S. Food and Drug Administration (FDA) for its AMDS Hybrid Prosthesis designed to treat DeBakey Type 1 dissections when malperfusion occurs. This HDE ensures select patients can be treated with the device before the FDA makes its final approval decision.
The AMDS Hybrid Prosthesis was designed to help clinicians treat DeBakey Type 1 dissections complicated by malperfusion. It works as a complement to hemiarch replacement, preserving the native arch and making reinterventions possible if needed. 
READ MORE >

In Case You Missed It

FDA clears first dedicated tricuspid surgical valve

The Edwards Lifesciences Triformis Resilia is the first dedicated surgical tricuspid valve on the market cleared with data from off-label use of mitral valves.

READ MORE >
The Edwards Lifesciences Triformis Resilia surgical tricuspid valve top and side views..
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FDA clears first dedicated tricuspid surgical valve

Share on Twitter Share on Facebook Share on Linkedin
The Edwards Lifesciences Triformis Resilia surgical tricuspid valve top and side views..
The Edwards Lifesciences Triformis Resilia is the first dedicated surgical tricuspid valve on the market cleared with data from off-label use of mitral valves.
READ MORE >

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