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Imaging trends in cardio-oncology | New FDA approvals | Patient sues hospital, cardiology practice | New surgery guidelines

News You Need to Know Today
Imaging trends in cardio-oncology | New FDA approvals | Patient sues hospital, cardiology practice | New surgery guidelines
Friday, October 10, 2025
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Today's News and Trends

Multimodality imaging is more important than ever to the field of cardio-oncology

“Multimodality imaging in cardio-oncology is something many of us in the field are truly excited about," Daniel Addison, MD, told Cardiovascular Business. He noted that modalities other than echocardiography are starting to play a much larger role in the treatment of these patients.

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As cancer therapies become increasingly targeted and complex, the need for sophisticated cardiovascular monitoring has grown in parallel. Cardiovascular Business spoke with Daniel Addison, MD, director of the cardio-oncology program at The Ohio State University and chair of the American Heart Association’s (AHA) Cardiac Imaging Committee, who said the use of multimodality imaging is transforming how clinicians manage cardiovascular risk in cancer patients and survivors.
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Multimodality imaging is more important than ever to the field of cardio-oncology

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As cancer therapies become increasingly targeted and complex, the need for sophisticated cardiovascular monitoring has grown in parallel. Cardiovascular Business spoke with Daniel Addison, MD, director of the cardio-oncology program at The Ohio State University and chair of the American Heart Association’s (AHA) Cardiac Imaging Committee, who said the use of multimodality imaging is transforming how clinicians manage cardiovascular risk in cancer patients and survivors.
“Multimodality imaging in cardio-oncology is something many of us in the field are truly excited about," Daniel Addison, MD, told Cardiovascular Business. He noted that modalities other than echocardiography are starting to play a much larger role in the treatment of these patients.
READ MORE >

FDA approves subcutaneous diuretic treatment for heart failure-related edema

The newly approved drug-device combination helps patients manage their own treatment from the comfort of home. 

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The Lasix ONYU device was cleared by the FDA as a new treatment option for heart-failure related edema. It is a new drug-device combination from SQ Innovation, for adult patients with chronic heart failure.
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FDA approves subcutaneous diuretic treatment for heart failure-related edema

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The Lasix ONYU device was cleared by the FDA as a new treatment option for heart-failure related edema. It is a new drug-device combination from SQ Innovation, for adult patients with chronic heart failure.
The newly approved drug-device combination helps patients manage their own treatment from the comfort of home. 
READ MORE >

Florida patient sues hospital, cardiology practice for alleged negligence after leg amputation

The patient alleges she experienced significant delays in care after being rushed to the hospital for acute limb ischemia. She also says no vascular surgeons were available, limiting her treatment options.

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American Heart Association and Joint Commission launch new Comprehensive Heart Attack Center certification.
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Florida patient sues hospital, cardiology practice for alleged negligence after leg amputation

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American Heart Association and Joint Commission launch new Comprehensive Heart Attack Center certification.
The patient alleges she experienced significant delays in care after being rushed to the hospital for acute limb ischemia. She also says no vascular surgeons were available, limiting her treatment options.
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FDA approves Zoll's newest defibrillator-monitor

The device, based on years of user feedback, is now cleared for use in both EMS and hospital settings.

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The U.S. Food and Drug Administration (FDA) granted pre-market approval (PMA) clearance for Zoll Zenix defibrillator-monitor for EMS and hospital use. It incorporates new technology and features based on years of user feedback.
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FDA approves Zoll's newest defibrillator-monitor

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The U.S. Food and Drug Administration (FDA) granted pre-market approval (PMA) clearance for Zoll Zenix defibrillator-monitor for EMS and hospital use. It incorporates new technology and features based on years of user feedback.
The device, based on years of user feedback, is now cleared for use in both EMS and hospital settings.
READ MORE >

New expert guidelines examine the use of temporary MCS during heart surgery

Three leading medical societies collaborated on the new document, providing detailed recommendations that cover a wide variety of technologies and clinical scenarios.

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IVUS guidance during DES implantation boosts long-term outcomes in new study
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New expert guidelines examine the use of temporary MCS during heart surgery

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IVUS guidance during DES implantation boosts long-term outcomes in new study
Three leading medical societies collaborated on the new document, providing detailed recommendations that cover a wide variety of technologies and clinical scenarios.
READ MORE >

Featured Articles

Pushback against Trump's $100K visa fee continues with new lawsuit

As a new lawsuit targets the unpopular policy, the American College of Cardiology and other medical societies worry that $100,000 fees will make the ongoing physician shortage much worse.

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Money dollar economics payment
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Pushback against Trump's $100K visa fee continues with new lawsuit

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Money dollar economics payment
As a new lawsuit targets the unpopular policy, the American College of Cardiology and other medical societies worry that $100,000 fees will make the ongoing physician shortage much worse.
READ MORE >

Cardiologist dies after choking on flight—family’s lawsuit points to alleged negligence

According to the lawsuit, the doctor followed a strict vegetarian diet and choked after he was served meat. The family also claims the airline delayed care by waiting too long to perform an emergency landing.

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healthcare AI and aviation
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Cardiologist dies after choking on flight—family’s lawsuit points to alleged negligence

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healthcare AI and aviation
According to the lawsuit, the doctor followed a strict vegetarian diet and choked after he was served meat. The family also claims the airline delayed care by waiting too long to perform an emergency landing.
READ MORE >

FDA clears new AI model for MAC detection in routine imaging results

The advanced algorithm was designed to detect and evaluate mitral annular calcification on routine, non-gated CT scans. It is now available as part of Carebricks, a generative AI platform from Bunkerhill Health. 

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robot reviewing heart data
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FDA clears new AI model for MAC detection in routine imaging results

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robot reviewing heart data
The advanced algorithm was designed to detect and evaluate mitral annular calcification on routine, non-gated CT scans. It is now available as part of Carebricks, a generative AI platform from Bunkerhill Health. 
READ MORE >

‘Every second counts’: New Viz.ai platform brings the entire heart attack team together

The new platform provides users with real-time access to high-quality electrocardiograms and patient data. The goal is to ensure everyone is on the same page at all times, with no unnecessary delays.

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Viz.ai Viz ACS
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‘Every second counts’: New Viz.ai platform brings the entire heart attack team together

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Viz.ai Viz ACS
The new platform provides users with real-time access to high-quality electrocardiograms and patient data. The goal is to ensure everyone is on the same page at all times, with no unnecessary delays.
READ MORE >

In Case You Missed It

Mavacamten fails to boost outcomes for patients with nonobstructive HCM

The drug, already approved by the FDA to treat obstructive HCM, failed to outperform a placebo after 48 weeks.

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pharmaceutical drug approval process
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Mavacamten fails to boost outcomes for patients with nonobstructive HCM

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pharmaceutical drug approval process
The drug, already approved by the FDA to treat obstructive HCM, failed to outperform a placebo after 48 weeks.
READ MORE >

FDA approves treatment of rare genetic disorder in children as young as 1 year old

Evinacumab-dgnb, sold by Regeneron under the brand name Evkeeza, can now be used to treat homozygous familial hypercholesterolemia in much younger patients.

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Evinacumab-dgnb is sold by Regeneron under the brand name Evkeeza
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FDA approves treatment of rare genetic disorder in children as young as 1 year old

Share on Twitter Share on Facebook Share on Linkedin
Evinacumab-dgnb is sold by Regeneron under the brand name Evkeeza
Evinacumab-dgnb, sold by Regeneron under the brand name Evkeeza, can now be used to treat homozygous familial hypercholesterolemia in much younger patients.
READ MORE >

In Other News

Private radiology practice will pay $3.25M to settle class-action lawsuit over cyberattack

Greenville, North Carolina-based Eastern Radiologists is denying any wrongdoing, deciding to settle the matter to avoid protracted litigation. 

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money cybersecurity ransomware health IT data breach hacker
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Private radiology practice will pay $3.25M to settle class-action lawsuit over cyberattack

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money cybersecurity ransomware health IT data breach hacker
Greenville, North Carolina-based Eastern Radiologists is denying any wrongdoing, deciding to settle the matter to avoid protracted litigation. 
READ MORE >

Planned Parenthood sues to block Missouri’s request for abortion records

The Missouri attorney general has demanded details on patient care, communications between providers and pregnant women, maintenance records and more in an effort to identify state residents who have sought abortions. 

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Missouri state house capitol Jefferson City
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Planned Parenthood sues to block Missouri’s request for abortion records

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Missouri state house capitol Jefferson City
The Missouri attorney general has demanded details on patient care, communications between providers and pregnant women, maintenance records and more in an effort to identify state residents who have sought abortions. 
READ MORE >

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