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Nonfatal adverse events after PCI are associated with an increased risk of two-year mortality. That risk is especially high, it seems, when patients are hospitalized for heart failure symptoms such as shortness of breath and edema. 

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The American College of Radiology recently gathered 25 different medical societies to discuss how to save academic radiology. 

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Mass General experts have created a program to pinpoint intimate partner violence, using inputs including radiology reports, imaging and diagnoses to aid in detection. 

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The institution has reportedly suspended multiple members of its staff and is implementing shift-change procedures in the wake of the incident. 

In its complaint, Tallahassee Memorial HealthCare said it cleared an unnamed female patient for discharge on Oct. 6, 2025. Despite setting her up with transportation and coordinating with family, she refused to leave. 

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Copilot Health will be able to use information such as medical histories, lab results and data from wearables to answer complicated healthcare questions. Microsoft said patients who use the app can rest assured all data shared with the AI is encrypted and can be deleted at any time. 

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Jennifer L. Jackman, 67, was vacationing in the South Pacific when the fatal incident occurred. She has been with the APG since 2019, serving as COO since 2023.

Insulet Corporation has announced a voluntary recall for specific lots of the pods associated with its Omnipod 5 Automated Insulin Delivery System

Small tears were found on the inside of some of Insulet Corporation's Omnipod 5 pods. The issue was linked to a total of 18 serious adverse events.

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Many of the details are unknown, as an investigation is ongoing. The National Association on Drug Abuse Programs said it became aware of an invasion of its network in January 2026. The nonprofit supports 35,000 people—mainly Medicaid enrollees—in the state of New York. 

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Adverse event reports for food, drugs, vaccines, dietary supplements and medical devices will soon be available in one place. The U.S. Food and Drug Administration said the change will simplify reporting for consumers and allow it to react in real-time to FOIA requests.

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The randomized COBRRA trial included more than 2,700 patients with acute symptomatic pulmonary embolism or proximal deep-vein thrombosis. 

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Researchers noted that these requirements are more common for Black and Hispanic patients, creating a critical barrier to guideline-recommended care.

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Nonfatal adverse events after PCI are associated with an increased risk of two-year mortality. That risk is especially high, it seems, when patients are hospitalized for heart failure symptoms such as shortness of breath and edema.