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Congenital Quadricuspid Aortic Valve (QAV) malformation is a relatively rare cardiac valve malformation, especially with abnormal coronary opening and severe stenosis of CoronaryArteryDisease (CAD). The pati.
The long-term prognosis of patients with coronaryarterydisease (CAD) with diffuse long lesion underwent coronaryartery bypass graft (CABG) or percutaneous coronary intervention (PCI) remains worse. Here, we.
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Hunter Mehaffey, MD, a cardiothoracic surgeon from West Virginia University, will examine results comparing two treatment options Transcatheter vs. Surgical Aortic Valve Replacement in Medicare Beneficiaries with Aortic Stenosis and Significant CoronaryDisease.
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In this study, we aimed to evaluate the association of pan-immune-inflammation value (PIV) with major cardiovascular and cerebrovascular events (MACCE) in stable coronaryarterydisease patients undergoing on-.
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Her heart failure was due to the fistula as she had no coronaryarterydisease on coronary angiogram. She had cardiothoracic surgery for fistula repair. Postoperatively, she developed complete heart block requiring a permanent pacemaker.
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I think especially with the recent changes in guidelines and the recommendation to use CT for screening of coronaryarterydisease, we expect to see this trend really impact the way CT is used in the future.” A 2021 study published in Radiology: Cardiothoracic Imaging focused on cardiac imaging trends over a decade.
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