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What is Cardiac Magnetic Resonance Imaging?

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Cardiac magnetic resonance imaging (CMR), also known as cardiac MRI, is a non-invasive diagnostic imaging technique that provides detailed information about the structure and function of the heart. It utilizes a powerful magnetic field and radio waves to create high-resolution images of the heart, allowing healthcare professionals to evaluate cardiac anatomy, assess myocardial function, and detect various cardiovascular conditions. CMR works by aligning the hydrogen atoms in the body's tissues using a strong magnetic field. When radio waves are applied, the hydrogen atoms emit signals that are captured by specialized detectors, enabling the creation of detailed images. By manipulating different imaging parameters, such as magnetic field strength and timing, CMR can provide a wealth of information about the heart's structure and function. One of the main applications of CMR is the assessment of myocardial function. It can accurately measure the heart's pumping capacity

(Dr Ramji Mehrotra) What are Inherited Cardiac Conditions?

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Inherited cardiac conditions are a group of cardiovascular disorders that are caused by genetic mutations or abnormalities passed down from parents to their children. These conditions can affect the structure or function of the heart and may occur at various stages of life, from infancy to adulthood. Understanding the nature of inherited cardiac conditions is crucial for early detection, proper management, and preventive measures. One prominent example of an inherited cardiac condition is hypertrophic cardiomyopathy (HCM) . HCM is characterized by the thickening of the heart muscle, particularly in the left ventricle. This abnormal thickening can disrupt the heart's pumping ability and lead to symptoms such as chest pain, shortness of breath, and palpitations. In some cases, HCM can cause sudden cardiac arrest, especially during intense physical activity. According to Dr. Ramji Mehrotra , leading cardiac surgeon in NCR region , genetic mutations in genes responsible for the str