Advanced Cardiovascular Care Center

Advanced Cardiovascular Care Center offers cardiac services in a warm, comforting, relaxing atmosphere. The practice is committed to high quality patient care in an ever-changing health care environment.

The practice operates under the direction of Dr. Annie Varughese, Board-Certified in Cardiology and leading cardiology specialist providing treatment for heart attacks, angina, hypertension and all aspects of cardiology. The well-trained cardiology staff offers a variety of comprehensive, state-of-the-art services to diagnose, treat and manage heart disease. Our cardiac specialists improve the lives of thousands of patients every year using advanced surgical and non-surgical procedures.

The goal is to provide state-of-the-art cardiology care in a personal setting for our patients. We provide information for you and your family so you can understand the problem, tests and any recommended treatments.

We thank you for selecting Advanced Cardiovascular Care Center for you or your loved ones. We appreciate any suggestions how we might improve our service for you.

The services offered by Advanced Cardiovascular Care Centre are listed below.

Click the service to know more about the service and request an appointment to get the service.

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Heart Doctors in Houston

Marfan syndrome is a genetic disorder that affects the body’s connective tissue. Connective tissue holds all the body’s cells, organs and tissue together which plays an important role in helping the body grow and develop properly. It this tissue is damaged, many body systems are affected, including the heart, blood vessels, bones, tendons, cartilage, eyes, nervous system, skin and lungs.

People with Marfan syndrome are usually tall and thin with disproportionately long arms, legs, fingers and toes. The damage caused by Marfan syndrome can be mild or severe. If your heart or blood vessels are affected, the condition can become life-threatening.

How common is Marfan syndrome?

About 1 in 5,000 people have Marfan syndrome, including men and women of all races and ethnic groups. About 3 out of 4 people with Marfan syndrome inherit it. But some people with Marfan syndrome are the first in their family to have it; when this happens it is called a spontaneous mutation. There is a 50 percent chance that a person with Marfan syndrome will pass along the genetic mutation each time they have a child.

Causes of Marfan syndrome:

Marfan syndrome is caused by a defect in the gene that encodes the structure of fibrillin and the elastic fibers, a major component of connective tissue. This gene is called fibrillin-1 or FBN1.

In most cases, Marfan syndrome is inherited. The pattern is called “autosomal dominant,” meaning it occurs equally in men and women and can be inherited from just one parent with Marfan syndrome. People who have Marfan syndrome have a 50 percent chance of passing along the disorder to each of their children.

In 25 percent of cases, a new gene defect occurs due to an unknown cause. Marfan syndrome is also referred to as a “variable expression” genetic disorder, because not everyone with Marfan syndrome has the same symptoms to the same degree. Marfan syndrome is present at birth. However, it may not be diagnosed until adolescence or young adulthood.

Signs and Symptoms of Marfan syndrome:

Sometimes Marfan syndrome is so mild, few if any, symptoms occur. In most cases, the disease progresses with age and symptoms of Marfan syndrome become noticeable as changes in connective tissue occur. The symptoms of Marfan syndrome differ from one person to the next, depending on which body part is affected and to what degree. Symptoms may include:

  • Thin, long fingers and toes
  • Sunken or protruding chest
  • Long, narrow face, Scoliosis
  • Family history of the condition
  • Enlarged aorta, mitral valve prolapsed
  • Loose and flexible joints, often prone to dislocation
  • Proportionately small lower jaw and narrow, highly arched palate
  • Usually, tall lean stature with disproportionate long arms and legs
  • Visual problems, such as nearsightedness (myopia) or dislocation of the ocular lens

Diagnosis of Marfan syndrome:

Gene testing is not readily available, but can be organised for some families who meet the diagnostic criteria. A specific collection of major characteristic features must be present to establish the syndrome. A confirmed diagnosis requires coordinated evaluation by a cardiologist, ophthalmologist, orthopaedic surgeon and geneticist, all experienced with the Marfan syndrome. The condition is diagnosed using a number of tests, including:

  • Genetic data
  • Echocardiogram
  • Eye examination
  • Physical examination
  • Skeletal tests such as x-rays

Treatments for Marfan syndrome:

Treatment usually includes medications to keep your blood pressure low to reduce the strain on weakened blood vessels. Depending on the severity of your symptoms and the part of your body that’s affected, surgery may be necessary.

Marfan’s syndrome can’t be cured. Treatments typically focus on lessening the impact of various symptoms.

Seek counsel from our Heart Doctors in Houston if you suspect you are suffering from Marfan syndrome for the best treatment options for you.

Visit us at: www.Advancedcardiodr.com |Call on: +1 281-866-7701.

Ischemic Heart Disease – Advanced Cardio Vascularcare Center

Ischemic Heart Disease or coronary heart disease is a heart issue created by narrowing of the coronary arteries. This causes less blood and oxygen to achieve the heart. Being that the heart is a muscle, it relies on upon a consistent supply of oxygen and nutrients to course through the coronary arteries. At the point when the coronary arteries get to be stopped up by fat and cholesterol stores and can’t supply enough blood to the heart, the outcome is ischemic heart disease. There are real risk factors for adding to this sort of Ischemic heart disease.

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In any case, there are natural elements that you can dispose of to decrease your shots:

Age: Substantial rates of the individuals who kick the bucket of coronary heart disease are age 65 or more seasoned.

Sex: Typically men are at more serious danger of showing some kindness assault than ladies. They additionally have a tendency to have heart assaults prior in life than ladies.

Smoking: Smoking duplicates the danger of a heart assault versus a non-smoker.

High Blood Cholesterol: As blood cholesterol levels expand, so does the danger of coronary heart disease.

Hypertension: High blood pressure constrained the heart to overexert its muscles, which makes it extend and debilitate after some time.

Physical Inactivity: Regular, moderate movement is valuable for the best possible course of blood in the body.

Stoutness: An abundance measure of weight strains the heart and raises the blood pressure and blood cholesterol levels.

Diabetes: The vicinity of diabetes has an unfriendly influence on the heart in light of the fact that diabetes straightforwardly influences cholesterol and triglyceride levels. At the point when glucose levels are hoisted, the danger of heart disease is incredibly expanded.

Seek counsel from our Heart Specialist in Houston if you suspect you are suffering from Ischemic Heart Disease or coronary heart disease for the best treatment options for you.

Contact Advanced Cardio at www.advancedcardiodr.com and get the treatment with the best and advanced doctors.

Hypertrophic cardiomyopathy (HCM)

Hypertrophic cardiomyopathy (HCM) is a disease in which the heart muscle (myocardium) becomes abnormally thick (hypertrophied). The thickened heart muscle can make it harder for the heart to pump blood. Hypertrophic cardiomyopathy is very common and can affect people of any age. About one out of every 500 people has HCM. It affects men and women equally.

Other Names for Hypertrophic Cardiomyopathy

  • Asymmetric Septal Hypertrophy
  • Familial Hypertrophic Cardiomyopathy
  • Hypertrophic Obstructive Cardiomyopathy
  • Hypertrophic Non-obstructive Cardiomyopathy
  • Idiopathic Hypertrophic Sub-aortic Stenosis (IHSS)

Causes of Hypertrophic Cardiomyopathy:

HCM is a genetic condition caused by a change or mutation in one or more genes and is passed on through families. Each child of someone with HCM has a 50 per cent chance of inheriting the condition. HCM is a common cause of sudden cardiac arrest (SCA) in young people, including young athletes.

HCM also can affect the heart’s mitral valve, causing blood to leak backward through the valve. Sometimes, the thickened heart muscle doesn’t block blood flow out of the left ventricle. This is called non-obstructive hypertrophic cardiomyopathy. The entire ventricle may thicken, or the thickening may happen only at the bottom of the heart. The right ventricle also may be affected.

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Symptoms of HCM:

Many people with HCM don’t experience any symptoms. However, the following symptoms may occur during physical activity:

You may find that you never have any serious problems related to your condition, and with treatment, your symptoms should be controlled. However some people may find that their symptoms worsen or become harder to control in later life.

The area of heart muscle that is affected by HCM and the amount of stiffening that occurs will determine how the symptoms affect you.

For some people, a number of other conditions can develop as a result of having HCM. These may include abnormal heart rhythms, or arrhythmias, including heart block and endocarditis.

Other symptoms that might occur, at any time, include:

  • Chest pain
  • Palpitations
  • Shortness of breath
  • High blood pressure
  • Light headedness and fainting

 

Diagnosis of Hypertrophic Cardiomyopathy:

The health care provider will perform a physical exam and listen to the heart and lungs with a stethoscope. Signs may include abnormal heart sounds or a heart murmur. These sounds may change with different body positions, High blood pressure, the pulse in your arms and neck will also be checked. The doctor may feel an abnormal heartbeat in the chest.

Close family members of people who have been diagnosed with hypertrophic cardiomyopathy may be screened for the condition. Tests used to diagnose heart muscle thickness, problems with blood flow, or leaky heart valves (mitral valve regurgitation) may include:

  • Echocardiography, ECG
  • Cardiac catheterization
  • MRI of the heart, Chest X-ray
  • Transesophageal echocardiogram (TEE)
  • 24-hour Holter monitor (heart rhythm monitor)

Risk Factors include:

Any strenuous exercise that increases after load (i.e., heavy weight lifting/training) can theoretically increase the magnitude of LV hypertrophy over time and thus worsen obstruction in subjects with pre-existing HCM. Risk factors for the development of end-stage HCM (manifesting as LV systolic dysfunction and LV dilation) include younger age of onset/presentation of HCM, a family history of HCM, increased ventricular wall thickness, along with the presence of certain genetic mutations in certain individuals.

Treatment of HCM:

At present there is no cure for HCM, but treatments are available to help control your symptoms and prevent complications. Your treatment will depend on how your heart is affected and what symptoms you have. You may need:

  • A Pacemaker – to control your heart rate
  • Medicines – to help control your blood pressure, abnormal heart rhythms
  • An ICD – if you are at risk of having a life threatening abnormal heart rhythm

Seek counsel from our Houston Cardiologist if you suspect you are suffering from Hypertrophic Cardiomyopathy (HCM) for the best treatment options for you.

Visit us at: www.advancedcardiodr.com|Call: +1 281-866-7701.