(Q22.4) Congenital tricuspid stenosis

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258 814 in individuals diagnosis congenital tricuspid stenosis confirmed
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5 601 deaths with diagnosis congenital tricuspid stenosis
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2% mortality rate associated with the disease congenital tricuspid stenosis

Diagnosis congenital tricuspid stenosis is diagnosed Men are 2.44% more likely than Women

132 569

Men receive the diagnosis congenital tricuspid stenosis

3 043 (2.3 %)

Died from this diagnosis.

100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
0
126 245

Women receive the diagnosis congenital tricuspid stenosis

2 558 (2.0 %)

Died from this diagnosis.

Risk Group for the Disease congenital tricuspid stenosis - Men and Women aged 0

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In Men diagnosis is most often set at age 0-79
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Less common in men the disease occurs at Age 80-95+Less common in women the disease occurs at Age 80-95+
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In Women diagnosis is most often set at age 0-79

Disease Features congenital tricuspid stenosis

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Absence or low individual and public risk
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Congenital tricuspid stenosis - what does this mean

Congenital tricuspid stenosis is a congenital heart defect in which the tricuspid valve is abnormally narrow, restricting the flow of blood from the right atrium to the right ventricle. it is usually caused by abnormal development of the tricuspid valve leaflets, or fusion of the leaflets, which can lead to a narrowing of the valve opening. it can also be caused by a thickening of the valve leaflets or a narrowing of the valve opening as a result of a congenital heart defect or other heart condition.

What happens during the disease - congenital tricuspid stenosis

Congenital tricuspid stenosis is a condition in which the tricuspid valve, located between the right atrium and right ventricle of the heart, is abnormally narrow. this leads to increased pressure in the right atrium, forcing the right ventricle to work harder to pump blood through the narrowed valve. this can cause symptoms such as shortness of breath, fatigue, and swelling in the legs and abdomen. in some cases, the condition may be caused by a genetic mutation that affects the development of the tricuspid valve during fetal development. in other cases, the cause of the condition may be unknown.

Clinical Pattern

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How does a doctor diagnose

  • Perform a physical exam to assess for signs and symptoms of tricuspid stenosis.
  • Obtain an echocardiogram to measure the pressure gradient across the tricuspid valve.
  • Perform a Doppler echocardiogram to assess the flow of blood across the tricuspid valve.
  • Perform a cardiac catheterization to measure the pressure gradient across the tricuspid valve.
  • Perform an MRI or CT scan to assess the anatomy of the tricuspid valve.
  • Perform genetic testing to identify any genetic mutations that may be associated with tricuspid stenosis.

Treatment and Medical Assistance

Main goal of the treatment: To reduce the risk of complications associated with Congenital Tricuspid Stenosis.
  • Medication to reduce the severity of symptoms
  • Surgery to repair the tricuspid valve
  • Regular monitoring of the heart rate and rhythm
  • Regular follow-up with a cardiologist
  • Lifestyle modifications to reduce stress on the heart
  • Regular exercise and physical activity
  • Healthy diet to maintain a healthy weight
  • Avoiding smoking and alcohol
  • Reducing salt intake
  • Avoiding certain medications that can worsen the condition
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15 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Congenital tricuspid stenosis - Prevention

Congenital tricuspid stenosis can be prevented by avoiding exposure to certain environmental factors, such as certain drugs and viruses, during pregnancy. additionally, prenatal care and regular check-ups can help detect the condition early and allow for prompt treatment.