Secondary pulmonary arterial hypertension digital illustration

Secondary pulmonary arterial hypertension Save


ICD-10 code: I27.21

Disease category: I27.2: Other secondary pulmonary hypertension

Understanding Secondary Pulmonary Arterial Hypertension

Secondary pulmonary arterial hypertension (PAH) is a condition characterized by high blood pressure in the pulmonary arteries, which are the blood vessels that carry blood from the heart to the lungs. Unlike primary PAH, which has no identifiable cause, secondary PAH is associated with an underlying medical condition or certain risk factors.

Secondary PAH can occur as a result of various underlying conditions, such as:

  1. Connective tissue diseases: Conditions like systemic lupus erythematosus, scleroderma, and rheumatoid arthritis can lead to secondary PAH.
  2. HIV infection: People living with HIV/AIDS are at an increased risk of developing PAH.
  3. Liver disease: Certain liver conditions, such as cirrhosis or portal hypertension, can contribute to the development of PAH.
  4. Left heart diseases: Conditions that affect the left side of the heart, such as heart failure or valve disease, can lead to PAH.
  5. Chronic lung diseases: Conditions like chronic obstructive pulmonary disease (COPD) or interstitial lung disease can cause PAH.

Secondary PAH can also arise from risk factors such as long-term use of certain medications, exposure to toxins like methamphetamine or cocaine, or a history of blood clots in the lungs.

Common symptoms of secondary PAH may include shortness of breath, fatigue, chest pain, dizziness, and swelling in the ankles, legs, or abdomen. If you experience any of these symptoms, it is important to consult with a healthcare professional for a proper diagnosis.

Diagnosing secondary PAH involves various tests, including echocardiograms, pulmonary function tests, and cardiac catheterization. These tests help healthcare providers evaluate the function of the heart and lungs, as well as measure the pressure in the pulmonary arteries.

It's crucial to remember that secondary PAH is a serious condition that requires proper medical management. Treatment options may include addressing the underlying cause, managing symptoms, and improving overall cardiovascular health.

In conclusion, secondary pulmonary arterial hypertension is a condition characterized by high blood pressure in the pulmonary arteries, which is often associated with an underlying medical condition or specific risk factors. Recognizing the symptoms and seeking medical attention promptly is important for proper diagnosis and management of this condition.

Treatment of Secondary pulmonary arterial hypertension:

Treatment Options for Secondary Pulmonary Arterial Hypertension

Secondary pulmonary arterial hypertension (PAH) is a serious condition that occurs as a result of an underlying medical condition or disease. It is characterized by high blood pressure in the arteries of the lungs, which can lead to heart failure if left untreated. Fortunately, there are several treatment options avail...

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