Secondary pulmonary hypertension

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Secondary Pulmonary Hypertension
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Synonyms
Pronounce
Specialty Pulmonology, Cardiology
Symptoms Shortness of breath, fatigue, chest pain, swelling of the legs
Complications Right-sided heart failure, arrhythmia
Onset
Duration
Types
Causes Underlying heart or lung conditions, chronic thromboembolic disease
Risks
Diagnosis Echocardiography, Right heart catheterization
Differential diagnosis
Prevention
Treatment Treat underlying cause, oxygen therapy, medication
Medication Anticoagulants, Vasodilators, Diuretics
Prognosis
Frequency
Deaths


Secondary pulmonary hypertension (SPH) is a complex type of pulmonary hypertension that arises as a consequence of other medical conditions. These conditions can include diseases of the left heart, lung diseases, and chronic thromboembolic disease. Unlike primary pulmonary hypertension, which is considered idiopathic, secondary pulmonary hypertension has identifiable causes.

Causes[edit | edit source]

Secondary pulmonary hypertension is caused by an increase in pressure in the pulmonary arteries due to an underlying condition. Common causes include:

  • Heart failure - particularly failure of the left side of the heart which leads to increased pressure in the pulmonary circulation.
  • Chronic obstructive pulmonary disease (COPD) - which can cause hypoxia leading to vasoconstriction and increased pulmonary artery pressures.
  • Interstitial lung disease - leading to decreased lung function and hypoxia.
  • Chronic thromboembolic disease - obstruction of pulmonary vessels can lead to increased resistance against which the right heart has to pump.

Symptoms[edit | edit source]

Symptoms of secondary pulmonary hypertension may include:

  • Dyspnea (shortness of breath)
  • Fatigue
  • Chest pain
  • Swelling of the legs (due to right heart failure)
  • Syncope (fainting spells)

Diagnosis[edit | edit source]

Diagnosis of secondary pulmonary hypertension typically involves:

  • Echocardiography - to estimate the pulmonary artery pressures and assess the function of the heart.
  • Right heart catheterization - the definitive test for measuring the pressure in the pulmonary arteries and assessing the severity of pulmonary hypertension.

Treatment[edit | edit source]

Treatment of secondary pulmonary hypertension focuses on managing the underlying cause. This can include:

  • Oxygen therapy - to manage hypoxia.
  • Medications such as anticoagulants to prevent thromboembolic events, vasodilators to lower pulmonary artery pressure, and diuretics to reduce fluid overload.
  • In severe cases, lung transplantation or heart-lung transplantation may be considered.

Prognosis[edit | edit source]

The prognosis for patients with secondary pulmonary hypertension varies depending on the underlying cause and the severity of the condition. Early diagnosis and management of the primary disease are crucial for improving outcomes.

See also[edit | edit source]


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Contributors: Prab R. Tumpati, MD