Tula, Tula, Russian Federation
Russian Federation
Tula, Tula, Russian Federation
UDC 61
Idiopathic pulmonary hypertension (IPH) is a rare but severe disease characterized by increased pressure in the pulmonary artery without an obvious cause or in connection with other known diseases. This form of hypertension be-longs to group 1 of pulmonary hypertension according to the classification of the World Organization on Pulmonary Hypertension (WHO) and is characterized by a severe clinical picture, progressive course and high mortality rate. The relevance of studying IPH is determined by the need for early diagnosis and the de-velopment of effective treatment methods, since this disease significantly worsens the quality of life of patients and leads to complications from the cardiovascular system.
idiopathic pulmonary hypertension, dyspnea, right ventricular failure, endotheli-al dysfunction, pulmonary vascular remodeling.
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