Abstract
Idiopathic (primary) pulmonary arterial hypertension – a rare progressive disease that shortens life, usually diagnosed at a late stage. Therefore, it is critical to have a low threshold for suspicion of pulmonary hypertension (PH) and to refer patients to specialized centers for diagnostic evaluation and treatment as early as possible. Echocardiography is the method of choice for pulmonary hypertension assessing. Aim of the study. To determine the reason for the late diagnosis of idiopathic pulmonary arterial hypertension.Material and methods. Using the developed questionnaire, 41 patients, men and women aged 18 years and older, who were reliably diagnosed with idiopathic pulmonary arterial hypertension, were interviewed.Results and discussion. The diagnosis of idiopathic pulmonary arterial hypertension in clinical practice is made on average 7.1±6.0 years from the onset of the first symptoms of the disease. In 95% of cases, the onset of idiopathic pulmonary arterial hypertension begins with shortness of breath on exertion. Most often, the development of the disease was preceded by an acute respiratory viral infection. All patients underwent diagnostic echocardiography at the time of their first visit, but the diagnosis was established in only 56% of patients.Conclusions. Reasons for late diagnosis of idiopathic pulmonary arterial hypertension: the nature of the disease at its onset and errors in diagnosis.