10 mmHg≤ mean right atrial pressure (mRAP) ≤20 mmHg;
The subjects had severe idiopathic pulmonary hypertension (mean pulmonary arterial pressure \> 45 mmHg);
WHO grade III or IV;
NT-proBNP≥650 ng/L;
The subjects were informed of the nature of the study and agreed to all the requirements for participating in the study. They signed the informed consent form and agreed to complete the follow-up and the examinations required for the follow-up.
You may not be if
Local or systemic sepsis or other acute infection;
Severe coagulopathy;
Allergy to nickel and/or titanium and/or nickel/titanium-based materials;
Patients with contraindications to antiplatelet, coagulant or thrombotic therapy;
Intolerance to contrast media;
Have participated in other drug or device clinical trials during the same period;
Glomerular filtration rate (GFR) \< 50 mL/min;
Patients with severe liver dysfunction (alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \> 3 times the upper limit of normal);
The patient had malignant arrhythmia;
The patient did not receive standardized drug therapy (triple sequential therapy) according to the Chinese guidelines for the diagnosis and treatment of pulmonary hypertension within 3 months;
Women who are pregnant, planning to become pregnant (within 12 months) or breastfeeding;
