Abstract
Chronic thromboembolic pulmonary hypertension (CTEPH) results from recurrence or incomplete resolution of a pulmonary embolism. CTEPH is much more common than is commonly believed. If left untreated, it can lead to right ventricular failure and death. It is critical that all patients with pulmonary hypertension (PH) be screened for CTEPH, as this form of PH is potentially treatable. Pulmonary endarterectomy (PEA) is the operation of choice for the treatment of CTEPH. Different levels of thromboembolic lesions cause different complexity of performing PEA. Higher levels are considered hard cases. Even in technically operable patients, the risk-benefit ratio of PEA should be considered due to the high operative risk. Patients who are not indicated for PEA are candidates for balloon pulmonary angioplasty (BPA) Ballon pulmonary angioplasty in CTEPH is indicated: for patients who are recognized as inoperable due to concomitant diseases; with residual or recurrent PH after PEA; as well as with surgically inaccessible lesions of the LA branches; after ineffective medical treatment; patients who were denied open surgery; patients who do not have contraindications for performing BPA.
This review is devoted to the clinical history of the disease, endovascular treatment of the CTEPH, balloon pulmonary angioplasty performed either alone or in combination with PEA.
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About the authors
- Komoliddin Kh. Rakhmonov, Cand. Med. Sci., Cardiovascular Surgeon; ORCID
- Kakhaber E. Diasamidze, Dr. Med. Sci., Leading Researcher; ORCID
- Baizak A. Sagymbaev, Physician for X-ray Endovascular Diagnostics and Treatment; ORCID