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Updated: Jan 1, 2026

Catheter-based Endovascular Angioplasty for Fibrosing Mediastinitis-associated Pulmonary Vein Stenosis
Published on: August 26, 2025
Balloon pulmonary angioplasty for chronic thromboembolic pulmonary hypertension
1Division of Cardiovascular Medicine, Toho University Ohashi Medical Center, 2-22-36 Ohashi, Meguro-ku, Tokyo, Japan. ikedanobutaka@yahoo.co.jp.
Insights
Balloon pulmonary angioplasty (BPA) offers a promising new treatment for chronic thromboembolic pulmonary hypertension (CTEPH), particularly for patients with inoperable disease or those not suitable for pulmonary endarterectomy.
Area of Science:
- Cardiology
- Pulmonology
- Interventional Radiology
Background:
- Chronic thromboembolic pulmonary hypertension (CTEPH) is a severe condition caused by organized blood clots in pulmonary arteries.
- Pulmonary endarterectomy (PEA) is a standard treatment for proximal CTEPH, but it is not suitable for all patients.
- Riociguat is the only FDA-approved medication for CTEPH, recommended for inoperable cases or post-PEA residual disease.
Purpose of the Study:
- To review the history, indications, procedures, and complications of Balloon Pulmonary Angioplasty (BPA).
- To evaluate BPA as a potential alternative treatment for CTEPH.
- To discuss the future outlook of BPA in managing CTEPH.
Main Methods:
- Literature review of existing studies on BPA for CTEPH.
- Analysis of procedural techniques and outcomes associated with BPA.
- Summary of complications and management strategies for BPA.
Main Results:
- BPA is emerging as a viable and promising treatment option for CTEPH.
- The procedure shows potential benefits, especially for patients with inoperable CTEPH.
- Understanding BPA's history and techniques is crucial for its application.
Conclusions:
- Balloon Pulmonary Angioplasty (BPA) represents a significant advancement in CTEPH treatment.
- Further research and experience are needed to fully establish BPA's role and optimize its use.
- BPA may offer a valuable alternative for patients unsuitable for PEA or medical therapy alone.
Abstract:
Chronic thromboembolic pulmonary hypertension (CTEPH) is classified as Group-4 pulmonary hypertension caused by organized thrombi in pulmonary arteries. Pulmonary endarterectomy (PEA) has been shown to improve the symptoms and prognoses of patients with proximal CTEPH. The soluble guanylate cyclase stimulator (riociguat) is the sole FDA-licensed drug for the treatment of CTEPH, and guidelines recommend its use for patients with inoperable CTEPH or residual or recurrent pulmonary hypertension following PEA. Balloon pulmonary angioplasty (BPA) is a new procedure, but it is a promising alternative to PEA, especially in patients with inoperable CTEPH. This review summarizes the history, indications, procedures and complications of BPA. Finally, we discuss the future perspective of BPA for better management of CTEPH.
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