INTRODUCTION Pulmonary vein stenosis (PVS) is a rare complication of pulmonary vein isolation for the treatment of atrial fibrillation. Endovascular treatment is an effective treatment, although there is little experience worldwide. OBJECTIVE The objective of the present study was to report early efficacy and safety of pulmonary vein angioplasty (PVA) METHOS Single center retrospective study at a general hospital. All adult patients undergoing PVA were included. Baseline characteristics and technical aspects of PVA were recorded. Efficacy was defined as the ability to dilate pulmonary veins and reduction in stenosis by angiography and transesophageal echocardiography (TEE). RESULTS From December 2022 to May 2023, 7 PVA were performed in 3 patients. Two of those patients had a history of multiple pulmonary vein (PV) isolation due to recurrent atrial fibrillation. Time from last PV isolation to diagnosis was approximately 6 months in all cases and very early (15 days) for the restenosis. All patients referred to a delay in diagnosis. Hemoptysis was present in all cases. PVA was performed for native stenosis (n=5) and restenosis (N=2) after stenting. The upper left pulmonary vein was affected more frequently (n=4), followed by right upper PV (n=2) and left lower PV (n=1). Right lower PV was not affected in any case. One patient presented with three PVS, which later presented with restenosis in two PV stents. The remaining two patients presented with single PVS in the upper left PV. All patients had a diagnosis with contrast computed tomography showing severe stenosis (n=5 PV) and occlusion (n=2 veins). Both occlusions were on the same patient and on the same PV, both before and after stenting. All procedures were performed under general anesthesia with TEE guidance, and through the right femoral vein. TEE confirmed PV occlusion in only one PV. After transseptal puncture, PVA was performed with coronary equipment including a guiding catheter and a 0.014’’ guide wire. Only in the first PVA, a simultaneous pulmonary artery injection was performed for visualizing the PV in a levophase. A dedicated 0.014’’ guidewire for chronic total occlusion was used in the case of PV occlusion. All native PVS were treated with bare metal balloon expandable stents that were 6 mm (n=2), 7 mm (n=1) or 10 mm (n=2) in diameter. Stent size was chosen based on computed tomography and angiography. Both stent restenosis occurred at PV treated with a 6 mm stent, and were subsequently treated with a 7 mm drug coated balloon. All PVA showed satisfactory results with reduction in TEE velocity (mean reduction was 33%). One patient experienced cardiac tamponade after stenting of a lower left PV with a 10 mm stent. All patients experienced improvement in symptoms without any mortality. One patient experienced pericarditis with mild pericardial effusion CONCLUSION In this early experience of patients with PVS, PVA is effective and safe. Larger registries are needed to confirm early experience. Restenosis was associated with small stents. |