Dzudovic Boris, Djuric Ivica, Matijasevic Jovan, Jovic Zoran, Darocha Szymon, Obradovic Slobodan
Clinic of Cardiology, Military Medical Academy, Belgrade, Serbia.
Institute for Pulmonary Disease, Novi Sad, Serbia.
Cardiol J. 2025;32(3):234-238. doi: 10.5603/cj.103142. Epub 2025 May 13.
Balloon pulmonary angioplasty (BPA) and pulmonary endarterectomy (PEA) are established treatments for chronic thromboembolic pulmonary hypertension (CTEPH). In cases where BPA is ineffective, stent implantation emerges as salvage therapy. However, stent implantation during BPA remains a subject of debate.
This seven-year case series in Serbia, where PEA is unavailable, examines outcomes in 10 CTEPH patients undergoing BPA with coronary-type stent implantation during BPA. Objectives include assessing the feasibility, safety, and efficacy of this combined approach, identifying optimal patient selection criteria. Criteria for stent placement included persistent unsatisfactory flow post-multiple balloon dilatations. Follow-up assessments were via repeat pulmonary angiography.
Stents were successfully deployed, demonstrating sustained patency in 14 of 15 stents over an average 21.5-month (ranging from 11 up to 82 months) follow-up. Outcomes revealed significant reductions in mean pulmonary artery pressure, improvements in WHO Functional Class, and enhanced 6-minute walking distance. For the first 6 months, patients received daily clopidogrel 75 mg and rivaroxaban 15 mg, without significant bleeding. Dual therapy for pulmonary hypertension was consistently upheld. During the follow-up period, no stent thrombosis, restenosis, or other severe acute or chronic complications were observed; however, in one case, additional balloon stent post-dilatation was required.
Coronary-type stent implantation during BPA for selected CTEPH patients, though not a primary treatment, proved valuable, offering a potential solution when BPA alone falls short. This case series emphasizes the need to refine patient selection criteria for this emerging therapeutic avenue.
球囊肺动脉血管成形术(BPA)和肺动脉内膜剥脱术(PEA)是治疗慢性血栓栓塞性肺动脉高压(CTEPH)的既定方法。在BPA无效的情况下,支架植入成为挽救治疗手段。然而,BPA期间的支架植入仍是一个有争议的话题。
在塞尔维亚进行的这项为期七年的病例系列研究中,由于无法进行PEA,研究了10例接受BPA并在BPA期间植入冠状动脉型支架的CTEPH患者的治疗结果。目标包括评估这种联合方法的可行性、安全性和有效性,确定最佳的患者选择标准。支架置入标准包括多次球囊扩张后血流持续不理想。通过重复肺动脉造影进行随访评估。
支架成功置入,在平均21.5个月(11至82个月)的随访中,15个支架中的14个显示出持续通畅。结果显示平均肺动脉压显著降低,世界卫生组织功能分级改善,6分钟步行距离增加。在最初的6个月里,患者每天服用75毫克氯吡格雷和15毫克利伐沙班,无明显出血。持续维持肺动脉高压的双重治疗。在随访期间,未观察到支架血栓形成、再狭窄或其他严重的急性或慢性并发症;然而,有1例患者需要额外进行球囊支架后扩张。
对于选定的CTEPH患者,在BPA期间植入冠状动脉型支架虽然不是主要治疗方法,但被证明是有价值的,当单独使用BPA不足时提供了一种潜在的解决方案。这个病例系列强调了需要完善这种新兴治疗途径的患者选择标准。