Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Front Immunol. 2022 Mar 11;13:828863. doi: 10.3389/fimmu.2022.828863. eCollection 2022.
To investigate the long-term efficacy of percutaneous transluminal pulmonary angioplasty (PTPA) in patients with Takayasu arteritis (TA) and pulmonary artery stenosis and pulmonary hypertension (PH).
Data from 183 lesions from 79 surgeries performed on 32 patients with TA and PH were analyzed. Symptoms, laboratory investigation results, World Health Organization (WHO) functional class, 6-min walk distance (6 MWD), hemodynamic parameters, and prognosis were analyzed at baseline and follow-up.
The mean (± SD) age of the 32 patients (28 female, 4 male) was 42.8 ± 11.9 years, and the median follow-up was 49.5 months (interquartile range, 26-71 months). Compared with baseline, changes in total bilirubin, N-terminal pro-brain natriuretic peptide (NT-proBNP) level, 6 MWD, and WHO score functional class demonstrated significant differences (<0.001). Echocardiography findings, right and left ventricular diameter, tricuspid annular plane systolic excursion, and estimated pulmonary artery systolic pressure were all improved (=0.016, <0.001, <0.001, =0.005, respectively). Importantly, repeat right heart catheterization revealed that mean pulmonary artery pressure, pulmonary vascular resistance, and cardiac index also improved significantly at follow-up (<0.001, <0.001, and =0.011, respectively). Pulmonary angiography revealed post-procedure restenosis in 64 (35.0%) lesions underwent PTPA within three to six months. Among three patients who underwent stent implantation, one experienced restenosis. Two patients died during the follow-up period, one from aggravation of right heart failure after lung infection, and the other in a traffic accident.
Results of this study indicated that PTPA significantly improved clinical symptoms, exercise tolerance, and hemodynamic parameters in patients with TA pulmonary artery stenosis and PH. More importantly, reperfusion pulmonary edema significantly decreased, and no patient died of PTPA-related complications with guidance from the pressure wire.
探讨经皮腔内肺血管成形术(PTPA)治疗大动脉炎(TA)并肺动脉狭窄和肺动脉高压(PH)患者的长期疗效。
分析了 32 例 PH 合并 TA 患者 79 次手术 183 处病变的数据。分析了基线和随访时的症状、实验室检查结果、世界卫生组织(WHO)功能分级、6 分钟步行距离(6MWD)、血流动力学参数和预后。
32 例(28 例女性,4 例男性)患者的平均(±SD)年龄为 42.8±11.9 岁,中位随访时间为 49.5 个月(四分位距,26-71 个月)。与基线相比,总胆红素、N 末端脑利钠肽前体(NT-proBNP)水平、6MWD 和 WHO 心功能分级均有显著变化(<0.001)。超声心动图发现右、左心室直径、三尖瓣环平面收缩期位移和估测肺动脉收缩压均有改善(=0.016,<0.001,<0.001,=0.005,分别)。重要的是,重复右心导管检查显示,平均肺动脉压、肺血管阻力和心指数在随访时也有显著改善(<0.001,<0.001,和=0.011,分别)。肺动脉造影显示,在 PTPA 后 3-6 个月,64 处病变(35.0%)出现再狭窄。在 3 例接受支架植入术的患者中,1 例出现再狭窄。在随访期间,有 2 例患者死亡,1 例死于肺部感染后右心衰竭加重,另 1 例死于交通事故。
本研究结果表明,PTPA 显著改善了 TA 肺动脉狭窄和 PH 患者的临床症状、运动耐量和血流动力学参数。更重要的是,在压力导丝的指导下,再灌注肺水肿明显减少,没有患者因 PTPA 相关并发症而死亡。