Rong Xing, Ye Qiaofang, Wang Qiaoyu, Wang Jiajun, Zhu Qiongjun, Chen Youran, Wu Rongzhou
Children's Heart Center, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Institute of Cardiovascular Development and Translational Medicine, Wenzhou Medical University, Wenzhou, China.
Front Cardiovasc Med. 2021 Nov 11;8:693414. doi: 10.3389/fcvm.2021.693414. eCollection 2021.
Transcatheter closure is an important treatment for patent ductus arteriosus (PDA) complicated with moderate and severe pulmonary arterial hypertension (PAH). This report presents our experience with transcatheter closure of PDA complicated with moderate and severe PAH. The 49 cases of PDA complicated with moderate and severe PAH were collected in the Second Affiliated Hospital and Yuying Children's Hospital from January 2014 to December 2019 with transcatheter closure of PDA and follow-up. All patients were invited for transthoracic echocardiography, electrocardiogram, and thoracic radiography check-up. Device implantation was successful in 48 of 49 patients (98.0%). Among them, 30 cases were in the PAH after defect correction (CD) group, and 19 examples were in the Non-PAH after defect correction (NCD) group. Pulmonary systolic pressure, left atrial diameter, and left ventricular end-diastolic diameter immediately after interventional therapy and 6 months later were lower than the pre-operative levels ( < 0.05). The incidence of the immediate residual shunt (RS) in this study was 34.9%, most of which were minimal amount shunt. RS disappeared in all patients within 1 year of therapy. Four patients had thrombocytopenia and one patient had left pulmonary artery stenosis. No other serious adverse event occurred during the follow-up period. The pressure gradient tricuspid valve regurgitation (PGTI) and the right heart catheterization (RHC) consistency points were 93.75% (15/16) and were within the 95% consistency limit by the Bland-Altman method. The Logistic regression analysis concluded that the pre-operative Pp/Ps and the narrowest diameter of PDA are risk factors for post-operative PAH ( < 0.05). The cut-off point of the pre-operative Pp/Ps and the narrowest diameter of PDA were calculated to be 0.595 and 4.75 mm, respectively. Interventional occlusion in children with PDA complicated with moderate and severe PAH is safe, effective, and has few complications. Targeted drug therapy has a good clinical effect. The narrowest diameter of PDA and the pre-operative Pp/Ps may be one of the risk factors of residual PAH after interventional therapy.
经导管封堵术是治疗合并中重度肺动脉高压(PAH)的动脉导管未闭(PDA)的重要方法。本报告介绍了我们对合并中重度PAH的PDA进行经导管封堵术的经验。2014年1月至2019年12月,在附属第二医院和育英儿童医院收集了49例合并中重度PAH的PDA患者,对其进行了PDA经导管封堵术及随访。所有患者均接受了经胸超声心动图、心电图和胸部X线检查。49例患者中有48例(98.0%)成功植入封堵器。其中,30例在缺损矫正后PAH(CD)组,19例在缺损矫正后非PAH(NCD)组。介入治疗后即刻及6个月后的肺动脉收缩压、左心房直径和左心室舒张末期直径均低于术前水平(P<0.05)。本研究中即刻残余分流(RS)的发生率为34.9%,大部分为微量分流。所有患者的RS在治疗1年内消失。4例患者出现血小板减少,1例患者出现左肺动脉狭窄。随访期间未发生其他严重不良事件。三尖瓣反流压差(PGTI)与右心导管检查(RHC)的一致性点为93.75%(15/16),采用Bland-Altman法在95%一致性界限内。Logistic回归分析得出术前Pp/Ps和PDA最窄直径是术后PAH的危险因素(P<0.05)。术前Pp/Ps和PDA最窄直径的截断点分别计算为0.595和4.75mm。对合并中重度PAH的PDA患儿进行介入封堵安全、有效,并发症少。靶向药物治疗有良好的临床效果。PDA最窄直径和术前Pp/Ps可能是介入治疗后残余PAH的危险因素之一。