Percutaneous transluminal pulmonary angioplasty for Takayasu arteritis‐associated pulmonary hypertension: A single‐arm meta‐analysis

医学 肺动脉 内科学 经皮 心脏病学 肺动脉高压 荟萃分析 血管成形术 动脉炎 置信区间 血管阻力 随机对照试验 血流动力学 外科
作者
Ming‐Li Sun,Yongjian Zhu,Yu‐Ping Zhou,Xi‐Jie Zhu,Yinjian Yang,Chun‐Yan Cheng,Ke‐Yi Mei,Xian‐Mei Li,Chao Liu,Xi‐Qi Xu,Kai Sun,Zhi‐Cheng Jing
出处
期刊:Catheterization and Cardiovascular Interventions [Wiley]
卷期号:102 (3): 558-567 被引量:1
标识
DOI:10.1002/ccd.30773
摘要

Abstract Background The efficacy and safety of percutaneous transluminal pulmonary angioplasty (PTPA) for Takayasu arteritis‐associated pulmonary hypertension (TA‐PH) remain unclear. Objectives To examine the efficacy and safety of PTPA in TA‐PH. Methods PubMed, Embase, and the Cochrane Central Register of Controlled Trials Library were searched from inception to August 18, 2022, for articles investigating the efficacy and safety of PTPA for TA‐PH. The primary efficacy outcomes were pulmonary vascular resistance (PVR) changes from baseline to re‐evaluation and 6‐minute walking distance (6MWD). The safety outcome was procedure‐related complications. Results Five articles comprising 104 patients with TA‐PH who underwent PTPA were included. The scores of article quality, as assessed using the methodological index for nonrandomized studies tool, were high, ranging from 13 to 15 points. The pooled treatment effects of PVR (weighted mean difference [WMD]: −4.8 WU; 95% confidence interval [CI]: −6.0 to −3.5 WU; I 2 = 0.0%), 6MWD (WMD: 101.9 m; 95% CI: 60.3–143.6 m; I 2 = 70.4%) significantly improved. Procedure‐related complications, which predominantly present as pulmonary artery injury and pulmonary injury, occurred in 32.0% of the included patients. Periprocedural death occurred in one patient (1.0%, 1/100). Conclusions Patients with TA‐PH could benefit from PTPA in terms of hemodynamics and exercise tolerance, at the expense of procedure‐related complications. PTPA should be encouraged to enhance the treatment response in TA‐PH. These findings need to be confirmed by further studies, ideally, randomized controlled trials. Registration PROSPERO CRD42022354087.

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