Division of Cardiology, Nanjing First Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Center for Public Health and Epidemic Preparedness & Response, Health Science Center, Peking University, Shanghai, People's Republic of China.
EuroIntervention. 2023 Oct 23;19(8):684-694. doi: 10.4244/EIJ-D-23-00349.
Long-term clinical outcomes after pulmonary artery denervation (PADN) in patients with Group 1 pulmonary arterial hypertension (PAH) have not been reported.
We aimed to investigate the effect of PADN on 1-year outcomes in patients with PAH.
In the multicentre PADN-CFDA trial, 128 patients with Group 1 PAH were randomly assigned to PADN plus a phosphodiesterase-5 inhibitor (PDE-5i) versus a sham PADN procedure plus a PDE-5i. The principal endpoint of interest for the present study was clinical worsening at 1 year after randomisation, the composite of worsening of PAH (increase in WHO functional class, need for additional PAH treatments or PAH-related hospitalisation), atrial septostomy, listing for lung transplantation, or all-cause death.
One-year clinical follow-up was available in all patients. At 1 year, clinical worsening had occurred in 3 (4.8%) patients in the PADN plus PDE-5i group and in 15 patients (23.1%) in the sham plus PDE-5i group (adjusted hazard ratio: 0.17; 95% confidence interval [CI]: 0.05-0.60; p=0.006), driven by significantly increased rates of PAH-related hospitalisations, worsening functional class and the requirement for additional PAH treatments in the sham group. Results were consistent in high-risk, intermediate-risk and low-risk patients (p=0.186). Patients treated with PADN plus PDE-5i had an improvement in the between-group change in the six-minute walking distance (6MWD) from baseline to 1 year of 81.2 m (95% CI: 50.3-112.2; p<0.001) compared with PDE-5i treatment alone.
In this multicentre sham-controlled randomised trial, PADN treatment for Group 1 PAH significantly reduced clinical worsening and improved the 6MWD during 1-year follow-up in patients treated with a PDE-5i.
目前尚未有关于肺动脉去神经术(PADN)治疗 1 型肺动脉高压(PAH)患者长期临床转归的报道。
本研究旨在评估 PADN 对 PAH 患者 1 年转归的影响。
多中心的 PADN-CFDA 试验中,128 例 1 型 PAH 患者被随机分为 PADN 联合磷酸二酯酶-5 抑制剂(PDE-5i)治疗组和假手术联合 PDE-5i 治疗组。本研究的主要终点为随机分组后 1 年时的临床恶化,包括 PAH 恶化(WHO 功能分级恶化、需要额外的 PAH 治疗或 PAH 相关住院治疗、房间隔造口术、肺移植登记或全因死亡)。
所有患者均完成 1 年的临床随访。1 年后,PADN 联合 PDE-5i 治疗组有 3 例(4.8%)患者出现临床恶化,而假手术联合 PDE-5i 治疗组有 15 例(23.1%)患者出现临床恶化(调整后的风险比:0.17;95%置信区间 [CI]:0.05-0.60;p=0.006),这主要归因于假手术组中 PAH 相关住院治疗、功能分级恶化和需要额外的 PAH 治疗的发生率显著增加。在高危、中危和低危患者中,结果一致(p=0.186)。与 PDE-5i 单药治疗相比,PADN 联合 PDE-5i 治疗组患者的 6 分钟步行距离(6MWD)从基线到 1 年的组间变化有显著改善,差值为 81.2 m(95%CI:50.3-112.2;p<0.001)。
在这项多中心假手术对照随机试验中,对于接受 PDE-5i 治疗的 1 型 PAH 患者,PADN 治疗可显著降低临床恶化发生率,并改善 1 年随访期间的 6MWD。