Chazova I E, Arkhipova O A, Martynyuk T V
A.L. Myasnikov Research Institute of Cardiology of National Medical Research Center of Cardiology of the Ministry of Health of the Russian Federation, Moscow, Russia.
Ter Arkh. 2019 Mar 10;91(1):24-31. doi: 10.26442/00403660.2019.01.000024.
Assess the prevalence, clinical course, current therapy, and mortality in patients with pulmonary arterial hypertension (PAH) in the National Registry.
In the prospective study we included patients over 18 years of age with diagnosed PAH [idiopathic PAH (IPAH); Drug- and Toxin-Induced Pulmonary Hypertension; inherited PAH; PAH associated with congenital heart disease (PAH-CHD); PAH associated with systemic connective tissue disease (PAH-CTD); PAH associated with HIV infection (PAH-HIV); with portal pulmonary hypertension (portoPAH)]. The observation was carried out in 15 expert centers of Russia from 01.01.2012 to 31.12.2017.
Our registry included 470 patients with PAH: IPAH - 41.5%, PAH-CHD - 36%, PAH-CTD - 19.5%, inherited PAH - 0.4%, portoPAH - 1.9%, PAH-HIV - 0.4%, Drug- and Toxin-Induced PAH - 0.4%. The prevalence among women was 84%. The mean age at the time of patient enrollment in the registry for the overall group of PAH was 42.7±15.3 years. The distance in the 6-minute walking test was 361.3±129.3 m. Among all patients with PAH, 65% had functional class (FC) III/IV at the time of diagnosis, among IPAH - 62%. 69.9% received PAH-specific therapy, of which 62.1% - monotherapy, 32.7% - dual combination therapy, and 5.2% triple therapy. Sildenafil is the most commonly prescribed drug in the regimen of monotherapy. 31.6% of patients were treated with bosentan, 6.4% - riociguat, 3.4% - ambrisentan, 2.1% - macitentan and 2.0% iloprost. Survival of patients with PAH was 98.9% at 1 year of follow-up, 94.1% at 3 years and 86.0% at 5 years.
The registry data indirectly indicates the need to increase efforts aimed at improving the diagnosis of systemic connective tissue diseases in adults, as well as congenital heart defects in children for timely surgical treatment. In recent years, PAH-specific drugs of the new generation have been introduced into clinical practice, but currently in Russia there are no parenteral prostanoids, which are recommended for the most severe patients.
评估国家登记处肺动脉高压(PAH)患者的患病率、临床病程、当前治疗方法及死亡率。
在这项前瞻性研究中,我们纳入了年龄超过18岁且已确诊PAH的患者[特发性PAH(IPAH);药物和毒素诱导的肺动脉高压;遗传性PAH;与先天性心脏病相关的PAH(PAH-CHD);与系统性结缔组织病相关的PAH(PAH-CTD);与HIV感染相关的PAH(PAH-HIV);门静脉性肺动脉高压(portoPAH)]。观察于2012年1月1日至2017年12月31日在俄罗斯的15个专家中心进行。
我们的登记处纳入了470例PAH患者:IPAH占41.5%,PAH-CHD占36%,PAH-CTD占19.5%,遗传性PAH占0.4%,portoPAH占1.9%,PAH-HIV占0.4%,药物和毒素诱导的PAH占0.4%。女性患病率为84%。PAH总体组患者登记时的平均年龄为42.7±15.3岁。6分钟步行试验的距离为361.3±129.3米。在所有PAH患者中,65%在诊断时为功能分级(FC)III/IV级,IPAH患者中这一比例为62%。69.9%的患者接受了PAH特异性治疗,其中62.1%为单药治疗,32.7%为双联联合治疗,5.2%为三联治疗。西地那非是单药治疗方案中最常用的药物。31.6%的患者接受波生坦治疗,6.4%接受利奥西呱治疗,3.4%接受安立生坦治疗,2.1%接受马昔腾坦治疗,2.0%接受伊洛前列素治疗。PAH患者随访1年时的生存率为98.9%,3年时为94.1%,5年时为86.0%。
登记处数据间接表明,需要加大力度改善成人系统性结缔组织疾病以及儿童先天性心脏缺陷的诊断,以便及时进行手术治疗。近年来,新一代PAH特异性药物已引入临床实践,但目前在俄罗斯没有肠外前列腺素类药物,而这类药物被推荐用于病情最严重的患者。