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根据俄罗斯国家登记处,不同形式肺动脉高压初诊患者的临床和仪器特征。

Clinical and Instrumental Characteristics of Newly Diagnosed Patients with Various Forms of Pulmonary Hypertension according to the Russian National Registry.

机构信息

Federal State Budgetary Institution, National Medical Research Center of Cardiology of the Ministry of Healthcare of Russian Federation, Russia.

Scientific Research Institute of Clinical Cardiology named after A.L. Myasnikov, Russia.

出版信息

Biomed Res Int. 2020 Jun 14;2020:6836973. doi: 10.1155/2020/6836973. eCollection 2020.

Abstract

AIM

To study demographic and clinical characteristics and to give a comparative description of the functional and hemodynamic status, profile of concomitant pathology in patients with various forms of pulmonary arterial hypertension (PAH), and chronic thromboembolic pulmonary hypertension (CTEPH) according to the Russian National Registry.

METHODS

During the period from January 01, 2012, till January 01, 2019, 1105 patients aged >18 years with verified diagnosis of PAH and CTEPH, who were subsequently observed at 15 PH expert centers of the Russian Federation in the 52 provinces, are included in the Russian registry on the basis of the Federal State Budgetary Institution of Cardiology of the Ministry of Healthcare of Russia. All newly diagnosed patients ( = 727) were entered into the registry database (NCT03707561). A comparative analysis of demographic and clinical characteristics, profile of concomitant pathology, and parameters of a comprehensive examination of patients was performed.

RESULTS

Among newly diagnosed patients, 67% had PAH and 28.3% had CTEPH. In the PAH group, 40.9% of patients had idiopathic arterial PAH (IPAH), 36.6% had PAH associated with simple congenital heart disease (PAH-CHD), 19.3% had PAH associated with systemic connective tissue disease (PAH-CTD), 1.8% had portal pulmonary hypertension (PoPH), 0.6% had PAH associated with HIV infection (PAH-HIV), 0.4% had heritable PAH (HPAH), and 0.4% had drug/toxin-induced PAH. At the time of diagnosis, PAH patients were younger than patients with CTEPH (45.2 ± 14.9; 52.6 ± 15.3 years, respectively) ( < 0.05). At the time of diagnosis, 71% PAH and 77% CTEPH patients had WHO FC III/IV. Mean (±SD) 6MWD was significantly less in CTEPH vs. the PAH group 331.3 ± 110.3 vs. 361.8 ± 135.7 m ( = 0.0006). Echo data showed a comparable sPAP between groups; CTEPH population had a more pronounced increase in the area of the right atrium (S) (24 [20; 32] cm and 19 [15; 26] cm, respectively), and a significant decrease in FAC (24.7 [22, 4; 29.0] and 29.0 [23.0; 31.0] %, respectively) as compared to the PAH group. RHC showed a comparable increase of sPAP and mPAP in PAH and CTEPH groups. 15.2% of patients with IPAH and HPAH demonstrated positive results in the acute vasoreactivity testing. CTEPH patients were more often obese and suffered from arterial hypertension and right heart failure. Deep venous thrombosis was significantly more often observed in patients with CTEPH (53%). The most common concomitant pathology was erosive-ulcerative lesion of the stomach/duodenum, less often of the esophagus (23.5% and 44.5%, respectively).

CONCLUSION

According to the Russian registry in patients with PAH and IPAH, the diagnosis is established at a younger age in comparison with the European registries. CTEPH patients are characterized by more severe functional status, pronounced signs of right heart failure taking into account the older age and the spectrum of comorbid pathology, which limits the possibility of surgical treatment. An increase in the number of expert centers participating in the registry is the key to improving early diagnosis of PH and optimal follow-up according to common standards in order to timely optimize therapy and reduce mortality of patients.

摘要

目的

根据俄罗斯国家登记处,研究各种形式的肺动脉高压(PAH)和慢性血栓栓塞性肺动脉高压(CTEPH)患者的人口统计学和临床特征,并对其功能和血流动力学状态、伴随病理特征进行比较描述。

方法

在 2012 年 1 月 1 日至 2019 年 1 月 1 日期间,根据俄罗斯联邦卫生部联邦国家预算机构心脏病学研究所,在俄罗斯联邦 52 个省份的 15 个 PH 专家中心对 1105 名年龄大于 18 岁且确诊为 PAH 和 CTEPH 的患者进行了观察,并将其纳入俄罗斯登记处。所有新诊断的患者(n=727)均被纳入登记数据库(NCT03707561)。对患者的人口统计学和临床特征、伴随病理特征以及综合检查参数进行了比较分析。

结果

在新诊断的患者中,67%患有 PAH,28.3%患有 CTEPH。在 PAH 组中,40.9%的患者患有特发性动脉性 PAH(IPAH),36.6%的患者患有与单纯先天性心脏病相关的 PAH(PAH-CHD),19.3%的患者患有与系统性结缔组织病相关的 PAH(PAH-CTD),1.8%的患者患有门静脉高压(PoPH),0.6%的患者患有与 HIV 感染相关的 PAH(PAH-HIV),0.4%的患者患有遗传性 PAH(HPAH),0.4%的患者患有药物/毒素诱导的 PAH。在诊断时,PAH 患者比 CTEPH 患者年轻(45.2±14.9;52.6±15.3 岁)(<0.05)。在诊断时,71%的 PAH 患者和 77%的 CTEPH 患者患有世界卫生组织功能分级(WHO FC)III/IV 级。与 PAH 组相比,CTEPH 组的 6MWD 明显更短,分别为 331.3±110.3m 和 361.8±135.7m(=0.0006)。超声心动图数据显示两组间的 sPAP 相当;CTEPH 组的右心房(S)面积增大更为明显(24[20;32]cm 和 19[15;26]cm),FAC 显著降低(24.7[22,4;29.0]和 29.0[23.0;31.0]%),与 PAH 组相比差异有统计学意义。右心导管检查显示 PAH 和 CTEPH 组的 sPAP 和 mPAP 均有类似的升高。15.2%的 IPAH 和 HPAH 患者急性血管反应性试验阳性。CTEPH 患者更常肥胖,且患有动脉高血压和右心衰竭。深静脉血栓形成在 CTEPH 患者中更为常见(53%)。最常见的伴随病理为胃/十二指肠侵蚀性溃疡性病变,食管病变较少见(分别为 23.5%和 44.5%)。

结论

根据俄罗斯 PAH 和 IPAH 登记处的数据,与欧洲登记处相比,PAH 和 IPAH 的诊断年龄较小。CTEPH 患者的功能状态更严重,考虑到年龄较大和伴发病理谱,右心衰竭的表现更为明显,这限制了手术治疗的可能性。增加参与登记处的专家中心数量是改善 PH 早期诊断和根据共同标准进行最佳随访的关键,以便及时优化治疗,降低患者死亡率。

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