特发性肺动脉高压患者血管反应性检测的流行及特点。

IF 2.1 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Annals of Thoracic Medicine Pub Date : 2025-01-01 Epub Date: 2025-01-11 DOI:10.4103/atm.atm_189_24
Goncharova Natalia, Kirill Lapshin, Aelita Berezina, Irina Zlobina, Anton Ryzhkov, Zhaneta Matakaeva, Elizaveta Andreeva, Olga Moiseeva
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引用次数: 0

摘要

基于急性血管反应试验结果(VRT)的特发性肺动脉高压(IPAH)/HPAH/DPAH(遗传性肺动脉高压/药物性肺动脉高压)II-III功能分类(FC) (WHO)患者治疗策略的选择。VRT阳性(VRT+)是钙通道阻滞剂治疗的指征。在所有PH亚型中,长期血管应答者表现出持续的低风险状态和最高的生存率。该研究的目的是:表征IPAH患者的VRT表现,以及VRT阳性、阴性和因医生决定未进行VRT的患者之间的表现差异。方法:2008 - 2023年间,166例IPAH成年患者(44.2±15.3岁,男性34例)纳入前瞻性单中心研究。VRT采用吸入伊洛前列素。VRT阳性以既定的Sitbon标准定义。进行标准基线肺动脉高压(PAH)评估,包括心肺运动试验(CPET)。使用ESC/ERS(欧洲心脏病学会/欧洲呼吸学会)2015年风险量表评估风险状态。采用Kaplan-Mayer法评估生存率。结果:85例(51.2%)患者行VRT治疗。26.7%的患者由于医生的决定而未做VRT (ND VRT), 15.4%的患者由于技术上的无能,16.2%的患者由于IV FC (WHO)。26例(15.6%)患者VRT阳性。与VRT+相比,VRT阴性患者血流动力学和运动耐量更差,n端脑型利钠肽(NT-proBNP)水平更高,右心扩张。与已完成VRT的患者相比,由于医生的决定而进行ND VRT的患者通常年龄大于60岁,具有较高的体重指数、右心衰症状、呕血、心律失常、高NT-proBNP和高危血流动力学标准。VRT +组与ND VRT组的CPET参数相似。在1.76年的随访中,50%的VRT +患者出现血管反应性丧失和PAH恶化。血管反应性丧失的患者在基线上表现为中度危险标准。VRT +组5年生存率为97%,VRT -组为61%,无VRT组为53%。结论:医生的决定是IPAH患者不做VRT的最常见原因。基线时存在的中等高危标准与由于医生的决定而未进行VRT、VRT阴性和随访期间血管反应性丧失有关。CPET应该更广泛地用于检测低风险或VRT +患者PAH进展的早期迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vasoreactive testing prevalence and characteristics in patients with idiopathic pulmonary arterial hypertension.

Introduction: The choice of treatment strategy in patients with idiopathic pulmonary arterial hypertension (IPAH)/HPAH/DPAH (Hereditary pulmonary arterial hypertension/ Drug-induced pulmonary arterial hypertension) II-III functional class (FC) (WHO) based on an acute vasoreactive testing result (VRT). Positive VRT (VRT+) is an indication for calcium channel blockers therapy. Long-term vasoresponders demonstrate sustained low-risk status and the highest survival among all PH subtypes.

The study aimed: To characterize VRT performance in IPAH patients and differences in presentation between patients with positive, negative VRT, and patients with not done VRT due to physicians' decision.

Methods: One hundred and sixty-six adult IPAH patients (44.2 ± 15.3 years, 34 males) comprised into prospective single-center study between 2008 and 2023 years. Inhaled iloprost was used for VRT. Positive VRT was defined with established Sitbon criteria. Standard baseline pulmonary arterial hypertension (PAH) evaluation including cardiopulmonary exercise test (CPET) was performed. Risk status was evaluated using ESC/ERS (European Society of Cardiology/European Respiratory Society) risk scale 2015. Survival was assessed with the Kaplan-Mayer method.

Results: Eighty-five (51.2%) patients underwent VRT. VRT not done (ND VRT) due to the physicians' decision in 26.7% patients, due to the technical inability in 15.4% and IV FC (WHO) in 16.2% patients. Positive VRT registered in 26 (15.6%) patients. Patients with negative VRT demonstrated worse hemodynamics and exercise tolerance, higher N-terminal pro-brain-type natriuretic peptide (NT-proBNP) level, and right heart dilatation compared with VRT+. Patients with ND VRT due to the physicians decision were often older than 60 years, had higher body mass index, symptoms of right heart failure, hemoptysis, arrhythmias, high NT-proBNP, and hemodynamic criteria of high risk in comparison with patients with done VRT. Some CPET parameters were similar between VRT + group and patients ND VRT group. Loss of vasoreactivity and PAH worsening were detected in 50% of VRT + patients in a 1.76 year of follow-up. Patients with vasoreactivity loss exhibited the criteria of intermediate risk at a baseline. Five-year survival was 97% in VRT + group in comparison with 61% in VRT - and 53% in ND VRT group.

Conclusions: Physicians' decision was the most common reason for not doing VRT in IPAH patients. Intermediate high-risk criteria presence at a baseline were associated with not done VRT due to physicians decision, negative VRT, and the vasoreactivity loss during the follow-up. CPET should be used more widely to detect the early signs of PAH progression in low risk or VRT + patients.

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来源期刊
Annals of Thoracic Medicine
Annals of Thoracic Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-RESPIRATORY SYSTEM
CiteScore
4.10
自引率
4.30%
发文量
19
审稿时长
>12 weeks
期刊介绍: The journal will cover studies related to multidisciplinary specialties of chest medicine, such as adult and pediatrics pulmonology, thoracic surgery, critical care medicine, respiratory care, transplantation, sleep medicine, related basic medical sciences, and more. The journal also features basic science, special reports, case reports, board review , and more. Editorials and communications to the editor that explore controversial issues and encourage further discussion by physicians dealing with chest medicine.
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