Cardiology Department, Rouen University Hospital, F-76000 Rouen, France.
Centre de Compétence en hypertension pulmonaire 27/76, Centre Hospitalier Universitaire Charles Nicolle, F76000 Rouen, France.
Eur Heart J. 2024 Sep 14;45(35):3274-3288. doi: 10.1093/eurheartj/ehae467.
Based on retrospective studies, the 2022 European guidelines changed the definition of post-capillary pulmonary hypertension (pcPH) in heart failure (HF) by lowering the level of mean pulmonary artery pressure (mPAP) and pulmonary vascular resistance (PVR). However, the impact of this definition and its prognostic value has never been evaluated prospectively.
Stable left HF patients with the need for right heart catheterization were enrolled from 2010 to 2018 and prospectively followed up in this multicentre study. The impact of the successive pcPH definitions on pcPH prevalence and subgroup [i.e. isolated (IpcPH) vs. combined pcPH (CpcPH)] was evaluated. Multivariable Cox regression analysis was used to assess the prognostic value of mPAP and PVR on all-cause death or hospitalization for HF (primary outcome).
Included were 662 HF patients were (median age 63 years, 60% male). Lowering mPAP from 25 to 20 mmHg resulted in +10% increase in pcPH prevalence, whereas lowering PVR from 3 to 2 resulted in +60% increase in CpcPH prevalence (with significant net reclassification improvement for the primary outcome). In multivariable analysis, both mPAP and PVR remained associated with the primary outcome [hazard ratio (HR) 1.02, 95% confidence interval (CI) 1.00-1.03, P = .01; HR 1.07, 95% CI 1.00-1.14, P = .03]. The best PVR threshold associated with the primary outcome was around 2.2 WU. Using the 2022 definition, pcPH patients had worse survival compared with HF patients without pcPH (log-rank, P = .02) as well as CpcPH compared with IpcPH (log-rank, P = .003).
This study is the first emphasizing the impact of the new pcPH definition on CpcPH prevalence and validating the prognostic value of mPAP > 20 mmHg and PVR > 2 WU among HF patients.
基于回顾性研究,2022 年欧洲指南通过降低平均肺动脉压(mPAP)和肺血管阻力(PVR)水平,改变了心力衰竭(HF)中毛细血管后肺动脉高压(pcPH)的定义。然而,这一定义的影响及其预后价值从未得到前瞻性评估。
本多中心前瞻性研究纳入了 2010 年至 2018 年需要进行右心导管检查的稳定型左心 HF 患者,并进行随访。评估连续 pcPH 定义对 pcPH 患病率和亚组(即单纯性 pcPH[IpcPH]与合并性 pcPH[CpcPH])的影响。多变量 Cox 回归分析用于评估 mPAP 和 PVR 对全因死亡或 HF 住院(主要终点)的预后价值。
共纳入 662 例 HF 患者(中位年龄 63 岁,60%为男性)。将 mPAP 从 25mmHg 降低至 20mmHg 会导致 pcPH 患病率增加 10%,而将 PVR 从 3 降低至 2 会导致 CpcPH 患病率增加 60%(主要终点的净重新分类改善有显著意义)。多变量分析显示,mPAP 和 PVR 均与主要终点相关[风险比(HR)1.02,95%置信区间(CI)1.00-1.03,P=0.01;HR 1.07,95%CI 1.00-1.14,P=0.03]。与主要终点相关的最佳 PVR 阈值约为 2.2WU。使用 2022 年的定义,pcPH 患者的生存率较无 pcPH 的 HF 患者更差(对数秩检验,P=0.02),且 CpcPH 患者较 IpcPH 患者更差(对数秩检验,P=0.003)。
本研究首次强调了新的 pcPH 定义对 CpcPH 患病率的影响,并验证了 mPAP>20mmHg 和 PVR>2WU 在 HF 患者中的预后价值。