Patel Jignesh K, Rao Youlan, Strachan Paul
Division of Pulmonary and Critical Care Medicine, Department of Medicine, State University of New York at Stony Brook, Stony Brook, NY, USA.
Biostatistics, United Therapeutics Corporation, Research Triangle Park, NC, USA.
Heart Lung Circ. 2018 Feb;27(2):183-189. doi: 10.1016/j.hlc.2017.02.015. Epub 2017 Mar 22.
The clinical impact of pulmonary capillary wedge pressure (PCWP) on long-term mortality among patients with pulmonary arterial hypertension (PAH) has been incompletely reported, particularly in relation to concomitant treprostinil administration. The goal of this study was to assess the impact of PCWP on long-term mortality in PAH patients treated with parenteral treprostinil.
We studied a cohort of 743 patients with PAH treated with parenteral treprostinil therapy. The long-term all-cause mortality was compared in patients with baseline mean PCWP≤8mmHg, 8<PCWP≤11mmHg, and PCWP>11mmHg over 4-year follow-up.
Of the 743 patients studied, 280 patients (37.7%) had a baseline mean PCWP ≤ 8mmHg, 233 patients (31.4%) had a mean PCWP of >8mmHg and ≤11mmHg, and 230 patients (31.0%) had a mean PCWP >11mmHg. While patients with higher PCWP had higher mean right atrial and PA pressures, no difference was noted in cardiac output and pulmonary vascular resistance (PVR). All-cause mortality was similar between patients with PCWP≤8mmHg, 8<PCWP≤11mmHg, and PCWP>11mmHg at 1 year (10.4% vs 9.9% vs 10.0%, p=0.980) and 4 years (16.8% vs 21.9% vs 19.2%, p=0.353) respectively. In multivariate analysis, PCWP was not independently predictive of 4-year all-cause mortality [HR 1.00, 95%CI 0.95-1.05, p=0.98 (permmHg)]. Predictors of 4-year mortality included older age [HR 1.02, 95%CI 1.00-1.03, p=0.0091 (per year)], non-Caucasian race, and higher PVR [HR 1.06, 95% CI 1.04-1.08, p<0.0001 (per Woods Unit)].
In this study of patients with PAH receiving parenteral treprostinil, PCWP was not associated with long-term all-cause mortality. Further studies examining prognostic indicators in patients with PAH optimised on guideline-based therapies are warranted.
肺动脉高压(PAH)患者中肺毛细血管楔压(PCWP)对长期死亡率的临床影响报道并不完整,尤其是与曲前列尼尔联合使用的情况。本研究的目的是评估PCWP对接受肠外曲前列尼尔治疗的PAH患者长期死亡率的影响。
我们研究了一组接受肠外曲前列尼尔治疗的743例PAH患者。在4年的随访中,比较了基线平均PCWP≤8mmHg、8<PCWP≤11mmHg和PCWP>11mmHg患者的长期全因死亡率。
在研究的743例患者中,280例(37.7%)基线平均PCWP≤8mmHg,233例(31.4%)平均PCWP>8mmHg且≤11mmHg,230例(31.0%)平均PCWP>11mmHg。虽然PCWP较高的患者平均右心房和肺动脉压力较高,但心输出量和肺血管阻力(PVR)无差异。PCWP≤8mmHg、8<PCWP≤11mmHg和PCWP>11mmHg的患者1年时全因死亡率相似(分别为10.4%对9.9%对10.0%,p=0.980),4年时分别为16.8%对21.9%对19.2%,p=0.353。在多变量分析中,PCWP不能独立预测4年全因死亡率[风险比1.00,95%置信区间0.95-1.05,p=0.98(每mmHg)]。4年死亡率的预测因素包括年龄较大[风险比1.02,95%置信区间1.00-1.03,p=0.0091(每年)]、非白种人种族和较高的PVR[风险比1.06,95%置信区间1.04-1.08,p<0.0001(每伍兹单位)]。
在这项针对接受肠外曲前列尼尔治疗的PAH患者的研究中,PCWP与长期全因死亡率无关。有必要进一步研究基于指南治疗优化的PAH患者的预后指标。