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卵圆孔未闭在肺动脉高压患者中的作用。

Effect of Patent Foramen Ovale in Patients With Pulmonary Hypertension.

作者信息

Sharan Lauren, Stackhouse Kathryn, Awerbach Jordan D, Bashore Thomas M, Krasuski Richard A

机构信息

Duke University Medical Center, Durham, North Carolina.

Beth Israel Deaconess Hospital, Boston, Massachusetts.

出版信息

Am J Cardiol. 2018 Aug 1;122(3):505-510. doi: 10.1016/j.amjcard.2018.04.014. Epub 2018 May 1.

Abstract

Septostomy reduces right ventricular (RV) workload at the expense of hypoxemia in patients with advanced pulmonary hypertension (PH). A patent foramen ovale (PFO) may serve as a "natural" septostomy, but the incidence and impact of a PFO in PH remains uncertain. We prospectively examined echocardiograms in 404 PH patients referred for initial hemodynamic assessment. Patients included had saline bubble injection and if negative repeatinjection after Valsalva maneuver. Echocardiographic and hemodynamic data were examined. Survival was modeled using Kaplan-Meier method. Eisenmenger syndrome or known atrial shunts other than PFO were excluded: 292 patients met entry criteria. A PFO was identified in 16.8% of the entire cohort, 22.9% of pulmonary arterial hypertension (PAH) patients, and 8.6% of Dana Point group 2 PH patients. Right atrial to pulmonary capillary wedge pressure difference was lowest in the latter group (-7.9 ± 7.1 vs -1.7 ± 5.5 mm Hg for all others, p <0.01). Patients with a PFO were younger (53.9 vs 58.6 years, p = 0.02). A PFO was more often present with moderately or severely dilated (p = 0.01) or dysfunctional (p = 0.03) RVs. Six year survival was unchanged by PFO presence for all patients, including those with PAH. Proportional hazards analysis found only age and functional class independently predicted survival (p <0.01). A PFO is identified less often in Dana Point group 2 PH, likely due to inability of Valsalva maneuver to overcome right atrial to pulmonary capillary wedge pressure difference. In conclusion, the incidence of a PFO in the PH population increases with more dilated and dysfunctional RVs, suggesting that the PFO may be stretched open rather than congenital. The presence of a PFO does not impact survival in PH or PAH.

摘要

对于晚期肺动脉高压(PH)患者,房间隔造口术虽能减轻右心室(RV)负荷,但会以低氧血症为代价。卵圆孔未闭(PFO)可能起到“天然”房间隔造口术的作用,但PFO在PH中的发生率及影响仍不确定。我们对404例因初始血流动力学评估而转诊的PH患者的超声心动图进行了前瞻性检查。纳入的患者接受了生理盐水气泡注射检查,若结果为阴性,则在Valsalva动作后重复注射。对超声心动图和血流动力学数据进行了检查。采用Kaplan-Meier方法对生存情况进行建模。排除艾森曼格综合征或除PFO外已知的心房分流:292例患者符合纳入标准。在整个队列中,16.8%的患者发现有PFO,肺动脉高压(PAH)患者中这一比例为22.9%,达纳点2组PH患者中为8.6%。后一组患者的右心房与肺毛细血管楔压差值最低(-7.9±7.1 mmHg,其他所有患者为-1.7±5.5 mmHg,p<0.01)。有PFO的患者更年轻(53.9岁对58.6岁,p = 0.02)。PFO更常出现在中度或重度扩张(p = 0.01)或功能不全(p = 0.03)的右心室患者中。对于所有患者,包括PAH患者,PFO的存在对6年生存率无影响。比例风险分析发现,只有年龄和功能分级能独立预测生存情况(p<0.01)。在达纳点2组PH患者中,PFO的检出率较低,可能是由于Valsalva动作无法克服右心房与肺毛细血管楔压差值。总之,PH人群中PFO的发生率随右心室扩张和功能不全程度增加而升高,提示PFO可能是被撑开而非先天性的。PFO的存在不影响PH或PAH患者的生存。

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