Increase of pulmonary artery wedge pressure above 15 mm Hg in patients with pre-capillary pulmonary hypertension

Julien Wain-Hobson , Rémi Sabatier , Mamadou Koné , Damien Legallois , Thérèse Lognoné , Ziad Dahdouh , Farzin Beygui , Gilles Grollier , Paul Milliez , Emmanuel Bergot , Vincent Roule
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引用次数: 2

Abstract

Aims

Daily practice shows that patients with pre-capillary pulmonary hypertension (PH) may develop a secondary elevation of their pulmonary artery wedge pressure (PAWP) above the 15 mm Hg limit. This phenomenon has not been precisely described yet. We aimed at identifying factors present at initial diagnosis that could predict this secondary elevation of PAWP, its possible causes and impact on survival.

Methods and results

We included 90 patients followed between 2004 and 2011 in our center. At the end of follow-up (3.0 ± 1.6 years), patients were divided into two groups according to the successive PAWP measurements (always ≤ 15 mm Hg or > 15 mm Hg on at least one right heart catheterization (RHC)). Demographical, biological, echographic and hemodynamical data at first RHC were compared. Possible causes for PAWP > 15 mm Hg were searched. A Kaplan–Meier method was used to assess differences in survival. One third of our cohort developed an elevation of PAWP above 15 mm Hg and patients with idiopathic pulmonary arterial hypertension were at smaller risk (OR 0.20 [0.05–0.82]; p = 0.026). We did not identify any other baseline predictive factors. We highlighted several possible causes and factors that may unmask an underlying left ventricular diastolic dysfunction. Survival was not different between both groups (p = 0.42).

Conclusion

Secondary elevation of PAWP in pre-capillary PH was frequent but less observed in idiopathic PH. We detailed many possible causes that can be sought, many of which may be related to an underlying left ventricular diastolic dysfunction.

毛细血管前肺动脉高压患者肺动脉楔压升高15 mm Hg以上
目的:日常实践表明,毛细血管前肺动脉高压(PH)患者的肺动脉楔压(PAWP)可能继发性升高,超过15毫米汞柱的限制。这种现象还没有得到精确的描述。我们的目的是确定存在于初始诊断的因素,可以预测继发性paap升高,其可能的原因和对生存的影响。方法与结果本中心2004 - 2011年随访患者90例。在随访结束(3.0±1.6年)时,根据连续的paap测量值将患者分为两组(总是≤15 mm Hg或>至少一次右心导管(RHC)时,血压为15mm Hg。比较首次RHC的人口学、生物学、超声和血流动力学数据。PAWP的可能原因检查15mm Hg。Kaplan-Meier法评估生存差异。我们的队列中有三分之一的患者paap升高超过15 mm Hg,特发性肺动脉高压患者的风险较小(OR 0.20 [0.05-0.82];P = 0.026)。我们没有发现任何其他基线预测因素。我们强调了几个可能的原因和因素可能揭示潜在的左心室舒张功能障碍。两组生存率无差异(p = 0.42)。结论继发性paap升高在毛细血管前PH中较为常见,但在特发性PH中较少观察到。我们详细介绍了许多可能的原因,其中许多可能与潜在的左室舒张功能障碍有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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