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慢性阻塞性肺疾病(COPD)合并重度肺动脉高压和轻至中度气流受限患者的肺动脉高压特异性药物治疗

Pulmonary Arterial Hypertension-Specific Drug Therapy in COPD Patients with Severe Pulmonary Hypertension and Mild-to-Moderate Airflow Limitation.

作者信息

Calcaianu George, Canuet Matthieu, Schuller Armelle, Enache Irina, Chaouat Ari, Kessler Romain

机构信息

Service de Pneumologie, Nouvel Hx00F4;pital Civil, Universitx00E9; de Strasbourg, Strasbourg, France.

出版信息

Respiration. 2016;91(1):9-17. doi: 10.1159/000441304. Epub 2015 Oct 23.

Abstract

BACKGROUND

Patients with severe pulmonary hypertension (PH) associated with chronic obstructive pulmonary disease (COPD) present a poor outcome. Specific PH treatment could improve the clinical and hemodynamic status of these patients but may worsen arterial blood gases.

OBJECTIVES

Our study retrospectively included 28 patients with severe precapillary PH (mean pulmonary arterial pressure >35 mm Hg) associated with mild-to-moderate COPD [forced expiratory volume in 1 s (FEV1) >50% predicted]. All patients underwent specific pulmonary arterial hypertension (PAH) treatment as mono-, bi- or triple therapy.

METHODS

Our single-center study was conducted based on retrospective data of 537 right heart catheterizations (RHCs) performed on patients with COPD from January 2004 to June 2014. An echocardiography, comprehensive blood tests, pulmonary function tests, and a high-resolution computed tomography were performed before the RHCs. All patients underwent RHC with a Swan-Ganz catheter.

RESULTS

Compared to baseline, patients treated with specific PAH drugs showed a significant increase in cardiac index at long term (2.5 ± 0.7 liters/min/m2 at baseline vs. 3.2 ± 0.6 liters/min/m2 at 6/12 months; p = 0.003) as well as a decrease in pulmonary vascular resistance in the long term (8.4 ± 4.2 Wood units at baseline vs. 5 ± 1.7 Wood units at 6/12 months; p = 0.008). There was a slight decrease in arterial oxygen tension (PaO2) after 3 months of treatment (-2.4 ± 7.21 mm Hg; p = 0.066). During a median follow-up of 3 years, 12 patients (42.8%) died (including all causes of death).

CONCLUSIONS

This preliminary report suggests that the use of specific PH therapy in severe PH associated with mild-to-moderate COPD can improve pulmonary hemodynamic parameters, with worsening of PaO2, which had no clinical significance and did not lead to specific PAH therapy withdrawal in any patient.

摘要

背景

患有与慢性阻塞性肺疾病(COPD)相关的重度肺动脉高压(PH)的患者预后较差。特异性PH治疗可改善这些患者的临床和血流动力学状况,但可能会使动脉血气恶化。

目的

我们的研究回顾性纳入了28例患有与轻至中度COPD相关的重度毛细血管前PH(平均肺动脉压>35 mmHg)的患者[1秒用力呼气容积(FEV1)>预测值的50%]。所有患者均接受了作为单一、双重或三联疗法的特异性肺动脉高压(PAH)治疗。

方法

我们的单中心研究基于2004年1月至2014年6月期间对COPD患者进行的537次右心导管检查(RHC)的回顾性数据开展。在RHC之前进行了超声心动图、全面血液检查、肺功能测试和高分辨率计算机断层扫描。所有患者均使用Swan-Ganz导管进行RHC。

结果

与基线相比,接受特异性PAH药物治疗的患者长期心脏指数显著增加(基线时为2.5±0.7升/分钟/平方米,6/12个月时为3.2±0.6升/分钟/平方米;p = 0.003),长期肺血管阻力也降低(基线时为8.4±4.2 Wood单位,6/12个月时为5±1.7 Wood单位;p = 0.008)。治疗3个月后动脉血氧张力(PaO2)略有下降(-2.4±7.21 mmHg;p = 0.066)。在中位随访3年期间,12例患者(42.8%)死亡(包括所有死因)。

结论

这份初步报告表明,在与轻至中度COPD相关的重度PH中使用特异性PH治疗可改善肺血流动力学参数,同时伴有PaO2恶化,这无临床意义,且未导致任何患者停用特异性PAH治疗。

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