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Treatment of exercise pulmonary hypertension improves pulmonary vascular distensibility

机译:运动性肺动脉高压的治疗可改善肺血管扩张性

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摘要

Exercise pulmonary hypertension (ePH) is an underappreciated form of exertional limitation. Despite normal resting pulmonary artery pressures, patients with ePH demonstrate early pulmonary vascular changes with reduced pulmonary arterial compliance (PAC) and vascular distensibility (α). Recent data suggest that targeted vasodilator therapy may improve hemodynamics in ePH, but it is not well-known whether such medications alter pulmonary vascular distensibility. Thus, we sought to evaluate if vasodilator therapy improved α a marker of early pulmonary vascular disease in ePH. Ten patients performed supine exercise right heart catheterization (exRHC) with bicycle ergometer to peak exercise. Patients diagnosed with ePH were treated with pulmonary vasodilators. A repeat symptom-limited exercise RHC was performed at least six months after therapy. Patients with ePH had evidence of early pulmonary vascular disease, as baseline PAC and α were reduced. After pulmonary vasodilator therapy, a number of peak exercise hemodynamics statistically improved, including a decrease of total pulmonary resistance and pulmonary vascular resistance, while cardiac output increased. Importantly, vasodilator therapy partially reversed the pathogenic decreases of α at the time of repeat exRHC. Pulmonary vascular distensibility, α, a marker of early pulmonary vascular disease, improves in ePH after therapy with pulmonary vasodilators.
机译:运动性肺动脉高压(ePH)是一种运动受限的低估形式。尽管静息肺动脉压力正常,ePH患者仍表现出早期肺血管变化,肺动脉顺应性(PAC)和血管扩张性(α)降低。最近的数据表明靶向血管扩张剂治疗可以改善ePH的血液动力学,但这类药物是否会改变肺血管扩张性尚不清楚。因此,我们试图评估血管扩张剂治疗能否改善ePH中早期肺血管疾病的标志物α。 10例患者使用自行车测功仪进行了仰卧运动右心导管检查(exRHC),以达到最大运动量。诊断为ePH的患者接受了肺血管扩张剂治疗。治疗后至少六个月进行了症状受限的重复运动RHC。 ePH患者有早期肺血管疾病的证据,因为基线PAC和α降低。肺血管扩张剂治疗后,许多峰值运动血流动力学统计改善,包括总肺阻力降低和肺血管阻力降低,而心输出量增加。重要的是,在重复exRHC时,血管扩张剂治疗可部分逆转α的致病性降低。肺血管扩张性,α,早期肺血管疾病的标志,在用肺血管扩张药治疗后,ePH改善。

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