Therapeutic limitations of oral medications to normalize hemodynamics in patients with pulmonary artery hypertension

H. Shimokawahara, H. Matsubara, K. Hayashi, T. Nishihara, M. Tsuji, T. Naito, M. Shigetoshi, I. Tabuchi, M. Munemasa
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Abstract

Background: Pulmonary arterial hypertension (PAH) has a poor prognosis despite the available therapeutic options. Normalization of hemodynamics would be needed to obtain the good prognosis. Aims and Objectives: We aimed to investigate the determinants in PAH patients for normalization of hemodynamics only with oral drugs. Methods: We retrospectively reviewed 190 patients with PAH treated at a single referral center. Hemodynamic parameters were investigated before and after treatments. All the patients were divided into a good control group with mean pulmonary arterial pressure (mPAP)<30mmHg and a poor control group with mPAP≧30mmHg at follow-up. Results: Eighty-two patients were idiopathic/heritable, 65 patients were connective tissue disease, 22 patients congenital heart disease and 21 patients were portal hypertension. mPAP decreased significantly from baseline to follow-up (51±18.7 mmHg to 34.1±15.2 mmHg, p Conclusions: To achieve normalization of hemodynamics in PAH, parenteral prostanoid should be used in cases with baseline mPAP exceeding 40mmHg.
口服药物使肺动脉高压患者血流动力学正常化的治疗局限性
背景:肺动脉高压(PAH)的预后较差,尽管现有的治疗方案。血流动力学的正常化将需要获得良好的预后。目的和目的:我们的目的是研究PAH患者仅通过口服药物使血流动力学正常化的决定因素。方法:我们回顾性分析了在单一转诊中心治疗的190例PAH患者。观察治疗前后血流动力学参数。随访时将患者分为平均肺动脉压(mPAP)<30mmHg的良好对照组和平均肺动脉压≧30mmHg的不良对照组。结果:特发性/遗传性82例,结缔组织病65例,先天性心脏病22例,门静脉高压症21例。从基线到随访,mPAP明显下降(51±18.7 mmHg至34.1±15.2 mmHg), p结论:为了使PAH血流动力学正常化,对于基线mPAP超过40mmHg的病例,应采用前列腺素外注射。
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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