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

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

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