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肺动脉高压:药物治疗和潜在的肺动脉去神经治疗。

Pulmonary arterial hypertension: pharmacologic therapies and potential pulmonary artery denervation treatment.

机构信息

Department of Cardiology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.

出版信息

EuroIntervention. 2013 May;9 Suppl R:R149-54. doi: 10.4244/EIJV9SRA25.

DOI:10.4244/EIJV9SRA25
PMID:23732148
Abstract

Pulmonary arterial hypertension (PAH) is a group of diseases related to progressively increasing pulmonary vascular resistance, a high incidence of right ventricular failure and premature death. Only a limited number of pharmaceutical therapies have proven to be beneficial for PAH. These therapies improve symptoms, exercise capacity, and haemodynamics; however, the clinical relevance of these effects has been challenged. Therefore, the effect of currently approved treatment options remains inconclusive. Conversely, several new drugs for various aetiologies and clinical stages are expected to provide significant advances for the treatment of PAH. Moreover, percutaneous pulmonary artery denervation treatment may lead to a new therapeutic orientation in patients with PAH. The aim of this review is to present the new developments in PAH treatment, provide a brief overview of future directions in the field and discuss the potential future prospects of these innovative therapies.

摘要

肺动脉高压(PAH)是一组与肺动脉阻力逐渐增加、右心衰竭发生率高和过早死亡相关的疾病。仅有少数药物治疗被证明对 PAH 有益。这些治疗方法可以改善症状、运动能力和血液动力学,但这些效果的临床意义受到了挑战。因此,目前批准的治疗方案的效果仍不确定。相反,针对各种病因和临床阶段的几种新药有望为 PAH 的治疗提供重大进展。此外,经皮肺动脉去神经治疗可能为 PAH 患者带来新的治疗方向。本综述旨在介绍 PAH 治疗的新进展,简要概述该领域的未来方向,并讨论这些创新疗法的潜在前景。

相似文献

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Pulmonary arterial hypertension: pharmacologic therapies and potential pulmonary artery denervation treatment.肺动脉高压:药物治疗和潜在的肺动脉去神经治疗。
EuroIntervention. 2013 May;9 Suppl R:R149-54. doi: 10.4244/EIJV9SRA25.
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Pulmonary Artery Denervation by Determining Targeted Ablation Sites for Treatment of Pulmonary Arterial Hypertension.通过确定靶向消融部位进行肺动脉去神经支配治疗肺动脉高压
Circ Cardiovasc Interv. 2017 Oct;10(10). doi: 10.1161/CIRCINTERVENTIONS.117.005812.
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Percutaneous pulmonary artery denervation completely abolishes experimental pulmonary arterial hypertension in vivo.经皮肺动脉去神经支配术可完全消除体内实验性肺动脉高压。
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Tadalafil as monotherapy and in combination regimens for the treatment of pulmonary arterial hypertension.他达拉非作为单一疗法和联合治疗方案治疗肺动脉高压。
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Pulmonary arterial hypertension in pregnant women.孕妇肺动脉高压。
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Long-term treatment with oral sildenafil is safe and improves functional capacity and hemodynamics in patients with pulmonary arterial hypertension.口服西地那非长期治疗对肺动脉高压患者是安全的,并能改善其功能容量和血流动力学。
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Current therapeutics and practical management strategies for pulmonary arterial hypertension.肺动脉高压的当前治疗方法和实用管理策略。
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Future perspectives in pulmonary arterial hypertension.肺动脉高压的未来展望
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引用本文的文献

1
EXPRESS: Statement on imaging and pulmonary hypertension from the Pulmonary Vascular Research Institute (PVRI).快报:肺血管研究所(PVRI)关于影像学与肺动脉高压的声明。
Pulm Circ. 2019 Mar 18;9(3):2045894019841990. doi: 10.1177/2045894019841990.