用瑞西奎特替代西地那非和序贯联合治疗特发性肺动脉高压长期有效治疗的可能性:病例报告

S. A. Musashaykhova, Z. Valieva, A. Osokina, I. Korobkova, V. Gramovich, N. Danilov, T. Martynyuk
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引用次数: 0

摘要

特发性肺动脉高压(idiopathic pulmonary arterial hypertension, IPAH)是一种病因不明的严重危及生命的心血管疾病,其现代病理治疗由于肺部微血管血管的逆向重塑而取得了积极的临床效果。作用于发病机制主要靶点的高效特异性治疗药物现已被引入临床实践。本文报道一例2014年确诊的IPAH患者,WHO分级初始功能等级为III级,在用西地那非替代原有治疗后,在使用可溶性鸟苷酸环化酶刺激剂瑞西奎特5年的基础上,进一步实施ambrisentan和selexipag的序次联合治疗策略,显示出了较高的长期疗效和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possibilities of long-term effective treatment of idiopathic pulmonary arterial hypertension by replacing sildenafil with riociguat and using sequential combination therapy: case report
Modern pathogenetic therapy of idiopathic pulmonary arterial hypertension (IPAH), a severe life-threatening cardiovascular disease of unknown etiology, leads to a positive clinical effect due to reverse remodeling of the vessels of the microvasculature of the lungs. Highly effective drugs of specific therapy that act on the main targets of pathogenesis have now been introduced into clinical practice.The presented clinical case of a patient with diagnosed in 2014 IPAH with an initial functional class III according to the WHO classification demonstrates high long-term efficacy and safety of specific therapy based on the use of the soluble guanylate cyclase stimulator riociguat for 5 years after replacing previous therapy with sildenafil with further implementation of the strategy of sequential combination therapy due to the addition of ambrisentan and selexipag.
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