The place of tadalafil in the treatment of PAH in the light of new clinical guidelines of the Eurasian Association of Cardiologists

T. Martynyuk
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Abstract

Pulmonaryarterialhypertension(PAH)isalife-threateningcardiovascular disease that is characterized by a marked increase in pulmonary vascular resistance and pulmonary artery pressure due to obstructive remodeling of the pulmonary vascular bed with the development of right ventricular heart failure as a cause of premature mortality. Impaired synthesis and reduced bioavailability of nitric oxide is one of the key pathophysiological mechanisms of the development and progression of the disease. The review paper presents key data from the evidence base on the clinical use of tadalafil, a phosphodiesterase type 5 inhibitor (PDE5), which in August 2023 approved by the Pharmaceutical Committee of the Russian Ministry of Health for the indication – treatment of patients with PAH. Tadacardil from Canonpharma Production is the first and only drug in Russian practice today with the active substance tadalafil with the registered indication “PAH”, approved in the Eurasian Guidelines for the diagnosis and treatment of pulmonary hypertension 2023 and available on the territory of the Russian Federation and the EAEU. Tadacardil is indicated for use in adult patients with PAH functional class II and III according to the WHO classification to increase exercise tolerance. The efficacy of tadalafil has been shown in idiopathic PAH and PAH associated with connective tissue diseases. The recommended dose is 40 mg (2 tablets of 20 mg) once a day. The paper describes the mechanism of action and pharmacological effects of PDE5 inhibitors, features of the pharmacokinetics of tadalafil in comparison with other drugs of the class. The advantages of Tadacardil from Canonpharma Production are the proven effecacy of use in patients with PAH, ease of use due to a single dose of 2 tablets of 20 mg once a day in a standard dose; good tolerability and favorable safety profile; proven bioequivalence to the reference drug. In light of the new Eurasian recommendations for the diagnosis and treatment of PH, tadalafil has a wide field for clinical use, which will improve the treatment options for patients with PAH both in mono- and combination therapy.
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从欧亚心脏病学家协会新临床指南看他达拉非在 PAH 治疗中的地位
肺动脉高压(PAH)是一种危及生命的心血管疾病,其特点是由于肺血管床的阻塞性重塑导致肺血管阻力和肺动脉压力明显增加,并导致右心室心力衰竭,是过早死亡的原因之一。一氧化氮合成障碍和生物利用率降低是该病发生和发展的关键病理生理机制之一。这篇综述论文介绍了他达拉非临床应用证据库中的关键数据,他达拉非是一种磷酸二酯酶5型抑制剂(PDE5),于2023年8月获得俄罗斯卫生部制药委员会批准,用于 PAH 患者的治疗。佳能制药生产的 "他达卡地尔 "是目前俄罗斯第一种也是唯一一种活性物质为他达拉非的药物,注册适应症为 "PAH",已获得《2023年欧亚肺动脉高压诊断和治疗指南》批准,可在俄罗斯联邦和欧亚经济联盟境内使用。根据世界卫生组织的分类,他达卡地尔适用于 PAH 功能分级 II 级和 III 级的成年患者,以提高运动耐量。他达拉非对特发性 PAH 和伴有结缔组织疾病的 PAH 具有疗效。推荐剂量为 40 毫克(2 片,每片 20 毫克),每天一次。本文介绍了 PDE5 抑制剂的作用机制和药理作用,以及他达拉非与其他同类药物相比的药代动力学特点。Canonpharma公司生产的他达卡地尔的优势在于:经证实可用于PAH患者,疗效显著;标准剂量为每天一次,每次2片,每次20毫克,使用方便;具有良好的耐受性和良好的安全性;经证实与参比药物具有生物等效性。根据新的欧亚 PH 诊断和治疗建议,他达拉非的临床应用前景广阔,这将改善 PAH 患者的治疗选择,无论是单药治疗还是联合治疗。
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