Chang Sung A, Kim Hyung Kwan, Chang Hyuk Jae, Kim Duk Kyung
Division of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Division of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Korean Circ J. 2019 Apr;49(4):353-360. doi: 10.4070/kcj.2018.0281. Epub 2018 Dec 10.
Udenafil, a new phosphodiesterase-5 inhibitor (PDE5i), has been used to treat erectile dysfunction. Given the proven benefit of PDE5i in pulmonary arterial hypertension (PAH), we evaluated serial hemodynamic changes after single udenafil administration to determine the appropriate therapeutic dose.
Eighteen patients were randomly allocated into one of 3 groups: placebo, udenafil 50 mg (U50), and udenafil 100 mg (U100). Diagnosis for inclusion was idiopathic PAH or PAH associated with connective tissue disease. Patients with any contraindication to PDE5i, and/or PDE5i treatment in the past 1 month were excluded. Continuous hemodynamic monitoring was performed by placing a Swan-Ganz catheter. Information on cardiac index (CI), mean pulmonary arterial pressure (mPAP), mean systemic arterial pressure (mSAP), pulmonary arterial wedge pressure (PAWP), and pulmonary vascular resistance index (PVRI) was obtained for 4 hours after drug administration.
The mPAP significantly decreased in both the U50 and U100 (-11 mmHg and -8 mmHg from baseline, respectively, p<0.1). The mSAP also decreased in both U50 and U100; however, the decrease was greater in the U100 (Δ=-8.5 mmHg and Δ=-14.0 mmHg). CI increased in the U50, but decreased in the U100. Although PVRI decreased in both, statistical significance was only achieved in the U50 compared to placebo. PAWP was stable during monitoring. U50 had at least 4 hour-effect after administration. Only 2 patients with U100 experienced mild adverse events.
This is the first demonstration of the acute hemodynamic changes induced by udenafil. U50 is considered an optimal dose for treating PAH with more than 4-hour treatment effect.
ClinicalTrials.gov Identifier: NCT01553721.
伐地那非是一种新型磷酸二酯酶5抑制剂(PDE5i),已用于治疗勃起功能障碍。鉴于PDE5i在肺动脉高压(PAH)治疗中的已证实益处,我们评估了单次服用伐地那非后的系列血流动力学变化,以确定合适的治疗剂量。
18例患者被随机分为3组之一:安慰剂组、伐地那非50mg组(U50)和伐地那非100mg组(U100)。纳入诊断标准为特发性PAH或与结缔组织病相关的PAH。排除有任何PDE5i禁忌证和/或在过去1个月内接受过PDE5i治疗的患者。通过放置Swan-Ganz导管进行连续血流动力学监测。给药后4小时获取心脏指数(CI)、平均肺动脉压(mPAP)、平均体动脉压(mSAP)、肺动脉楔压(PAWP)和肺血管阻力指数(PVRI)信息。
U50组和U100组的mPAP均显著降低(分别较基线降低11mmHg和8mmHg,p<0.1)。U50组和U100组的mSAP也均降低;然而,U100组的降低幅度更大(Δ=-8.5mmHg和Δ=-14.0mmHg)。U50组CI升高,而U100组CI降低。虽然两组的PVRI均降低,但与安慰剂组相比,仅U50组具有统计学意义。监测期间PAWP稳定。U50给药后至少有4小时的效应。U100组仅2例患者出现轻度不良事件。
这是首次证明伐地那非引起的急性血流动力学变化。U50被认为是治疗PAH的最佳剂量,治疗效果超过4小时。
ClinicalTrials.gov标识符:NCT01553721。