Muraoka Hironori, Imamura Teruhiko, Hatano Masaru, Maki Hisataka, Yao Atsushi, Kinugawa Koichiro, Komuro Issei
Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.
Int Heart J. 2015;56(4):471-3. doi: 10.1536/ihj.15-007. Epub 2015 Jun 18.
Although endothelin receptor antagonists (ERAs) including bosentan and ambrisentan are essential tools for the treatment of pulmonary arterial hypertension (PAH), each agent has a specific adverse effect with non-negligible frequency, ie, liver dysfunction for bosentan and peripheral edema for ambrisentan. These adverse effects often hinder the titration of the doses of ERAs up to the therapeutic levels. Portopulmonary hypertension, which is complicated with liver cirrhosis and successive portal hypertension, is one of the PAHs refractory to general anti-PAH agents because of the underlying progressed liver dysfunction and poor systemic condition. We here present a patient with portopulmonary hypertension, which was treated safely by combination therapy that included low-dose bosentan and ambrisentan, minimizing the adverse effects of each ERA. Combination therapy including different types of ERAs at each optimal dose may become a breakthrough to overcome portopulmonary hypertension in the future.
尽管包括波生坦和安立生坦在内的内皮素受体拮抗剂(ERA)是治疗肺动脉高压(PAH)的重要药物,但每种药物都有特定的不良反应,且发生频率不可忽视,即波生坦会导致肝功能障碍,安立生坦会引起外周水肿。这些不良反应常常阻碍ERA剂量滴定至治疗水平。肝肺综合征合并肝硬化及继发性门静脉高压,是PAH的一种类型,由于潜在的肝功能进行性损害和全身状况不佳,对一般抗PAH药物难治。我们在此报告一例肝肺综合征患者,通过低剂量波生坦和安立生坦联合治疗安全有效,将每种ERA的不良反应降至最低。未来,每种ERA以最佳剂量联合治疗可能成为攻克肝肺综合征的突破口。