Verlinden Nathan J, Benza Raymond L, Raina Amresh
Cardiovascular Institute, Allegheny General Hospital, Pittsburgh, PA, USA.
Division of Cardiovascular Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Pulm Circ. 2020 Dec 9;10(4):2045894020945523. doi: 10.1177/2045894020945523. eCollection 2020 Oct-Dec.
The combination of bosentan and sildenafil is commonly used to treat patients with pulmonary arterial hypertension (PAH); however, there is evidence of a significant drug interaction between these two medications. We sought to evaluate the safety and efficacy of transitioning patients with PAH from the combination of bosentan and sildenafil to alternative therapy. A retrospective database review was performed on 16 patients with PAH who were treated with the combination of bosentan and sildenafil and transitioned to alternative treatment at our center. Invasive and non-invasive patient parameters were collected at baseline and after transition. 56.3% of patients were in World Health Organization functional class (WHO FC) III and a majority of patients (68.7%) were on background prostacyclin therapy. The most common reason for transition was concern for a drug interaction in seven patients (43.8%). The most common transition was bosentan to macitentan in eight patients (50%). Fifteen patients (93.8%) tolerated the transition after a median follow-up of 6.5 months with minor adverse events occurring in four patients (25%). In 11 patients, 6-min walk distance (6MWD) was unchanged comparing baseline to post transition measurements with a median change of +8 m (range: -50 to + 70; P = 0.39). Nine patients (81.8%) had stable (within 15% margin) or significant improvement (increase by ≥15%) in 6MWD after transition. All patients demonstrated stable or improved WHO FC after transition. There were no significant changes after transition in hemodynamics, N-terminal pro-brain natriuretic peptide (NT-proBNP) values, or Registry to Evaluate Early and Long-Term PAH Disease Management (REVEAL) risk scores. In our study, transitioning patients from bosentan and sildenafil to alternative therapy was safe and resulted in clinical stability.
波生坦和西地那非联合用药常用于治疗肺动脉高压(PAH)患者;然而,有证据表明这两种药物之间存在显著的药物相互作用。我们旨在评估PAH患者从波生坦和西地那非联合用药转换为替代疗法的安全性和有效性。对16例接受波生坦和西地那非联合治疗并在我们中心转换为替代治疗的PAH患者进行了回顾性数据库分析。在基线和转换后收集患者的有创和无创参数。56.3%的患者属于世界卫生组织功能分级(WHO FC)III级,大多数患者(68.7%)接受前列环素背景治疗。转换的最常见原因是7例患者(43.8%)担心药物相互作用。最常见的转换是8例患者(50%)从波生坦转换为马昔腾坦。15例患者(93.8%)在中位随访6.5个月后耐受了转换,4例患者(25%)出现轻微不良事件。11例患者中,转换前后6分钟步行距离(6MWD)无变化,中位变化为+8米(范围:-50至+70;P = 0.39)。9例患者(81.8%)在转换后6MWD稳定(在15%范围内)或显著改善(增加≥15%)。所有患者在转换后WHO FC均稳定或改善。转换后血流动力学、N末端脑钠肽前体(NT-proBNP)值或评估PAH疾病早期和长期管理注册研究(REVEAL)风险评分均无显著变化。在我们的研究中,PAH患者从波生坦和西地那非转换为替代疗法是安全的,并导致了临床稳定性。