Sheth Abhijat, Park John E S, Ong Yee Ean, Ho Timothy B, Madden Brendan P
Department of Cardiothoracic surgery, St Georges Hospital, London SW17 0QT, UK.
Vascul Pharmacol. 2005 Jan;42(2):41-5. doi: 10.1016/j.vph.2004.11.005. Epub 2005 Jan 18.
Sildenafil, a phosphodiesterase type-5 inhibitor, offers potential to treat pulmonary hypertension associated with a variety of conditions. We assessed the early impact of sildenafil on a cohort of patients referred to our unit who had severe pulmonary hypertension secondary to chronic thromboembolic disease which was not amenable to pulmonary thromboendarterectomy and who also had coexisting left ventricular dysfunction. Six patients were studied. Diagnosis of pulmonary embolic disease was made by ventilation perfusion scanning and/or CT pulmonary angiography. All patients were anticoagulated with oral coumarin derivatives and none were considered suitable for pulmonary thromboendarterectomy. Pulmonary hypertension was diagnosed by right heart catheterisation and each patient had Medical Research Council (MRC) dyspnoea score and New York Heart Association (NYHA) class noted and 2D echocardiography prior to commencement of sildenafil 50 mg three times a day. After 6 weeks of sildenafil therapy, right heart catheterisation and 2D echocardiography were repeated, and MRC dyspnoea score, NYHA class and exercise capacity were recorded. All patients demonstrated an improvement in mean pulmonary artery pressure, mean pulmonary capillary wedge pressure, MRC dyspnoea score, NYHA class and gas transfer. No adverse effects of sildenafil were noted. Our data suggests that sildenafil is an effective and well-tolerated therapy for patients with severe pulmonary hypertension associated with pulmonary thromboembolic disease and impaired left ventricular function, producing beneficial effects as early as 6 weeks.
西地那非是一种5型磷酸二酯酶抑制剂,具有治疗多种疾病相关肺动脉高压的潜力。我们评估了西地那非对一组转诊至我院的患者的早期影响,这些患者患有慢性血栓栓塞性疾病继发的严重肺动脉高压,无法进行肺动脉血栓内膜剥脱术,且同时存在左心室功能障碍。对6例患者进行了研究。通过通气灌注扫描和/或CT肺动脉造影诊断肺栓塞疾病。所有患者均口服香豆素衍生物进行抗凝,且均不被认为适合进行肺动脉血栓内膜剥脱术。通过右心导管检查诊断肺动脉高压,在开始每日3次服用50 mg西地那非之前,记录每位患者的医学研究委员会(MRC)呼吸困难评分、纽约心脏协会(NYHA)心功能分级以及二维超声心动图结果。西地那非治疗6周后,重复进行右心导管检查和二维超声心动图检查,并记录MRC呼吸困难评分、NYHA心功能分级和运动能力。所有患者的平均肺动脉压、平均肺毛细血管楔压、MRC呼吸困难评分、NYHA心功能分级和气体交换均有改善。未观察到西地那非的不良反应。我们的数据表明,西地那非对于患有与肺血栓栓塞性疾病和左心室功能受损相关的严重肺动脉高压的患者是一种有效且耐受性良好的治疗方法,早在6周时就能产生有益效果。