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口服西地那非在重度肺动脉高压中的作用:临床疗效及剂量反应关系

Role of oral sildenafil in severe pulmonary arterial hypertension: clinical efficacy and dose response relationship.

作者信息

Garg Naveen, Sharma Mukesh Kumar, Sinha Nakul

机构信息

Department of Cardiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Raibareli Road, Lucknow, India.

出版信息

Int J Cardiol. 2007 Sep 3;120(3):306-13. doi: 10.1016/j.ijcard.2006.10.017. Epub 2006 Dec 15.

Abstract

BACKGROUND

Sildenafil (phosphodiesterase type 5 inhibitor) has been shown to be effective in pulmonary arterial hypertension (PAH). We evaluated the efficacy and safety of oral sildenafil in patients of severe PAH with special emphasis on dose response relationship, time of onset of clinical response and its effects on different haemodynamic parameters.

METHODS

Forty-four patients of severe PAH of either idiopathic pulmonary arterial hypertension [23 (51.7%)] or Eisenmenger syndrome [21 (48.3%)] were studied. All patients underwent six-minute walk test (SMWT) and echocardiography, while some also underwent cardiac catheterization. Sildenafil was started after a test dose and was gradually increased up to a target dose of 300 mg/day. Patients were followed-up 2 weekly for 10 weeks and monthly thereafter for functional class assessment and SMWT. Echocardiography and cardiac catheterization were repeated after at least 1 month of achieving maximal sildenafil dose (target dose or maximally tolerated dose). Drug safety and tolerability were assessed by monitoring patients for adverse effects including fundus examination.

RESULTS

Mean follow-up duration was 18.7+/-8.8 months (range 7-30 months). Mean maximum dose achieved was 276.1+/-62.2 mg/day (range 75-300 mg/day). A significant improvement in NYHA class (2.54+/-0.5 vs. 1.31+/-0.4, p=0.0001) and in SMWT distance (247.4+/-74.7 vs. 366.3+/-93.8 m, p=0.0001) was noted. All patients reported "feeling better" within 2 weeks of starting 12.5 mg thrice a day sildenafil. Marked improvement was noticed at 150 mg/day dose. Some minor additional benefit was noticed with further increase in the dose up to 225 mg/day. No further benefit was noted in improvement of NYHA class and SMWT distance by further increasing the dose of sildenafil. Haemoptysis as well as chest pain, if present, were also improved. On follow-up cardiac catheterization, a significant reduction in mean pulmonary arterial pressure (from 67.0+/-10.2 to 56.9+/-9.5 mm Hg, p=0.001), PVRI (from 19.5+/-7.0 to 11.1+/-6.9 WU m2, p=0.0001) and PVR/SVR ratio (0.6+/-0.3 vs. 0.4+/-0.2, p=0.013) with increase in cardiac index (2.9+/-1.1 l/min vs. 3.7+/-1.1 l/min, p=0.008) was noted. Systemic as well as pulmonary arterial oxygen saturations also improved significantly. Sildenafil was generally well tolerated, except for rhinorrhoea in 2, bodyache in 1 and headache in 1 patient. No visual symptom or change in fundus examination was noted.

CONCLUSIONS

Oral sildenafil improves functional capacity, haemodynamic parameters and is safe in patients with severe PAH. Benefits start as early as 2 weeks. The effects are dose related. A target dose of 150 mg/day appears to be optimal. Being very effective, widely available, relatively inexpensive, and very easy to use and very well tolerated without any major side effect, sildenafil may qualify as a first line medication for these patients.

摘要

背景

西地那非(5型磷酸二酯酶抑制剂)已被证明对肺动脉高压(PAH)有效。我们评估了口服西地那非对重度PAH患者的疗效和安全性,特别关注剂量反应关系、临床反应的起效时间及其对不同血流动力学参数的影响。

方法

对44例重度PAH患者进行研究,其中特发性肺动脉高压23例(51.7%),艾森曼格综合征21例(48.3%)。所有患者均接受6分钟步行试验(SMWT)和超声心动图检查,部分患者还接受了心导管检查。在给予试验剂量后开始服用西地那非,并逐渐增加至目标剂量300mg/天。患者每2周随访一次,共10周,此后每月随访一次,以评估功能分级和SMWT。在达到最大西地那非剂量(目标剂量或最大耐受剂量)至少1个月后,重复进行超声心动图和心导管检查。通过监测患者的不良反应(包括眼底检查)来评估药物的安全性和耐受性。

结果

平均随访时间为18.7±8.8个月(范围7 - 30个月)。平均达到的最大剂量为276.1±62.2mg/天(范围75 - 300mg/天)。纽约心脏协会(NYHA)分级(2.54±0.5对1.31±0.4,p = 0.0001)和SMWT距离(247.4±74.7对366.3±93.8m,p = 0.0001)有显著改善。所有患者在开始每日3次服用12.5mg西地那非后的2周内均报告“感觉好转”。在150mg/天的剂量时观察到明显改善。剂量进一步增加至225mg/天时,有一些轻微额外益处。进一步增加西地那非剂量在改善NYHA分级和SMWT距离方面未观察到进一步益处。咯血以及胸痛(如有)也有所改善。在随访心导管检查时,平均肺动脉压显著降低(从67.0±10.2降至56.9±9.5mmHg,p = 0.001),肺血管阻力指数(PVRI)(从19.5±7.0降至11.1±6.9WU m2,p = 0.0001)和PVR/SVR比值(0.6±0.3对0.4±0.2,p = 0.013)降低,心脏指数增加(2.9±1.1l/min对3.7±1.1l/min,p = 0.008)。体循环和肺动脉血氧饱和度也显著改善。西地那非总体耐受性良好,2例出现鼻漏,1例出现身体疼痛,1例出现头痛。未观察到视觉症状或眼底检查变化。

结论

口服西地那非可改善重度PAH患者的功能能力、血流动力学参数,且安全。益处最早在2周时出现。效果与剂量相关。150mg/天的目标剂量似乎是最佳的。西地那非非常有效、广泛可得、相对便宜、易于使用且耐受性良好,无任何主要副作用,可能有资格作为这些患者的一线用药。

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