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终末期结节病中的肺动脉高压:西地那非的治疗效果?

Pulmonary hypertension in end-stage pulmonary sarcoidosis: therapeutic effect of sildenafil?

作者信息

Milman Nils, Burton Christopher M, Iversen Martin, Videbaek Regitze, Jensen Claus V, Carlsen Jørn

机构信息

Department of Cardiology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

出版信息

J Heart Lung Transplant. 2008 Mar;27(3):329-34. doi: 10.1016/j.healun.2007.11.576.

Abstract

BACKGROUND

The objectives of this study were to assess the frequency and severity of pulmonary hypertension (PH) and the effect of sildenafil treatment in patients with recalcitrant pulmonary sarcoidosis.

METHODS

This investigation was a single-center, retrospective study of all patients (n = 25) with end-stage pulmonary sarcoidosis referred for lung transplantation. Hemodynamic measurements were evaluated by right-side cardiac catheterization in 24 of 25 patients. Sildenafil treatment for patients with sarcoidosis-associated PH was introduced in April 2004.

RESULTS

The study group of 24 patients (16 men, 8 women) had a median age of 45 (range 35 to 58) years, and duration of sarcoidosis of 11 (range 2 to 38) years. Mean pulmonary arterial pressure (MPAP) was median 36 (range 18 to 73) mm Hg. PH (MPAP >25 mm Hg) was present in 19 of 24 patients (79%). Sildenafil was administered to 12 of 13 patients at a dose of 150 (range 75 to 225) mg/day for 4 (range 1 to 12) months. Sildenafil treatment was associated with reductions in MPAP of -8 mm Hg (CI -1 to -15 mm Hg), and PVR -4.9 Wood units (CI -7.2 to -2.6 Wood units). Cardiac output and cardiac index also increased during treatment (p = 0.01, respectively). There were no consistent changes in 6-minute walk distance.

CONCLUSIONS

Patients with severe pulmonary sarcoidosis have a high prevalence of PH. Sildenafil treatment was associated with significant improvements in hemodynamic parameters.

摘要

背景

本研究的目的是评估顽固性肺结节病患者肺动脉高压(PH)的发生率和严重程度,以及西地那非治疗的效果。

方法

本研究为单中心回顾性研究,纳入了所有因终末期肺结节病转诊接受肺移植的患者(n = 25)。25例患者中的24例通过右侧心导管检查评估血流动力学指标。2004年4月开始对结节病相关PH患者采用西地那非治疗。

结果

研究组24例患者(16例男性,8例女性),中位年龄45岁(范围35至58岁),结节病病程11年(范围2至38年)。平均肺动脉压(MPAP)中位数为36 mmHg(范围18至73 mmHg)。24例患者中有19例(79%)存在PH(MPAP > 25 mmHg)。13例患者中的12例接受了西地那非治疗,剂量为150 mg/天(范围75至225 mg/天),治疗4个月(范围1至12个月)。西地那非治疗使MPAP降低了8 mmHg(可信区间 -1至 -15 mmHg),肺血管阻力降低了4.9 Wood单位(可信区间 -7.2至 -2.6 Wood单位)。治疗期间心输出量和心脏指数也有所增加(p值分别为0.01)。6分钟步行距离没有持续变化。

结论

严重肺结节病患者中PH的患病率很高。西地那非治疗使血流动力学参数有显著改善。

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