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波生坦联合西地那非治疗艾森曼格综合征的随机、安慰剂对照、双盲试验。

Combination therapy with bosentan and sildenafil in Eisenmenger syndrome: a randomized, placebo-controlled, double-blinded trial.

机构信息

Department of Cardiology, Copenhagen University Hospital, Section 2014, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.

出版信息

Eur Heart J. 2010 May;31(9):1124-31. doi: 10.1093/eurheartj/ehq011. Epub 2010 Mar 3.

DOI:10.1093/eurheartj/ehq011
PMID:20202971
Abstract

AIMS

To evaluate the efficacy of combining the dual endothelin receptor antagonist, bosentan, and the phosfodiesterase-5-inhibitor, sildenafil, in patients with Eisenmenger syndrome.

METHODS AND RESULTS

The study was a randomized, placebo-controlled, double-blinded, cross-over design. Patients with Eisenmenger syndrome (n = 21) were treated open label with bosentan for 9 months. After 3 months, sildenafil/placebo was added for 3 months, and a cross-over was performed for the last 3 months. At baseline and after 3, 6, and 9 months, patients were examined with 6 min walk test, oxygen saturations, N-terminal pro-brain natriuretic peptide, New York Heart Association (NYHA) classification, cardiac catheterization, and magnetic resonance imaging. The primary endpoint was changed in 6 min walk distance (MWD). Bosentan improved the 6 MWD (377 vs. 414 m, P = 0.001), pulmonary vascular resistance (PVR) (28 vs. 22 wood, P = 0.01), and pulmonary blood flow (2.6 vs. 3.5 L/min, P = 0.01). Adding sildenafil to bosentan did not improve the 6 MWD significantly (21 vs. 8 m, P = 0.48), but increased saturation at rest (2.9 vs. -1.8%, P < 0.01).

CONCLUSION

In Eisenmenger syndrome, treatment with bosentan significantly improved walking distance, pulmonary blood flow, and PVR. Adding sildenafil to bosentan did not significantly improve walking distance but did increase saturation at rest. http://www.ClinicalTrial.gov: NCT00303004.

摘要

目的

评估联合应用双重内皮素受体拮抗剂波生坦和磷酸二酯酶-5 抑制剂西地那非治疗艾森曼格综合征患者的疗效。

方法和结果

该研究采用随机、安慰剂对照、双盲、交叉设计。艾森曼格综合征患者(n = 21)接受波生坦开放标签治疗 9 个月。3 个月后,加入西地那非/安慰剂治疗 3 个月,并进行最后 3 个月的交叉。在基线和 3、6 和 9 个月时,患者接受 6 分钟步行测试、氧饱和度、N 端脑利钠肽前体、纽约心脏协会(NYHA)分级、心导管检查和磁共振成像检查。主要终点为 6 分钟步行距离(MWD)的变化。波生坦改善了 6 MWD(377 对 414 m,P = 0.001)、肺血管阻力(PVR)(28 对 22 伍德,P = 0.01)和肺血流量(2.6 对 3.5 L/min,P = 0.01)。将西地那非加入波生坦治疗并未显著改善 6 MWD(21 对 8 m,P = 0.48),但显著提高了静息时的饱和度(2.9 对 -1.8%,P < 0.01)。

结论

在艾森曼格综合征中,波生坦治疗显著改善了步行距离、肺血流量和 PVR。将西地那非加入波生坦治疗并未显著改善步行距离,但显著提高了静息时的饱和度。http://www.ClinicalTrial.gov:NCT00303004。

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