Washington Chad W, Derdeyn Colin P, Dhar Rajat, Arias Eric J, Chicoine Michael R, Cross DeWitte T, Dacey Ralph G, Han Byung Hee, Moran Christopher J, Rich Keith M, Vellimana Ananth K, Zipfel Gregory J
Departments of 1 Neurological Surgery.
Radiology, Washington University School of Medicine, Saint Louis, Missouri.
J Neurosurg. 2016 Feb;124(2):318-27. doi: 10.3171/2015.2.JNS142752. Epub 2015 Aug 28.
Studies show that phosphodiesterase-V (PDE-V) inhibition reduces cerebral vasospasm (CVS) and improves outcomes after experimental subarachnoid hemorrhage (SAH). This study was performed to investigate the safety and effect of sildenafil (an FDA-approved PDE-V inhibitor) on angiographic CVS in SAH patients.
A2-phase, prospective, nonrandomized, human trial was implemented. Subarachnoid hemorrhage patients underwent angiography on Day 7 to assess for CVS. Those with CVS were given 10 mg of intravenous sildenafil in the first phase of the study and 30 mg in the second phase. In both, angiography was repeated 30 minutes after infusion. Safety was assessed by monitoring neurological examination findings and vital signs and for the development of adverse reactions. For angiographic assessment, in a blinded fashion, pre- and post-sildenafil images were graded as "improvement" or "no improvement" in CVS. Unblinded measurements were made between pre- and post-sildenafil angiograms.
Twelve patients received sildenafil; 5 patients received 10 mg and 7 received 30 mg. There were no adverse reactions. There was no adverse effect on heart rate or intracranial pressure. Sildenafil resulted in a transient decline in mean arterial pressure, an average of 17% with a return to baseline in an average of 18 minutes. Eight patients (67%) were found to have a positive angiographic response to sildenafil, 3 (60%) in the low-dose group and 5 (71%) in the high-dose group. The largest degree of vessel dilation was an average of 0.8 mm (range 0-2.1 mm). This corresponded to an average percentage increase in vessel diameter of 62% (range 0%-200%).
The results from this Phase I safety and proof-of-concept trial assessing the use of intravenous sildenafil in patients with CVS show that sildenafil is safe and well tolerated in the setting of SAH. Furthermore, the angiographic data suggest that sildenafil has a positive impact on human CVS.
研究表明,抑制磷酸二酯酶-V(PDE-V)可减轻实验性蛛网膜下腔出血(SAH)后的脑血管痉挛(CVS)并改善预后。本研究旨在调查西地那非(一种经美国食品药品监督管理局批准的PDE-V抑制剂)对SAH患者血管造影显示的CVS的安全性和疗效。
开展了一项两阶段、前瞻性、非随机的人体试验。SAH患者在第7天接受血管造影以评估是否存在CVS。存在CVS的患者在研究的第一阶段给予10mg静脉注射西地那非,第二阶段给予30mg。在两个阶段中,输注后30分钟重复进行血管造影。通过监测神经学检查结果、生命体征以及不良反应的发生情况来评估安全性。对于血管造影评估,以盲法将西地那非给药前后的图像评为CVS“改善”或“未改善”。在西地那非给药前后的血管造影之间进行非盲测量。
12例患者接受了西地那非治疗;5例患者接受10mg,7例接受30mg。未出现不良反应。对心率或颅内压无不良影响。西地那非导致平均动脉压短暂下降,平均下降17%,平均18分钟后恢复至基线水平。8例患者(67%)血管造影显示对西地那非有阳性反应,低剂量组3例(60%),高剂量组5例(71%)。最大血管扩张程度平均为0.8mm(范围0 - 2.1mm)。这相当于血管直径平均增加62%(范围0% - 200%)。
这项评估静脉注射西地那非用于CVS患者的I期安全性和概念验证试验结果表明,西地那非在SAH情况下是安全且耐受性良好的。此外,血管造影数据表明西地那非对人类CVS有积极影响。