Dhar Rajat, Washington Chad, Diringer Michael, Zazulia Allyson, Jafri Hussain, Derdeyn Colin, Zipfel Gregory
Division of Neurocritical Care, Department of Neurology, Washington University in St. Louis, 660 S Euclid Avenue, St. Louis, MO, 63110, USA.
Department of Neurosurgery, Washington University in St. Louis, St. Louis, MO, 63110, USA.
Neurocrit Care. 2016 Oct;25(2):201-4. doi: 10.1007/s12028-016-0243-0.
The phosphodiesterase-5 inhibitor sildenafil has been shown to attenuate delayed cerebral ischemia (DCI) and improve neurologic function in experimental subarachnoid hemorrhage (SAH). We recently demonstrated that it could improve cerebral vasospasm (CVS) in humans after SAH. However, successful therapies for DCI must also restore cerebral blood flow (CBF) and/or autoregulatory capacity. In this study, we tested the effects of sildenafil on CBF in SAH patients at-risk for DCI.
Six subjects with angiographically confirmed CVS received 30-mg of intravenous sildenafil (mean 9 ± 2 days after aneurysmal SAH). Each underwent (15)O-PET imaging to measure global and regional CBF at baseline and post-sildenafil.
Mean arterial pressure declined by 10 mm Hg on average post-sildenafil (8 %, p = 0.01), while ICP was unchanged. There was no change in global CBF (mean 34.5 ± 7 ml/100g/min at baseline vs. 33.9 ± 8.0 ml/100g/min post-sildenafil, p = 0.84). The proportion of brain regions with low CBF (<25 ml/100g/min) was also unchanged after sildenafil infusion.
Infusion of sildenafil does not lead to a change in global or regional perfusion despite a significant reduction in cerebral perfusion pressure. While this could reflect the ineffectiveness of sildenafil-induced proximal vasodilatation to alter brain perfusion, it also suggests that cerebral autoregulatory function was preserved in this group. Future studies should assess whether sildenafil can restore or enhance autoregulation after SAH.
磷酸二酯酶-5抑制剂西地那非已被证明可减轻实验性蛛网膜下腔出血(SAH)后的迟发性脑缺血(DCI)并改善神经功能。我们最近证明,它可以改善SAH后人类的脑血管痉挛(CVS)。然而,成功治疗DCI还必须恢复脑血流量(CBF)和/或自动调节能力。在本研究中,我们测试了西地那非对有DCI风险的SAH患者CBF的影响。
6名经血管造影证实有CVS的受试者接受了30mg静脉注射西地那非(动脉瘤性SAH后平均9±2天)。每人在基线和注射西地那非后均接受(15)O-PET成像,以测量全脑和局部CBF。
注射西地那非后平均动脉压平均下降10mmHg(8%,p = 0.01),而颅内压未改变。全脑CBF无变化(基线时平均为34.5±7ml/100g/min,注射西地那非后为33.9±8.0ml/100g/min,p = 0.84)。注射西地那非后,脑血流量低(<25ml/100g/min)的脑区比例也未改变。
尽管脑灌注压显著降低,但注射西地那非不会导致全脑或局部灌注的改变。虽然这可能反映了西地那非诱导的近端血管扩张改变脑灌注无效,但也表明该组患者的脑自动调节功能得以保留。未来的研究应评估西地那非是否能恢复或增强SAH后的自动调节功能。