Thomas J E, Rosenwasser R H
Department of Neurological Surgery, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Neurosurgery. 1999 Jan;44(1):48-57; discussion 57-8. doi: 10.1097/00006123-199901000-00026.
The chronic delayed type of cerebral vasoconstriction that occurs after aneurysmal subarachnoid hemorrhage (SAH) is now the most important cause of mortality and neurological morbidity for patients who initially survive the rupture of cerebral aneurysms. Although intravascular volume expansion and cardiac performance enhancement have had a profound impact on the treatment of the chronic delayed type of cerebral vasoconstriction, this form of treatment is not tolerated by all patients and is unhelpful in some. A more specific and more reliable treatment for this condition has not been previously reported. Previous work in an animal model has demonstrated the efficacy of nitric oxide-donating compounds in reversing severe cerebral vasoconstriction when delivered to the adventitial side of the blood vessel. A clinical study was initiated after receiving approval from the United States Food and Drug Administration and the institutional review board.
Three cases of prompt and substantial reversal of medically refractory vasospasm occurring after aneurysmal SAH in humans using an intrathecally administered nitric oxide donor and clinical, angiographic, and ultrasonographic documentation are presented. All patients developed severe vasospasm refractory to medical treatment 5 to 12 days after sustaining aneurysmal SAH. All patients manifested stupor of new onset (Glasgow Coma Scale score of 7) and new focal neurological deficit (hemiplegia). The condition was angiographically demonstrated in all cases.
The patients were treated with intrathecally administered sodium nitroprusside, which caused the reversal of vasospasm, which was documented by angiography and transcranial Doppler ultrasonography up to 54 hours later and also by dramatic clinical improvement. Complications related to intracranial pressure elevation, changes in vital signs, and hemodynamic parameters were not observed during or after the procedures. Radiographic evidence of the reversal of vasospasm and brain ischemia was obtained. The clinical outcomes of the treated patients were excellent. All patients presented with hemiplegia and stupor that resolved or markedly improved (within several days, two patients; within 12 hours, one patient). All three patients were discharged and were living at home at the time of manuscript submission.
These preliminary observations suggest that sodium nitroprusside delivered by an intrathecal route of administration may be a useful treatment for severe vasospasm complicating SAH in humans.
动脉瘤性蛛网膜下腔出血(SAH)后发生的慢性迟发性脑血管收缩,是最初在脑动脉瘤破裂后存活下来的患者死亡和神经功能障碍的最重要原因。尽管血管内容量扩充和心脏功能增强对慢性迟发性脑血管收缩的治疗产生了深远影响,但这种治疗形式并非所有患者都能耐受,且对部分患者无效。此前尚未报道过针对这种情况更具体、更可靠的治疗方法。先前在动物模型中的研究表明,当将释放一氧化氮的化合物输送到血管外膜侧时,其在逆转严重脑血管收缩方面具有疗效。在美国食品药品监督管理局和机构审查委员会批准后,启动了一项临床研究。
本文报告了3例人类动脉瘤性SAH后发生的药物难治性血管痉挛通过鞘内注射一氧化氮供体迅速且显著逆转的病例,并提供了临床、血管造影和超声检查记录。所有患者在动脉瘤性SAH后5至12天出现严重的药物难治性血管痉挛。所有患者均出现新发昏迷(格拉斯哥昏迷量表评分为7分)和新的局灶性神经功能缺损(偏瘫)。所有病例均通过血管造影证实了病情。
患者接受鞘内注射硝普钠治疗,血管痉挛得以逆转,血管造影和经颅多普勒超声在54小时后记录了这一情况,临床症状也有显著改善。在治疗过程中及治疗后均未观察到与颅内压升高、生命体征变化和血流动力学参数相关的并发症。获得了血管痉挛和脑缺血逆转的影像学证据。治疗患者的临床结局良好。所有患者均表现为偏瘫和昏迷,均已缓解或明显改善(两名患者在数天内;一名患者在12小时内)。所有三名患者均已出院,在撰写本文时均在家中生活。
这些初步观察结果表明,鞘内给药的硝普钠可能是治疗人类SAH并发严重血管痉挛的有效方法。