Section of Neurosurgery, Department of Neuroscience, Uppsala University , Uppsala , Sweden.
Anesthesiology and Intensive Care, Department of Surgical Sciences, Uppsala University , Uppsala , Sweden.
Front Neurol. 2014 Jun 2;5:89. doi: 10.3389/fneur.2014.00089. eCollection 2014.
Cerebral ischemia is the leading cause of morbidity and mortality following aneurysmal subarachnoid hemorrhage (SAH). Although 70% of the patients show angiographic vasospasm only 30% develop symptomatic vasospasm defined as delayed cerebral ischemia (DCI). Early detection and management of reversible ischemia is of critical importance in patients with SAH. Using a bedside Xenon enhanced computerized tomography (Xenon-CT) scanner makes it possible to measure quantitative regional Cerebral blood flow (CBF) bedside in the neurointensive care setting and intracerebral microdialysis (MD) is a method that offers the possibility to monitor the metabolic state of the brain continuously. Here, we present results from nine SAH patients with both MD monitoring and bedside Xenon-CT measurements. CBF measurements were performed within the first 72 h following bleeding. Six out of nine patients developed DCI at a later stage. Five out of six patients who developed DCI had initial global CBF below 26 ml/100 g/min whereas one had 53 ml/100 g/min. The three patients who did not develop clinical vasospasm all had initial global CBF above 27 ml/100 g/min. High lactate/pyruvate (L/P) ratio was associated with lower CBF values in the area surrounding the catheter. Five out of nine patients had L/P ratio ≥25 and four of these patients had CBF ≤ 22 ml/100 g/min. These preliminary results suggest that patients with initially low global CBF on Xenon-CT may be more likely to develop DCI. Initially low global CBF was accompanied with metabolic disturbances determined by the MD. Most importantly, pathological findings on the Xenon-CT and MD could be observed before any clinical signs of DCI. Combining bedside Xenon-CT and MD was found to be useful and feasible. Further studies are needed to evaluate if DCI can be detected before any other signs of DCI to prevent progress to infarction.
脑缺血是蛛网膜下腔出血(SAH)后发病率和死亡率的主要原因。尽管 70%的患者表现出血管造影性血管痉挛,但只有 30%的患者出现有症状的血管痉挛,即迟发性脑缺血(DCI)。在 SAH 患者中,早期发现和处理可逆转的缺血至关重要。使用床边氙增强计算机断层扫描(Xenon-CT)扫描仪可实现在神经重症监护环境下床边测量定量区域性脑血流(CBF),而颅内微透析(MD)是一种连续监测脑代谢状态的方法。在这里,我们报告了 9 例同时进行 MD 监测和床边氙 CT 测量的 SAH 患者的结果。CBF 测量在出血后 72 小时内进行。9 例患者中有 6 例在后期发生 DCI。6 例发生 DCI 的患者中有 5 例初始全脑 CBF 低于 26ml/100g/min,而 1 例为 53ml/100g/min。未发生临床血管痉挛的 3 例患者初始全脑 CBF 均高于 27ml/100g/min。高乳酸/丙酮酸(L/P)比值与导管周围区域的 CBF 值较低有关。9 例患者中有 5 例 L/P 比值≥25,其中 4 例 CBF≤22ml/100g/min。这些初步结果表明,氙 CT 上初始全脑 CBF 较低的患者可能更容易发生 DCI。氙 CT 上初始全脑 CBF 较低伴 MD 确定的代谢紊乱。最重要的是,在任何 DCI 的临床迹象之前,都可以观察到 Xenon-CT 和 MD 的病理发现。床边氙 CT 和 MD 的结合被发现是有用和可行的。需要进一步的研究来评估是否可以在任何其他 DCI 迹象之前检测到 DCI,以防止进展为梗塞。