Kroppenstedt Stefan-Nikolaus, Thomale Ulrich-Wilhelm, Griebenow Martin, Sakowitz Oliver W, Schaser Klaus-Dieter, Mayr Petra S, Unterberg Andreas W, Stover John F
Department of Neurosurgery, Charité, Virchow Medical Center, Humboldt University, Berlin, Germany.
Crit Care Med. 2003 Aug;31(8):2211-21. doi: 10.1097/01.CCM.0000080482.06856.62.
Reduction of cerebral perfusion during the early phase after traumatic brain injury is followed by a later phase of normal to increased perfusion. Thus, pharmacologically elevating mean arterial blood pressure with the aim of improving cerebral perfusion may exert different time-dependent effects on cortical perfusion, microcirculation, tissue oxygenation and brain edema formation after traumatic brain injury.
Randomized, placebo-controlled trial.
Experimental laboratory at a university hospital.
A total of 37 male Sprague-Dawley rats subjected to a focal cortical contusion.
At 4 or 24 hrs after focal traumatic brain injury, mean arterial blood pressure was increased to 120 mm Hg for 90 mins by infusing norepinephrine. In rats receiving physiologic saline, mean arterial blood pressure remained unchanged. In the first series, pericontusional cortical perfusion was measured using the laser Doppler flowmetry scanning technique before injury and before, during, and after the infusion period. In a second series, intracranial and cerebral perfusion pressure and intraparenchymal perfusion and tissue oxygen measured within the contused and pericontusional cortex were recorded continuously before, during, and after norepinephrine infusion. Changes in cortical microcirculation were investigated by orthogonal polarization spectral imaging. At the end of each experiment, hemispheric swelling and water content were determined gravimetrically.
At 4 and 24 hrs after traumatic brain injury, intravenous norepinephrine significantly increased pericontusional cortical perfusion, which was also reflected by an increase in diameters and flow velocities of pericontusional arterioles and venules. Cerebral perfusion pressure and intraparenchymal perfusion and tissue oxygen were significantly increased during norepinephrine infusion at 4 and 24 hrs. Hemispheric swelling and water content showed no difference between the groups.
After cortical impact injury, early and late intravenous norepinephrine infusion pressure-dependently increased cerebral perfusion and tissue oxygenation without aggravating or reducing brain edema formation. Future studies are warranted to determine long-term changes of short and prolonged norepinephrine-induced increases in mean arterial blood pressure and cerebral perfusion pressure.
创伤性脑损伤后早期脑灌注减少,随后进入灌注正常至增加的后期阶段。因此,以改善脑灌注为目的通过药物升高平均动脉血压,可能会对创伤性脑损伤后的皮质灌注、微循环、组织氧合和脑水肿形成产生不同的时间依赖性影响。
随机、安慰剂对照试验。
大学医院的实验实验室。
总共37只雄性Sprague-Dawley大鼠,均遭受局灶性皮质挫伤。
在局灶性创伤性脑损伤后4小时或24小时,通过输注去甲肾上腺素将平均动脉血压升高至120 mmHg并维持90分钟。接受生理盐水的大鼠,其平均动脉血压保持不变。在第一组实验中,使用激光多普勒血流仪扫描技术在损伤前以及输注期之前、期间和之后测量挫伤周围皮质灌注。在第二组实验中,在去甲肾上腺素输注之前、期间和之后,连续记录挫伤和挫伤周围皮质内的颅内和脑灌注压、实质内灌注和组织氧含量。通过正交偏振光谱成像研究皮质微循环的变化。在每个实验结束时,通过重量法测定半球肿胀和含水量。
在创伤性脑损伤后4小时和24小时,静脉注射去甲肾上腺素显著增加了挫伤周围皮质灌注,这也表现为挫伤周围小动脉和小静脉直径及流速的增加。在4小时和24小时去甲肾上腺素输注期间,脑灌注压、实质内灌注和组织氧含量显著增加。两组之间半球肿胀和含水量无差异。
在皮质撞击损伤后,早期和晚期静脉注射去甲肾上腺素均能压力依赖性地增加脑灌注和组织氧合,而不会加重或减轻脑水肿形成。有必要进行进一步研究以确定短期和长期去甲肾上腺素诱导的平均动脉血压和脑灌注压升高的长期变化。