Zweckberger Klaus, Erös Christian, Zimmermann Ricarda, Kim Seong-Woong, Engel Doortje, Plesnila Nikolaus
Laboratory of Experimental Neurosurgery, Department of Neurosurgery and Institute for Surgical Research, University of Munich Medical Center-Grosshadern, Munich, Germany.
J Neurotrauma. 2006 Jul;23(7):1083-93. doi: 10.1089/neu.2006.23.1083.
The timing of decompressive craniectomy for the treatment of increased intracranial pressure (ICP) after traumatic brain injury (TBI) is a widely discussed clinical issue. Although we showed recently that early decompression is beneficial following experimental TBI, it remains unclear to what degree decompression craniectomy reduces secondary brain damage and if craniectomy is still beneficial when it is delayed by several hours as often inevitable during daily clinical practice. The aim of the current study was therefore to investigate the influence of craniectomy on secondary contusion expansion and brain edema formation and to determine the therapeutic window of craniectomy. Male C57/Bl6 mice were subjected to controlled cortical impact injury. Contusion volume, brain edema formation, and opening of the blood-brain barrier were investigated 2, 6, 12, and 24 h and 7 days after trauma. The effect of decompression craniectomy on secondary brain damage was studied in control mice (closed skull) and in animals craniotomized immediately or with a delay of 1, 3, or 8 h after trauma. Twenty-four hours after trauma, the time point of maximal lesion expansion (+60% vs. 15 min after trauma) and brain edema formation (+3.0% water content vs. sham), contusion volume in craniotomized mice did not show any secondary expansion; that is, contusion volume was similar to that observed in mice sacrificed immediately after trauma (18.3 +/- 5.3 vs. 22.2 +/- 1.4 mm(3)). Furthermore, brain edema formation was reduced by 52% in craniotomized animals. The beneficial effect of craniectomy was still present even when treatment was delayed by up to 3 h after trauma (p < 0.05). The current study clearly demonstrates that early craniectomy prevents secondary brain damage and significantly reduces brain edema formation after experimental TBI. Evaluation of early craniectomy as a therapeutic option after TBI in humans may therefore be indicated.
外伤性脑损伤(TBI)后行减压性颅骨切除术治疗颅内压(ICP)升高的时机是一个广泛讨论的临床问题。尽管我们最近表明,实验性TBI后早期减压有益,但减压性颅骨切除术能在多大程度上减少继发性脑损伤,以及当在日常临床实践中经常不可避免地延迟数小时进行颅骨切除术时是否仍然有益,仍不清楚。因此,本研究的目的是探讨颅骨切除术对继发性挫伤扩展和脑水肿形成的影响,并确定颅骨切除术的治疗窗。雄性C57/Bl6小鼠接受控制性皮质撞击损伤。在创伤后2、6、12和24小时以及7天,研究挫伤体积、脑水肿形成和血脑屏障开放情况。在对照小鼠(闭合颅骨)以及创伤后立即或延迟1、3或8小时进行开颅手术的动物中,研究减压性颅骨切除术对继发性脑损伤的影响。创伤后24小时,即最大损伤扩展的时间点(创伤后+60% 与15分钟时相比)和脑水肿形成(含水量+3.0% 与假手术组相比),开颅小鼠的挫伤体积未显示任何继发性扩展;也就是说,挫伤体积与创伤后立即处死的小鼠中观察到的体积相似(18.3±5.3 与22.2±1.4 mm³)。此外,开颅动物的脑水肿形成减少了52%。即使在创伤后延迟长达3小时进行治疗,颅骨切除术的有益效果仍然存在(p<0.05)。本研究清楚地表明,早期颅骨切除术可预防实验性TBI后的继发性脑损伤,并显著减少脑水肿形成。因此,可能有必要评估早期颅骨切除术作为人类TBI后一种治疗选择的可行性。