Department of Neuroscience, Section of Neurosurgery, Uppsala University Hospital, Uppsala, Sweden.
Department of Clinical Neurosciences, Neurosurgical Unit, Division of Anaesthesia, University of Cambridge, Addenbrooke's Hospital, Cambridge, United Kingdom.
Crit Care Med. 2018 Mar;46(3):e235-e241. doi: 10.1097/CCM.0000000000002930.
The three centers in this study have different policies regarding cerebral perfusion pressure targets and use of vasopressors in traumatic brain injury patients. The aim was to determine if the different policies affected the estimation of cerebral perfusion pressure which optimizes the strength of cerebral autoregulation, termed "optimal cerebral perfusion pressure."
Retrospective analysis of prospectively collected data.
Three neurocritical care units at university hospitals in Cambridge, United Kingdom, Groningen, the Netherlands, and Uppsala, Sweden.
A total of 104 traumatic brain injury patients were included: 35 each from Cambridge and Groningen, and 34 from Uppsala.
None.
In Groningen, the cerebral perfusion pressure target was greater than or equal to 50 and less than 70 mm Hg, in Uppsala greater than or equal to 60, and in Cambridge greater than or equal to 60 or preferably greater than or equal to 70. Despite protocol differences, median cerebral perfusion pressure for each center was above 70 mm Hg. Optimal cerebral perfusion pressure was calculated as previously published and implemented in the Intensive Care Monitoring+ software by the Cambridge group, now replicated in the Odin software in Uppsala. Periods with cerebral perfusion pressure above and below optimal cerebral perfusion pressure were analyzed, as were absolute difference between cerebral perfusion pressure and optimal cerebral perfusion pressure and percentage of monitoring time with a valid optimal cerebral perfusion pressure. Uppsala had the highest cerebral perfusion pressure/optimal cerebral perfusion pressure difference. Uppsala patients were older than the other centers, and age is positively correlated with cerebral perfusion pressure/optimal cerebral perfusion pressure difference. Optimal cerebral perfusion pressure was significantly lower in Groningen than in Cambridge. There were no significant differences in percentage of monitoring time with valid optimal cerebral perfusion pressure. Summary optimal cerebral perfusion pressure curves were generated for the combined patient data for each center. These summary curves could be generated for Groningen and Cambridge, but not Uppsala. The older age of the Uppsala patient cohort may explain the absence of a summary curve.
Differences in optimal cerebral perfusion pressure calculation were found between centers due to demographics (age) and treatment (cerebral perfusion pressure targets). These factors should be considered in the design of trials to determine the efficacy of autoregulation-guided treatment.
本研究中的三个中心在创伤性脑损伤患者的脑灌注压目标和血管加压剂使用方面有不同的政策。目的是确定不同的政策是否会影响脑灌注压的估计,从而优化脑自动调节的强度,称为“最佳脑灌注压”。
前瞻性收集数据的回顾性分析。
英国剑桥、荷兰格罗宁根和瑞典乌普萨拉的三所神经重症监护病房。
共纳入 104 例创伤性脑损伤患者:剑桥和格罗宁根各 35 例,乌普萨拉 34 例。
无。
在格罗宁根,脑灌注压目标大于或等于 50 毫米汞柱且小于 70 毫米汞柱;在乌普萨拉,脑灌注压目标大于或等于 60 毫米汞柱;在剑桥,脑灌注压目标大于或等于 60 毫米汞柱,或最好大于或等于 70 毫米汞柱。尽管方案存在差异,但每个中心的中位脑灌注压均高于 70 毫米汞柱。最佳脑灌注压如前所述计算,并由剑桥组在 Intensive Care Monitoring+软件中实施,现在在乌普萨拉的 Odin 软件中得到复制。分析了脑灌注压高于和低于最佳脑灌注压的时间段,以及脑灌注压与最佳脑灌注压之间的绝对差值和监测时间内有效最佳脑灌注压的百分比。乌普萨拉的脑灌注压/最佳脑灌注压差值最高。乌普萨拉患者比其他中心的年龄大,年龄与脑灌注压/最佳脑灌注压差值呈正相关。与剑桥相比,格罗宁根的最佳脑灌注压显著降低。有效最佳脑灌注压监测时间百分比无显著差异。为每个中心的合并患者数据生成了最佳脑灌注压汇总曲线。这些汇总曲线可用于格罗宁根和剑桥,但不能用于乌普萨拉。乌普萨拉患者队列的年龄较大可能解释了汇总曲线的缺失。
由于人口统计学因素(年龄)和治疗因素(脑灌注压目标),不同中心之间的最佳脑灌注压计算存在差异。在设计试验以确定自动调节引导治疗的疗效时,应考虑这些因素。