Biomedical Engineering, Faculty of Engineering, University of Manitoba, Winnipeg, Canada.
Section of Neurosurgery, Department of Surgery, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Acta Neurochir (Wien). 2022 Dec;164(12):3107-3118. doi: 10.1007/s00701-022-05366-9. Epub 2022 Sep 26.
Impaired cerebrovascular reactivity following moderate/severe traumatic brain injury (TBI) has emerged as a key potential driver of morbidity and mortality. However, the major contributions to the literature so far have been solely focused on single point measures of long-term outcome. Therefore, it remains unknown whether cerebrovascular reactivity impairment, during the acute phase of TBI, is associated with failure to improve in outcome across time.
Cerebrovascular reactivity was measured using three intracranial pressure-based surrogate metrics. For each patient, % time spent above various literature-defined thresholds was calculated. Patients were dichotomized based on outcome transition into Improved vs Not Improved between 1 and 3 months, 3 and 6 months, and 1 and 6 months, based on the Glasgow Outcome Scale-Extended (GOSE). Univariate and multivariable logistic regression analyses were performed, adjusting for the International Mission for Prognosis and Analysis of Clinical Trials (IMPACT) variables.
Seventy-eight patients from the Winnipeg Acute TBI Database were included in this study. On univariate logistic regression analysis, higher % time with cerebrovascular reactivity metrics above clinically defined thresholds was associated with a lack of clinical improvement between 1 and 3 months and 1 and 6 months post injury (p < 0.05). These relationships held true on multivariable logistic regression analysis.
Our study demonstrates that impaired cerebrovascular reactivity, during the acute phase of TBI, is associated with failure to improve clinically over time. These preliminary findings highlight the significance that cerebrovascular reactivity monitoring carries in outcome recovery association in moderate/severe TBI.
中度/重度创伤性脑损伤(TBI)后脑血管反应性受损已成为发病率和死亡率的一个关键潜在驱动因素。然而,迄今为止,文献的主要贡献仅集中在长期预后的单点测量上。因此,尚不清楚 TBI 急性期的脑血管反应性受损是否与随时间改善的预后失败有关。
使用三种基于颅内压的替代指标来测量脑血管反应性。对于每个患者,计算超过各种文献定义的阈值的时间百分比。根据格拉斯哥预后评分扩展版(GOSE),根据 1 至 3 个月、3 至 6 个月和 1 至 6 个月的结局变化,将患者分为改善组和未改善组。进行单变量和多变量逻辑回归分析,并调整国际预后和分析临床试验(IMPACT)变量。
本研究纳入了温尼伯急性 TBI 数据库中的 78 名患者。在单变量逻辑回归分析中,脑血管反应性指标超过临床定义阈值的时间百分比较高与受伤后 1 至 3 个月和 1 至 6 个月的临床改善缺乏相关(p<0.05)。多变量逻辑回归分析也证实了这些关系。
我们的研究表明,TBI 急性期的脑血管反应性受损与随时间临床改善失败有关。这些初步发现强调了在中度/重度 TBI 中,脑血管反应性监测对预后恢复关联的重要性。