Department of Neurosurgery, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Neuroscience, Karolinska Institutet, Bioclinicum J5:20, 171 64 , Solna, Stockholm, Sweden.
Neurocrit Care. 2023 Feb;38(1):60-70. doi: 10.1007/s12028-022-01609-w. Epub 2022 Sep 27.
Preventing intracranial hematoma expansion has been advertised as a possible treatment opportunity in traumatic brain injury (TBI). However, the time course of hematoma expansion, and whether the expansion affects outcome, remains poorly understood. In light of this, the aim of this study was to use 3D volume rendering to determine how traumatic intracranial hematomas expand over time and evaluate its impact on outcome.
Single-center, population-based, observational cohort study of adults with moderate-to-severe TBI. Hematoma expansion was defined as the change in hematoma volume from the baseline computed tomography scan until the lesion had stopped progressing. Volumes were calculated by using semiautomated volumetric segmentation. Functional outcome was measured by using the 12 month Glasgow outcome scale (GOS).
In total, 643 patients were included. The mean baseline hematoma volume was 4.2 ml, and the subsequent mean hematoma expansion was 3.8 ml. Overall, 33% of hematomas had stopped progressing within 3 h, and 94% of hematomas had stopped progressing within 24 h of injury. Contusions expanded significantly more, and for a longer period of time, than extra-axial hematomas. There was a significant dose-response relationship between hematoma expansion and 12 month GOS, even after adjusting for known outcome predictors, with every 1-ml increase in hematoma volume associated with a 6% increased risk of 1-point GOS deduction.
Hematoma expansion is a driver of unfavorable outcome in TBI, with small changes in hematoma volume also impacting functional outcome. This study also proposes a wider window of opportunity to prevent lesion progression than what has previously been suggested.
在创伤性脑损伤(TBI)中,防止颅内血肿扩大已被宣传为一种可能的治疗机会。然而,血肿扩大的时间过程以及扩大是否影响结果仍知之甚少。有鉴于此,本研究旨在使用 3D 容积渲染来确定外伤性颅内血肿随时间的扩展方式,并评估其对结果的影响。
这是一项单中心、基于人群的、观察性队列研究,纳入了成年人中度至重度 TBI。血肿扩大定义为从基线 CT 扫描到病变停止进展时血肿体积的变化。通过半自动容积分割计算体积。功能结局通过 12 个月格拉斯哥结局量表(GOS)进行测量。
共纳入 643 例患者。平均基线血肿体积为 4.2ml,随后的平均血肿扩大为 3.8ml。总体而言,33%的血肿在 3 小时内停止进展,94%的血肿在受伤后 24 小时内停止进展。挫伤比轴外血肿扩展得更多,持续时间更长。血肿扩大与 12 个月 GOS 之间存在显著的剂量反应关系,即使在调整了已知的结局预测因素后也是如此,血肿体积每增加 1ml,GOS 降低 1 分的风险就会增加 6%。
血肿扩大是 TBI 不良结局的驱动因素,血肿体积的微小变化也会影响功能结局。本研究还提出了比先前建议更广泛的防止病变进展的机会窗口。