Tollefsen Marie Hexeberg, Vik Anne, Skandsen Toril, Sandrød Oddrun, Deane Susan Frances, Rao Vidar, Moen Kent Gøran
Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway; Department of Neurosurgery, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
World Neurosurg. 2018 Jun;114:e209-e217. doi: 10.1016/j.wneu.2018.02.167. Epub 2018 Mar 7.
We aimed to examine the effect of preinjury antithrombotic medication on clinical and radiologic neuroworsening in traumatic brain injury (TBI) and study the effect on outcome.
A total of 184 consecutive patients ≥50 years old with moderate and severe TBI admitted to a level 1 trauma center were included. Neuroworsening was assessed clinically by using the Glasgow Coma Scale (GCS) score and radiologically by using the Rotterdam CT score on repeated time points. Functional outcome was assessed with the Glasgow Outcome Scale Extended 6 months after injury.
The platelet inhibitor group (mean age, 77.3 years; n = 43) and the warfarin group (mean age, 73.2 years; n = 20) were significantly older than the nonuser group (mean age, 63.7 years; n = 121; P ≤ 0.001). In the platelet inhibitor group 74% and in the warfarin group, 85% were injured by falls. Platelet inhibitors were not significantly associated with clinical or radiologic neuroworsening (P = 0.37-1.00), whereas warfarin increased the frequency of worsening in GCS score (P = 0.001-0.028) and Rotterdam CT score (P = 0.004). In-hospital mortality was higher in the platelet inhibitor group (28%; P = 0.030) and the warfarin group (50%; P < 0.001) compared with the nonuser group (13%). Platelet inhibitors did not predict mortality or worse outcome after adjustment for age, preinjury disability, GCS score, and Rotterdam CT score, whereas warfarin predicted both mortality and worse outcome.
In this study of patients with moderate and severe TBI, preinjury platelet inhibitors did not cause neuroworsening or predict higher mortality or worse outcome. In contrast, preinjury warfarin caused neuroworsening and was an independent risk factor for mortality and worse outcome at 6 months. Hence, fall prevention and liberal use of computed tomography examinations is important in this patient group.
我们旨在研究伤前抗血栓药物对创伤性脑损伤(TBI)患者临床和影像学神经功能恶化的影响,并探讨其对预后的作用。
纳入了184例年龄≥50岁、因中度和重度TBI入住一级创伤中心的连续患者。通过格拉斯哥昏迷量表(GCS)评分进行临床神经功能恶化评估,并在多个时间点通过鹿特丹CT评分进行影像学评估。在伤后6个月,使用格拉斯哥扩展预后量表评估功能预后。
血小板抑制剂组(平均年龄77.3岁;n = 43)和华法林组(平均年龄73.2岁;n = 20)的年龄显著高于未使用抗血栓药物组(平均年龄63.7岁;n = 121;P≤0.001)。血小板抑制剂组74%以及华法林组85%的患者因跌倒受伤。血小板抑制剂与临床或影像学神经功能恶化无显著相关性(P = 0.37 - 1.00),而华法林会增加GCS评分恶化频率(P = 0.001 - 0.028)以及鹿特丹CT评分恶化频率(P = 0.004)。与未使用抗血栓药物组(13%)相比,血小板抑制剂组(28%;P = 0.030)和华法林组(50%;P < 0.001)的院内死亡率更高。在校正年龄、伤前残疾情况、GCS评分和鹿特丹CT评分后,血小板抑制剂不能预测死亡率或更差的预后,而华法林则可预测死亡率和更差的预后。
在这项针对中度和重度TBI患者的研究中,伤前使用血小板抑制剂不会导致神经功能恶化,也不会预测更高的死亡率或更差的预后。相比之下,伤前使用华法林会导致神经功能恶化,并且是6个月时死亡率和更差预后的独立危险因素。因此,对于该患者群体,预防跌倒和广泛使用计算机断层扫描检查非常重要。