Tawil Isaac, Stein Deborah M, Mirvis Stuart E, Scalea Thomas M
Division of Trauma/Critical Care, Department of Surgery, University of New Mexico, Albuquerque, New Mexico, USA.
J Trauma. 2008 Apr;64(4):849-53. doi: 10.1097/TA.0b013e318160c08a.
Outcome in patients with traumatic brain injury (TBI) is often affected by secondary insults including posttraumatic cerebral infarction (PTCI). The incidence of PTCI after TBI was previously reported to be 2% with no mortality impact. We suspected that recent advances in imaging modalities and treatment might affect incidence and outcome. We sought to define the incidence and mortality impact of PTCI. We also identified risk factors associated with PTCI.
We retrospectively reviewed all patients admitted between 2004 and 2006 with severe TBI (brain Abbreviated Injury Scale [AIS] score >2, Glasgow Coma Scale score [GCS] <9). Demographics, injury specifics, and clinical data were abstracted. All brain imaging studies were reviewed with an attending trauma radiologist. Statistical analysis of outcome data were performed using chi and Student's t test and multivariate analysis was performed using logistic regression to identify independent risk factors.
Of the 384 patients identified with severe TBI; 93% sustained a blunt injury, 75% were men. Mortality was 21%, and 48% had a brain AIS score of 5. Mean age was 36 years (11-90 years), admission GCS score was 5 (3-8), and Injury Severity Score was 32 (9-75). Thirty-one (8%) had a confirmed PTCI. The PTCI group had a significantly increased mortality (45% vs. 19%, p < 0.002), hospital length of stay (LOS) (25 days vs. 18 days, p < 0.02), and intensive care unit LOS (21 days vs. 15 days, p < 0.03). In multivariate analysis, sex, age, Injury Severity Score, Revised Trauma Score, admission GCS, and brain AIS were not associated with PTCI; whereas the presence of blunt cerebral vascular injury [odds ratio (OR) 4.0, 95% confidence interval (CI) 1.9-8.7], the need for craniotomy (OR 3.0, 95% CI 1.2-6.9), or treatment with recombinant factor VIIa (OR 3.1, 95% CI 1.1-8.0) were each independently associated with an increased risk of PTCI.
The incidence of PTCI in patients with severe TBI is higher after severe brain injury than previously thought. PTCI has a significant impact on mortality and LOS. The presence of a blunt cerebral vascular injury, the need for craniotomy, or treatment with factor VIIa are risk factors for PTCI. Recognition of this secondary brain insult and the associated risk factors may help identify the group at risk and tailor management of patients with severe TBI.
创伤性脑损伤(TBI)患者的预后常受包括创伤后脑梗死(PTCI)在内的继发性损伤影响。先前报道TBI后PTCI的发生率为2%,且对死亡率无影响。我们怀疑成像方式和治疗方面的最新进展可能会影响其发生率和预后。我们试图明确PTCI的发生率及对死亡率的影响。我们还确定了与PTCI相关的危险因素。
我们回顾性分析了2004年至2006年间收治的所有重度TBI患者(脑损伤简略评分[AIS]>2,格拉斯哥昏迷量表评分[GCS]<9)。提取了人口统计学、损伤细节及临床数据。所有脑部影像学检查均由主治创伤放射科医生进行复查。使用卡方检验和学生t检验对预后数据进行统计分析,并使用逻辑回归进行多变量分析以确定独立危险因素。
在384例确诊为重度TBI的患者中,93%为钝性损伤,75%为男性。死亡率为21%,48%的患者脑AIS评分为5分。平均年龄36岁(11 - 90岁),入院时GCS评分为5分(3 - 8分),损伤严重程度评分为32分(9 - 75分)。31例(8%)确诊为PTCI。PTCI组的死亡率(45%对19%,p<0.002)、住院时间(LOS)(25天对18天,p<0.02)及重症监护病房住院时间(21天对15天,p<0.03)均显著增加。在多变量分析中,性别、年龄、损伤严重程度评分、修订创伤评分、入院时GCS及脑AIS与PTCI无关;而钝性脑血管损伤的存在(比值比[OR]4.0,95%置信区间[CI]1.9 - 8.7)、开颅手术需求(OR 3.0,95% CI 1.2 - 6.9)或重组因子VIIa治疗(OR 3.1,95% CI 1.1 - 8.0)均各自独立与PTCI风险增加相关。
重度TBI患者中PTCI的发生率在严重脑损伤后高于先前认为的水平。PTCI对死亡率和住院时间有显著影响。钝性脑血管损伤的存在、开颅手术需求或因子VIIa治疗是PTCI的危险因素。认识到这种继发性脑损伤及其相关危险因素可能有助于识别高危人群并对重度TBI患者进行针对性管理。