Department of Surgery, San Francisco General Hospital, San Francisco, California 94110, USA.
J Trauma Acute Care Surg. 2013 May;74(5):1223-9; discussion 1229-30. doi: 10.1097/TA.0b013e31828b7fa1.
Clotting factor abnormalities underlying acute traumatic coagulopathy are poorly understood, with application of traditional regression techniques confounded by colinearity. We hypothesized that principal components analysis (PCA), a pattern-finding and data reduction technique, would identify clinically predictive patterns in the complex clotting factor milieu after trauma.
Plasma was prospectively collected from 163 critically injured trauma patients. Prothrombin; factors V, VII, VIII, IX, X; D-dimer; activated and native protein C; and antithrombin III levels were assayed and subjected to nonlinear PCA to identify principal components (PCs).
Of 163 patients, 19.0% were coagulopathic on admission. PCA identified 3 significant PCs, accounting for 67.5% of overall variance. PC1 identified global clotting factor depletion; PC2 the activation of protein C and fibrinolysis; and PC3 factor VII elevation and VIII depletion. PC1 score correlated with penetrating injury and injury severity, predicting coagulopathy (odds ratio [OR], 4.67; p < 0.001) and mortality (OR, 1.47; p = 0.032). PC2 score correlated with injury severity, acidosis, and shock, and significantly predicted ventilator-associated pneumonia (OR, 1.59; p = 0.008), acute lung injury (OR, 2.24; p < 0.001), multiorgan failure (OR, 1.83; p = 0.002), and mortality (OR, 1.62; p = 0.006) but was not associated with international normalized ratio (INR)-based or partial thromboplastin time (PTT)-based coagulopathy (p > 0.200). PC3 did not significantly predict outcomes.
PCA identifies distinct patterns of coagulopathy: depletion coagulopathy predicts mortality and INR/PTT elevation, while fibrinolytic coagulopathy predicts infection, end-organ failure, and mortality, without detectable differences in INR or PTT. While depletion coagulopathy is intuitive, fibrinolytic coagulopathy may be a distinct but often overlapping entity with differential effects on outcomes.
急性创伤性凝血病的凝血因子异常目前了解甚少,传统回归技术的应用受到共线性的干扰。我们假设主成分分析(PCA)是一种发现模式和数据简化技术,可以识别创伤后复杂凝血因子环境中的临床预测模式。
前瞻性收集 163 例严重创伤患者的血浆。检测凝血酶原、因子 V、VII、VIII、IX、X;D-二聚体;激活和天然蛋白 C;抗凝血酶 III 水平,并进行非线性 PCA 以识别主成分(PC)。
163 例患者中,19.0%入院时存在凝血异常。PCA 确定了 3 个显著的 PC,占总方差的 67.5%。PC1 确定了整体凝血因子耗竭;PC2 确定了蛋白 C 和纤维蛋白溶解的激活;PC3 确定了因子 VII 升高和 VIII 耗竭。PC1 评分与穿透性损伤和损伤严重程度相关,预测凝血异常(比值比[OR],4.67;p<0.001)和死亡率(OR,1.47;p=0.032)。PC2 评分与损伤严重程度、酸中毒和休克相关,显著预测呼吸机相关性肺炎(OR,1.59;p=0.008)、急性肺损伤(OR,2.24;p<0.001)、多器官功能衰竭(OR,1.83;p=0.002)和死亡率(OR,1.62;p=0.006),但与 INR 或 PTT 为基础的凝血异常无关(p>0.200)。PC3 评分与结局无显著相关性。
PCA 确定了不同的凝血异常模式:耗竭性凝血异常预测死亡率和 INR/PTT 升高,而纤维蛋白溶解性凝血异常预测感染、终末器官衰竭和死亡率,INR 或 PTT 无明显差异。虽然耗竭性凝血异常是直观的,但纤维蛋白溶解性凝血异常可能是一种不同但经常重叠的实体,对结局有不同的影响。