Choi Phillip A, Parry Phillip V, Bauer Joshua S, Zusman Benjamin E, Panczykowski David M, Puccio Ava M, Okonkwo David O
University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Neurosurgery. 2017 Jan 1;80(1):98-104. doi: 10.1227/NEU.0000000000001401.
At present, guidelines are lacking on platelet transfusion in patients with a traumatic intracranial bleed and history of antiplatelet therapy. The aspirin and P2Y 12 response unit (ARU and PRU, respectively) assays detect the effect of aspirin and P2Y 12 inhibitors in the cardiac population.
To describe the reversal of platelet inhibition after platelet transfusion using the ARU and PRU assays in patients with traumatic brain injury.
Between 2010 and 2015, we conducted a prospective comparative cohort study of patients presenting with a positive head computed tomography and a history of antiplatelet therapy. ARU and PRU assays were performed on admission and 6 hours after transfusion, with a primary end point of detection of disinhibition after platelet transfusion.
One hundred seven patients were available for analysis. Seven percent of patients taking aspirin and 27% of patients taking clopidogrel were not therapeutic on admission per the ARU and PRU, respectively. After platelet transfusion, 51% of patients on any aspirin and 67% of patients on any clopidogrel failed to be reversed. ARU increased by 71 ± 76 per unit of apheresis platelets for patients taking any aspirin, and PRU increased by 48 ± 46 per unit of apheresis platelets for patients taking any clopidogrel.
A significant percentage of patients taking aspirin or clopidogrel were not therapeutic and thus would be unlikely to benefit from a platelet transfusion. In patients with measured platelet inhibition, a single platelet transfusion was not sufficient to reverse platelet inhibition in almost half.
目前,对于有创伤性颅内出血且有抗血小板治疗史的患者,缺乏血小板输注指南。阿司匹林和P2Y12反应单位(分别为ARU和PRU)检测可检测阿司匹林和P2Y12抑制剂在心脏疾病人群中的作用。
描述使用ARU和PRU检测评估创伤性脑损伤患者血小板输注后血小板抑制的逆转情况。
2010年至2015年期间,我们对头部计算机断层扫描阳性且有抗血小板治疗史的患者进行了一项前瞻性比较队列研究。入院时及输血后6小时进行ARU和PRU检测,主要终点为检测血小板输注后抑制作用的解除。
107例患者可供分析。根据ARU和PRU检测,分别有7%服用阿司匹林的患者和27%服用氯吡格雷的患者入院时未达到治疗效果。血小板输注后,服用任何剂量阿司匹林的患者中有51%以及服用任何剂量氯吡格雷的患者中有67%未能实现抑制作用的逆转。服用任何剂量阿司匹林的患者,每单位单采血小板的ARU增加71±76,服用任何剂量氯吡格雷的患者,每单位单采血小板的PRU增加48±46。
相当比例服用阿司匹林或氯吡格雷的患者未达到治疗效果,因此不太可能从血小板输注中获益。在检测到血小板抑制的患者中,单次血小板输注几乎不足以逆转近半数患者的血小板抑制作用。