Briggs Alexandra, Gates Jonathan D, Kaufman Richard M, Calahan Christopher, Gormley William B, Havens Joaquim M
Brigham and Women's Hospital, Boston, Massachusetts.
Brigham and Women's Hospital, Boston, Massachusetts.
J Surg Res. 2015 Feb;193(2):802-6. doi: 10.1016/j.jss.2014.08.016. Epub 2014 Aug 13.
Both aspirin therapy and trauma impair platelet function. Platelet dysfunction is associated with worse outcomes in patients with traumatic intracranial hemorrhage (ICH). Platelet transfusion is often used to limit progression of ICH in patients on aspirin, but has not been shown to improve platelet function or outcomes. We hypothesized that platelet transfusion would improve aspirin-induced, but not trauma-induced, platelet dysfunction.
In this prospective trial, blood samples were collected from patients evaluated in our level 1 trauma center with traumatic ICH, at the time of arrival and at the next clinical laboratory draw after admission. Patients on aspirin therapy were transfused one apheresis unit of platelets. Platelet function was assessed using a Multiplate multiple electrode aggregometer. Platelet activation was induced by collagen (COL) and arachidonic acid (AA). Agonist responses are reported as area under the aggregation curve in units (U). Reference ranges for agonist response were provided by the manufacturer, based on studies of healthy controls.
Seventeen patients with isolated ICH were enrolled, twelve taking aspirin and five not taking aspirin. All patients on aspirin received platelet transfusion. Median admission platelet function in patients taking aspirin was abnormal in response to both agonists. After transfusion, median platelet function in response to AA improved from 19.0 U to 26.0 U (P = 0.012), whereas there was no improvement in the COL response. In patients not on aspirin, platelet response to COL was abnormal at both time points.
Patients with isolated ICH have trauma-induced platelet dysfunction. In addition, patients on aspirin have drug-induced abnormalities in platelet response to AA. Platelet transfusion improves aspirin-induced, but not trauma-induced, platelet dysfunction.
阿司匹林治疗和创伤均会损害血小板功能。血小板功能障碍与创伤性颅内出血(ICH)患者的不良预后相关。血小板输注常用于限制服用阿司匹林患者的ICH进展,但尚未显示能改善血小板功能或预后。我们推测血小板输注可改善阿司匹林诱导的而非创伤诱导的血小板功能障碍。
在这项前瞻性试验中,于患者抵达时及入院后的下一次临床实验室采血时,从我们一级创伤中心评估的创伤性ICH患者采集血样。服用阿司匹林治疗的患者输注一个单采血小板单位。使用Multiplate多电极凝集仪评估血小板功能。通过胶原(COL)和花生四烯酸(AA)诱导血小板活化。激动剂反应以单位(U)的凝集曲线下面积报告。激动剂反应的参考范围由制造商根据对健康对照的研究提供。
纳入17例单纯性ICH患者,12例服用阿司匹林,5例未服用阿司匹林。所有服用阿司匹林的患者均接受了血小板输注。服用阿司匹林患者入院时对两种激动剂的血小板功能中位数均异常。输血后,对AA的血小板功能中位数从19.0 U改善至26.0 U(P = 0.012),而对COL的反应无改善。未服用阿司匹林的患者在两个时间点对COL的血小板反应均异常。
单纯性ICH患者存在创伤诱导的血小板功能障碍。此外,服用阿司匹林的患者对AA的血小板反应存在药物诱导的异常。血小板输注可改善阿司匹林诱导的而非创伤诱导的血小板功能障碍。