Division of Neurointerventional Surgery, Ascension Columbia St. Mary's Hospital, Milwaukee, WI, USA; University of Iowa, Department of Radiology, Iowa City, IA, USA.
Division of Neurointerventional Radiology, Neuroscience Institute, Abbott Northwestern Hospital, Minneapolis, MN, USA.
Clin Neurol Neurosurg. 2020 Aug;195:106038. doi: 10.1016/j.clineuro.2020.106038. Epub 2020 Jun 23.
The pathophysiology of delayed cerebral ischemia (DCI) after aneurysmal subarachnoid hemorrhage (aSAH) may include platelet activation and microthrombi formation. Antiplatelet therapy may reduce the incidence of DCI and improve clinical outcomes after aSAH. This study compared outcomes among aSAH patients receiving aspirin monotherapy versus dual antiplatelet therapy (DAPT).
Aneurysmal subarachnoid hemorrhage patients treated at a single institution between November 2011 and December 2017 were divided according to whether they received aspirin monotherapy or DAPT after endovascular treatment. Baseline characteristics and outcomes of the groups were compared, including incidences of delayed cerebral ischemia, bleeding complications, symptomatic vasospasm, in-hospital mortality, and functional status 6 months after discharge.
During the study period, 142 patients met study inclusion criteria, of which 123 were treated with aspirin monotherapy (87 %) and 19 were treated with DAPT (13 %). There was no statistically significant difference between the aspirin monotherapy and DAPT groups with respect to incidences of delayed cerebral ischemia (4.9 vs 10.5 %; p = 0.32), symptomatic vasospasm (13.0 vs 15.8 %; p = 0.74), or good clinical outcome at 6-month follow up (73.3 vs 66.7 %; p = 0.56). The DAPT group experienced a higher incidence of in-hospital mortality (21 vs 5.7 %; p = 0.02), but DAPT did not remain independently predictive of this outcome on regression analysis. There was a trend toward a higher bleeding complication rate in the DAPT group (0.8 vs 5.3 %; p = 0.13).
DAPT does not reduce the incidence of DCI or improve outcomes in aSAH patients, and may increase the risk of clinically significant bleeding complications.
动脉瘤性蛛网膜下腔出血(aSAH)后迟发性脑缺血(DCI)的病理生理学可能包括血小板激活和微血栓形成。抗血小板治疗可能会降低 DCI 的发生率并改善 aSAH 后的临床结局。本研究比较了接受阿司匹林单药治疗与双联抗血小板治疗(DAPT)的 aSAH 患者的结局。
2011 年 11 月至 2017 年 12 月,在一家机构接受治疗的 aSAH 患者根据血管内治疗后是否接受阿司匹林单药治疗或 DAPT 分为两组。比较两组的基线特征和结局,包括迟发性脑缺血、出血并发症、症状性血管痉挛、住院死亡率以及出院后 6 个月的功能状态。
在研究期间,142 名患者符合研究纳入标准,其中 123 例接受阿司匹林单药治疗(87%),19 例接受 DAPT(13%)。阿司匹林单药治疗组和 DAPT 组在迟发性脑缺血发生率(4.9%与 10.5%;p=0.32)、症状性血管痉挛发生率(13.0%与 15.8%;p=0.74)或 6 个月随访时的良好临床结局(73.3%与 66.7%;p=0.56)方面无统计学差异。DAPT 组住院死亡率较高(21%与 5.7%;p=0.02),但回归分析显示 DAPT 不是这一结局的独立预测因素。DAPT 组出血并发症发生率有升高趋势(0.8%与 5.3%;p=0.13)。
DAPT 不能降低 aSAH 患者 DCI 的发生率或改善结局,反而可能增加临床显著出血并发症的风险。