Wiśniewski Adam, Sikora Joanna, Karczmarska-Wódzka Aleksandra, Bugieda Joanna, Filipska Karolina, Ślusarz Robert
Department of Neurology, Faculty of Medicine, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, 85-094 Bydgoszcz, Poland.
Experimental Biotechnology Research and Teaching Team, Department of Transplantology and General Surgery, Faculty of Medicine, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, 85-094 Bydgoszcz, Poland.
Brain Sci. 2021 Feb 18;11(2):257. doi: 10.3390/brainsci11020257.
Previous studies have revealed that high platelet reactivity while on clopidogrel may affect the severe course and worse prognosis of ischemic stroke. However, the above findings were based on a single measurement of platelet function. We aimed to investigate whether the dynamics of platelet reactivity over time would more accurately determine its actual impact on clinical outcome.
We enrolled 74 ischemic stroke subjects, taking a dose of 75 mg a day of clopidogrel to this prospective, single-center, and observational study. The determination of platelet function was based on the impedance aggregometry 6-12 h after the first dose of clopidogrel and 48 h later. We defined a favorable dynamics of platelet reactivity as a decrease in values at least equal to the median obtained in the entire study. The clinical condition was assessed by the National Institutes of Health Stroke Scale on the first, third, and ninetieth days and the functional status by modified Rankin Scale, respectively.
A favorable dynamics of platelet reactivity was associated with the mild clinical condition and favorable functional status, both early and late. Early neurological deterioration was related to unfavorable dynamics of platelet reactivity over time. In multivariate regression models, we found that unfavorable dynamics of platelet reactivity, alone and combined with a high baseline value of platelet reactivity, is an independent predictor of a severe clinical condition, the risk of deterioration, and poor early and late prognosis.
We highlighted that dynamics of platelet reactivity over time predict the clinical course and prognosis of stroke better than a single value.
既往研究表明,服用氯吡格雷时血小板高反应性可能会影响缺血性卒中的严重病程及预后。然而,上述发现是基于对血小板功能的单次测量。我们旨在研究血小板反应性随时间的动态变化是否能更准确地确定其对临床结局的实际影响。
我们纳入了74例缺血性卒中患者,进行这项前瞻性、单中心观察性研究,患者每日服用75毫克氯吡格雷。血小板功能的测定基于首次服用氯吡格雷后6 - 12小时以及48小时后的阻抗聚集法。我们将血小板反应性的良好动态变化定义为其值下降至少等于整个研究中获得的中位数。分别在第1天、第3天和第90天通过美国国立卫生研究院卒中量表评估临床状况,并通过改良Rankin量表评估功能状态。
血小板反应性的良好动态变化与早期和晚期的轻度临床状况及良好功能状态相关。早期神经功能恶化与血小板反应性随时间的不良动态变化有关。在多变量回归模型中,我们发现血小板反应性的不良动态变化,单独以及与血小板反应性的高基线值相结合,是严重临床状况、恶化风险以及早期和晚期不良预后的独立预测因素。
我们强调,血小板反应性随时间的动态变化比单一值能更好地预测卒中的临床病程和预后。