Merlino Giovanni, Nesi Lorenzo, Vergobbi Pietro, Scanni Marco Domenico, Pez Sara, Marziali Alessandro, Tereshko Yan, Sportelli Giuseppe, Lorenzut Simone, Janes Francesco, Gigli Gian Luigi, Valente Mariarosaria
Stroke Unit, Department of Head-Neck and Neuroscience, Udine University Hospital, Udine, Italy.
Clinical Neurology, Udine University Hospital, Udine, Italy.
Front Neurol. 2023 Jul 17;14:1212712. doi: 10.3389/fneur.2023.1212712. eCollection 2023.
It is unknown whether alteplase is effective and safe in patients with mild acute ischemic stroke (AIS). Determining whether symptoms are "disabling" or not is a crucial factor in the management of these patients. This study aimed to investigate the efficacy and safety of alteplase in patients with mild, non-disabling AIS.
We included all consecutive patients admitted for AIS at our institution from January 2015 to May 2022 who presented a baseline NIHSS score of 0-5 and fit the criteria to receive intravenous thrombolysis. In order to select only subjects with non-disabling AIS, we excluded patients who scored more than 1 point in the following NIHSS single items: vision, language, neglect, and single limb. Patients who scored at least 1 point in the NIHSS consciousness item were excluded as well. This study is a retrospective analysis of a prospectively collected database.
After the application of the exclusion criteria, we included 319 patients, stratified into patients receiving and not receiving alteplase based on non-disabling symptoms. The two groups were comparable regarding demographic and clinical data. Rates of a 3-month favorable outcome, defined as a 3-month mRS score of 0-1, were similar, being 82.3% and 86.1% in the treated and untreated patients, respectively. Hemorrhagic complications and mortality occurred infrequently and were not affected by alteplase treatment.
This observational study suggests that the use of alteplase, although safe, is not associated with a better outcome in highly selected patients with non-disabling AIS.
对于轻度急性缺血性卒中(AIS)患者,阿替普酶是否有效及安全尚不清楚。确定症状是否“致残”是这些患者管理中的关键因素。本研究旨在调查阿替普酶在轻度、非致残性AIS患者中的疗效和安全性。
我们纳入了2015年1月至2022年5月在我院因AIS入院的所有连续患者,这些患者的基线美国国立卫生研究院卒中量表(NIHSS)评分为0 - 5分且符合接受静脉溶栓的标准。为了仅选择非致残性AIS患者,我们排除了在以下NIHSS单项中得分超过1分的患者:视力、语言、偏侧忽视和单肢。NIHSS意识项得分至少为1分的患者也被排除。本研究是对前瞻性收集的数据库进行的回顾性分析。
应用排除标准后,我们纳入了319例患者,根据非致残症状分为接受和未接受阿替普酶治疗的患者。两组在人口统计学和临床数据方面具有可比性。3个月良好结局的发生率,定义为3个月改良Rankin量表(mRS)评分为0 - 1分,相似,治疗组和未治疗组分别为82.3%和86.1%。出血并发症和死亡率发生率较低,且不受阿替普酶治疗的影响。
这项观察性研究表明,在经过高度筛选的非致残性AIS患者中,使用阿替普酶虽然安全,但并未带来更好的结局。