Department of Emergency, Can Tho S.I.S General Hospital, Can Tho, Vietnam.
Eur Rev Med Pharmacol Sci. 2023 Jul;27(14):6554-6562. doi: 10.26355/eurrev_202307_33126.
Globally, there are more than six million deaths due to cerebrovascular disease, which is the second leading cause of death. Although the imaging findings of magnetic resonance imaging (MRI) are more accurate than computed tomography for acute ischemic stroke (AIS), it is uncommon in recombinant tissue plasminogen activator (rTPA) treatment. Alteplase is not only strongly recommended treatment for acute ischemic stroke within 4.5 hours, but also decreases the disability and mortality rate. Besides, low-dose rTPA was associated with significant reductions in symptomatic intracerebral hemorrhage (sICH), compared with standard one. However, the benefits of low-dose rTPA for the treatment of AIS without large vessel occlusion (LVO) have not been fully demonstrated. We evaluated whether the low-dose rTPA in AIS without LVO could improve prognosis in patients three months post-treatment.
This was a cross-sectional study on patients with AIS treated within 4.5 hours of symptom onset admitted to Can Tho S.I.S General Hospital between February 2019 and July 2021. The eligibility criteria were patients aged > 18 years treated with low-dose rTPA (0.6 mg/kg) and screened by 3T MRI. Patients with a pre-hospital modified Rankin score (mRS) ≥ 2 points, intracranial hemorrhage, LVO, or ≥ 3 microbleeds on brain MRI were excluded. The primary outcomes were the favorable outcome rate at three months and safety, which were evaluated by the rates of intracranial hemorrhage and mortality at three months.
This study enrolled 92 eligible patients between February 2019 and July 2021. Their National Institute of Health Stroke Scale (NIHSS) scores were 7.5 ± 3.7 at admission, 3.3 ± 3.5 at discharge or seven days after discharge, and 2.2 ± 2.8 at three months. Their mRS were 2.9 ± 0.8 at admission, 1.4 ± 1.3 at discharge or seven days after discharge, and 1.1 ± 1.1 at three months. Elevated cardiac enzymes, age ≥ 75 years, and body mass index ≥ 25 were associated with increased poor outcomes at three months. While AIS was more common in men than women, a similar number of men (33.3%) and women had poor mRS. Three patients had complications associated with low-dose rTPA treatment: one (1.1%) had intracranial hemorrhage, one (1.1%) had new infarcts, and one (1.1%) had gastrointestinal bleeding. No deaths occurred within three months.
Our study indicates the efficacy and safety of low-dose rTPA treatment for AIS without LVO within 4.5 hours. Patient selection for rTPA by 3T MRI decreased complications and mortality.
在全球范围内,有超过 600 万人死于脑血管疾病,这是第二大致死原因。尽管磁共振成像(MRI)的影像学发现比急性缺血性脑卒中(AIS)的计算机断层扫描更准确,但在重组组织型纤溶酶原激活剂(rTPA)治疗中并不常见。阿替普酶不仅强烈推荐用于发病 4.5 小时内的急性缺血性脑卒中治疗,还可降低残疾和死亡率。此外,与标准剂量相比,低剂量 rTPA 与症状性颅内出血(sICH)的显著减少相关。然而,低剂量 rTPA 治疗无大血管闭塞(LVO)的 AIS 的益处尚未得到充分证实。我们评估了无 LVO 的 AIS 患者接受低剂量 rTPA 治疗后三个月的预后是否会得到改善。
这是一项在 2019 年 2 月至 2021 年 7 月期间就诊于芹苴市 S.I.S 综合医院、发病 4.5 小时内接受治疗的 AIS 患者的横断面研究。入选标准为年龄>18 岁、接受低剂量 rTPA(0.6mg/kg)治疗且经 3T MRI 筛选的患者。排除发病前改良 Rankin 量表(mRS)评分≥2 分、颅内出血、LVO 或脑 MRI 上有≥3 个微出血的患者。主要结局是三个月时的良好预后率和安全性,通过三个月时的颅内出血率和死亡率来评估。
本研究纳入了 2019 年 2 月至 2021 年 7 月间的 92 名符合条件的患者。他们的入院时美国国立卫生研究院卒中量表(NIHSS)评分为 7.5±3.7,出院时或出院后 7 天为 3.3±3.5,三个月时为 2.2±2.8。入院时 mRS 评分为 2.9±0.8,出院时或出院后 7 天为 1.4±1.3,三个月时为 1.1±1.1。心脏酶升高、年龄≥75 岁和体重指数≥25 与三个月时预后不良相关。AIS 患者中男性多于女性,但男性和女性的 mRS 预后不良比例相似,分别为 33.3%和 33.3%。有 3 例患者出现与低剂量 rTPA 治疗相关的并发症:1 例(1.1%)发生颅内出血,1 例(1.1%)发生新梗死,1 例(1.1%)发生胃肠道出血。三个月内无死亡病例。
本研究表明,发病 4.5 小时内接受低剂量 rTPA 治疗无 LVO 的 AIS 安全有效。通过 3T MRI 选择 rTPA 治疗可降低并发症和死亡率。