Department of Neurology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Eur Rev Med Pharmacol Sci. 2022 Feb;26(3):779-786. doi: 10.26355/eurrev_202202_27986.
To investigate the safety and efficacy of intravenous thrombolysis with recombinant tissue plasminogen activator (rt-PA) in patients with acute ischemic stroke (AIS) and cerebral microbleeds (CMBs) and analyze the risk factors for hemorrhagic transformation (HT).
The clinical data of 220 patients with CMB within the first 4.5 h after the onset of acute ischemic stroke treated in our hospital from September 2018 to December 2019 were retrospectively analyzed. Then, these patients were evenly assigned into two groups based on whether the intravenous thrombolysis with rt-PA was adopted or not. Next, the neurological deficit was scored using the National Institute of Health stroke scale (NIHSS) before and after treatment, the modified Rankin scale (mRs) score of patients was recorded at 90 d after treatment, and the incidence rate and death rate of intracranial hemorrhage (ICH) after treatment were recorded and evaluated. Additionally, the univariate and logistic regression analyses were employed for the risk factors for HT in patients after thrombolysis.
The NIHSS score declined to (7.08±3.75) points and (7.83±4.22) points at 24 h after treatment and (3.67±3.63) points and (4.92±3.87) points at 7 d after treatment, respectively, in Thrombolysis group and Control group, which were significantly lower than those before treatment (p<0.05). The NIHSS score displayed no statistically significant difference between the two groups at 24 h after treatment (p=0.165), whereas it was markedly lower in Thrombolysis group than that in Control group at 7 d after treatment (p=0.015). At 90 d after treatment, there were 98 (89.1%) and 79 (71.8%) cases of good prognosis in Thrombolysis group and Control group, respectively, and the difference was statistically significant between the two groups (p=0.002). Besides, the number of patients with SICH and aSICH was 3 and 2 (2.7% vs. 1.8%, p=0.651) and 9 and 4 (8.2% vs. 3.6%, p=0.152) in Thrombolysis group and Control group, respectively, and the number of deaths was 7 and 5 (6.4% vs. 4.5%, p=0.553) in the two groups, showing no statistically significant difference. The results of univariate and multivariate analyses revealed that the time from stroke onset to thrombolysis, baseline NIHSS score, and history of atrial fibrillation were independent risk factors affecting the HT of patients undergoing intravenous thrombolysis [odds ratio (OR) =1.330, 95% confidence interval (95% CI) =1.079-1.851, p=0.019; OR=1.592, 95% CI=1.025-2.767, p=0.010; OR=2.428, 95% CI=1.814-3.643, p=0.016].
Compared with those undergoing no intravenous thrombolysis with rt-PA, patients with acute ischemic stroke and CMB who received intravenous thrombolysis with rt-PA exhibit significantly improved short-term neurological function recovery and long-term prognosis, but the incidence and mortality rates of ICH have no statistically significant differences. Moreover, the time from stroke onset to thrombolysis, baseline NIHSS score, and history of atrial fibrillation are independent risk factors affecting the HT of patients treated with intravenous thrombolysis.
探讨重组组织型纤溶酶原激活剂(rt-PA)静脉溶栓治疗急性缺血性脑卒中(AIS)合并脑微出血(CMB)患者的安全性和有效性,并分析出血转化(HT)的危险因素。
回顾性分析 2018 年 9 月至 2019 年 12 月我院收治的 220 例 CMB 发病 4.5 h 内的患者的临床资料,根据是否采用重组组织型纤溶酶原激活剂静脉溶栓治疗将患者分为两组,分别为溶栓组和对照组。治疗前后采用美国国立卫生研究院卒中量表(NIHSS)评分评估神经功能缺损程度,治疗后 90 d 采用改良 Rankin 量表(mRs)评分评估患者的预后,记录并评估治疗后颅内出血(ICH)的发生率和死亡率。采用单因素和 Logistic 回归分析影响溶栓后 HT 的危险因素。
溶栓组和对照组治疗后 24 h 的 NIHSS 评分分别下降至(7.08±3.75)分和(7.83±4.22)分,治疗后 7 d 的 NIHSS 评分分别下降至(3.67±3.63)分和(4.92±3.87)分,均明显低于治疗前(P<0.05)。治疗后 24 h 两组 NIHSS 评分比较差异无统计学意义(P=0.165),但治疗后 7 d 溶栓组 NIHSS 评分明显低于对照组(P=0.015)。治疗后 90 d 时,溶栓组和对照组的预后良好率分别为 89.1%(98/110)和 71.8%(79/110),两组比较差异有统计学意义(P=0.002)。溶栓组和对照组 SICH 和 aSICH 发生率分别为 2.7%(3/110)和 1.8%(2/110)(P=0.651)、8.2%(9/110)和 3.6%(4/110)(P=0.152),死亡率分别为 6.4%(7/110)和 4.5%(5/110)(P=0.553),两组比较差异均无统计学意义。单因素和多因素分析结果显示,发病至溶栓时间、基线 NIHSS 评分和心房颤动史是影响溶栓患者 HT 的独立危险因素[比值比(OR)=1.330,95%置信区间(95%CI)=1.079-1.851,P=0.019;OR=1.592,95%CI=1.025-2.767,P=0.010;OR=2.428,95%CI=1.814-3.643,P=0.016]。
与未接受 rt-PA 静脉溶栓治疗的患者相比,接受 rt-PA 静脉溶栓治疗的急性缺血性脑卒中合并 CMB 患者短期神经功能恢复和长期预后明显改善,但 ICH 的发生率和死亡率无统计学差异。此外,发病至溶栓时间、基线 NIHSS 评分和心房颤动史是影响溶栓患者 HT 的独立危险因素。