Shahid Sufyan, Saeed Humza, Iqbal Minahil, Batool Ayesha, Masood Muhammad Bilal, Ahmad Muhammad Husnain, Rehman Aqeeb Ur, Aemaz Ur Rehman Muhammad, Sultan Fahd
Khawaja Muhammad Safdar Medical College, Sialkot, Pakistan.
Rawalpindi Medical University, Rawalpindi, Pakistan.
J Stroke Cerebrovasc Dis. 2025 Mar;34(3):108230. doi: 10.1016/j.jstrokecerebrovasdis.2025.108230. Epub 2025 Jan 9.
Intravenous alteplase (ALT) is the standard treatment for acute ischemic stroke (AIS). However, recent trials comparing other tissue plasminogen activators (tPAs) like tenecteplase (TNK) and reteplase with ALT have yielded conflicting results. This necessitated a network meta-analysis to compare the efficacy and safety of various tPAs in AIS patients.
We searched MEDLINE, Embase, and CENTRAL (until September 15, 2024) for randomized controlled trials (RCTs) comparing TNK or reteplase (any dose) with ALT (0.9 mg/kg) in AIS patients. A frequentist network meta-analysis was performed using risk ratio (RR) and 95 % CI for each comparison, and P-scores ranked treatments. Analyses were done using R Software 4.4.1.
Sixteen RCTs (9259 patients, 62.1 % males) were included. Reteplase 18+18 mg significantly improved excellent functional recovery (mRS 0-1) (RR: 1.13; p < 0.01) and independent ambulation (mRS 0-2) at 3 months (RR: 1.07; p < 0.01) compared to ALT. The 0.25 mg/kg TNK group also showed improved functional recovery (mRS 0-1) (RR: 1.06; p < 0.01). For safety, 0.1 mg/kg TNK was associated with a higher incidence of symptomatic intracranial hemorrhage (s-ICH) (RR: 7.27; p < 0.01). No significant differences in ICH or all-cause mortality were found between ALT and other treatments. Reteplase 18+18 mg ranked highest for functional recovery (P-score=0.9638) and ambulation (P-score=0.9749), while ALT ranked highest for s-ICH (P-score=0.8060). No significant differences were observed between reteplase and TNK.
Reteplase 18+18 mg and TNK 0.25 mg/kg demonstrated higher efficacy and comparable safety to ALT. Larger trials are needed to further explore these agents as alternatives to ALT.
静脉注射阿替普酶(ALT)是急性缺血性卒中(AIS)的标准治疗方法。然而,最近比较其他组织纤溶酶原激活剂(tPA)如替奈普酶(TNK)和瑞替普酶与ALT的试验结果相互矛盾。这就需要进行一项网状Meta分析,以比较各种tPA在AIS患者中的疗效和安全性。
我们检索了MEDLINE、Embase和CENTRAL(截至2024年9月15日),以查找在AIS患者中比较TNK或瑞替普酶(任何剂量)与ALT(0.9mg/kg)的随机对照试验(RCT)。对每次比较使用风险比(RR)和95%置信区间进行频率学派网状Meta分析,并通过P值对治疗进行排序。使用R软件4.4.1进行分析。
纳入了16项RCT(9259例患者,男性占62.1%)。与ALT相比,瑞替普酶18 + 18mg在3个月时显著改善了良好的功能恢复(改良Rankin量表评分0 - 1)(RR:1.13;p < 0.01)和独立行走能力(改良Rankin量表评分0 - 2)(RR:1.07;p < 0.01)。0.25mg/kg的TNK组也显示出功能恢复改善(改良Rankin量表评分0 - 1)(RR:1.06;p < 0.01)。在安全性方面,0.1mg/kg的TNK与症状性颅内出血(s - ICH)的发生率较高相关(RR:7.27;p < 0.01)。在ALT与其他治疗之间,未发现颅内出血或全因死亡率有显著差异。瑞替普酶18 + 18mg在功能恢复(P值 = 0.9638)和行走能力(P值 = 0.9749)方面排名最高,而ALT在s - ICH方面排名最高(P值 = 0.8060)。在瑞替普酶和TNK之间未观察到显著差异。
瑞替普酶18 + 18mg和TNK 0.25mg/kg显示出比ALT更高的疗效和相当的安全性。需要进行更大规模的试验,以进一步探索这些药物作为ALT替代药物的可能性。