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January 16, 2026Clinical and Applied Thrombosis/Hemostasis2 citationsOpen Access

Efficacy and Safety of Intravenous Thrombolytics in Ischemic Stroke Beyond the 4.5-Hour Time Window: A Systematic Review and Meta-Analysis

MWMuhammad Hassan WaseemZAZain ul AbideenDGDua Ghori

Key Result

Intravenous thrombolytics administered beyond 4.5 hours for acute ischemic stroke improved excellent functional outcomes (RR 1.22; 95% CI 1.13-1.31) but increased the risk of symptomatic ICH.

Key Points

  • This meta-analysis evaluates the effectiveness and safety of intravenous thrombolytics administered beyond the traditional 4.5-hour window in ischemic stroke.
  • Systematic review of randomized trials
  • Literature search on PubMed, Cochrane, and ScienceDirect
  • Pooled analysis of risk ratios using a random effects model
  • IV thrombolytics significantly improved excellent functional outcomes (RR = 1.22) and good outcomes (RR = 1.11) compared to control.
  • Increased risk of symptomatic intracranial hemorrhage (RR = 2.28) and any intracranial hemorrhage (RR = 1.22).
  • Mortality rates showed no significant difference (RR = 1.10).

Study Design

Type

Meta-Analysis (n=3,602)

Structured PICO

Do intravenous thrombolytics administered beyond the 4.5-hour time window improve functional outcomes in patients with acute ischemic stroke?

P
Population
3,602 patients with acute ischemic stroke from 13 randomized trials evaluating intravenous thrombolytics administered beyond the 4.5-hour window.
I
Intervention
Intravenous thrombolytics (tenecteplase or alteplase) administered beyond the 4.5-hour time window.
C
Comparator
Control group
O
Outcome
Excellent and good functional outcomeshard clinical

Intravenous thrombolytics administered beyond the 4.5-hour window in acute ischemic stroke improve functional outcomes but carry a significantly higher risk of symptomatic intracranial hemorrhage.

Main Result

Relative Risk: 1.22 (95% CI 1.13–1.31)

p-value: p=<0.00001

Abstract

Background Stroke significantly impacts global health, and IV thrombolytics such as tenecteplase and alteplase are time sensitive. While they show promise beyond 4.5 h, evidence is inconclusive. This meta-analysis assesses IVT's efficacy and safety past 4.5 h. Methods PubMed, Cochrane Central, and ScienceDirect were searched till August 2025. The risk ratios (RR) were pooled along with 95% confidence intervals under the random effect model using the Review Manager version 5.4.1. Results Thirteen randomized trials involving 3602 patients were analyzed. Compared to the control group, IVT significantly improved the rates of excellent (RR = 1.22; 95%CI: 1.13, 1.31;p < 0.00001; I 2 = 0%) and good (RR = 1.11; 95%CI: 1.06, 1.18;p < 0.0001; I 2 = 0%) functional outcomes. However, the risk of symptomatic (RR = 2.28; 95%CI:1.35, 3.85;p = 0.002; I 2 = 0%) and any (RR = 1.22; 95%CI:1.01, 1.46;p = 0.04; I 2 = 13%) intracranial hemorrhage (ICH) was also higher with IVT; mortality rates, however, showed no significant difference (RR = 1.10; 95%CI:0.89, 1.36;p = 0.35). TNK at 0.25 mg/kg did not improve functional outcomes or increase the risk of ICH. Similarly, low-dose 0.60 mg/kg alteplase did not significantly enhance functional outcomes or raise the risk of ICH, while alteplase at 0.90 mg/kg showed results consistent with the overall IVT group. Conclusion IVT administered beyond the 4.5-h window in acute ischemic stroke significantly improved excellent and good functional outcomes. Although the use of IVT was associated with a higher risk of symptomatic and any ICH, the mortality rates remained comparable. Further high-quality randomized trials are necessary to confirm and reinforce these results.

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Cite This Study

Waseem et al. (2026) conducted a meta-analysis in Acute ischemic stroke (n=3,602). Intravenous Thrombolytics vs. Control was evaluated on Excellent functional outcomes (RR 1.22, 95% CI 1.13-1.31, p=<0.00001). Intravenous thrombolytics administered beyond 4.5 hours for acute ischemic stroke improved excellent functional outcomes (RR 1.22; 95% CI 1.13-1.31) but increased the risk of symptomatic ICH.

synapsesocial.com/papers/6969d488940543b977709610https://doi.org/10.1177/10760296251414133
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