Key result
Higher SBP above 110 mmHg linked to ~2% higher ICH risk per mmHg with tenecteplase.
Why the study?
Intracranial haemorrhage is a significant complication of fibrinolytic therapy for STEMI, and risk factors following tenecteplase administration were not fully characterized.
What are the clinical risk factors for intracranial haemorrhage following tenecteplase administration in patients with STEMI?
Meta-Analysis (n=15,954)
Yes
What are the clinical risk factors for intracranial haemorrhage following tenecteplase administration in patients with STEMI?
Odds Ratio: 1.02 (95% CI 1.01–1.03)
p-value: p=<.0001
Dose reduction of tenecteplase in older patients and strict optimization of systolic blood pressure prior to administration may reduce the risk of intracranial haemorrhage in STEMI patients.
Strict pre-tenecteplase SBP control below 110 mmHg may reduce ICH risk in STEMI; extends meta-analytic support for BP optimization in thrombolysis.
BACKGROUND AND AIMS: Intracranial haemorrhage (ICH) is a significant complication of fibrinolytic therapy for ST-elevation myocardial infarction (STEMI). The risk factors for ICH following tenecteplase (TNK) administration were evaluated, and a clinical risk prediction tool was developed. METHODS: A pooled individual patient data analysis from STEMI patients who received weight-adjusted TNK with a consistent blood pressure exclusion criterion of >180/110 mmHg in six randomized controlled trials (ASSENT-2, ASSENT-3, ASSENT-3 PLUS, ASSENT-4 PCI, STREAM, STREAM-2) was undertaken. Logistic regression was used to model risk factors, and a nomogram was developed for individual risk prediction. RESULTS: Among 15 954 patients, 169 developed ICH. Above a systolic blood pressure (SBP) threshold of 110 mmHg, each 1 mmHg increase conferred a 2% relative increase in ICH risk [adjusted odds ratio (aOR) 1.02, 95% confidence interval (CI) 1.01-1.03; P < .0001]; risk accelerated sharply beyond 160 mmHg. With increasing dose, the likelihood of ICH increased with age, rising from 1% per year (30 mg TNK) to nearly 7% per year with 50 mg. The multivariable model incorporating age, sex, SBP, body weight, and TNK dose with the age-dose interaction demonstrated good discrimination (C index 0.718; 95% CI 0.68-0.76). Female sex conferred a 49% increased ICH risk (aOR 1.49, 95% CI 1.06-2.11; P = .023), and each 5 kg decrease in body weight was associated with 16% increased odds of ICH (aOR 1.16, 95% CI 1.03-1.30; P = .014). CONCLUSIONS: Dose reduction of TNK in older patients and SBP optimization before fibrinolytic administration represent modifiable strategies to potentially reduce ICH.
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Armstrong et al. (2026) conducted a meta-analysis in ST-elevation myocardial infarction (STEMI) (n=15,954). Higher systolic blood pressure (>110 mmHg) vs. Lower systolic blood pressure was evaluated on Intracranial haemorrhage (ICH) (aOR 1.02, 95% CI 1.01-1.03, p=<.0001). In STEMI patients receiving tenecteplase, each 1 mmHg increase in systolic blood pressure >110 mmHg significantly increased the risk of intracranial haemorrhage (aOR 1.02; 95% CI 1.01-1.03; P<.0001).
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