ATTENTION-IA
Intra-arterial tenecteplase after successful endovascular recanalisation in patients with acute posterior circulation arterial occlusion (ATTENTION-IA): multicentre randomised controlled trial
Clinical Question
Does intra-arterial tenecteplase administered after successful thrombectomy improve clinical outcomes in posterior circulation stroke?
Bottom Line
Intra-arterial tenecteplase after successful thrombectomy for posterior circulation stroke did not significantly improve functional outcomes at 90 days and was associated with a non-significant increase in symptomatic intracranial hemorrhage.
Major Points
- Multicentre, randomized controlled trial of 208 patients with acute posterior circulation stroke and successful endovascular recanalization (eTICI ≥2b50).
- Intra-arterial tenecteplase (0.025 mg/kg) did not significantly increase the proportion of patients with mRS 0–1 at 90 days compared with control (34.6% vs. 26.0%; P=0.12).
- Symptomatic intracranial hemorrhage occurred more often in the tenecteplase group (8.3% vs. 3.1%; RR 2.70, 95% CI 0.76–9.60).
- No significant difference in 90-day mortality (27.9% vs. 26.9%).
- Subgroup analysis suggested a potential benefit in patients with NIHSS 10–19, but not NIHSS ≥20.
Design
Study Type: Multicentre randomized controlled trial
Randomization: 1
Blinding: Open-label with blinded outcome assessment
Enrollment Period: January 24 to August 24, 2023
Follow-up Duration: 90 days
Centers: 31
Countries: China
Sample Size: 208
Analysis: Intention-to-treat and modified intention-to-treat; Poisson regression and ordinal logistic regression (adjusted), using STATA 15.0
Inclusion Criteria
- Age ≥18 years
- NIHSS ≥10
- Acute occlusion of vertebral artery (V4), basilar artery, or P1 segment of PCA
- Successful endovascular recanalization (eTICI ≥2b50)
- Onset-to-recanalization time ≤24 hours
Exclusion Criteria
- Prestroke mRS >1
- Intracranial hemorrhage on imaging before thrombectomy
- pc-ASPECTS <6
- Severe renal or hepatic dysfunction
- Allergy to tenecteplase
Baseline Characteristics
| Characteristic | Control | Active |
|---|---|---|
| Age | 67.3 ± 10.8 | 65.0 ± 11.3 |
| Male | 70.2% | 80.8% |
| NIHSS | 20 (IQR 14–35) | 19 (IQR 12–35) |
| Hypertension | 84.6% | 70.2% |
| Diabetes | 27.9% | 27.9% |
| Received IVT | 24.0% | 26.9% |
Arms
| Field | Tenecteplase | Control |
|---|---|---|
| Intervention | Intra-arterial tenecteplase 0.025 mg/kg (max 2.5 mg) infused over 10 seconds post-thrombectomy | Standard care without additional intra-arterial thrombolytic therapy after thrombectomy |
| Duration | Single administration after recanalization | Standard care |
Outcomes
| Outcome | Type | Control | Intervention | HR / OR / RR | P-value |
|---|---|---|---|---|---|
| Proportion of patients with modified Rankin Scale score 0–1 at 90 days | Primary | 26.0% | 34.6% | RR 1.36 (95% CI 0.92-2.02) | 0.12 |
| Proportion with mRS 0–2 at 90 days | Secondary | 40.4% | 38.5% | 0.76 | |
| Reperfusion (patency on CTA or MRA) at 24–72 hours | Secondary | 91.4% | 90.0% | 0.70 | |
| Symptomatic ICH | Adverse | 3.1% | 8.3% | 2.7 | 0.11 |
| All-cause mortality (90d) | Adverse | 26.9% | 27.9% | 1.04 | 0.85 |
Subgroup Analysis
Subgroup analysis showed a higher proportion of mRS 0–1 in the tenecteplase group among patients with baseline NIHSS 10–19 (RR 1.64, 95% CI 1.02–2.62), but not in those with NIHSS ≥20 (RR 0.75, 95% CI 0.38–1.50)
Criticisms
- Open-label design may introduce bias despite blinded outcome adjudication
- Sample size was relatively small and underpowered for definitive conclusions
- Limited generalizability outside Chinese population
- Numerical baseline imbalance in hypertension
- Lack of perfusion imaging post-intervention to confirm sustained reperfusion
Funding
Funded by Fundamental Research Funds for the Central Universities; sponsor had no role in trial design, data collection, or manuscript writing
Based on: ATTENTION-IA (BMJ, 2025)
Authors: Wei Hu, Chunrong Tao, Li Wang, ..., Xinfeng Liu
Citation: BMJ 2025;388:e080489
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