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Updated: Jul 24, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
Thrombolytic Therapy for Central Retinal Artery Occlusion in an Academic Multi-Site Stroke Centre
Nour Alhayek1, Jacob M Sobczak1, Aimen Vanood1
1Department of Neurology, Mayo Clinic College of Medicine and Science, Scottsdale, Arizona, USA.
Insights
Central retinal artery occlusion (CRAO) treatment with thrombolysis showed varied outcomes. This study found no significant visual acuity benefit compared to conservative care, suggesting a need for randomized trials.
Area of Science:
- Ophthalmology
- Neurology
- Vascular Medicine
Background:
- Central retinal artery occlusion (CRAO) is a critical condition causing severe vision loss, often treated as an acute ischemic stroke.
- Recent guidelines suggest time-windows for thrombolysis in CRAO, mirroring acute cerebral stroke protocols.
Purpose of the Study:
- To review the academic stroke center's experience with intravenous (IVT) and intra-arterial thrombolysis (IAT) for CRAO.
- To compare visual acuity outcomes in thrombolysed CRAO patients versus a matched conservative therapy cohort.
Main Methods:
- Retrospective review of CRAO patients treated between 1997 and 2022.
- Collected demographic, clinical, thrombolysis timeline, and concurrent therapy data.
- Compared 3-month visual acuity between thrombolysed and conservatively treated patients.
Main Results:
- Thrombolysis was given to 3.55% of CRAO admissions (20 patients: 13 IVT, 7 IAT).
- IVT achieved ≥2 Snellen lines improvement in 25%; IAT in 42%. Intracranial hemorrhage occurred in 7.6% of IVT cases.
- No significant difference in 3-month visual acuity was found between thrombolysis and conservative therapy groups.
Conclusions:
- Acute CRAO management remains heterogeneous.
- Thrombolysis did not demonstrate a clear benefit in this series, highlighting the need for randomized trials.
- Further research is required to establish optimal hyperacute CRAO management strategies.
Abstract:
Central retinal artery occlusion (CRAO) is a subtype of acute ischaemic stroke leading to severe visual loss. A recent American Heart Association scientific statement proposed time-windows for thrombolysis in CRAO similar to acute ischaemic cerebral strokes. We aimed to review our academic multi-site stroke centre experience with intravenous (IVT) and intra-arterial thrombolysis (IAT) in CRAO between 1997 and 2022. Demographic, clinical characteristics, thrombolysis timeline, concurrent therapies, complications, and 3-month follow-up visual acuity (VA) were collected. The thrombolysed cohort follow-up VA was compared with an age, gender and baseline VA matched cohort of CRAO patients that received conservative therapies. Thrombolytic therapy was administered to 3.55% (n = 20) of CRAO admissions; 13 IVT (mean age 68, 61.5% male, 12 alteplase and 1 tenecteplase, all embolic aetiology, 1 CRAO mimic) and 7 IAT (mean age 55, 85.7% male, 3 post-operative and 3 embolic). Additional conservative CRAO-targeting therapies was received by 60%. The median time from onset of visual loss to IVT was 158 minutes (range 67-260). Improvement by at least two Snellen lines was achieved by 25% with 12.5% improving to 20/100 or better. Intracranial haemorrhage post IVT occurred in 1/13 (7.6%). The median time from onset of visual loss to IAT was 335 minutes. Improvement by at least two Snellen lines was achieved by 42%. No difference in 3-month VA was noted between patients that received thrombolysis, either alone (n = 8) or combined with other therapies, and those that received conservative therapies. Our results suggest that the management of acute CRAO remains heterogeneous. The lack of obvious benefit of thrombolysis in our small series supports the need for randomizsd clinical trials comparing thrombolysis to placebo to guide hyperacute CRAO management.
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