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  3. Early Thrombolysis and Outcomes in Central Retinal Artery Occlusion: An Individual Participant Data Meta-Analysis.
 

Early Thrombolysis and Outcomes in Central Retinal Artery Occlusion: An Individual Participant Data Meta-Analysis.

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BORIS DOI
10.48620/90914
Publisher DOI
10.1161/STROKEAHA.124.049955
PubMed ID
40832714
Description
Background
This individual participant data meta-analysis aimed to determine whether time to treatment influences the effect of intraarterial thrombolysis (IAT), intravenous thrombolysis, and conservative standard therapy on visual outcomes in nonarteritic central retinal artery occlusion.Methods
We searched MEDLINE, CENTRAL, and Embase up to June 2023 for studies reporting treatment modality and peri-treatment best-corrected visual acuity (BCVA) for ≥5 participants, excluding patients with nonsevere vision loss (BCVA <1.0 logarithm of the minimum angle of resolution [logMAR]) or treated after 24 hours of symptom onset. The primary outcome was recovery from severe vision loss (final BCVA <1.0 logMAR). We used mixed-effect models and local polynomial regression to investigate nonlinear relationships between time to treatment and recovery from severe vision loss.Results
Of 4074 screened studies, individual participant data were sought from 52, with 35 contributing individual participant data for 1038 participants. In total, 783 patients met inclusion criteria (age, 64.8±13.3 years; 35.5% female; baseline BCVA, 2.3±0.5 logMAR). For every hour decrease in time to treatment, thrombolysis was associated with greater improvement in BCVA (intraarterial, 0.02 logMAR [95% CI, 0-0.04]; intravenous, 0.04 logMAR [95% CI, 0.00-0.07]) than conservative standard therapy (0.01 logMAR [95% CI, 0-0.02]). A nonlinear relationship was detected for intraarterial thrombolysis with a changepoint at 8 hours (95% CI, 6.7-9.4). Thrombolysis was associated with increased recovery from severe vision loss compared with conservative standard therapy (intraarterial within 6 hours: odds ratio, 2.72 [95% CI, 1.02-7.28], 27.2% versus 12.0%; intravenous within 4.5 hours: odds ratio, 3.32 [95% CI, 1.24-8.92], 28.8% versus 11.1%). Findings were consistent in subgroup analysis restricted to patients receiving recombinant tissue-type plasminogen activator. Monte-Carlo simulations showed that a randomized controlled trial would require 95 participants per group to achieve 80% power to detect an odds ratio of 3.0 for recovery from severe vision loss.Conclusions
Early intervention in nonarteritic central retinal artery occlusion is associated with improvement in visual recovery, with intraarterial thrombolysis and intravenous thrombolysis outperforming nonthrombolytic treatments. These findings warrant confirmation in sufficiently powered randomized controlled trials.
Date of Publication
2025-11
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
odds ratio
•
perfusion
•
plasminogen
•
retinal artery
•
visual acuity
Language(s)
en
Contributor(s)
Xie, Jim S
Zaslavsky, Kirill
Chaban, Yuri
Lusterio, Adrien
Kaur, Hargun
Motekalem, Yasmin
Zeraatkar, Dena
Popovic, Marko M
Althaus, Katharina
Malbin, Brett
Nolte, Christian H
Scheitz, Jan F
Pettersen, Jacqueline A
Leker, Ronen R
Kim, Joonhyung
Woo, Se Joon
Chen, Celia
Feltgen, Nicolas
Khrlobyan, Manya
Sangha, Navdeep
Jurado, Elena A
Arnold, Marcel
Clinic of Neurology
Mattle, Heinrich
Heldner, Mirjam R.orcid-logo
Clinic of Neurology
Nedelmann, Max G
Cordonnier, Charlotte
Spitzer, Martin S
Poli, Sven
Hametner, Christian
Baumgartner, Philipp
Wegener, Susanne
Kook, Lucas
Shahjouei, Shima
Dumitrascu, Oana M
Margolin, Edward
Additional Credits
Clinic of Neurology
Series
Stroke
Publisher
Lippincott, Williams & Wilkins
ISSN
1524-4628
0039-2499
Access(Rights)
restricted
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