Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion

Ethan K Sobol,1,2 Yu Sakai,3 Danielle Wheelwright,3 Carl S Wilkins,1,2 Amanda Norchi,1 Michael G Fara,4 Christopher Kellner,3 James Chelnis,1 J Mocco,3 Richard B Rosen,1,2 Reade A De Leacy,3 Gareth MC Lema1,2 1Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029,...

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Autores principales: Sobol EK, Sakai Y, Wheelwright D, Wilkins CS, Norchi A, Fara MG, Kellner C, Chelnis J, Mocco J, Rosen RB, De Leacy RA, Lema GMC
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Lenguaje:EN
Publicado: Dove Medical Press 2021
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spelling oai:doaj.org-article:45d940185dcb4e41b4535cf9257d49dd2021-12-02T14:12:25ZIntra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion1177-5483https://doaj.org/article/45d940185dcb4e41b4535cf9257d49dd2021-02-01T00:00:00Zhttps://www.dovepress.com/intra-arterial-tissue-plasminogen-activator-for-central-retinal-artery-peer-reviewed-article-OPTHhttps://doaj.org/toc/1177-5483Ethan K Sobol,1,2 Yu Sakai,3 Danielle Wheelwright,3 Carl S Wilkins,1,2 Amanda Norchi,1 Michael G Fara,4 Christopher Kellner,3 James Chelnis,1 J Mocco,3 Richard B Rosen,1,2 Reade A De Leacy,3 Gareth MC Lema1,2 1Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA; 2Department of Ophthalmology, New York Eye and Ear Infirmary of Mount Sinai, New York, NY, 10003, USA; 3Department of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA; 4Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USACorrespondence: Gareth MC LemaDepartment of Ophthalmology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USATel +1 212-241-0939Fax +1 212-824-2325Email gareth.lema@mssm.eduPurpose: To investigate the benefit of early intra-arterial tissue plasminogen activator (IAT) for treatment of central retinal artery occlusion (CRAO).Patients and Methods: Fifteen eyes of 15 patients presenting with acute CRAO were included in this retrospective consecutive interventional case series. Patients were excluded if treatment with IAT was not initiated within 12 hours. The diagnosis was confirmed by an ophthalmologist. IAT was performed via a transfemoral arterial approach. Tissue plasminogen activator (tPA) was infused into the ophthalmic artery in aliquots up to 3mg to a maximum of 22mg. Paracentesis was done at the ophthalmologist’s discretion. The primary outcome measure was visual acuity after three weeks. Adverse events were recorded during treatment and follow-up visits.Results: After treatment with IAT, there was a statistically significant improvement in visual acuity, with a mean change of − 0.76 (SD 0.91; range − 2.4 to 0.85) logMAR (p=0.006). Vision improved by 3 or more lines in 53%, and of these, the mean Snellen visual acuity improvement was > 6 lines. Notably, 4 patients (27%) improved from CF or worse to 20/80 or better. The mean dose of tPA used was 17mg and the mean time to treatment was 8.83 hours (range: 5.5 to 12 hours). There were no statistically significant differences based on time to treatment, dose of tPA, or use of a paracentesis. No major adverse events were recorded.Conclusion: IAT was safe and showed significant visual improvement in this small uncontrolled study. Larger studies and efforts to decrease time to treatment should be initiated to optimize outcomes.Keywords: CRAO, tPA, intervention, treatment, ophthalmic arterySobol EKSakai YWheelwright DWilkins CSNorchi AFara MGKellner CChelnis JMocco JRosen RBDe Leacy RALema GMCDove Medical Pressarticlecraotpainterventiontreatmentophthalmic arteryOphthalmologyRE1-994ENClinical Ophthalmology, Vol Volume 15, Pp 601-608 (2021)
institution DOAJ
collection DOAJ
language EN
topic crao
tpa
intervention
treatment
ophthalmic artery
Ophthalmology
RE1-994
spellingShingle crao
tpa
intervention
treatment
ophthalmic artery
Ophthalmology
RE1-994
Sobol EK
Sakai Y
Wheelwright D
Wilkins CS
Norchi A
Fara MG
Kellner C
Chelnis J
Mocco J
Rosen RB
De Leacy RA
Lema GMC
Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion
description Ethan K Sobol,1,2 Yu Sakai,3 Danielle Wheelwright,3 Carl S Wilkins,1,2 Amanda Norchi,1 Michael G Fara,4 Christopher Kellner,3 James Chelnis,1 J Mocco,3 Richard B Rosen,1,2 Reade A De Leacy,3 Gareth MC Lema1,2 1Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA; 2Department of Ophthalmology, New York Eye and Ear Infirmary of Mount Sinai, New York, NY, 10003, USA; 3Department of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA; 4Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USACorrespondence: Gareth MC LemaDepartment of Ophthalmology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USATel +1 212-241-0939Fax +1 212-824-2325Email gareth.lema@mssm.eduPurpose: To investigate the benefit of early intra-arterial tissue plasminogen activator (IAT) for treatment of central retinal artery occlusion (CRAO).Patients and Methods: Fifteen eyes of 15 patients presenting with acute CRAO were included in this retrospective consecutive interventional case series. Patients were excluded if treatment with IAT was not initiated within 12 hours. The diagnosis was confirmed by an ophthalmologist. IAT was performed via a transfemoral arterial approach. Tissue plasminogen activator (tPA) was infused into the ophthalmic artery in aliquots up to 3mg to a maximum of 22mg. Paracentesis was done at the ophthalmologist’s discretion. The primary outcome measure was visual acuity after three weeks. Adverse events were recorded during treatment and follow-up visits.Results: After treatment with IAT, there was a statistically significant improvement in visual acuity, with a mean change of − 0.76 (SD 0.91; range − 2.4 to 0.85) logMAR (p=0.006). Vision improved by 3 or more lines in 53%, and of these, the mean Snellen visual acuity improvement was > 6 lines. Notably, 4 patients (27%) improved from CF or worse to 20/80 or better. The mean dose of tPA used was 17mg and the mean time to treatment was 8.83 hours (range: 5.5 to 12 hours). There were no statistically significant differences based on time to treatment, dose of tPA, or use of a paracentesis. No major adverse events were recorded.Conclusion: IAT was safe and showed significant visual improvement in this small uncontrolled study. Larger studies and efforts to decrease time to treatment should be initiated to optimize outcomes.Keywords: CRAO, tPA, intervention, treatment, ophthalmic artery
format article
author Sobol EK
Sakai Y
Wheelwright D
Wilkins CS
Norchi A
Fara MG
Kellner C
Chelnis J
Mocco J
Rosen RB
De Leacy RA
Lema GMC
author_facet Sobol EK
Sakai Y
Wheelwright D
Wilkins CS
Norchi A
Fara MG
Kellner C
Chelnis J
Mocco J
Rosen RB
De Leacy RA
Lema GMC
author_sort Sobol EK
title Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion
title_short Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion
title_full Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion
title_fullStr Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion
title_full_unstemmed Intra-Arterial Tissue Plasminogen Activator for Central Retinal Artery Occlusion
title_sort intra-arterial tissue plasminogen activator for central retinal artery occlusion
publisher Dove Medical Press
publishDate 2021
url https://doaj.org/article/45d940185dcb4e41b4535cf9257d49dd
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