Cargando…

Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity

AIM: This study aimed to assess the diagnostic ramifications of vascular occlusion of the ocular vein and artery as a first thrombotic event associated with factor V Leiden (FVL) and/or prothrombin gene (PTG) heterozygosity. METHODS: Patients with ocular vein (n=191) and artery (n=74) occlusion, fre...

Descripción completa

Detalles Bibliográficos
Autores principales: Schockman, Samantha, Glueck, Charles J, Hutchins, Robert K, Patel, Jaykumar, Shah, Parth, Wang, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396423/
https://www.ncbi.nlm.nih.gov/pubmed/25897198
http://dx.doi.org/10.2147/OPTH.S80714
_version_ 1782366577518182400
author Schockman, Samantha
Glueck, Charles J
Hutchins, Robert K
Patel, Jaykumar
Shah, Parth
Wang, Ping
author_facet Schockman, Samantha
Glueck, Charles J
Hutchins, Robert K
Patel, Jaykumar
Shah, Parth
Wang, Ping
author_sort Schockman, Samantha
collection PubMed
description AIM: This study aimed to assess the diagnostic ramifications of vascular occlusion of the ocular vein and artery as a first thrombotic event associated with factor V Leiden (FVL) and/or prothrombin gene (PTG) heterozygosity. METHODS: Patients with ocular vein (n=191) and artery (n=74) occlusion, free of cardioembolic etiologies, were sequentially referred from vitreoretinal specialists for measurement of thrombophilia-hypofibrinolysis and compared to 110 healthy normal controls. RESULTS: Of the 265 patients, 29 (11%; 17 women, 12 men) of all referred ocular vascular occlusion (OVO) cases were found to be heterozygous for FVL and/or PTG, including 16 with FVL, 12 with PTG, and 1 with both. Of the 29 cases, 16 had central retinal vein occlusion (CRVO), 2 branch retinal vein occlusion (BRVO), 5 nonarteritic anterior ischemic optic neuropathy (NA-AION), 3 retinal artery occlusion (RAO), 2 amaurosis fugax (AF), and 1 had both CRVO and RAO. Of the 16 FVL cases, 15 (94%) had OVO as a first thrombotic event without prior deep venous thrombosis (DVT) or pulmonary embolism (PE); 6 (38%) also had other thrombotic events, including recurrent miscarriage, osteonecrosis, ischemic stroke, and/or ischemic colitis; and 5 (31%) had immediate family members with previous venous thromboembolism (VTE). Of the 12 PTG cases, 9 (75%) had OVO as a first thrombotic event, 5 (42%) experienced VTE other than DVT or PE, and 6 (50%) had immediate family members with VTE. In one patient with both FVL and PTG, DVT occurred before BRVO. Of the 17 women with FVL and/or PTG mutations, 7 (41%) experienced ≥1 miscarriage, 6 (35%) were on estrogen therapy, and 1 (6%) was on clomiphene. CONCLUSION: Of the 265 patients with OVO, 29 (11%) had FVL and/or PTG, and 83% of these 29 cases presented with OVO as their first thrombotic event. By diagnosing thrombophilia as an etiology for OVO, the ophthalmologist opens a window to family screening and preventive therapy.
format Online
Article
Text
id pubmed-4396423
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-43964232015-04-20 Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity Schockman, Samantha Glueck, Charles J Hutchins, Robert K Patel, Jaykumar Shah, Parth Wang, Ping Clin Ophthalmol Original Research AIM: This study aimed to assess the diagnostic ramifications of vascular occlusion of the ocular vein and artery as a first thrombotic event associated with factor V Leiden (FVL) and/or prothrombin gene (PTG) heterozygosity. METHODS: Patients with ocular vein (n=191) and artery (n=74) occlusion, free of cardioembolic etiologies, were sequentially referred from vitreoretinal specialists for measurement of thrombophilia-hypofibrinolysis and compared to 110 healthy normal controls. RESULTS: Of the 265 patients, 29 (11%; 17 women, 12 men) of all referred ocular vascular occlusion (OVO) cases were found to be heterozygous for FVL and/or PTG, including 16 with FVL, 12 with PTG, and 1 with both. Of the 29 cases, 16 had central retinal vein occlusion (CRVO), 2 branch retinal vein occlusion (BRVO), 5 nonarteritic anterior ischemic optic neuropathy (NA-AION), 3 retinal artery occlusion (RAO), 2 amaurosis fugax (AF), and 1 had both CRVO and RAO. Of the 16 FVL cases, 15 (94%) had OVO as a first thrombotic event without prior deep venous thrombosis (DVT) or pulmonary embolism (PE); 6 (38%) also had other thrombotic events, including recurrent miscarriage, osteonecrosis, ischemic stroke, and/or ischemic colitis; and 5 (31%) had immediate family members with previous venous thromboembolism (VTE). Of the 12 PTG cases, 9 (75%) had OVO as a first thrombotic event, 5 (42%) experienced VTE other than DVT or PE, and 6 (50%) had immediate family members with VTE. In one patient with both FVL and PTG, DVT occurred before BRVO. Of the 17 women with FVL and/or PTG mutations, 7 (41%) experienced ≥1 miscarriage, 6 (35%) were on estrogen therapy, and 1 (6%) was on clomiphene. CONCLUSION: Of the 265 patients with OVO, 29 (11%) had FVL and/or PTG, and 83% of these 29 cases presented with OVO as their first thrombotic event. By diagnosing thrombophilia as an etiology for OVO, the ophthalmologist opens a window to family screening and preventive therapy. Dove Medical Press 2015-04-03 /pmc/articles/PMC4396423/ /pubmed/25897198 http://dx.doi.org/10.2147/OPTH.S80714 Text en © 2015 Schockman et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Schockman, Samantha
Glueck, Charles J
Hutchins, Robert K
Patel, Jaykumar
Shah, Parth
Wang, Ping
Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity
title Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity
title_full Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity
title_fullStr Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity
title_full_unstemmed Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity
title_short Diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor V Leiden and prothrombin gene heterozygosity
title_sort diagnostic ramifications of ocular vascular occlusion as a first thrombotic event associated with factor v leiden and prothrombin gene heterozygosity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396423/
https://www.ncbi.nlm.nih.gov/pubmed/25897198
http://dx.doi.org/10.2147/OPTH.S80714
work_keys_str_mv AT schockmansamantha diagnosticramificationsofocularvascularocclusionasafirstthromboticeventassociatedwithfactorvleidenandprothrombingeneheterozygosity
AT glueckcharlesj diagnosticramificationsofocularvascularocclusionasafirstthromboticeventassociatedwithfactorvleidenandprothrombingeneheterozygosity
AT hutchinsrobertk diagnosticramificationsofocularvascularocclusionasafirstthromboticeventassociatedwithfactorvleidenandprothrombingeneheterozygosity
AT pateljaykumar diagnosticramificationsofocularvascularocclusionasafirstthromboticeventassociatedwithfactorvleidenandprothrombingeneheterozygosity
AT shahparth diagnosticramificationsofocularvascularocclusionasafirstthromboticeventassociatedwithfactorvleidenandprothrombingeneheterozygosity
AT wangping diagnosticramificationsofocularvascularocclusionasafirstthromboticeventassociatedwithfactorvleidenandprothrombingeneheterozygosity