Case Report
Open Access
Acute Branch Retinal Artery Occlusion and
OCT Angiography Imaging
Courtney M Crawford1*, Okezie C Igboeli2
1North Texas Retina Consultants, Fort Worth TX
2Department of Ophthalmology, Carl R. Darnall Army Medical Center, Fort Hood, TX
2Department of Ophthalmology, Carl R. Darnall Army Medical Center, Fort Hood, TX
*Corresponding author: Courtney Crawford, M.D., North Texas Retina Consultants, 101 Chuckwagon Trail, Fort Worth TX 76087, Tel: 817-441-1212;
Fax: 817-441-2851; E-mail:
@
Received: 12 September, 2016; Accepted: 25 September, 2016; Published: 04 October, 2016
Citation: Crawford CM, Igboeli OC (2016) Acute Branch Retinal Artery Occlusion and OCT Angiography Imaging. Int J Open Access
Ophthal 1(2): 2. DOI: 10.15226/2474-9249/1/2/00106
Abstract
A 70year old male presented with a 2day history of sudden
painless decreased vision in the right eye. Other than presbyopia
and senile cataracts, there was no significant past ocular history. His
past medical history was significant for a cerebral vascular event
of unclear origin several years prior. Evaluation revealed a branch
retinal artery occlusion. Optical Coherence Tomography (OCT)
angiography was employed as part of the evaluation process. We
describe the OCT-angiographic findings in acute branch retinal artery
occlusion.
Introduction
Retinal vascular disease is a significant cause of decreased
vision and blindness. OCT has emerged as an invaluable imaging
modality in the evaluation of retinal vascular diseases and is often
used in guiding andassessing treatments for retinal vascular
diseases.Jia Y et al, recently reported OCT angiography as a
safe alternative to conventional fluorescein angiography. While
OCT angiography has been studied since 2006, the commercial
availability of angiography-enabled OCT systems began in late
2014 and these systems are in use in Europe and Asia. In this
article we present the case of a patient found to have a Branch
Retinal Artery Occlusion (BRAO) and the OCT angiographic
findings in acute BRAO.
Case Report
A 70 year old Caucasian male presented to the New England
Eye Center with a chief complaint of decreased vision in the right
eye. He reported the onset, about two days prior to presentation,
of sudden painless decreased in vision in the right eye which he
described as a sudden appearance of a dark spot inferiorly in
the right eye. His past medical history is significant for systemic
hypertension and a cerebral vascular event of uncertain origin
several years prior which resolved without clinical sequelae.
His ocular history was significant for presbyopia, and senile
cataracts in both eyes. Review of systems was significant only for
hypertension. On exam visual acuity was OD 20/40+3 PH 20/25,
OS 20/30-3 PH 20/20-2. Intraocular Pressure was measured OD
16, OS 17. The patient had a visual field defect inferonasally in the right eye. There was no afferent pupillary defect and ocular
motility was full. On slit lamp exam the anterior chamber was
unremarkable in both eyes. Fundus exam revealed a superior
temporal area of retinal whitening superior to the arcades and
a Hollenhurst plaque was visualized superior to disc in the right
eye. Fundus exam of the left eye revealed normal appearing
macula and vessels.
Multimodal imaging techniques (i.e. fundus color photographs, OCT), were used to confirm the diagnosis of branch retinal artery occlusion (BRAO). OCT angiography was performed on the day of presentation using the prototype AngioVue OCT angiography (OCTA) system on the commercially-available Avanti SD-OCT device (Optovue, Inc, Fremont, CA), which used a SSADA software algorithm to generate OCT angiograms. The AngioVue OCTA system operated at 70,000 A-scans per second to acquire OCTA volumes consisting of 304x304 A-scans in approximately 2.6 seconds. Orthogonal registration and merging of two consecutive scan volumes were used to obtain optic disc angiography of the affected eye.
En-face sectioning was performed to visualize the various levels of ischemia; decreased perfusion was noted and can be seen superficial to the nerve head, within the peripapillary capillaries, and angio choroid (Figure 1). Increased retinal thickening corresponding to areas of ischemia is noted within the inner retinal layers (Figure 2).
Upon completion of his ophthalmic exam, the patient was admitted to the stroke service of the hospital were a complete stroke work up was completed to include echocardiography, neuro-imaging, and systemic labs all of which were unremarkable.
Multimodal imaging techniques (i.e. fundus color photographs, OCT), were used to confirm the diagnosis of branch retinal artery occlusion (BRAO). OCT angiography was performed on the day of presentation using the prototype AngioVue OCT angiography (OCTA) system on the commercially-available Avanti SD-OCT device (Optovue, Inc, Fremont, CA), which used a SSADA software algorithm to generate OCT angiograms. The AngioVue OCTA system operated at 70,000 A-scans per second to acquire OCTA volumes consisting of 304x304 A-scans in approximately 2.6 seconds. Orthogonal registration and merging of two consecutive scan volumes were used to obtain optic disc angiography of the affected eye.
En-face sectioning was performed to visualize the various levels of ischemia; decreased perfusion was noted and can be seen superficial to the nerve head, within the peripapillary capillaries, and angio choroid (Figure 1). Increased retinal thickening corresponding to areas of ischemia is noted within the inner retinal layers (Figure 2).
Upon completion of his ophthalmic exam, the patient was admitted to the stroke service of the hospital were a complete stroke work up was completed to include echocardiography, neuro-imaging, and systemic labs all of which were unremarkable.
Discussion
Branch retinal artery occlusion is a common ocular condition.
Fluorescein angiography is considered the gold standard
diagnostic test, although it is often omitted in clinical care since
the fundus exam is adequate for diagnosis and the test has risks,
albeit low associated with it, such as allergic reaction to the
flourescein dye. Acute and chronic BRAO have been described
using SD-OCT. Shah, et al. described SD-OCT findings of a single
Figure 1: A. Fundus color photograph with sectoral retinal whitening
along superior arcade B. Avanti angiography of superficial retina with
sectoral decreased perfusion. C. Avanti angiography of deep retina
with sectoral decreased perfusion. D. Avanti angiography of Choroid
with decreased perfusion.
Figure 2: A. Cirrus HD 5 Line Raster. B. Cirrus HD with retinal edema
of inner retina.
case of acute BRAO including hyperreflectivity and increased
thickness of the inner retinal layers of the superior retina
compared to the inferior retina.
Yu, et al. studied SD-OCT in 35 acute BRAO and 38 chronic BRAO. Acute findings included:
1. Thickening and hyperreflectivity of inner retinal layers, including NFL/GCL
2. Acute middle maculopathy d/t ischemia of the intermediate and deep retinal capillary plexuses
3. Diffuse thickening and hyper reflectivity of both inner and middle retinal layers d/t ischemia of inner and superficial, intermediate, and deep capillary plexuses.
Chronic BRAO finding include thinning and atrophy of retinal layers corresponding to acute lesions when present. Overall superficial and deep capillary ischemia occurred in 78% of eyes, isolated deep capillary ischemia or paracentral acute middle maculopathy occurred in 22%.
Ahmed, et al. characterized emboli on SD-OCT in 11 cases of acute BRAO. Findings include flake of highly reflective, yet transparent material, oriented with its edge towards the direction of flow and positioned in the middle of the artery was seen in 3 cases. Reflectivity profile of the blood above and below the flake on SD-OCT and FA were normal.
This paper is the first published case report of OCT angiographic findings in acute branch retinal artery occlusion. These findings can be correlated with previously described findings on OCT. The OCT of the affected area showed thickening of the inner retinal layers consistent with previous descriptions. En face OCT angiogram of the nerve head revealed diffuse ischemia in the areas corresponding to intraluminal plaques. In the future we anticipate that OCT angiography could replace fluorescein angiography as the gold standard diagnostic test and might be more quickly and easily performed as part of routine clinical care. Future studies should directly compare OCT angiography to fluorescein angiography, enroll a large number of patients, and further examine OCT angiography findings as a potential to guide prognosis and therapy.
Yu, et al. studied SD-OCT in 35 acute BRAO and 38 chronic BRAO. Acute findings included:
1. Thickening and hyperreflectivity of inner retinal layers, including NFL/GCL
2. Acute middle maculopathy d/t ischemia of the intermediate and deep retinal capillary plexuses
3. Diffuse thickening and hyper reflectivity of both inner and middle retinal layers d/t ischemia of inner and superficial, intermediate, and deep capillary plexuses.
Chronic BRAO finding include thinning and atrophy of retinal layers corresponding to acute lesions when present. Overall superficial and deep capillary ischemia occurred in 78% of eyes, isolated deep capillary ischemia or paracentral acute middle maculopathy occurred in 22%.
Ahmed, et al. characterized emboli on SD-OCT in 11 cases of acute BRAO. Findings include flake of highly reflective, yet transparent material, oriented with its edge towards the direction of flow and positioned in the middle of the artery was seen in 3 cases. Reflectivity profile of the blood above and below the flake on SD-OCT and FA were normal.
This paper is the first published case report of OCT angiographic findings in acute branch retinal artery occlusion. These findings can be correlated with previously described findings on OCT. The OCT of the affected area showed thickening of the inner retinal layers consistent with previous descriptions. En face OCT angiogram of the nerve head revealed diffuse ischemia in the areas corresponding to intraluminal plaques. In the future we anticipate that OCT angiography could replace fluorescein angiography as the gold standard diagnostic test and might be more quickly and easily performed as part of routine clinical care. Future studies should directly compare OCT angiography to fluorescein angiography, enroll a large number of patients, and further examine OCT angiography findings as a potential to guide prognosis and therapy.
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