Peripapillary and Macular Vascular Changes of Unilateral Anterior Ischemic Optic Neuropathy: An Optical Coherence Tomography Angiography Study

Omar Said

Status: Completed

Conditions: Non-arteritic Ischemic Optic Neuropathy

Treatments: Diagnostic Test: Optical Coherence Tomography Angiography

Study type: Observational

Funder types: Other

Identifiers

NCT06031350

EOM64

Details and patient eligibility

About

This series aims at studying the peripapillary and macular vascular changes in subjects with unilateral anterior ischemic optic neuropathy via Optical Coherence Tomography Angiography (OCTA).

Full description

After approval of the local institutional ethics committee and local institutional review board, This study was conducted upon 30 patients diagnosed with acute NAION attending at Ophthalmology outpatient clinic in Fayoum University Hospitals. The participants were informed about the objectives of the study, the examination, investigations and the confidentiality of their information and their right not to participate in the study. OCT and OCTA was done for all subjects and control group with Optovue, Inc., Fremont, CA, USA. Patients were examined on presentation, after 6 weeks and lastly after 3 months. OCT was used for evaluation of Central macular thickness (CMT), nerve fiber layer thickness (NFLT) and ganglion cell complex (GCC). OCTA was done for quantitative evaluation of vessel density in the following: optic nerve head and peripapillary area, macular superficial vessel density, macular deep vessel density and foveal avascular zone. Vessel density was reported as the percentage of the total area that was occupied by blood vessels. All parameters were calculated automatically by the machine software. Poor quality scans and those with motion artifacts were excluded. Statistical analysis was performed using SPSS software (version 22; SPSS, Chicago, IL, USA). The data were presented as the mean ± SD values. P-value <0.05 was considered significant.

Enrollment: 30 patients

Sex: All

Ages: Under 40 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients diagnosed with unilateral NAION and acute or sudden painless drop of vision.
• A normal fellow eye.
• Age ≥ 40 years old.

Exclusion criteria

• Arteritic type of AION.
• NAION patients in chronic phase.
• Acute phase NAION patients with any other optic neuropathy in the other eye.
• Eyes with opaque media.
• Elevated intraocular pressure (>22 mmHg).
• Refractive errors greater than 6 diopters of spherical equivalent.
• Poor cooperation with fixation or the OCTA examination.

Trial design

30 participants in 2 patient groups

Diseased eyes

Description:

The 30 diseased eyes of the patients were considered the case group.

Treatment:

Diagnostic Test: Optical Coherence Tomography Angiography

Fellow eyes

Description:

The 30 fellow eyes of the patients were considered the control group.

Treatment:

Diagnostic Test: Optical Coherence Tomography Angiography