Background
This study was done to evaluate macular perfusion changes following intravitreal bevacizumab injections for diabetic macular edema (DME) using spectral domain optical coherence tomography angiography (SD-OCTA).
Methods
This study was a prospective noncomparative interventional case series. Treatment naïve patients with DME were recruited at Cairo University retina clinic and underwent full ophthalmological examination and SD-OCTA scanning at baseline and after 3 intravitreal bevacizumab injections. Both the 6X6 and 3X3-mm macular scan protocols were used. Pre and post-treatment OCTA images were automatically aligned using a commercially available retina alignment software (i2k Align Retina software) then the fractal dimension (FD), vascular density (VD), and skeleton VD changes were obtained at the full retinal thickness (Full) and superficial (SCP) and deep (DCP) capillary plexuses after processing images using a semi-automated program. The foveal avascular zone (FAZ) was manually measured and FD was calculated using the FracLac plugin of ImageJ.
Results
Forty eyes of 26 patients were included. Following injections, there was an 8.1% increase in FAZ, 1.3% decrease in FD-Full and FD-SCP, 1.9% decrease in FD-DCP, 8% decrease in VD-Full, 9.1% decrease in VD-SCP, 10.6% decrease in VD-DCP, 13.3% decrease in skeleton VD-Full, 12.5% decrease in skeleton VD-SCP, and 16.3% decrease in skeleton VD-DCP in the 6X6 mm macular area, and a 2.6% decrease in FD-Full, 3.4% decrease in FD-SCP, 11.5% decrease in VD-Full, 14.3% decrease in VD-SCP, and 25.1% decrease in skeleton VD-SCP in the 3X3 mm macular area which were all statistically significant (p<0.05). There was also an 8.3% increase in the FAZ, 18.5% decrease in skeleton VD-Full, 2.6% decrease in FD-DCP, 8.8% decrease in VD-DCP, and 19.7% decrease in skeleton VD-DCP in the 3X3 mm macular area but these were not statistically significant (p>0.05). Using univariate and multivariate analysis, the pre-treatment FD, VD, and skeleton VD at each capillary layer significantly negatively correlated with the change in FD, VD, and skeleton VD at the corresponding capillary layer respectively (p>0.05).
Conclusion
OCTA is a useful non-invasive tool for quantitative evaluation of macular perfusion changes following DME treatment.
Trial Registration
Trial registered at ClinicalTrials.gov on August 11, 2017 (Study ID: NCT03246152).