More research needed to ‘realize the full potential of OCTA’ for diabetic retinopathy
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Key takeaways:
- OCTA can identify early evidence of microvascular change and help assess diseases such as diabetic retinopathy.
- Expert consensus and validation of metrics is needed for OCTA to “have true clinical utility.”
Despite the promise of OCTA as a valuable tool in the evaluation of diabetic retinopathy and its complications, challenges remain and more research is needed to standardize its use in clinical trials, according to a published review.
“Numerous studies have confirmed that OCTA can be used to identify the earliest evidence of microvascular change and provide quantitative assessment of the extent of diseases such as DR and its common complications, including [diabetic macular ischemia (DMI)],” Nadia K. Waheed, MD, MPH, retina specialist and associate professor at Tufts University School of Medicine, and colleagues wrote in Progress in Retinal and Eye Research.
“OCTA has been shown to be more sensitive than physician examination or fundus imaging and detects capillary loss earlier than when the clinical lesions of DR become apparent, indicating its sensitivity and promise as a tool for assessing DMI.”
Waheed and colleagues reviewed the potential use of OCTA for DR, aiming to provide guidance for future research, support for development of new treatments and improved understanding of DR and associated complications.
According to researchers, several OCTA metrics have potential for use in clinical trials of DR, diabetic macular edema and DMI, including foveal avascular zone, vessel density, extrafoveal avascular zones and neovascularization.
“In order for OCTA to have true clinical utility, it is critical to establish a consensus among experts and to validate OCTA metrics through research and clinical trials for its use in DR,” they wrote.
Researchers also identified several challenges associated with use of OCTA for these conditions, including variability at the patient level, as well as variability among devices, noting: “As a relatively new technology, there is still a lack of standardized tools and procedures to address common imaging problems like artifacts, segmentation errors and image focus.”
Waheed and colleagues highlighted the use of wide-field OCTA imaging to assess peripheral retinal vasculature and aid in predicting DR progression, as well as automated methods and algorithms for analysis of OCTA images, which will benefit efficiency and standardization of results.
“When we have solved these issues and established a common set of OCTA procedures for use in clinical trials, it will be possible to realize the full potential of OCTA as a robust and regulator-accepted clinical trial endpoint,” they wrote.