ZEISS Retina Workflow Redefined

Don’t Overlook the Utility of OCT Angiography in These Common Disease States

22 January 2025
Image of Rishi Singh, MD
About the expert Rishi Singh, MD Dr. Singh is Vice President and Chief Medical Officer of Martin North and South Hospitals at Cleveland Clinic Martin Health in Stuart, Florida. He is also Professor of Ophthalmology at the Cleveland Clinic Lerner College of Medicine in Cleveland, Ohio.

When presentations covering the use of OCT angiography (OCTA) first appeared on the podium, many retina specialists correctly surmised that the modality was best suited to answering questions posed by curious academics and clinical researchers. Many of us were unsure what to make of OCTA images—and even if we had been experts in image capture and interpretation, so few of us had OCTA platforms in the clinic that such skills would be rendered moot.

Today the widespread availability of OCTA has changed the playing field. Platforms such as ZEISS CIRRUS 5000 and ZEISS CIRRUS 6000 both run ZEISS AngioPlex OCT Angiography, which allows these platforms to capture up to 100,000 A-scans per second in service of generating OCTA images that depict microvascular flow patterns.

The best part? All parties are happy when retina specialists choose OCTA. For patients, OCTA image capture is fast and comfortable. For providers, OCTA offers a new means by which to characterize anatomy, allowing a more nuanced understanding of disease. For payors, OCTA is less expensive than fluorescein angiography (FA), as outlined by the Academy in a recent memo1.

Still, many providers curious about OCTA have yet to implement it into their workflows. If that sounds like you (or if you’re a provider looking to expand your use of OCTA), then weigh whether any or all of the below uses of OCTA could enhance your clinical care and optimize your workflow.

OCTA as a Safer, Faster, and Less Invasive Means of Depicting Microvascular Structure in Neovascular Disease Patients

For many years, FA imaging produced some of the highest quality images of microvascular structures. While that remains true today (after all, the dawn of the OCTA era didn’t negatively affect the quality of FA as a technology), OCTA offers multiple advantages over FA that often make it my preferred imaging modality for many cases.

For starters, OCTA requires no dyes or injections. As small as the risk of an allergic response or injection-related complication may be during the capture of FA imaging, a provider eliminates those risks when opting for OCTA imaging.

As outlined above, OCTA imaging capture is fast. I order OCTA images and conventional OCT images in a single session without significantly disrupting my clinical workflow. Compared with the chair time FA imaging needs, the differences in efficiency become clear.

Patients, too, often prefer OCTA imaging to FA imaging. Discomforts such as nausea following FA imaging that have been documented in the literature1 are not an issue with OCTA imaging. This overall improved patient experience, at the very least, leads to a more pleasant visit for our patients.

  • Diabetic Retinopathy (DR)
    Diabetic Retinopathy (DR)
    Figure 1. While thickness maps generated by conventional OCT imaging show no signs of atypical anatomy (A), OCTA imaging shows microaneurysms and a foveal avascular zone (B).

    OCTA as a Tool for Diagnosing Diabetic Retinopathy and Assessing Treatment Effects

    Patients with vision complications due to diabetic retinopathy (DR) face the prospect of a severely diminished quality of life, particularly if they are working-age adults. Early diagnosis of DR and characterization of any response to treatment is key to quality health care—and OCTA can help.

    OCTA may aid in early detection of disease would otherwise go unnoticed by other imaging modalities. Figure 1a depicts en face OCT imaging of a diabetic patient. Macula thickness is within normal ranges, and a physician relying on OCT alone would be unlikely to diagnose DR. Figure 2b shows the same patient, but instead with an en face OCTA image. A foveal avascular zone is depicted, and microaneurysms that would otherwise go unobserved are seen.

    OCTA can guide treatment decisions in patients with DR. For example, patients who undergo panretinal photocoagulation for DR may experience improved vision, but neovascularization may still lurk in the background. By using OCTA in these patients, providers can determine whether further treatment (i.e., anti-VEGF therapy) is warranted, or if observation is a more appropriate plan.

OCTA as Screening Mechanism for GA Patients

Now that US providers have access to treatments for geographic atrophy (GA), patients who previously saw little purpose in visiting our clinics now occupy regular appointments in our schedules. GA patients are at risk of converting to exudative disease, and the sooner we detect conversion, the more effectively we can treat it.

When patients with possible GA first visit my clinic (or when patients diagnosed with GA transfer to my care), I capture a baseline OCTA image to screen for signs of neovascularization. This occurs alongside the capture of the OCT images I use for diagnosing and characterizing GA, and takes so little time that my clinic’s workflow is not disrupted.

As patients return for care, I capture OCTA images on each visit to screen for conversion to exudative disease. Before OCTA, such thorough screening would require FA imaging, which is expensive, time-consuming, and uncomfortable for patients.

Embracing the Latest Technology

We retina specialists embrace new technology by instinct: we’re drawn to innovation in much the same way our intellectual curiosity drove us to retina in the first place. By slowly integrating OCTA imaging into our clinical protocols, we familiarize ourselves with the modality’s nuances and learn how it can best improve our clinical decision-making.

Don’t sleep on OCTA—it’s the future of retinal clinical imaging, and might just be the technology that allows you to catch nascent disease in your vulnerable patients.

The statements of the author reflect only his personal opinions and do not necessarily reflect the opinions of any institution with whom he is affiliated.
The author has a contractual or other financial relationship with Carl Zeiss Meditec, Inc. and has received financial support.


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