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Probe of IRIS registry: Anti-VEGF injections key treatment for PDR

Digital EditionOphthalmology Times: October 1, 2020
Volume 45
Issue 16

DME diagnosis plays no role in determining whether patients will receive injection.

DME diagnosis plays no role in determining whether patients will receive injection.
Jeremiah Brown Jr, MD, MS

This article was reviewed by Jeremiah Brown Jr, MD, MS

A contemporary look at treatment patterns for proliferative diabetic retinopathy (PDR) shows that the vast majority of patients with PDR will receive an anti-VEGF injection regardless of whether they have diabetic macular edema (DME), said Jeremiah Brown Jr, MD, MS, at the 2020 virtual meeting of the American Society of Retina Specialists.

Brown presented the findings from a retrospective review conducted using data from the American Academy of Ophthalmology’s Intelligent Research in Sight (IRIS) registry, the nation’s first comprehensive eye disease clinical registry.

Related: Researchers advocate for intraoperative intravitreal steroid during cataract surgery in DME eyes​ ​

The study included 33,452 patients with PDR and new onset vitreous hemorrhage treated within 3 months who had a visit between June 2017 and June 2018.

Eighty percent of patients had a diagnosis of DME, and 84% of those patients received anti-VEGF treatment. However, 69% of patients with PDR alone also were given anti-VEGF therapy.

In addition, anti-VEGF treatment was received by approximately one-half of patients who underwent panretinal photocoagulation (PRP) or vitrectomy if they also had DME, and by approximately one-third of those without DME who were treated with PRP or vitrectomy.

Study data
“The data from this study show that treatment patterns for PDR have undergone a dramatic shift since the advent of anti-VEGF medications,” said Brown, who is in private practice at the Brown Retina Institute in San Antonio, Texas. “Ophthalmologists are no longer relying on a foundation of repetitive peripheral laser applications to treat PDR but instead are taking care of patients using anindividualized mix of anti-VEGF injections, PRP, and vitrectomy.”

Brown also pointed out that the “research also highlights the enormous value of the IRIS registry, which contains information from hundreds of thousands of patient visits, for enabling us to look into our practices and evaluate trends to improve patient care.”

Related: Clinical trial outcomes for macular edema don’t translate to ‘real-world’ settings​ ​

Providing context for undertaking the study, Brown noted there are some clear indications for treating DME with anti-VEGF medications, while the timing and the need for their use in the treatment of PDR are less clear.

Treatment foundation
“Our treatment for PDR was built on the foundation of the diabetic retinopathy study published in 1976 that established peripheral scatter laser photocoagulation as the standard of care,” he said. “More recently, Protocol S [NCT01489189] and the Clarity study showed similar visual outcomes could be achieved with anti-VEGF therapy. Our study sought to understand how the available options are being employed in the real world.”

Data on the use of PRP and vitrectomy showed that in the cohort of patients with PDR and DME, 30% were treated with PRP, 17% received PRP plus an anti-VEGF medication, and 20% underwent vitrectomy, of which approximately one-half also received an anti-VEGF injection.

Related: Managing the challenge of cataract surgery in eyes with diabetic macular edema

Among those patients who had PDR without DME, 35% received PRP, while 11% received PRP plus anti-VEGF injection, and 29% underwent vitrectomy, of which 36% of those also received anti-VEGF therapy.

Functional results similar
The study also analyzed visual acuity (VA) outcomes at 6 months following treatment, and the results showed that the percentage of patients achieving logMAR VA of 0.4 or better (approximately Snellen 20/50) was similar regardless of whether they received an anti-VEGF injection. Percentages of patients achieving logMAR VA of 0.4 or better were 59% in the anti-VEGF cohort, 65% among those treated with PRP alone, and 63% for patients who received both treatments.

Considering patients undergoing vitrectomy, approximately 50% achieved logMAR VA of 0.4 or better whether they had surgery alone or combined with anti-VEGF treatment.

Related: Identifying biomarkers to predict diabetic retinopathy progression


Brown concluded that it is interesting to see that the VA results are similar with or without anti-VEGF therapy “if we consider that retina specialists would be more likely to use an anti-VEGF agent in patients with more severe proliferative disease, more severe vitreous hemorrhage, or more ischemic appearing retinas, along with the fact that patients with longstanding DME may reach a plateau in their VA improvement because of foveal atrophy or persistent edema.”

“Therefore, it is encouraging to note that patients treated with anti-VEGF injections were able to achieve the same level of vision as the patients treated with PRP or vitrectomy alone who likely had milder hemorrhage,” he said.

Read more by Cheryl Guttman Krader


Jeremiah Brown Jr, MD, MS
Brown serves as an investigator, consultant, or member of speakers bureau for companies that market or are developing treatments for diabetic eye disease.

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