June 2021
Volume 62, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2021
Risk Factors for Acute Elevated Intraocular Pressure after Intravitreal Anti-VEGF Injections
Author Affiliations & Notes
  • Stephen LoBue
    Ophthalmology, SUNY Downstate Health Sciences University, New York, New York, United States
    Ophthalmology, Acuity Eye Group & Retina Institute Pasadena, Pasadena, California, United States
  • Abenet Michael
    Ophthalmology, SUNY Downstate Health Sciences University, New York, New York, United States
  • Alan Guagliardo
    Ophthalmology, Acuity Eye Group & Retina Institute Pasadena, Pasadena, California, United States
  • Tom Chang
    Ophthalmology, Acuity Eye Group & Retina Institute Pasadena, Pasadena, California, United States
  • Michael Davis
    Ophthalmology, Acuity Eye Group & Retina Institute Pasadena, Pasadena, California, United States
  • Steven Fish
    Ophthalmology, Acuity Eye Group & Retina Institute Pasadena, Pasadena, California, United States
  • Footnotes
    Commercial Relationships   Stephen LoBue, None; Abenet Michael, None; Alan Guagliardo, None; Tom Chang, None; Michael Davis, None; Steven Fish, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2021, Vol.62, 430. doi:
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    • Get Citation

      Stephen LoBue, Abenet Michael, Alan Guagliardo, Tom Chang, Michael Davis, Steven Fish; Risk Factors for Acute Elevated Intraocular Pressure after Intravitreal Anti-VEGF Injections. Invest. Ophthalmol. Vis. Sci. 2021;62(8):430.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To study the effects of intravitreal injection (IVI) on intraocular pressure (IOP) and to predict the patient population which may be most susceptible to acute elevations in IOP.

Methods : A three-month, prospective study of patients receiving IVI of anti-VEGF at the Acuity Eye Group. IOP was measured pre-injection as well as post-injection at 10-minute intervals up to 50 minutes. Patients with an IOP greater than 35mmHg at 30 minutes received an ACP. Patients with an IOP below 35mmHg were monitored without intervention.

Results : 617 patients were included, with a mean age of 73 years. Patients received IVI for diabetic retinopathy (n = 199), age-related macular degeneration (n= 355), and retinal vein occlusion (n = 63). Average pre-injection IOP was 16 +/-5 mmHg. Average post-injection IOP was 25, 27, 28, 27, and 29 mmHg at 10, 20, 30, 40, and 50 minutes respectively (P<.0001). The ACP group (n=17) had a pre-injection average IOP of 24 +/- 7 mmHg (p<.0001), and post-injection IOP of 47 +/- 10 and 44 +/- 9 mmHg at 10 and 20 minutes respectively (p<.0001). Overall, 33% of patients with a pre-injection IOP > 25 mmHg and 50% with a pre-injection IOP > 30 mmHg required ACP. A diagnosis of glaucoma was higher in the ACP group compared to the non-ACP, 82.3% vs 14.2% (p<0.0001), and a diagnosis of glaucoma suspect was also higher in the ACP group vs non-ACP, 17.6% vs 9.0 respectively ( p>0.05). Patients with a pre-injection IOP > 25 mmHg and a history of glaucoma had a 58.3% rate of ACP. The number of IVI were similar between the ACP and non-ACP group at 22 +/- 10 vs 19 +/- 11 injections, respectively. A 31-gauge needle had a higher incidence of ACP when pre-injection IOP > 25 versus 30-gauge, 42.9% vs 29.4% respectively (p>0.05).

Conclusions : IVI of anti-VEGF medication is associated with a transient but significant increase in IOP. Patients with a pre-injection IOP of 25mmHg or greater, combined with a history of glaucoma, may be at a higher risk of prolonged IOP increases and may benefit from prophylactic ACP.

This is a 2021 ARVO Annual Meeting abstract.

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