Baseline Predictors of Vitreomacular Adhesion/Traction Resolution Following an Intravitreal Injection of Ocriplasmin

Ophthalmic Surg Lasers Imaging Retina. 2016 Aug 1;47(8):716-23. doi: 10.3928/23258160-20160808-04.

Abstract

Background and objective: To determine factors predicting response to ocriplasmin (Jetrea; ThromboGenics, Iselin, NJ) response in patients with symptomatic vitreomacular adhesion (VMA).

Patients and methods: Combined analysis of two multicenter, prospective, randomized, double-masked trials of intravitreal ocriplasmin 125 µg injection versus placebo. Patients had vitreomacular traction with or without a full-thickness macular hole (FTMH). Multivariate logistic regression was used to determine factors influencing treatment response (complete VMA release [day 28] and non-surgical FTMH closure [month 6]).

Results: Younger age, presence of FTMH (odds ratio [OR] = 2.1; 95% confidence interval [CI], 1.1-3.7), VMA diameter of 1,500 µm or less (OR = 4.9; 95% CI, 2.0-12.4), phakic lens status (OR = 2.8; 95% CI, 1.5-5.2), and absence of epiretinal membrane (OR = 4.1; 95% CI, 2.2-7.9) predicted VMA resolution. FTMHs with apical diameter of 250 µm or less were more likely to close than larger holes (58.3% vs. 24.6%; P = .013). Both FTMH size groups had significantly greater chance of VMA resolution and FTMH closure versus controls.

Conclusion: Ocriplasmin is most effective in younger patients with focal VMA and without an epiretinal membrane. [Ophthalmic Surg Lasers Imaging Retina. 2016;47:716-723.].

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Female
  • Fibrinolysin / administration & dosage*
  • Follow-Up Studies
  • Humans
  • Intravitreal Injections
  • Macula Lutea / drug effects
  • Macula Lutea / pathology*
  • Male
  • Peptide Fragments / administration & dosage*
  • Prospective Studies
  • Retinal Perforations / diagnosis
  • Retinal Perforations / drug therapy*
  • Retinal Perforations / etiology
  • Time Factors
  • Tissue Adhesions / drug therapy
  • Tissue Adhesions / pathology
  • Tomography, Optical Coherence / methods
  • Treatment Outcome
  • Visual Acuity
  • Vitreous Body / drug effects
  • Vitreous Body / pathology*
  • Vitreous Detachment / complications
  • Vitreous Detachment / diagnosis
  • Vitreous Detachment / drug therapy*

Substances

  • Peptide Fragments
  • microplasmin
  • Fibrinolysin