OPTICAL COHERENCE TOMOGRAPHY FEATURES ASSOCIATED WITH VITREOMACULAR TRACTION RELEASE AND MACULAR HOLE SIZE PROGRESSION FOLLOWING TREATMENT WITH OCRIPLASMIN

Retina. 2024 Nov 1;44(11):1923-1930. doi: 10.1097/IAE.0000000000004205.

Abstract

Purpose: To evaluate OCT features for vitreomacular traction (VMT) release and change in macular hole (MH) size after treatment with ocriplasmin.

Methods: Patients who had undergone treatment with ocriplasmin for VMT with or without MH ≤400 µm were included. The main outcomes were VMT release and changes in minimum linear diameter MH size at 4 weeks in MHs that persisted. OCT features evaluated were central retinal thickness, vitreomacular adhesion length, posterior vitreous cortex (PVC) insertion angles 500 µm from the insertion points, and minimum linear diameter size.

Results: Sixty patients were included: 37 had isolated VMT and 23 VMT with a MH. Four weeks after ocriplasmin injection, the overall VMT release rate was 66.7% (40/60); 64.9% (24/37) in eyes with isolated VMT and 69.6% (16/23) in eyes with MH. VMT release was associated with younger age (P = 0.02). Macular hole closure was achieved in 26.1% (6/23) and was associated with a smaller ratio of the temporal to the nasal PVC angle (P < 0.01). Of the 17 persistent MHs, 76.5% (13/17) increased in minimum linear diameter size from baseline 186 (±78) to 358 (±133) µm (P < 0.001). Progression in minimum linear diameter size showed a negative linear association with the size of the nasal PVC angle (R2 = 0.39, P = 0.002) and a positive linear association with the ratio of the temporal to nasal PVC angle (R2 = 0.39, P = 0.002).

Conclusion: In patients with VMT-associated MHs, the risk of MH enlargement following ocriplasmin is negatively correlated with the nasal PVC angle size and is increased if the ratio of the temporal to nasal angle is >1.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Disease Progression
  • Female
  • Fibrinolysin* / administration & dosage
  • Fibrinolysin* / therapeutic use
  • Fibrinolytic Agents* / therapeutic use
  • Follow-Up Studies
  • Humans
  • Intravitreal Injections*
  • Macula Lutea / diagnostic imaging
  • Macula Lutea / pathology
  • Male
  • Middle Aged
  • Peptide Fragments* / administration & dosage
  • Peptide Fragments* / therapeutic use
  • Retinal Perforations* / diagnosis
  • Retinal Perforations* / drug therapy
  • Retrospective Studies
  • Tissue Adhesions / drug therapy
  • Tomography, Optical Coherence* / methods
  • Visual Acuity*
  • Vitreous Body* / diagnostic imaging
  • Vitreous Body* / drug effects
  • Vitreous Body* / pathology
  • Vitreous Detachment / diagnosis
  • Vitreous Detachment / drug therapy

Substances

  • microplasmin
  • Fibrinolysin
  • Peptide Fragments
  • Fibrinolytic Agents