Retreatment strategies following Small Incision Lenticule Extraction (SMILE): In vivo tissue responses

PLoS One. 2017 Jul 14;12(7):e0180941. doi: 10.1371/journal.pone.0180941. eCollection 2017.

Abstract

With any refractive correction, including Small Incision Lenticule Extraction (SMILE), there may be a residual refractive error that requires a retreatment. Here, we investigated the tissue responses following various retreatment procedures in a rabbit model of SMILE. All rabbits underwent a -6.00D correction with SMILE. Two weeks later, they underwent -1.00D enhancement by: (i) VisuMax Circle, followed by excimer ablation (S+C); (ii) secondary SMILE anterior to the primary procedure (S+SE); or (iii) surface ablation (S+P), and were examined for 28 days. S+P induced corneal edema and haze, and more CD11b- (23±6 cells) and TUNEL-positive (36±4 cells) cells in the central stromal superficial layers early post-operatively (p<0.001 compared to other procedures). The corneas appeared normal on day 28 after S+P, but had a lower number of keratocytes near the laser ablated plane compared to other procedures. S+SE and S+C did not induce corneal haze and resulted similar level of fibronectin. However, S+C resulted in more inflammatory (10±2 cells; p = 0.001) and apoptotic cells (25±2 cells; p<0.001) compared to S+SE (7±1 inflammatory cells and 21±3 apoptotic cells) early post-operatively. In conclusion, each SMILE retreatment method resulted in unique tissue responses. S+SE offers advantages, such as minimal inflammation and cell death, as well as maintaining a 'flap-less' surgery, over other procedures. However, depending on the degree of enhancement, the lenticule may become too thin to be extracted and the procedure becomes more difficult to perform than S+C and S+P. S+P can maintain corneal integrity by avoiding flap creation and is technically more simple to perform than the others, but the surgery needs to be supplemented with mitomycin-C in order to reduce inflammation and modulate better wound healing.

MeSH terms

  • Animals
  • Apoptosis
  • CD11b Antigen / metabolism
  • Cornea / diagnostic imaging
  • Cornea / metabolism
  • Cornea / pathology*
  • Corneal Stroma / surgery*
  • Fibronectins / metabolism
  • Ki-67 Antigen / metabolism
  • Lasers, Excimer*
  • Microscopy, Confocal
  • Photorefractive Keratectomy*
  • Rabbits
  • Tomography, Optical Coherence

Substances

  • CD11b Antigen
  • Fibronectins
  • Ki-67 Antigen

Grants and funding

This study was supported by National Research Foundation of Singapore-Funded Translational and Clinical Research Programme Grant (NMRC/TCR/002-SERI/2008). The funding was received by JSM. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.