June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Retinal nerve fiber layer (RNFL) thickness modification after internal limiting membrane (ILM) peeling: 45 months follow-up
Author Affiliations & Notes
  • Antonio Ciardella
    Policlinico Sant'Orsola Malpighi, Bologna, Italy
  • Nicole Balducci
    Policlinico Sant'Orsola Malpighi, Bologna, Italy
  • Alessandro Finzi
    Ophthalmology Unit, University of Bologna, Bologna, Italy
  • Mariachiara Morara
    Policlinico Sant'Orsola Malpighi, Bologna, Italy
  • Chiara Veronese
    Policlinico Sant'Orsola Malpighi, Bologna, Italy
  • Carlo Torrazza
    Policlinico Sant'Orsola Malpighi, Bologna, Italy
  • Roberto Gattegna
    Private practice, Rome, Italy
  • Tommaso Perossini
    Policlinico Sant'Orsola Malpighi, Bologna, Italy
  • Footnotes
    Commercial Relationships Antonio Ciardella, None; Nicole Balducci, None; Alessandro Finzi, None; Mariachiara Morara, None; Chiara Veronese, None; Carlo Torrazza, None; Roberto Gattegna, None; Tommaso Perossini, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 5119. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Antonio Ciardella, Nicole Balducci, Alessandro Finzi, Mariachiara Morara, Chiara Veronese, Carlo Torrazza, Roberto Gattegna, Tommaso Perossini; Retinal nerve fiber layer (RNFL) thickness modification after internal limiting membrane (ILM) peeling: 45 months follow-up. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):5119.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: To evaluate RNFL thickness modification after ILM peeling for idiopathic macular hole (MH) or epiretinal membrane (ERM) during a follow up period of 45 months.<br />

Methods: Interventional, prospective, non randomized case series. Twenty eyes of 20 patients (76,7±6,6 years) who underwent pars plana vitrectomy and brilliant blue G-assisted ILM peeling were evaluated 24,2±1.2 and 45,6±1,4 months after surgery. All the patients received a complete ophthalmic examination, autofluorescence, infrared and blue light images, peripapillary and macular SD-OCT (Spectralis HRA + OCT; Heidelberg Engineering, Heidelberg, Germany), visual field test (Humphrey central 30-2) in both eyes. Six peripapillar sector (superotemporal, temporal, inferotemporal, nasal, superonasal, inferonasal) and global RNFL thickness were evaluated. Data were compared with the data of the same patients obtained preoperatively and 1, 3 and 6 months postoperatively, that had already been analyzed in a previous study. Data were analyzed using Friedman, Wilcoxon and Spearman tests.<br />

Results: Best corrected visual acuity, expressed in LogMAR, significantly improved after surgery, remained stable at the 45 months follow-up (0,41±0,25 vs 0,12±0,2, p<0,01) and it was not statistically different from the early postoperative values. Sectoral and global RNFL thickness showed statistically significant modifications during the follow up period (p<0,0001). Specifically, after an initially significative increase of RNFL thickness in all the sectors, but the temporal one, 1 month post surgery, a progressive decrease of global, superotemporal, temporal and inferotemporal RNFL thickness was detectable 6 months after surgery. The RNFL thickness reduction in these sectors did not change after 24 and 45 months of follow-up (p< 0,001 when compared to preoparative values and p>0,05 when compared to 6 months values).

Conclusions: ILM peeling leads to significant peripapillar RNFL thickness modification in the early postoperavite period and it is not responsible for further retinal nerve fiber loss. The superotemporal, temporal and inferotemporal thickness reduction detectable 6 months after surgery did not change during a follow up period of 45 months.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×