July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Safety and efficacy of accelerated cornea cross-linking to arrest progression of corneal ectasia in a tertiary referral center in the UK
Author Affiliations & Notes
  • Borja Salvador Culla
    Ophthalmology, Royal Victoria Infirmary, Durham, North Carolina, United States
  • Afsara Ahmmed
    Ophthalmology, Royal Victoria Infirmary, Durham, North Carolina, United States
  • Nicola Roper
    Ophthalmology, Royal Victoria Infirmary, Durham, North Carolina, United States
  • Julie Mulroy
    Ophthalmology, Royal Victoria Infirmary, Durham, North Carolina, United States
  • David Tabibian
    Ophthalmology, Royal Victoria Infirmary, Durham, North Carolina, United States
  • Francisco Figueiredo
    Ophthalmology, Royal Victoria Infirmary, Durham, North Carolina, United States
    Institute of Genetic Medicine, Newcastle University,, Newcastle upon Tyne, United Kingdom
  • Footnotes
    Commercial Relationships   Borja Salvador Culla, None; Afsara Ahmmed, None; Nicola Roper, None; Julie Mulroy, None; David Tabibian, None; Francisco Figueiredo, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 345. doi:
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      Borja Salvador Culla, Afsara Ahmmed, Nicola Roper, Julie Mulroy, David Tabibian, Francisco Figueiredo; Safety and efficacy of accelerated cornea cross-linking to arrest progression of corneal ectasia in a tertiary referral center in the UK. Invest. Ophthalmol. Vis. Sci. 2019;60(9):345.

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

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Abstract

Purpose : Corneal collagen cross-linking (CXL) is nowadays the gold-standard procedure to stabilize progression ofectatic disorders. The initial Dresden protocol has been progressively replaced by new accelerated protocols that allow reduced treatment time without compromising safety and efficacy. We present our data on accelerated CXL from a tertiary Ophthalmology center in the UK.

Methods : Prospective non-randomized interventional clinical study including all consecutive patients with topographic evidence of progressing corneal ectatic disorder who underwent accelerated CXL (9mW/cm2for 10’; 5.4J/cm2). Outcomes regarding best-corrected visual acuity (BCVA; LogMAR), sphere, cylinder, spherical equivalent (SE), topographical indices and complications were collected preoperatively and at 1, 3, 6, 12, 18, and 24 months postoperatively and analyzed accordingly.

Results : 67 eyes of 58 patients (males=43; 74%) were included. Mean age was 21.1 years (SD 4.9, range 14-38). Mean follow-up time was 14.9 months (SD 6.49, range 3-34). 64 eyes (95.5%) were treated for keratoconus, 2 for pellucid marginal degeneration and 1 for post-LASIK ectasia. Mean preoperative BCVA was 0.4 (SD 0.4) and at last follow-up 0.3 (SD 0.4), with no statistically significant differences between timepoints (p>0.05). Subjective refraction values (sphere, cylinder and SE) did not show any statistically significant differences between timepoints (p>0.05). Mean pre-operative keratometric values were: K154.3D (SD 5.2), K246.1D (SD 9.2) and Km50.8D (SD 4.4), remaining stable at last follow-up: K156.4D (SD 6.4), K247.9D (SD 4.4) and Km52.2D (SD 5.0) (p>0.05). One eye (1.5%) presented a sterile corneal infiltrate 5 days after CXL that resolved completely after one month of intensive topical treatment with antibiotics and steroids, with no residual corneal scarring or haze.

Conclusions : Accelerated CXL successfully stabilized all corneal ectatic disorders in our study, and reduced surgical time, potentially increasing the efficiency of CXL. Our results confirm that progression of ectasia was successfully halted with CXL, with no serious complications. Accelerated CXL is a safe and effective alternative to the Dresden protocol.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

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