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Published on: November 12, 2015
Intrastromal corneal ring segment implantation in pediatric keratoconus: Up to 10 years of follow-up
Luis Fernández-Vega-Cueto1, Carlos Lisa1, Belén Alfonso-Bartolozzi1
1Cornea, Cataract & Refractive Surgery Department, Fernández-Vega Ophthalmological Institute, Oviedo, Spain.
Insights
Intrastromal corneal ring segment (ICRS) implantation significantly improved vision and refractive error in pediatric keratoconus patients. These positive outcomes were maintained long-term, establishing ICRS as a viable rehabilitation option.
Area of Science:
- Ophthalmology
- Corneal Surgery
- Pediatric Eye Care
Background:
- Keratoconus is a progressive corneal ectasia causing visual impairment.
- Pediatric patients with keratoconus require effective visual rehabilitation strategies.
- Intrastromal corneal ring segments (ICRS) offer a potential solution for improving vision in these patients.
Purpose of the Study:
- To evaluate the efficacy of Intrastromal corneal ring segment (ICRS) implantation for visual rehabilitation in pediatric patients diagnosed with keratoconus.
- To assess the long-term visual and refractive outcomes following ICRS implantation in this patient group.
Main Methods:
- A cohort of 107 eyes (85 patients) aged 18 years or younger with keratoconus underwent ICRS implantation.
- Preoperative and 1-, 5-, 7-, and 10-year postoperative data including uncorrected (UDVA) and corrected (CDVA) distance visual acuities, manifest refraction, and keratometry were collected.
- Treatment success was defined by visual and refractive improvement and stability over time.
Main Results:
- Significant improvements in UDVA (logMAR 0.64 to 0.34) and CDVA (logMAR 0.19 to 0.08) were observed one year postoperatively (P < 0.0001).
- 74.8% of eyes gained lines of CDVA, and 76.6% achieved a refractive cylinder <3.00 D one year postoperatively.
- High success rates (84.3%-88.9%) were maintained at 5-, 7-, and 10-year follow-ups, with less than 10% cumulative failure over 10 years.
Conclusions:
- ICRS implantation provides significant and durable visual and refractive benefits for pediatric keratoconus patients.
- The procedure is a safe and effective long-term visual rehabilitation option, maintaining improvements over a decade.
- ICRS implantation demonstrates a favorable safety profile with low cumulative failure rates in this pediatric cohort.
Abstract:
PurposeTo evaluate the Intrastromal corneal ring segment (ICRS) implantation for visual rehabilitation in pediatric patients with keratoconus.MethodsPatients aged ≤18 years with keratoconus who underwent ICRS implantation were included. Uncorrected (UDVA) and corrected (CDVA) distance visual acuities, manifest refraction and keratometry were recorded preoperatively and at 1-5-7- and 10-year postoperatively. Treatment was categorized as success, qualified success or failure based on short-term visual and refractive improvement, the visual and refractive stability and the comparison between the long-term follow-up and the preoperative.ResultsOne hundred seven eyes (85 patients) were included. All eyes were examined 1 year postoperatively, 89 at 5 years, 69 at 7 years and 36 at 10 years. UDVA (logMAR) changed from 0.64 ± 0.38 preoperatively to 0.34 ± 0.24 one year postoperatively (P < 0.0001). CDVA (logMAR) rose from 0.19 ± 0.15 to 0.08 ± 0.08 (P < 0.0001). No eyes lost lines of CDVA 1 year postoperatively compared to preoperative, and 74.8% of the eyes gained lines. Preoperatively, 61.7% of the eyes had a refractive cylinder ≥3.00 D; one year postoperatively, 76.6% had <3.00 D. The treatment was successful in most cases at 5-, 7- and 10-year follow-ups (84.3%, 85.5%, and 88.9%, respectively), qualified success in around 8% of the eyes, and treatment failed in 6 eyes represented a cumulative rate over the 10 years <10%ConclusionICRS implantation induced significant visual and refractive improvements, and in most eyes with available long-term follow-up, visual and refractive improvements were maintained, supporting ICRS as a long-term visual rehabilitation option in pediatric keratoconus.

