Primary Pediatric Keratoplasty: Etiology, Graft Survival, and Visual Outcome

Maria Emilia Xavier Dos Santos Araújo1, Namir Clementino Santos1, Luciene Barbosa de Souza1

  • 1Department of Ophthalmology and Visual Sciences, Paulista School of Medicine, São Paulo Hospital, Federal University of São Paulo - UNIFESP, São Paulo, Brazil.

Insights

Corneal transplantation in children, primarily for congenital glaucoma, shows improved visual acuity despite a 64.7% graft survival rate over 24 months. Graft failure is linked to rejection and early glaucoma.

Area of Science:

  • Ophthalmology
  • Pediatric Surgery

Background:

  • Corneal transplantation in pediatric patients presents unique challenges.
  • Understanding risk factors for graft failure is crucial for improving outcomes.

Purpose of the Study:

  • To evaluate the causes, visual results, and survival rates of corneal transplantation in children.
  • To identify risk factors associated with corneal graft failure in pediatric recipients.

Main Methods:

  • A retrospective review of medical records for children aged 7 years or younger undergoing primary penetrating keratoplasty.
  • Assessment of indications, graft survival using Kaplan-Meier analysis, and visual acuity (VA) improvement via preferential looking test and visual evoked potential.

Main Results:

  • Fifty-six transplants were performed in 43 children, with congenital glaucoma as the primary indication (29.4%).
  • Overall graft survival was 64.7% at 24 months post-transplant, with no significant difference between congenital and acquired opacity groups.
  • Significant visual acuity improvement was observed in both congenital and acquired groups (P = .0022 and P < .0001, respectively).

Conclusions:

  • Congenital glaucoma is a leading indication for pediatric corneal transplantation.
  • Despite challenges, corneal transplantation in children can achieve prolonged graft survival and improved vision.
  • Graft rejection and early-onset glaucoma are significant risk factors for corneal graft failure in pediatric patients.
Abstract

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