Abstract

To evaluate the efficacy of phacoemulsification combined with posterior capsulorhexis, core vitrectomy and ciliary sulcus intraocular lens (IOL) implantation in patients with Fuchs' heterochromic uveitis (FHU). A total of 18 eyes of 18 patients with FHU underwent cataract surgery were included in the study. 18 eyes with FHU underwent posterior capsulorhexis, core vitrectomy and poly (methyl methacrylate) (PMMA) IOL implantation in the ciliary sulcus. Subjects were chosen for this procedure based on an intraoperative vitreous haziness assessment, performed by indirect ophthalmoscopy. Patients with +2 or more vitreous haziness qualified for this procedure. Of the 83 eyes with FHU that underwent cataract surgery, 18 eyes (21.6%) of 18 patients were employed in the study. There were 11 (61.1%) men and 7 (38.9%) women in the study; ages ranged from 23 to 47, with a mean of 32.06 years. Follow-up ranged from 8 months to 49 months. There were no intraoperative complications except for peripheral iris bleeding in 7 eyes. There was no severe intraocular inflammation in any patient postoperatively. All patients had 0.05 or better logMAR visual acuity after corneal suture removal. Glaucoma developed in 2 patients. For the short term period, the main vision threatening problem was suture-induced astigmatism. Cataract surgery combined with posterior capsulorhexis, core vitrectomy and IOL implantation in the ciliary sulcus is safe and leads to good visual outcome due to the removal of the hazy vitreous in patients with FHU.

Highlights

  • Fuchs’ heterochromic uveitis (FHU) is a type of anterior uveitis with a chronic and insidious character

  • Materials and Methods: A total of 18 eyes of 18 patients with FHU underwent cataract surgery were included in the study. 18 eyes with FHU underwent posterior capsulorhexis, core vitrectomy and poly (PMMA) intraocular lens (IOL) implantation in the ciliary sulcus

  • Of the 83 eyes with FHU that underwent cataract surgery, 18 eyes (21.6%) of 18 patients were employed in the study

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Summary

Introduction

Fuchs’ heterochromic uveitis (FHU) is a type of anterior uveitis with a chronic and insidious character. It may present at any age but most often appears in young adults. Several studies have suggested that Toxoplasma gondii, chronic herpetic infection, and congenital Horner syndrome may be etiological factors of FHU [2]. Regardless of the etiology, this uveitic syndrome has several vision-impairing ocular complications such as cataracts, secondary glaucoma, and vitreous haze. The crucial problems that threaten vision are ocular inflammation, glaucoma, posterior capsular opacification (PCO) and vitreous haze [5]

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