Effects of twice-daily topical difluprednate 0.05% emulsion in a child with pars planitis

Paul A Kurz1, Lena V Chheda, Daryl E Kurz

  • 1Ohio State University, Havener Eye Institute, 915 Olentangy River Road, Columbus, OH 43212, USA. paul.kurz@osumc.edu

Insights

Topical difluprednate effectively controlled pars planitis (PP) in a child for one year. However, delayed ocular hypertension and cataracts developed, requiring treatment changes.

Area of Science:

  • Ophthalmology
  • Pediatric Ophthalmology

Background:

  • Pars planitis (PP) is a form of intermediate uveitis requiring management.
  • Topical corticosteroids are often used for ocular inflammation.

Observation:

  • A pediatric case of pars planitis (PP) was treated with twice-daily topical difluprednate.
  • Initial control of PP was achieved with difluprednate over a 12-month period.

Findings:

  • Sustained control of pars planitis (PP) was observed for one year.
  • Atypical steroid response manifested as delayed, recalcitrant ocular hypertension (OHT) and posterior subcapsular cataract (PSC) formation.
  • These complications necessitated discontinuation of difluprednate and initiation of alternative therapies.

Implications:

  • Topical difluprednate may serve as a short-term treatment option for pediatric pars planitis (PP).
  • Ophthalmologists must monitor for delayed adverse effects, including ocular hypertension (OHT) and cataract formation, during difluprednate therapy.
  • Awareness of potential serious complications is crucial for safe and effective management of pediatric ocular inflammation.
Abstract