Risk factors and critical thresholds for glucocorticoid-induced ocular adverse reactions in children: implications

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You Li1, Tingxin Cui1, Zhilang Lin1

  • 1Zhongshan Ophthalmic Center, Sun Yat-sen University, WHO Collaborating Centre for Eye Care and Vision, State Key Laboratory of Ophthalmology, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou.

Insights

Systemic glucocorticoid (GC) therapy in children risks ocular adverse drug reactions (ADRs) like cataracts and hypertension. Identifying risk factors and exposure thresholds is key to preventing vision loss in pediatric patients.

Area of Science:

  • Ophthalmology
  • Pediatrics
  • Pharmacology

Background:

  • Systemic glucocorticoid (GC) therapy is essential for pediatric inflammatory and neuromuscular diseases.
  • Prolonged GC use in children carries risks of severe ocular adverse drug reactions (ADRs), including posterior subcapsular cataract (PSCC) and steroid-induced ocular hypertension (SIOH).
  • These ADRs can cause irreversible vision impairment, adding to the burden of chronic conditions in children.

Purpose of the Study:

  • To identify specific risk factors and quantitative exposure thresholds for ocular ADRs in pediatric patients receiving GC therapy.
  • To guide optimized GC treatment strategies and timely ophthalmic monitoring in children.

Main Methods:

  • A retrospective case-control study involving 305 children with kidney disease treated with GCs (December 2020 - December 2022).
  • Participants were categorized into PSCC, SIOH, or control groups.
  • Logistic regression and Receiver Operating Characteristic (ROC) analysis were employed to identify risk factors and critical exposure thresholds.

Main Results:

  • Seven significant risk factors for PSCC were identified: younger age, longer GC duration, hypertension, growth retardation, vitamin D deficiency, immunosuppressant use, and oral methylprednisolone.
  • Critical thresholds for PSCC onset were GC treatment duration >5.6 months or cumulative dose >5,888 mg.
  • Higher daily GC dosage (>0.59 mg/kg/day), oral methylprednisolone, and growth retardation were significant risk factors for SIOH.

Conclusions:

  • This study elucidates key risk factors and establishes quantitative GC exposure thresholds for ocular ADRs in children.
  • Findings provide evidence-based guidance for ophthalmic screening and intervention timing in pediatric patients requiring long-term GC therapy.
  • Proactive monitoring and tailored GC management are crucial for mitigating vision-threatening complications and improving long-term outcomes.

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