June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Use of Immunosuppressive Medications for Treatment of Pediatric Intermediate Uveitis
Author Affiliations & Notes
  • Spencer Cope
    Division of Pediatrics Rheumatology, University of Utah, Salt Lake City, UT
  • Aimee Hersh
    Division of Pediatrics Rheumatology, University of Utah, Salt Lake City, UT
  • Akbar Shakoor
    Ophthalmology and Visual Sciences, John A. Moran Eye Center, Salt Lake City, UT
  • John Bohnsack
    Division of Pediatrics Rheumatology, University of Utah, Salt Lake City, UT
  • Albert Vitale
    Ophthalmology and Visual Sciences, John A. Moran Eye Center, Salt Lake City, UT
  • Footnotes
    Commercial Relationships Spencer Cope, None; Aimee Hersh, None; Akbar Shakoor, None; John Bohnsack, None; Albert Vitale, ACIONT (C), Bausch & Lomb (C), Teva (C)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 5201. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Spencer Cope, Aimee Hersh, Akbar Shakoor, John Bohnsack, Albert Vitale; Use of Immunosuppressive Medications for Treatment of Pediatric Intermediate Uveitis. Invest. Ophthalmol. Vis. Sci. 2013;54(15):5201.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract
 
Purpose
 

The optimal treatment strategy for pediatric patients with intermediate uveitis is not well known. The purpose of this study is to describe the demographics, clinical presentation, treatment, and outcomes of a cohort of pediatric patients with intermediate uveitis, with a particular focus on the use of immunosuppressive medications.

 
Methods
 

This retrospective cohort study included all pediatric intermediate uveitis patients treated in the Uveitis Clinic at the University of Utah Moran Eye Center from 1999-2012. Medical records were reviewed and data abstracted at specific time points including initial presentation, 6 months, 1 year, and then annually. Data abstracted included examination findings, disease related complications, and treatment including surgical interventions and immunosuppressive medications. Responsiveness was determined based on Standardization of Uveitis Nomenclature (SUN) definitions for grading inflammation, inactive disease, and remission. Summary statistics were used to describe this cohort.

 
Results
 

The mean age at presentation was 7.7 years (SD 3.1), 56% of subjects were male, 95% had bilateral involvement. 36 subjects had idiopathic disease; 3 subjects had an underlying condition (juvenile idiopathic arthritis (n=2), multiple sclerosis (n=1)). Average length of follow-up was 37 months (range (6-96) months). Out of 76 total eyes involved, findings at presentation included: snowballs (n=48, 63%), snowbanks (n=38, 50%), vitreous debris (n=32, 42%), and visual acuity < 20/50 (n=43, 57%). The most frequent disease complications were hypertony (n=45, 59%), cataracts (n=38, 50%), cystoid macular edema (n=30, 39%), visual acuity < 20/50 (n=46, 61%) and visual acuity < 20/200 (n=20, 26%). Common surgical treatments included periocular steroid injection (n=25 subjects, 64%) and pars plana vitrectomy (n=10, 26%). Oral steroids were received by 17 subjects (44%), and Table 1 describes immunosuppressive medication and responses. Overall, 49 subjects (64%) had inactive disease at their final follow-up visit, and 9 subjects (23%) achieved remission after at least 3 months off all medications.

 
Conclusions
 

In this cohort, patients treated with immunosuppressive therapy had interval improvement in their degree of inflammation. Prospective studies are needed to determine the best therapy for this high risk population.

 
 
Table 1. Use of immunosuppressive treatment for pediatric intermediate uveitis.
 
Table 1. Use of immunosuppressive treatment for pediatric intermediate uveitis.
 
Keywords: 746 uveitis-clinical/animal model • 555 immunomodulation/immunoregulation • 432 autoimmune disease  
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×