June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Descriptive Study of Ocular Surface changes in Patients with Congenital Glaucoma
Author Affiliations & Notes
  • Simone Finzi
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Ruth Santo
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Monique Matsuda
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Ernst Oltrogge
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Marcio Mendes
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Fernando Naves
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Rodrigo Azevedo
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Frederico Lazar
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Bruno Cardoso
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Alberto Betinjane
    Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil
  • Footnotes
    Commercial Relationships Simone Finzi, None; Ruth Santo, None; Monique Matsuda, None; Ernst Oltrogge, None; Marcio Mendes, None; Fernando Naves, None; Rodrigo Azevedo, None; Frederico Lazar, None; Bruno Cardoso, None; Alberto Betinjane, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 2576. doi:
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      Simone Finzi, Ruth Santo, Monique Matsuda, Ernst Oltrogge, Marcio Mendes, Fernando Naves, Rodrigo Azevedo, Frederico Lazar, Bruno Cardoso, Alberto Betinjane; Descriptive Study of Ocular Surface changes in Patients with Congenital Glaucoma. Invest. Ophthalmol. Vis. Sci. 2013;54(15):2576.

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

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Abstract
 
Purpose
 

Recent studies show a relationship between POAG and lacrimal dysfunction. Several factors may lead to alteration of the ocular surface (OS) in patients with primary congenital glaucoma (PCG). The purpouse of this study is to elaborate a clinical description of the ocular surface (OS) in patients with GCP

 
Methods
 

After informed consent, 34 patients diagnosed with PCG were included in the study. Ophthalmologic examination was performed, and clinical evaluation of OS. The patients were submitted to a questionnaire to evaluate symptoms of dry eye

 
Results
 

We examined 34 patients (60 eyes) diagnosed with PCG to 17.97 ± 7.91 years. 17 patients without use of eyedrop for at least 1 year and 17 patients using eye drops, these 9 patients (64%) using 3 or more drops. The patients had chronic use of eye drops with a mean of 6.07 ± 7.56 years. All patients underwent surgery. In the interview, 18 patients (52%) complained of dry eye. On examination it was observed: IOP OD: 14.62 ± 5.72 mmHg, OS: 12.55 ± 14.16 mmHg; pachymetry: OD: 567.37 ± 87.04 μ, OS: 555.92 ± 51.76 μ; Biometry OD : 25.80 ± 4.27 mm, OS: 23.99 ± 2.31 mm. In assessing the OS resulted: Schirmer Test OD = 25.93 ± 10.44 mm, OS: 23.28 ± 11.84 mm; BUT: OD = 11.26 ± 4.50 s, OS = 11.76 ± 11.76 s , Lacrimal Meniscus: OD = 0.82 ± 1.15 mm, OE: 0.77 ± 0.93 mm, no patient had a significant positive staining Rose Bengal.

 
Conclusions
 

Despite PCG is a rare disease and this study has a heterogeneous sample, our patients expressed mild symptoms of dry eye, but without clinical signs consistent with lacrimal dysfunction. Subjective evaluation of the questionnaire is controverted in children, but other factors beyond the chronic use of eye drops, as buphthalmos, lagophthalmos and anatomic alterations from surgery, may contribute to the symptoms of the disease in this patients sample

  
Keywords: 486 cornea: tears/tear film/dry eye • 576 lacrimal gland • 467 clinical laboratory testing  
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