April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Morphometric Analysis of the Macular Area in Retinitis Pigmentosa and Stargardt's Disease with Spectral Domain Optical Coherence Tomography
Author Affiliations & Notes
  • Igal M. Zand-Hadas
    Ophthalmology, Asociacion Para Evitar la Ceguera en Mexico, I.A.P, Mexico, Mexico
  • Juan Manuel Jiménez-Sierra
    Ophthalmology, Asociacion Para Evitar la Ceguera en Mexico, I.A.P, Mexico, Mexico
  • Ximena Ortega-Larrocea
    Ophthalmology, Asociacion Para Evitar la Ceguera en Mexico, I.A.P, Mexico, Mexico
  • Andrée Henaine-Berra
    Ophthalmology, Asociacion Para Evitar la Ceguera en Mexico, I.A.P, Mexico, Mexico
  • Gustavo Sánchez-Bermúdez
    Ophthalmology, Asociacion Para Evitar la Ceguera en Mexico, I.A.P, Mexico, Mexico
  • Virgilio Morales-Canton
    Ophthalmology, Asociacion Para Evitar la Ceguera en Mexico, I.A.P, Mexico, Mexico
  • Footnotes
    Commercial Relationships  Igal M. Zand-Hadas, None; Juan Manuel Jiménez-Sierra, None; Ximena Ortega-Larrocea, None; Andrée Henaine-Berra, None; Gustavo Sánchez-Bermúdez, None; Virgilio Morales-Canton, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 3693. doi:
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      Igal M. Zand-Hadas, Juan Manuel Jiménez-Sierra, Ximena Ortega-Larrocea, Andrée Henaine-Berra, Gustavo Sánchez-Bermúdez, Virgilio Morales-Canton; Morphometric Analysis of the Macular Area in Retinitis Pigmentosa and Stargardt's Disease with Spectral Domain Optical Coherence Tomography. Invest. Ophthalmol. Vis. Sci. 2011;52(14):3693.

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

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Abstract

Purpose: : To determine the retinal changes in the macular area in each of the retinal dystrophies with Spectral Domain optical coherence tomography (SD-OCT).

Methods: : Descriptive, transversal study. We took images of the macular area with SD-OCT in patients with retinitis pigmentosa (RP) and Stargardt’s disease (SD). We included 39 eyes of patients with retinal dystrophies: 31 eyes with RP and 8 eyes with SD. Each one of the patients had a diagnosis based on clinical examination; in all patients a retinal fluorescein angiography, electroretinogram and electrooculogram were performed. An SD-OCT (Spectralis®, Heidelberg Engineering) of the macular area was performed in all cases, using a macular cube. Central macular thickness (CMT), structural characteristics of the retina and retinal pigment epithelium (RPE) were analyzed. We made a correlation between the best corrected visual acuity (BCVA) and the findings in the macular area seen by SD-OCT.

Results: : We analyzed images of 39 eyes from 20 patients with SD-OCT (12 female, 8 male). Age ranged from 21 to 64 years. In eyes with RP, BCVA was 20/100, mean CMT of 227.2 µ. OCT findings showed RPE atrophy in 25 eyes (80.6%), hyper-reflective intraretinal deposits above the RPE in 15 eyes (48.3%) and epiretinal membrane (ERM) in 6 eyes (19.35%). Cystoid macular edema was observed in 8 eyes (25.8%) which correlated with a mean BCVA of 20/200. In SD, mean BCVA was 20/200, mean CMT of 62.87 µ. OCT findings showed RPE atrophy in 8 eyes (100%), increased visualization of choroidal vessels in 7 eyes (87.5%) and hyper-reflective intraretinal deposits in 7 eyes (87.5%). Four eyes had "bulls eye" RPE changes and 4 eyes had fundus flavimaculatus. Both RP and SD had a poor differentiation of the retinal layers.

Conclusions: : Our results suggest that SD-OCT shows characteristic findings in each one of these 2 inherited retinal diseases, which could help to identify each one of them.

Keywords: retinal degenerations: hereditary • imaging/image analysis: clinical • imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) 
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