May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Retinopathy in Adult Patients With Congenital Heart Disease
Author Affiliations & Notes
  • R.S. Wirthlin
    Ophthalmology, Jules Stein Eye Institute, Los Angeles, CA
  • C.W. Mango
    Ophthalmology, Jules Stein Eye Institute, Los Angeles, CA
  • A. Gupta
    Ophthalmology, Jules Stein Eye Institute, Los Angeles, CA
  • C.R. Gonzales
    Ophthalmology, Jules Stein Eye Institute, Los Angeles, CA
  • J. Perloff
    Adult Congenital Heart Disease Center, UCLA Medical Center, Los Angeles, CA
  • S.D. Schwartz
    Ophthalmology, Jules Stein Eye Institute, Los Angeles, CA
  • Footnotes
    Commercial Relationships  R.S. Wirthlin, None; C.W. Mango, None; A. Gupta, None; C.R. Gonzales, None; J. Perloff, None; S.D. Schwartz, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 5173. doi:
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      R.S. Wirthlin, C.W. Mango, A. Gupta, C.R. Gonzales, J. Perloff, S.D. Schwartz; Retinopathy in Adult Patients With Congenital Heart Disease . Invest. Ophthalmol. Vis. Sci. 2006;47(13):5173.

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

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Abstract

Purpose: : To determine the presence of retinal vascular disease and vascular anomalies in an adult population of patients with congenital heart disease (CHD).

Methods: : IRB–approved, prospective consecutive case series of four adult patients with congenital heart disease examined by a single observer at one institution. Wide–angle Optos® photography to document retinopathy.

Results: : Four patients were examined. Patient One was a 30 year–old woman with coarctation of the aorta, malposition of great arteries, double inlet single left ventricle status post 4 cardiac surgeries. Most recent surgery was 12 years prior to presentation. Visual acuity (VA) measured 20/20 OU. There were no ocular abnormalities. Patient Two was a 42 year–old man with non–restrictive ventricular septal defect, Eisenmenger syndrome, situs inversus, dextrocardia. VA measured 20/20 OD and 20/30 OS. There was evidence of retinal vascular tortuosity. Patient Three was a 37 year–old woman with coarctation of the aorta status post repair times two, most recently 6 years prior to presentation. VA measured 20/20 OU. There was evidence of retinal vascular tortuosity. Patient Four was a 61 year–old man with coarctation of the aorta 39 years status post repair. VA measured 20/20 OU. There was evidence retinal vascular tortuosity, arterial narrowing and arterial–venous crossing changes. 3 of 4 patients showed evidence of retinal vascular tortuosity.

Conclusions: : Adult patients with CHD status post repair may have retinal vascular abnormalities. In adult patients with retinal vascular tortuosity, CHD should be considered.

Keywords: retina • pathology: human 
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