April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Influence of corneal storage media on human corneal endothelial cell density during organ culture
Author Affiliations & Notes
  • Ingo Schmack
    Ophthalmology, University of Heidelberg, Heidelberg, Germany
  • Brigitte Erber
    Ophthalmology, University of Heidelberg, Heidelberg, Germany
  • Irina Voehringer
    Ophthalmology, University of Heidelberg, Heidelberg, Germany
  • Seda Ballikaya
    Ophthalmology, University of Heidelberg, Heidelberg, Germany
  • Gerd Auffarth
    Ophthalmology, University of Heidelberg, Heidelberg, Germany
  • Footnotes
    Commercial Relationships Ingo Schmack, None; Brigitte Erber, None; Irina Voehringer, None; Seda Ballikaya, None; Gerd Auffarth, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 2046. doi:
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      Ingo Schmack, Brigitte Erber, Irina Voehringer, Seda Ballikaya, Gerd Auffarth; Influence of corneal storage media on human corneal endothelial cell density during organ culture. Invest. Ophthalmol. Vis. Sci. 2014;55(13):2046.

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

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Abstract

Purpose: To evaluate the potential impact of two different storage media on corneal endothelial cell density during organ culture preservation.

Methods: Retrospective analysis of organ-cultured human corneas selected for corneal grafting over a period of 4 years. All corneal-scleral discs were organ-cultured for up to 4 weeks at 32 degrees C. Corneas were cultured either in storage medium 1, (Dulbecco Modified Eagle Medium, Biochrom; group 1) or medium 2 (CorneaMax Medium, Eurobio; group 2). Endothelial cell densities (ECD) were determined at the beginning and at the end of organ-culture preservation. In addition, the potential impact of sex, donor age, cause of death, death-to-cultivation interval, and organ-culture time was analyzed.

Results: Both groups did not show statistic significant differences in regard to initial endothelial cell density, donor age, death-to-cultivation interval, and organ-culture time. During organ-culture, endothelial cell density decreased significantly in both groups. The mean overall endothelial cell loss was 13.3% in group 1 and 9.9% in group 2, respectively. Differences were statistical significant between the two groups.

Conclusions: Organ-culture is well-established, standardized, and safe technique for preservation of human corneal tissue. Current storage media allow endothelial cell survival with sufficient endothelial cell densities for up to 4 to 5 weeks. However, slight differences may exist in regard to individual storage media.

Keywords: 481 cornea: endothelium • 483 cornea: storage • 467 clinical laboratory testing  
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