Abstract 99. Jahrestagung der DOG, 29. 9. - 2. 10. 01 im ICC, Berlin

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Autologous serum for the treatment of persistent epithelial defects after penetrating keratoplasty

1Ferreira de Souza R., 2Kruse F.; 1Seitz B.

1Dept. of Ophthalmology University Erlangen-Nuernberg, Erlangen; 2Dept. of Ophthalmology University Heidelberg, Heidelberg

Purpose: To show our first results of topical autologous serum for the treatment of persistent epithelial defects after penetrating keratoplasty (PK) and to analyze the safety and efficacy of this new therapeutic modality.
Methods: Between November 1999 and March 2001, 35 eyes with epithelial defects after PK refractory to conventional therapy (mean age 68±14 years) were treated with autologous serum. We investigated localization, size and duration of defects, the time period until complete epithelial closure in successful cases (</= 30 days) and the incidence of recurrences. After centrifugal separation of freshly taken blood the serum (100% concentrated) was kept in sterile dosing bottles at refrigerator temperature and was applied at an hourly interval during day time. Further topical and systemic medication was given according to the underlying diseases.
Results: On average, the epithelial defect was 5 mm long and 3 mm wide. All patients had been treated before with maximum topical therapy (including hyaluronic acid) for 10±10 days. The period of autologous serum treatment ranged between 4 and 38 days (13±9 days). In 28 of 35 eyes (80%) the epithelial closure was complete after 3 to 27 days (average10±6 days). During a mean follow-up of 7±4 months, 17% of eyes had a recurrence after 4 to 38 days and were treated successfully with secondary serum application (3x) or amniotic membrane transplantation (1x). Seven eyes (20%) considered to be non-responding clinically were treated with amniotic membrane transplantation (4x) or repeat PK (3x) after 7, 8, 11, 14, 15, 36 and 38 days.
Conclusion: Autologous serum seems to be safe and efficient for persistent epithelial defects after complicated PK thus avoiding more invasive treatment modalities, such as botulinum toxin application, tarsorrhaphy, amniotic membrane transplantation or repeat PK.




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