Abstract
Background
To evaluate antifungal chemotherapy in patients with fungal keratitis guided by in vivo confocal microscopy.
Methods
A total of 121 patients (121 eyes) with fungal keratitis were enrolled in this study. Confocal microscopy was performed in real time after topical and/or oral antifungal chemotherapy. Hyphal density and morphology, composition of inflammatory cells, and appearance of corneal stromal cells at the central and peripheral corneal lesions were recorded. Antifungal therapy discontinued at 1 week after hyphae and inflammatory cells could not be detected, and affected corneal stromal cells became visible.
Results
Successful outcomes were achieved in 110 patients (90.9%). By confocal microscopy, we observed the gradual decrease of hyphae-positive sites and hyphal density during the chemotherapy. The inflammatory cells reduced in number and heterogeneity, while corneal stromal cells recovered. The antifungal drugs were tapered according to the changes in hyphae, inflammatory cells, and corneal stromal cells. There was no fungal recurrence during the 2-month follow-up period. The other 11 patients (9.1%) had deteriorated infection within 1 week of antifungal therapy, and therefore were subjected to corneal transplantation.
Conclusions
In vivo confocal microscopy appears to be an effective approach to guide antifungal chemotherapy. It allows comprehensive evaluation of hyphae, inflammatory cells, and corneal stromal cells in real time, and provides valuable and objective information required in selecting and adjusting therapeutic regimens for the treatment of fungal keratitis.
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Acknowledgements
This study was supported in part by the National Natural Science Foundation of China (30630063, 30271394), Department of Science and Technology of Shandong Province (2004GG2202154), and Qingdao Municipal Science and Technology Bureau (02KGYSH-01). The authors thank Ms. Ping Lin for her editorial assistance.
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Shi, W., Li, S., Liu, M. et al. Antifungal chemotherapy for fungal keratitis guided by in vivo confocal microscopy. Graefes Arch Clin Exp Ophthalmol 246, 581–586 (2008). https://doi.org/10.1007/s00417-007-0719-x
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DOI: https://doi.org/10.1007/s00417-007-0719-x