Quantitative analysis of in vivo confocal microscopy images: A review

2013 ◽  
Vol 58 (5) ◽  
pp. 466-475 ◽  
Author(s):  
Dipika V. Patel ◽  
Charles N. McGhee
PLoS ONE ◽  
2021 ◽  
Vol 16 (6) ◽  
pp. e0252653
Author(s):  
Fan Xu ◽  
Yikun Qin ◽  
Wenjing He ◽  
Guangyi Huang ◽  
Jian Lv ◽  
...  

Purpose Infiltration of activated dendritic cells and inflammatory cells in cornea represents an important marker for defining corneal inflammation. Deep transfer learning has presented a promising potential and is gaining more importance in computer assisted diagnosis. This study aimed to develop deep transfer learning models for automatic detection of activated dendritic cells and inflammatory cells using in vivo confocal microscopy images. Methods A total of 3453 images was used to train the models. External validation was performed on an independent test set of 558 images. A ground-truth label was assigned to each image by a panel of cornea specialists. We constructed a deep transfer learning network that consisted of a pre-trained network and an adaptation layer. In this work, five pre-trained networks were considered, namely VGG-16, ResNet-101, Inception V3, Xception, and Inception-ResNet V2. The performance of each transfer network was evaluated by calculating the area under the curve (AUC) of receiver operating characteristic, accuracy, sensitivity, specificity, and G mean. Results The best performance was achieved by Inception-ResNet V2 transfer model. In the validation set, the best transfer system achieved an AUC of 0.9646 (P<0.001) in identifying activated dendritic cells (accuracy, 0.9319; sensitivity, 0.8171; specificity, 0.9517; and G mean, 0.8872), and 0.9901 (P<0.001) in identifying inflammatory cells (accuracy, 0.9767; sensitivity, 0.9174; specificity, 0.9931; and G mean, 0.9545). Conclusions The deep transfer learning models provide a completely automated analysis of corneal inflammatory cellular components with high accuracy. The implementation of such models would greatly benefit the management of corneal diseases and reduce workloads for ophthalmologists.


Eye ◽  
2006 ◽  
Vol 21 (5) ◽  
pp. 614-623 ◽  
Author(s):  
K H Weed ◽  
C J MacEwen ◽  
A Cox ◽  
C N J McGhee

2020 ◽  
Vol 45 (9) ◽  
pp. 1058-1064
Author(s):  
Tor Paaske Utheim ◽  
Xiangjun Chen ◽  
Otto Fricke ◽  
Linda Hildegard Bergersen ◽  
Neil Lagali

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Christine W. Sindt ◽  
D. Brice Critser ◽  
Trudy K. Grout ◽  
Jami R. Kern

This study was designed to identify whether topical fluorescein, a common ophthalmic tool, affects laser in vivo confocal microscopy of the cornea, a tool with growing applications. Twenty-five eye care specialists were asked to identify presence or absence of fluorescein in 99 confocal micrographs of healthy corneas. Responses were statistically similar to guessing for the epithelium (48% ± 14% of respondents correct per image) and the subbasal nerve plexus (49% ± 11% correct), but results were less clear for the stroma. Dendritic immune cells were quantified in bilateral images from subjects who had been unilaterally stained with fluorescein. Density of dendritic immune cells was statistically similar between the unstained and contralateral stained eyes of 24 contact lens wearers (P=.72) and of 10 nonwearers (P=.53). Overall, the results indicated that fluorescein staining did not interfere with laser confocal microscopy of corneal epithelium, subbasal nerves, or dendritic immune cells.


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