To compare the lesion characteristics of two different types of confocal scanning laser ophthalmoscopy (cSLO) autofluorescence (AF) images in central serous chorioretinopathy (CSC). The study included 63 eyes of 61 patients; 63 pairs of fundus autofluorescence (FAF) images were compared before CSC resolution in 63 eyes, FAF images of 31 eyes were also compared after CSC resolution. The lesion characteristics (brightness and composite pattern) were compared between Heidelberg Retina Angiograph 2 (HRA2; Heidelberg Engineering, Germany) and Optomap Tx (Optomap; Optos, Scotland) FAF images. The lesion composite pattern was categorized as diffuse or granular. Diffuse AF was defined as homogenously increased or decreased AF, and granular AF was defined as dot-like, coarse changes in AF. The mean disease duration and subretinal fluid (SRF) height in the spectral domain optical coherence tomography were compared according to the FAF image characteristics. Lesion brightness before CSC resolution was hypo-AF in 48 eyes (76.2 %), hyper-AF in three (4.8 %), and mixed-AF in 12 (19.0 %) in HRA2 FAF images. In comparison, nine (14.3 %) images were hypo-AF, 44 (69.8 %) were hyper-AF, and 10 (15.9 %) were mixed-AF in Optomap FAF images (P < 0.0001). There was no significant difference in lesion composite pattern between the two FAF image wavelengths. Patients with lesions that were hyper-AF in Optomap FAF and hypo-AF in HRA2 FAF had a shorter disease duration and greater SRF height (1 month, 281 um) than those who were hyper-AF in both Optomap and HRA2 images (26 months, 153 um; P = 0.004, 0.001). The two types of FAF images of CSC showed different lesion brightness before and after CSC resolution but demonstrated similar lesion composite patterns.
机构:
Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
2010 Retina & Macula Ctr, Tsim Sha Tsui, Kowloon, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
Lai, Timothy Y. Y.
Tang, Ziqi
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Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
Tang, Ziqi
Lai, Adrian C. W.
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2010 Retina & Macula Ctr, Tsim Sha Tsui, Kowloon, Hong Kong, Peoples R China
UNSW Sydney, Fac Med & Hlth, Kensington, NSW 2052, AustraliaChinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
Lai, Adrian C. W.
Szeto, Simon K. H.
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Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
Szeto, Simon K. H.
Lai, Ricky Y. K.
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2010 Retina & Macula Ctr, Tsim Sha Tsui, Kowloon, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
Lai, Ricky Y. K.
Cheung, Carol Y.
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Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
机构:
Chinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R China
Retina Macula Ctr, Kowloon, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R China
Lai, Timothy Y. Y.
Tang, Ziqi
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Chinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R China
Tang, Ziqi
Lai, Adrian C. W.
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Retina Macula Ctr, Kowloon, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R China
Lai, Adrian C. W.
Lai, Ricky Y. K.
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Retina Macula Ctr, Kowloon, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R China
Lai, Ricky Y. K.
Cheung, Carol Y.
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Chinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Ophthalmol Visual Sci, Hong Kong, Peoples R China