In-vivo quantification of bacterial keratitis with optical coherence tomography

Konstantopoulos, Aris, Fievez, Marina, Anderson, David and Hossain, Parwez (2010) In-vivo quantification of bacterial keratitis with optical coherence tomography. Investigative Ophthalmology & Visual Science, 52, (2), 1093-1097. (doi:10.1167/iovs.10-6067) (PMID:20926816)

Download

[file icon]PDF (Primary Research Paper) - Post print
Restricted to admin only

627Kb

Description/Abstract

PURPOSE: To quantify the human corneal inflammatory response in treated bacterial keratitis with long-wavelength anterior segment optical coherence tomography (AS-OCT).
METHODS: Patients with clinically suspected bacterial keratitis were recruited from the corneal service at Southampton Eye Unit, UK. Patients underwent AS-OCT and slit-lamp examination on presentation (day 0) and days 3, 7, and 14 of treatment. Corneal thickness (CT) in the infiltrated area, infiltrate thickness (IT), and infiltrate width (IW) were measured on high-resolution AS-OCT scans. Mean values for each day and rates of change for each interval were calculated and compared (one-way ANOVA, paired t-test).
RESULTS: Twenty-six eyes of 26 patients were recruited. Mean CT and IT on presentation were 905 μm and 388 μm, respectively. On days 3, 7, and 14, CT and IT decreased to 753 μm and 320 μm (P < 0.01), 678 μm and 296 μm (P < 0.01), and 584 μm and 207 μm (P < 0.01), respectively. Mean IW, 1498 μm on presentation, did not change during treatment (P > 0.30). Mean daily rate of CT reduction was faster in the early (days 0-3) compared to late (days 7-14) phase (4.49% vs. 1.33%, P = 0.006). Mean daily rate of IT reduction was no different in early, middle, and late phases (5.41% vs. 1.19% vs. 3.38%, P > 0.01). In the late phase, IT decreased faster than CT (3.38% vs. 1.33%, P = 0.003).
CONCLUSIONS: CT and IT decreased significantly by day 3 in resolving bacterial keratitis. The rapid early phase reduction in IT and CT was followed by rapid late phase IT reduction. This study demonstrates that serial AS-OCT examination can be used to monitor in vivo the clinical course of inflammatory disease.

Item Type:Article
ISSN:0146-0404 (print)
Subjects:R Medicine > RB Pathology
R Medicine > RE Ophthalmology
Divisions:University Structure - Pre August 2011 > School of Medicine > Infection, Inflammation and Repair
ePrint ID:181577
URI:http://eprints.soton.ac.uk/id/eprint/181577
Deposited On:19 Apr 2011 11:31
Last Modified:01 Jun 2011 04:23

Associated Staff Only: edit my ePrint