Studies in the diagnosis and pathophysiology of severe microbial keratitis

Background: Microbial keratitis (MK) is a major cause of blindness worldwide. Few studies have assessed the HRT3 in vivo confocal microscope (IVCM) in the diagnosis or management of MK. This PhD aimed to investigate these questions and was based in a high incidence setting for MK: Aravind Eye Hospit...

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Main Author: Chidambaram, J. D.
Other Authors: Burton, M. J. ; Holland, M. J.
Published: London School of Hygiene and Tropical Medicine (University of London) 2018
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.755896
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spelling ndltd-bl.uk-oai-ethos.bl.uk-7558962019-02-05T03:35:40ZStudies in the diagnosis and pathophysiology of severe microbial keratitisChidambaram, J. D.Burton, M. J. ; Holland, M. J.2018Background: Microbial keratitis (MK) is a major cause of blindness worldwide. Few studies have assessed the HRT3 in vivo confocal microscope (IVCM) in the diagnosis or management of MK. This PhD aimed to investigate these questions and was based in a high incidence setting for MK: Aravind Eye Hospital, Madurai, India. Methods: A prospective observational study of 252 severe MK patients was conducted with follow-up at days 7, 14 and 21 post-enrolment. Quantitative PCR of corneal swabs obtained at presentation validated transcriptome results. IVCM images were evaluated in this cohort for diagnostic accuracy, and ability to monitor outcome. Results: For fungal detection, HRT3 IVCM had a high sensitivity (85.7%; 95% CI: 82.2%– 88.6%) and specificity (81.4%; 95% CI: 76.0%–85.9%). For Acanthamoeba, the sensitivity was 88.2% (95% CI: 76.2%–94.6%) and specificity was 98.2% (95% CI: 94.9%–99.3%). Mean fungal branching angle in IVCM images was not significantly different for Fusarium sp. (59.7°; 95% CI: 57.7°–61.8°) versus Aspergillus sp. (63.3°; 95% CI: 60.8°–65.8°; p=0.07). At presentation, anterior corneal IVCM morphology associated with BK included bullae (OR 9.99, 95% CI: 3.11–32.06, p < 0.001), and in FK a honeycomb distribution of inflammatory cells (OR 2.74, 95%CI: 1.01–7.40, p=0.047). Poor outcomes in FK were associated with stellate interconnected cellular processes with no visible nuclei (OR 2.28, 95% CI: 1.03-5.06, p=0.043) in baseline IVCM images, and fungal filaments (OR 6.48, 95% CI:2.50-16.78, p < 0.001) or inflammatory cells in a honeycomb distribution (OR 5.24, 95% CI: 1.44-19.06, p=0.012) in final visit images. Conclusions: HRT3 IVCM can yield a high diagnostic accuracy. Fungal branching angle in IVCM images does not differentiate between Fusarium and Aspergillus keratitis. IVCM image morphologies may be associated with causative organism or clinical outcome in MK.London School of Hygiene and Tropical Medicine (University of London)10.17037/PUBS.04649231https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.755896http://researchonline.lshtm.ac.uk/4649231/Electronic Thesis or Dissertation
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description Background: Microbial keratitis (MK) is a major cause of blindness worldwide. Few studies have assessed the HRT3 in vivo confocal microscope (IVCM) in the diagnosis or management of MK. This PhD aimed to investigate these questions and was based in a high incidence setting for MK: Aravind Eye Hospital, Madurai, India. Methods: A prospective observational study of 252 severe MK patients was conducted with follow-up at days 7, 14 and 21 post-enrolment. Quantitative PCR of corneal swabs obtained at presentation validated transcriptome results. IVCM images were evaluated in this cohort for diagnostic accuracy, and ability to monitor outcome. Results: For fungal detection, HRT3 IVCM had a high sensitivity (85.7%; 95% CI: 82.2%– 88.6%) and specificity (81.4%; 95% CI: 76.0%–85.9%). For Acanthamoeba, the sensitivity was 88.2% (95% CI: 76.2%–94.6%) and specificity was 98.2% (95% CI: 94.9%–99.3%). Mean fungal branching angle in IVCM images was not significantly different for Fusarium sp. (59.7°; 95% CI: 57.7°–61.8°) versus Aspergillus sp. (63.3°; 95% CI: 60.8°–65.8°; p=0.07). At presentation, anterior corneal IVCM morphology associated with BK included bullae (OR 9.99, 95% CI: 3.11–32.06, p < 0.001), and in FK a honeycomb distribution of inflammatory cells (OR 2.74, 95%CI: 1.01–7.40, p=0.047). Poor outcomes in FK were associated with stellate interconnected cellular processes with no visible nuclei (OR 2.28, 95% CI: 1.03-5.06, p=0.043) in baseline IVCM images, and fungal filaments (OR 6.48, 95% CI:2.50-16.78, p < 0.001) or inflammatory cells in a honeycomb distribution (OR 5.24, 95% CI: 1.44-19.06, p=0.012) in final visit images. Conclusions: HRT3 IVCM can yield a high diagnostic accuracy. Fungal branching angle in IVCM images does not differentiate between Fusarium and Aspergillus keratitis. IVCM image morphologies may be associated with causative organism or clinical outcome in MK.
author2 Burton, M. J. ; Holland, M. J.
author_facet Burton, M. J. ; Holland, M. J.
Chidambaram, J. D.
author Chidambaram, J. D.
spellingShingle Chidambaram, J. D.
Studies in the diagnosis and pathophysiology of severe microbial keratitis
author_sort Chidambaram, J. D.
title Studies in the diagnosis and pathophysiology of severe microbial keratitis
title_short Studies in the diagnosis and pathophysiology of severe microbial keratitis
title_full Studies in the diagnosis and pathophysiology of severe microbial keratitis
title_fullStr Studies in the diagnosis and pathophysiology of severe microbial keratitis
title_full_unstemmed Studies in the diagnosis and pathophysiology of severe microbial keratitis
title_sort studies in the diagnosis and pathophysiology of severe microbial keratitis
publisher London School of Hygiene and Tropical Medicine (University of London)
publishDate 2018
url https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.755896
work_keys_str_mv AT chidambaramjd studiesinthediagnosisandpathophysiologyofseveremicrobialkeratitis
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