Literature DB >> 11888357

Corneal ulceration in pediatric patients: a brief overview of progress in topical treatment.

Serina Stretton1, Usha Gopinathan, Mark D P Willcox.   

Abstract

Pediatric microbial keratitis is a rare but potentially devastating condition. The condition is similar to adult microbial keratitis, but is often characterized by a more severe inflammatory response. The micro-organisms that cause microbial keratitis in children are similar to the causative agents in adults, with herpes simplex and bacteria being the predominant causative agents, and fungi being less frequent. Of the bacterial pathogens, Pseudomonas aeruginosa, Staphylococcus aureus and alpha-hemolytic streptococci are common. The risk factors for pediatric keratitis include colonization of the eyes during birth and trauma to the cornea. Certain microbial factors involved in microbial keratitis are common to all micro-organisms, including adhesion to the cornea, penetration into the cornea, destruction of the corneal stroma (usually by microbial and/or host proteases), and recruitment of white blood cells to help defend the eye. Specific inflammatory responses that occur during pediatric microbial keratitis are not known in detail, but it is likely that cytokines and polymorphonuclear leucocytes are major factors, as they are in adult microbial keratitis. Treatment for pediatric microbial keratitis is usually the same as treatment for adult microbial keratitis; topical application of antimicrobial agents initially, followed by application of anti-inflammatory agents. With pediatric microbial keratitis, extra care must be taken to ensure nontoxicity due to blood adsorption. New microbial keratitis treatments are being developed and these mainly focus on new antimicrobials, antivirulence agents (such as vaccination against microbial toxins) or specific anti-inflammatory agents. There remains a clear need for increased research into the specific responses during microbial keratitis in children which will help progress new therapies as well as the development of new antimicrobials, especially new antifungal therapies.

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Year:  2002        PMID: 11888357     DOI: 10.2165/00128072-200204020-00003

Source DB:  PubMed          Journal:  Paediatr Drugs        ISSN: 1174-5878            Impact factor:   3.022


  162 in total

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Journal:  Cornea       Date:  2000-01       Impact factor: 2.651

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3.  Postexposure vaccination with a virion host shutoff defective mutant reduces UV-B radiation-induced ocular herpes simplex virus shedding in mice.

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Journal:  Vaccine       Date:  1998-01       Impact factor: 3.641

4.  CD4+ T-cell type 1 and type 2 cytokines in the HSV-1 infected cornea.

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Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1999-05       Impact factor: 3.117

5.  Pseudomonas aeruginosa protease IV produces corneal damage and contributes to bacterial virulence.

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Journal:  Invest Ophthalmol Vis Sci       Date:  1998-03       Impact factor: 4.799

6.  Comparative studies on topical lomefloxacin and ciprofloxacin on ocular kinetic and experimental corneal ulcer.

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Journal:  J Ocul Pharmacol Ther       Date:  1999-12       Impact factor: 2.671

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Journal:  Ophthalmology       Date:  1983-02       Impact factor: 12.079

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Journal:  Invest Ophthalmol Vis Sci       Date:  1989-06       Impact factor: 4.799

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Journal:  Ophthalmology       Date:  1986-04       Impact factor: 12.079

10.  Pathogenesis of corneal infection: binding of Pseudomonas aeruginosa to specific phospholipids.

Authors:  N Panjwani; Z Zhao; M B Raizman; F Jungalwala
Journal:  Infect Immun       Date:  1996-05       Impact factor: 3.441

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  1 in total

1.  Paediatric bacterial keratitis cases in Shanghai: microbiological profile, antibiotic susceptibility and visual outcomes.

Authors:  J Hong; J Chen; X Sun; S X Deng; L Chen; L Gong; W Cao; X Yu; J Xu
Journal:  Eye (Lond)       Date:  2012-10-19       Impact factor: 3.775

  1 in total

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