Author/Authors :
Haghani ، I نويسنده Invasive Fungi Research Centre (IFRC) and Department of Medical Mycology and Parasitology, Scho ol of Medicine, Mazandaran Univ ersity of Medical Sciences, Sari, Iran , , Amirinia، F نويسنده Student Research Committee, School of Medicine, Mazandara n University of Medical Sciences, Sari, Iran , , Nowroozpoor-Dailami ، K نويسنده Department of Ophthalmology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran ,
Abstract :
Background and Purpose:
Fungal keratitis is a suppurative, ulcerative, and
sight-threatening infecti
on of the cornea that
sometimes leads to blindness. The aims of
this study were: recuperating facilities
for laboratory diagnosis, determining the
causative microorganisms, and comparing conventional
laboratory diagnostic tools and semi-nested PCR.
Materials and Methods:
Sampling was conducted in patients with suspected fungal keratitis.
Two corneal scrapings
specimens, one for direct smear and culture and
the other for semi- nested PCR were obtained.
Results:
Of the 40 expected cases of mycotic keratitis, calcofluor white staining showed positivity in 25%, culture in
17.5%, KOH in 10%, and semi-nested PCR in 27.5%. The
sensitivities of semi-nested PCR, KOH, and CFW were
57.1%, 28.5%, and 42% while the specificities were 78.7%, 94%, and 78.7%, respectively. The time taken for PCR
assay was 4 to 8 hours, whereas positive f
ungal cultures took at least 5 to 7 days.
Conclusion:
Due to the increasing incidence of fungal infections in people with weakened immune systems,
uninformed using of topical co
rticosteroids and improper use of contact lens
, fast diagnosis and accurate treatment of
keratomycosis seems to be essential
.
Therefore, according to the current study
, molecular methods can detect mycotic
keratitis early and correctly leading to appropriate treatment.