AI Article Synopsis

  • Interface infectious keratitis (IIK) is a new type of corneal infection that can occur after lamellar keratoplasty procedures, typically starting in the space between the graft and the host.
  • A study found 42 cases of IIK, mostly linked to endothelial keratoplasty, with fungi as the main pathogens and evidence of infection transmission from donor to host.
  • Treatments like topical and systemic antimicrobials were largely ineffective, but direct antifungal injections at the graft-host interface showed promise, while early excisional penetrating keratoplasty proved to be the most effective treatment method with better outcomes.

Article Abstract

Interface infectious keratitis (IIK) is a novel corneal infection that may develop after any type of lamellar keratoplasty. Onset of infection occurs in the virtual space between the graft and the host where it may remain localised until spreading with possible risk of endophthalmitis. A literature review identified 42 cases of IIK. Thirty-one of them occurred after endothelial keratoplasty and 12 after deep anterior lamellar keratoplasty. Fungi in the form of species were the most common microorganisms involved, with donor to host transmission of infection documented in the majority of cases. Donor rim cultures were useful to address the infectious microorganisms within few days after surgery. Due to the sequestered site of infection, medical treatment, using both topical and systemic antimicrobials drugs, was ineffective on halting the progression of the infection. Injection of antifungals, right at the graft-host interface, was reported successful in some cases. Spreading of the infection with development of endophthalmitis occurred in five cases after Descemet stripping automated endothelial keratoplasty with severe sight loss in three cases. Early excisional penetrating keratoplasty showed to be the treatment with the highest therapeutic efficacy, lowest rate of complications and greater visual outcomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579547PMC
http://dx.doi.org/10.1136/bjophthalmol-2018-312938DOI Listing

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