Understanding time course of DLK can help eliminate visual loss
Proper identification, staging and intervention is crucial.
by Eric J. Linebarger, MD; David R. Hardten, MD; Y. Ralph Chu, MD; and Richard L. Lindstrom, MD
Special to Ocular Surgery News
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September 1, 1999, Ocular Surgery News
http://www.OcularSurgerynews.com
---DLK also is known as shifting sands phenomenon or Sands of the Sahara Syndrome. (Figure 1)
---A striking characteristic of DLK is a white, granular appearance. (Figure 2)
With the volume of laser in situ keratomileusis (LASIK) procedures growing exponentially, there is an expanding role for ophthalmologists and other eye care providers to be aware of an uncommon post operative condition known as diffuse lamellar keratitis (DLK), which has the potential to derail an otherwise ideal outcome.
Understanding the time course of the disease, along with proper identification, staging and intervention, can help eliminate visual loss associated with this condition.
Background
Stage 1 DLK is defined by the presence of white, granular cells in the periphery of the lamellar flap, with sparing of the visual axis. (Figures 3A and 3B)
The first anecdotal reports of a mysterious post-LASIK inflammatory syndrome began to surface only a few years ago, which is when LASIK began to rise in popularity and acceptance among patients and physicians. Maloney and Smith were one of the first to report on this unusual syndrome at the 1997 American Academy of Ophthalmology meeting in Chicago.
The condition would eventually come to be known by a variety of names, including shifting sands phenomenon or sands of the Sahara syndrome, alluding to the white, granular appearance with waves of increased density (Figure 1).
Since then considerable amount of speculation has been focused on possible etiologies (Table). Anecdotal reports of case clusters seem to point the finger toward a contaminant in the lamellar interface introduced at the time of surgery.
Still more cases appear to be associated with epithelial defects at the time of surgery or even delayed epithelial abrasions occurring weeks or months later. This cumulative evidence suggests that no one agent is completely responsible for the syndrome, and that a multifactorial etiology is likely.
Despite efforts to eliminate potential causes of DLK, an increasing number of cases are being reported as the volume of LASIK procedures performed worldwide continues to grow. Although difficult to accurately document, the authors’ own experience suggests that the incidence of severe vision-threatening DLK cases may be in the range of 1 in 5,000, while very mild cases may be as frequent as 1 in 50.
The authors’ experience in a high-volume LASIK practice has provided significant insight into this elusive condition, along with a strategy to successfully identify and manage this uncommon yet potentially sight-threatening complication.
Our treatment strategy is threefold, and includes identifying cells in the lamellar interface, staging their location and severity, and intervening at the appropriate time.
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Thank you
Bill Trattler, MD
Miami, FL