Another marker, perhaps the most clinically useful, is the observation of epithelial microcysts. Microcysts are small, irregularly shaped high refractive inclusions that form in the basal layers of the epithelium and move towards the anterior surface of the cornea.
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| Figure 2.Corneal Microcysts (courtesy CCLRU Grading Scales) |
The technique for observing epithelial microcysts uses retro-illumination. The cornea is scanned with a 1mm wide slit beam on a slit-lamp biomicroscope. A magnification of at least 16x is required with marginal retro-illumination. Once observed, magnification is increased to 20-40x while keeping the inclusion centred in the beam and confirming that it shows reversed illumination as demonstrated in Figure 3. Microcysts are typically 10-50 microns in diameter and appear similar to micropunctate corneal staining.
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| Figure 3.Observation of Unreversed and Reversed Illumination (courtesy IACLE) |
Relatively low numbers of microcysts are observed in patients wearing silicone hydrogels if they are new to contact lens wear or have been wearing these lenses for some time (several months or longer). This is because, as has been demonstrated previously (6), the oxygen transmissibility of lenses is inversely proportional to the number of microcysts seen.
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| Figure 4.Relationship between microcyts and Dk/t for RGP and soft lenses (adapted from “Silicone Hydrogels: the rebirth of continuous wear contact wear” ed. Sweeney, DF) |
The number of microcysts is generally less than 10, a number commonly seen in non-lens wearers and with daily wear of lenses. Large number of microcysts however will be found in a significant proportion of our patients that we transfer from low Dk lenses particularly if worn on an extended wear basis, to high Dk SCLs. In these patients, as has been reported by Keay and colleagues (7), a spike or rebound effect will be observed with large numbers of microcysts observed in the cornea for up to one month after refitting. These large numbers of microcysts are seen to be spread across the cornea or they have been noticed to aggregate in a ring in the corneal mid-periphery. As microcysts move to the anterior surface of the cornea, areas of negative staining, or black spots, may be observed (best observed after instillation of fluorescein using a cobalt blue illumination with a Wratten yellow filter).
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| Figure 5. The typical trend in microcyst numbers when moving patients from low Dk to high Dk materials (adapted from “Silicone Hydrogels: the rebirth of continuous wear contact wear”, ed. Sweeney, DF) |
Such a trend has also been observed when patients are discontinued from low Dk extended wear. It has been suggested that the rebound is related to re-oxygenation of the corneal surface resulting in recovery of epithelial metabolism and so clearance of extra-cellular debris trapped in the deeper basal layers of the epithelium.
We have also had the opportunity in our long-term studies to monitor the levels of microcysts in our high Dk patients over a number of years and with patients on both a 6 and 30 night continuous wear schedule. We have observed no shift or increase in the low numbers of microcysts observed across time and nor have we seen any differences in the levels of microcysts observed with either a 6 or 30 night wear schedule.
When observing the corneal epithelium it is important also to ensure that microcysts are differentially diagnosed from the many other presentations with which they may be confused. The table below adapted from Keay et al (7) details a number of conditions that can have a similar appearance to microcysts and the main distinguishing feature by which to differentiate them from microcysts.
Table 2: Differential diagnosis with other epithelial events
| |
<Size (µm) |
Appearance |
Cause |
| Recurrent corneal erosion |
<15 to 100
|
Clear cysts |
Trauma often unknown |
| Microcystic edema |
<20 to 50
|
Clear cyst surrounding epithelial haze, > 200 |
Inflammatory origin |
| Epithelial infiltrates |
<100 to 500
|
Granular, dense centre |
Chemotactic stimulus |
| Vacuoles |
<20 to 50
|
Round, bubble-like, unreversed illumination |
Hypoxia |
| Mucin balls* |
<< 100
|
Spherical balls |
Surface interaction between lens and cornea |
| Punctate corneal staining |
<10 to 50
|
Fine opaque dots, positive stain |
Epithelial trauma (e.g. toxic or dehydration) |
| Microcysts |
<10 to 50
|
Small, irregular-shaped dots; reversed illumination (negative stain) |
Hypoxia |