The fluorescein pattern can be evaluated with both a Burton lamp and a biomicroscope.
Burton Lamp:
The traditional method of evaluating the fluorescein pattern is by use of an ultraviolet fluorescent lamp that utilizes a +5.00 D magnification lens to assist in viewing (
Fig. 5.2). This method has the following advantages:
However, the Burton lamp is very limited in its abilities. It does not allow for variable magnification or illumination. In addition, it is an ineffective method of observing the fluorescein pattern of rigid lens materials with ultraviolet-absorbing capabilities. Therefore, it would not be advantageous or appropriate to use this as the only method to evaluate a fluorescein pattern. However, it is a useful adjunct to the biomicroscope because of the overall field of view. This is especially beneficial in observing some of the more distinctive patterns, such as those pertaining to high corneal toricity and keratoconus.
Biomicroscope:
The most popular method of evaluating the fluorescein pattern of a rigid lens is with the biomicroscope. The primary advantage of this over other observational methods is flexibility. It allows the practitioner the opportunity to vary the magnification, illumination, and slit-beam width while observing the fluorescein pattern. Proper use of a biomicroscope for GP fitting and evaluation is essential for patient success.
As biomicroscopes vary considerably from manufacturer to manufacturer, it is important for a good illumination source and variable magnification to be present to effectively evaluate the fluorescein pattern. In fact, it has been determined that with many biomicroscopes it is not possible to use <10× magnification and still retain an adequate field of view.
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Once fluorescein has been properly instilled, the patient should be instructed to blink several times for adequate distribution on the eye. The fluorescein pattern should be initially observed under low magnification with a wide (diffuse) slit-beam and high-intensity illumination. The central and peripheral fluorescein pattern should be relatively easy to determine after several seconds. An optic section with the angle of illumination equal to 45 to 60 degrees can also be used to observe the pooling of tears in relation to the contact lens. It will appear as a green layer representing the outer layer of tears on the lens; then a wider dark layer, which is the contact lens; next another green layer, which represents the tear layer between the lens and cornea; and finally a bright grayish layer, the cornea.
22 The lens-to-cornea fitting relationship can be evaluated by viewing the thickness of the tear layer along the optic section.
Typically, the fluorescein pattern is viewed with the assistance of a cobalt blue filter, which, in effect, transmits blue light that will activate the fluorescein dye. It is important to use a Wratten no. 12 yellow filter (or equivalent) that can be attached to the observation system to serve as a barrier filter, screening out all but the wavelengths of interest.
25 The importance of the yellow filter cannot be underestimated since it makes an easily observable improvement in fluorescein pattern evaluation. The use of a yellow filter, in combination with a good illumination source, is especially important in the evaluation of GP materials that contain ultraviolet inhibitors because, as the material absorbs wavelengths that correspond to the illumination source, there is an apparent reduction or even absence of fluorescence behind the lens unless the appropriate filters and illumination source are used. It is hoped that biomicroscopic manufacturers will begin to incorporate the yellow filter into their respective instruments.
Pattern Evaluation:
The fluorescein pattern assumes a variety of forms. Areas of fluorescein pooling appear green; areas in which fluorescein is absent or where the tear layer is too thin to detect, having the contact lens in direct contact with the cornea, appear as dark or black. In between these extremes, the varying thickness of the tear layer is observed as varying shades of green.
An alignment fit is observed when the lens evenly contours the cornea with a light, even tear pooling (
Fig. 5.3). Apical clearance exists when a steep central fit with excessive fluorescence or central tear pooling is present (
Fig. 5.4). This can result in midperipheral bearing and sealoff with a reduced ability to remove cellular debris and mucus that may be an important precursor to rigid lens adherence to the cornea. Apical clearance has also been found to induce corneal steepening, even after short-term wear.
26 Apical bearing exists when there is direct contact of the lens against the central cornea or the amount of tear pooling is too shallow to detect
with the instillation of fluorescein (
Fig. 5.5). Excessive apical bearing can potentially result in corneal molding with resultant distortion or warpage. In addition, the gradual formation of a central corneal abrasion is also possible.
With corneal astigmatism greater than one diopter, a dumbbell-shaped fluorescein pattern will be observed (
Fig. 5.6). Typically, along the steeper meridian of the cornea, the tear layer thickness gradually increases toward the edge and the lens does not touch the cornea.
Along the flatter meridian, however, the tear layer thickness decreases toward the periphery and the lens comes in contact with the cornea at the edge of the optical zone. As corneal astigmatism increases, the difference in tear layer thickness between the two primary meridians becomes greater, the area of alignment becomes smaller, and the astigmatic, or dumbbell-shaped, fluorescein pattern becomes exaggerated.
27 If the cornea exhibits with-the-rule corneal astigmatism, the pooling is in the vertical meridian with alignment or bearing in the horizontal meridian. If the cornea exhibits against-the-rule astigmatism, the opposite is true: the pooling is in the horizontal meridian with alignment or bearing in the vertical meridian. In high corneal astigmatism—typically greater than two diopters—the use of a high-Dk material with a steeper than K base curve radius will result in excessive flexure and reduced visual acuity. In addition, the “rocking” of the lens during the blink process may result in discomfort, mechanical corneal staining, and possible lens adherence. The selection of a lower oxygen-permeable material, and perhaps a flatter base curve radius, is recommended. Another option would be a bitoric design, especially if the high amount of corneal toricity results in inferior decentration of the lens (see
Chapter 14).
It is important to evaluate the fluorescein pattern after the blink since the amount of pooling and bearing will vary during the blink process. If the lens is decentered, the position of the lens relative to the cornea must be considered prior to evaluating the fluorescein pattern. For example, an inferior decentering lens will typically exhibit excessive superior pooling since the flatter peripheral bevel is adjacent to the steeper central cornea.
The evaluation of the fluorescein pattern at the lens periphery is also beneficial. There should be sufficient clearance peripherally—typically greater than apically—to allow sufficient tear exchange and debris removal while avoiding mechanical irritation as the lens moves across the cornea. If fluorescein pooling is minimal or absent peripherally and seal-off exists, the peripheral curve(s) should be flattened.
Fluorescein pattern evaluation of the rigid lens-to-cornea fitting relationship should be performed both at the fitting visit and at all subsequent follow-up visits. A practitioner’s ability to properly assess fluorescein patterns occurs with experience and frequent evaluation. There are several educational resources available from the GP Lens Institute (www.gpli.info) including an educational CD-ROM entitled “GP Fitting, Evaluation, and Problem-Solving,” a GP Lens Management Guide, and a Fluorescein Pattern Identification laminated card. It would be erroneous to believe that fluorescein pattern evaluation is not as important with GP materials as with polymethylmethacrylate (PMMA) as a result of the reduction in edema-related complications. The lens material is only as good as the practitioner’s ability to properly evaluate it; a poor lens-to-cornea fitting relationship can result in numerous problems, including desiccation, adhesion, and abrasion. In particular, the fluorescein pattern evaluation is invaluable in the difficult-to-fit cases such as high corneal toricity, irregular/distorted corneas, and keratoconus.
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