OM t of c.iii - Vision Research Coordinating Center - Washington ...
OM t of c.iii - Vision Research Coordinating Center - Washington ...
OM t of c.iii - Vision Research Coordinating Center - Washington ...
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2/1/99 Chapter 1 Background page 1-15<br />
1. Flat, with primary lens support on the apex <strong>of</strong> the cornea (Hall, 1963), where the<br />
central optic zone <strong>of</strong> the lens actually touches or “bears on” the central corneal<br />
epithelium<br />
2. Steep, with lens support and bearing directed <strong>of</strong>f the apex and onto the paracentral<br />
cornea, with clearance (vaulting) <strong>of</strong> the apex <strong>of</strong> the cornea (Voss and Liberatore,<br />
1962); and<br />
3. Divided support, or “three-point touch,” with lens support and bearing shared<br />
between the corneal apex and the paracentral cornea.<br />
Most optometrists continue to use central corneal touch fitting since it is easier<br />
and appears to provide better vision, comfort, and wearing time. We have shown in a<br />
prospective survey <strong>of</strong> almost 1,600 keratoconus patients that 75% <strong>of</strong> the patients<br />
wearing rigid contact lenses are fitted with apical touch (Edrington et al., 1991). In<br />
addition, it has been argued (Kemmetmuller, 1962) that flat lenses delay the need for<br />
surgery by physically keeping the shape <strong>of</strong> the conus relatively flat. In contrast, it has<br />
been argued that the flat fitting method, which the majority <strong>of</strong> practitioners use today,<br />
may actually increase the risk <strong>of</strong> corneal compromise in the form <strong>of</strong> scarring.<br />
However, only one prospective randomized clinical trial has compared central<br />
corneal touch fitting to central corneal clearance fitting in keratoconus (Korb et al.,<br />
1982), and the results are inconclusive as to whether contact lenses influence the disease<br />
course directly.<br />
1.7 Tissue Changes in Keratoconus<br />
Keratoconus corneas are structurally and biochemically different from normal<br />
corneas. The distribution <strong>of</strong> stromal fibers is uneven. The results <strong>of</strong> a number <strong>of</strong><br />
investigations appear to indicate that there is an increase in intercellular substance and<br />
a decrease <strong>of</strong> total collagen accompanied by an increase <strong>of</strong> structural glycoproteins<br />
(Robert et al., 1970; Critchfield et al, 1988; Yue et al, 1984). However, others argue that<br />
correction for age negates these observations (Zimmermann et al., 1988). Teng (1963)<br />
demonstrated early changes in keratoconus in the basal epithelium indicating enzymes<br />
may be released from fragile basal epithelial cells which may cause fragmentation,<br />
fibrillation and liquefaction <strong>of</strong> the anterior stroma with invasion <strong>of</strong> fibroblasts and<br />
resultant scarring. Fibrin and fibrinogen are decreased in the epithelial basement<br />
membrane in keratoconus (Millin et al, 1986). In scarred areas <strong>of</strong> keratoconus corneas,<br />
collagen type III predominates (Maumenee, 1978; Newsome et al, 1981). Some studies<br />
have found high amounts <strong>of</strong> lysinonorleucine in keratoconus corneas indicating<br />
abnormal collagen cross linking (Cannon and Foster, 1978), while others have not