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shapes that approximate various types of irregular astigmatism more closely than the simple “football” model. These aberrations include such shapes as spherical aberration, coma, and trefoil. See Chapter 6 of this book and BCSC Section 13, Refractive Surgery, for further discussion.

Binocular States of the Eyes

The spherical equivalent of a refractive state is defined as the algebraic sum of the spherical component and half of the astigmatic component. Anisometropia refers to any difference in the spherical equivalents between the 2 eyes. Uncorrected anisometropia in children may lead to amblyopia, especially if 1 eye is hyperopic. Although adults may be annoyed by uncorrected anisometropia, they may be intolerant of initial spectacle correction. Unequal image size, or aniseikonia, may occur, and the prismatic effect of the glasses will vary in different directions of gaze, inducing anisophoria. Anisophoria may be more bothersome than aniseikonia for patients with spectacle-corrected anisometropias.

Aniseikonia can also be due to a difference in the shape of the images formed in the 2 eyes. The most common cause is the differential magnification inherent in the spectacle correction of anisometropia. Even though aniseikonia is difficult to measure, anisometropic spectacle correction can be prescribed in such a manner as to reduce aniseikonia. Making the front surface power of a lens less positive can reduce magnification. Decreasing center thickness also reduces magnification. Decreasing vertex distance diminishes the magnifying effect of plus lenses as well as the minifying effect of minus lenses. These effects become increasingly noticeable as lens power increases. Contact lenses may provide a better solution than spectacles for most patients with anisometropia, particularly children, in whom fusion may be possible.

Unilateral aphakia is an extreme example of hyperopic anisometropia arising from refractive ametropia. In the adult patient, spectacle correction produces an intolerable aniseikonia of about 25%; contact lens correction produces aniseikonia of about 7%, which is usually tolerated. If necessary, the clinician may reduce aniseikonia still further by adjusting the powers of contact lenses and simultaneously worn spectacle lenses to provide the appropriate minifying or magnifying effect via the Galilean telescope principle. For further information on correcting aphakia, see Chapters 3, 4, and 5.

Accommodation and Presbyopia

Accommodation is the mechanism by which the eye changes refractive power by altering the shape of its crystalline lens. The mechanisms that achieve this alteration have been described by Helmholtz. The posterior focal point is moved forward in the eye during accommodation (Fig 2-13A). Correspondingly, the far point moves closer to the eye (Fig 2-13B). Accommodative effort occurs when the ciliary muscle contracts in response to parasympathetic stimulation, thus allowing the zonular fibers to relax. The outward-directed tension on the lens capsule is decreased, and the lens becomes more convex. Accommodative response results from the increase in lens convexity (primarily the anterior surface). It may be expressed as the amplitude of accommodation (in diopters) or as the range of accommodation, the distance between the far point of the eye and the nearest point at which the eye can maintain focus (near point). It is evident that as the lens loses elasticity from the aging process, the accommodative response wanes (a condition called

presbyopia), even though the amount of ciliary muscle contraction (or accommodative effort) is virtually unchanged. For an eye with presbyopia, the amplitude is a more useful measurement for calculating the power requirement of the additional spectacle lens. For appraising an individual’s ability to perform a specific visual task, the range is more informative.

Figure 2-13 Emmetropia with accommodation stimulated. A, Parallel light rays now come to a point locus in front of the retina, forming a blurred image on the retina. B, Light rays emanating from a point on the retina focus to a near point in front of the eye, between optical infinity and the cornea. (Illustration b y C. H. Wooley.)

Glasser A, Kaufman PL. The mechanism of accommodation in primates. Ophthalmology. 1999;106(5):863–872.

Epidemiology of Refractive Errors

An interplay among corneal power, lens power, anterior chamber depth, and axial length determines an individual’s refractive status. All 4 elements change continuously as the eye grows. On average, babies are born with about 3.00 D of hyperopia. In the first few months of life, this hyperopia may increase slightly, but it then declines to an average of about 1.00 D of hyperopia by the end of the first year because of marked changes in corneal and lenticular powers, as well as axial length growth. By the end of the second year, the anterior segment attains adult proportions; however, the curvatures of the refracting surfaces continue to change measurably. One study found that average corneal power decreased 0.10–0.20 D and lens power decreased about 1.80 D between ages 3 years and 14 years.

From birth to age 6 years, the axial length of the eye grows by approximately 5 mm; thus, one might expect a high prevalence of myopia in infants. However, most children’s eyes are actually emmetropic, with only a 2% incidence of myopia at 6 years. This phenomenon is due to a stillundetermined mechanism called emmetropization. During this period of eye growth, a compensatory loss of 4.00 D of corneal power and 2.00 D of lens power keeps most eyes close to emmetropia. It appears that the immature human eye develops so as to reduce refractive errors.

American Academy of Ophthalmology. Refractive Management/Intervention Panel. Preferred Practice Pattern Guidelines. Refractive Errors. San Francisco: American Academy of Ophthalmology; 2002. Available at www.aao.org/ppp.

Lawrence MS, Azar DT. Myopia and models and mechanisms of refractive error control. Ophthalmol Clin North Am. 2002;15(1):127–133.

Prevent Blindness America; National Eye Institute. Vision Problems in the U.S.: Prevalence of Adult Vision Impairment and Age-Related Eye Disease in America. 5th ed. Chicago, IL: Prevent Blindness America; 2012.

Developmental Myopia

Myopia increases steadily with increasing age. In the United States, the prevalence of myopia has been estimated at 3% among children aged 5–7 years, 8% among those aged 8–10 years, 14% among those aged 11–12 years, and 25% among adolescents aged 12–17 years. In particular ethnic groups, a similar trend has been demonstrated, although the percentages in each age group may differ. Ethnic Chinese children have much higher rates of myopia at all ages. A national study in Taiwan found the prevalence was 12% among 6-year-olds and 84% among adolescents aged 16–18 years. Similar rates have been found in Singapore and Japan.

Different subsets of myopia have been characterized. Juvenile-onset myopia, defined as myopia with an onset between 7 years and 16 years of age, is due primarily to growth in axial length. Risk factors include esophoria, against-the-rule astigmatism, premature birth, family history, and intensive near work. In general, the earlier the onset of myopia is, the greater is the degree of progression. In the United States, the mean rate of childhood myopia progression is reported at about 0.50 D per year. In approximately 75% of teenagers, refractive errors stabilize at about age 15 or 16. In those whose errors do not stabilize, progression often continues into the 20s or 30s.

Adult-onset myopia begins at about 20 years of age, and extensive near work is a risk factor. A study of West Point cadets found myopia requiring corrective lenses in 46% at entrance, 54% after 1 year, and 65% after 2 years. The probability of myopic progression was related to the degree of initial refractive error. It is estimated that as many as 20%–40% of patients with low hyperopia or emmetropia who have extensive near-work requirements become myopic before age 25, compared with less than 10% of persons without such demands. Older Naval Academy recruits have a lower rate of myopia development than younger recruits over a 4-year curriculum (15% for 21-year-olds versus 77% for 18-year-olds). Some young adults are at risk for myopic progression even after a period of refractive stability. It has been theorized that persons who regularly perform considerable near work undergo a process similar to emmetropization for the customary close working distance, resulting in a myopic shift.

The etiologic factors concerning myopia are complex, involving both genetic and environmental factors. Regarding a genetic role, identical twins are more likely to have a similar degree of myopia than are fraternal twins, siblings, or parent and child. Identical twins separated at birth and having different work habits do not show significant differences in refractive error. Some forms of severe myopia suggest dominant, recessive, and even sex-linked inheritance patterns. However, studies of ethnic Chinese in Taiwan show an increase in the prevalence and severity of myopia over the span of 2 generations, a finding that implies that genetics alone are not entirely responsible for myopia. Some studies have reported that near work is not associated with a higher prevalence and progression of myopia, especially with respect to middle-distance activities such as tasks involving video displays. Higher educational achievement has been strongly associated with a higher prevalence of myopia. Poor nutrition has been implicated in the development of some refractive errors as well. Studies from Africa, for example, have found that children with malnutrition have an increased prevalence of high ametropia, astigmatism, and anisometropia.

Feldkämper M, Schaeffel F. Interactions of genes and environment in myopia. Dev Ophthalmol. 2003;37:34–49.

Fischer AJ, McGuire JJ, Schaeffel F, Stell WK. Lightand focus-dependent expression of the transcription factor ZENK in the chick retina. Nat Neurosci. 1999;2(8):706–712.

McCarty CA, Taylor HR. Myopia and vision 2020. Am J Ophthalmol. 2000;129(4):525–527.

Winawer J, Wallman J, Kee C. Differential responses of ocular length and choroidal thickness in chick eyes to brief periods of plus and minus lens-wear. Invest Ophthalmol Vis Sci Suppl. 1999;40:S963.