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Visual acuity (VA) is acuteness or clearness of vision. It depends on optical and neural factors, i.e., (i) the sharpness of the retinal focus within the eye, (ii) the intactness and functioning of the retina, and (iii) the sensitivity of the interpretative faculty of the brain.
A common cause of low visual acuity is refractive error (ametropia), or errors in how the light is refracted in the eyeball. Causes of refractive errors include aberrations in the shape of the eyeball, the shape of the cornea, and reduced flexibility of the lens. In the case of pseudomyopia, the aberrations are caused by muscle spasms. Too high or too low refractive error (in relation to the length of the eyeball) is the cause of nearsightedness (myopia) or farsightedness (hyperopia) (normal refractive status is referred to as emmetropia). Other optical causes are astigmatism or more complex corneal irregularities. These anomalies can mostly be corrected by optical means (such as eyeglasses, contact lenses, laser surgery, etc.).
Neural factors that limit acuity are located in the retina or the brain (or the pathway leading there). Examples for the first are a detached retina and macular degeneration, to name just two. A common impairment amblyopia caused by incorrect nerve pathway function connecting eye with brain is involved . In some cases, low visual acuity is caused by brain damage, such as from traumatic brain injury or stroke. When optical factors are corrected for, acuity can be considered as being a measure of neural well-functioning.
Visual acuity is typically measured while fixating, i.e. as a measure of central (or foveal) vision, for the reason that it is highest there. However, acuity in peripheral vision can be of equal (or sometimes higher) importance in everyday life. Acuity declines towards the periphery in an inverse-linear (i.e. hyperbolic) fashion.
Visual acuity is a measure of the spatial resolution of the visual processing system. VA is tested by requiring the person whose vision is being tested to identify so-called optotypes – stylized letters, Landolt rings, Lea symbols, or other patterns – on a printed chart (or some other means) from a set viewing distance. Optotypes are represented as black symbols against a white background (i.e. at maximum contrast). The distance between the person's eyes and the testing chart is set at a sufficient distance to approximate infinity in the way the lens attempts to focus (far acuity), or at a defined reading distance (near acuity).
Normal visual acuity is commonly referred to as 20/20 vision (even though acuity in normally sighted people is generally higher), the metric equivalent of which is 6/6 vision. At 20 feet or 6 meters, a human eye with nominal performance is able to separate contours that are approximately 1.75 mm apart. A vision of 20/40 corresponds to lower than nominal performance, a vision of 20/10 to better performance.
In the expression 20/x vision, the numerator (20) is the distance in feet between the subject and the chart, and the denominator (x) is the distance at which a person with 20/20 acuity would just discern the same optotype. Thus, 20/20 means "normal" vision and 20/40 means that a person with 20/20 vision would discern the same optotype from 40 feet away. This is equivalent to saying that with 20/40 vision, the person possesses half the resolution and needs twice the size to discern the optotype.
A simple and efficient way to state acuity is by solving the fraction to a decimal number. 20/20 then corresponds to an acuity (or a Visus) of 1.0 (see Expression below). 20/10 corresponds to 2.0, which is often attained by well-corrected healthy young subjects with binocular vision. Stating acuity as a decimal number is the standard in European countries, as required by the European norm (EN ISO 8596, previously DIN 58220).
The precise distance at which acuity is measured is not important as long as the size of the optotype on the retina is the same. That size is specified as a visual angle, which is the angle, at the eye, under which the optotype appears. For 20/20 = 1.0 acuity, the size of a letter on the Snellen chart or Landolt C chart is a visual angle of 5 arc minutes (1 arc min = 1/60 of a degree). By the design of a typical optotype (like a Snellen E or a Landolt C), the critical gap that needs to be resolved is 1/5 this value, i.e., 1 arc min. The latter is the value used in the international definition of visual acuity:
Acuity = 1/
Acuity is a measure of visual performance and is unrelated to the eyeglass prescription required to correct vision. Instead, an eye exam seeks to find the prescription that will provide the best corrected visual performance achievable. The resulting acuity may be greater or less than 20/20 = 1.0. Indeed, a subject diagnosed as having 20/20 vision will often actually have higher visual acuity because, once this standard is attained, the subject is considered to have normal (in the sense of undisturbed) vision and smaller optotypes are not tested.
Measuring visual acuity is by a psychophysical procedure and as such relates the physical characteristics of a stimulus to a subject's percept and his/her resulting responses. Measurement can be by using an eye chart, by optical instruments, or by computerized tests like the FrACT.
Care must be taken that viewing conditions correspond to the standard, like correct luminance of the eye chart, correct viewing distance, enough time for responding, obeying how many errors are allowed, etc. In European countries, these conditions are standardized by the European norm (EN ISO 8596, previously DIN 58220).
|1843||Vision test types are invented in 1843 by the German ophthalmologist Heinrich Kuechler (1811-1873), in Darmstadt, Germany. He argues for need to standardize vision tests and produces three reading charts to avoid memorization.|
|1854||Eduard Jäger von Jaxtthal, a Vienna oculist, makes improvements to eye chart test types that were developed by Heinrich Kuechler. He publishes, in German, French, English and other languages, a set of reading samples to document functional vision. He uses fonts that were available in the State Printing House in Vienna in 1854 and labels them with the numbers from that printing house catalogue, currently known as Jaeger numbers.|
|1862||Hermann Snellen, a Dutch ophthalmologist, publishes in Utrecht his "Optotypi ad visum determinandum", ("Probebuchstaben zur Bestimmung der Sehscharfe"), the first visual chart based on "Optotypes", advocating the need for standardized vision tests. Snellen's Optotypes are not identical to the test letters used today. They were printed in an 'Egyptian Paragon' font and were of a serif style.|
|1888||Edmund Landolt introduces the broken ring, now known as the Landolt ring, which later becomes an international standard.|
Rick Ferris et al. of the National Eye Institute chooses the LogMAR chart layout, implemented with Sloan letters, to establish a standardized method of visual acuity measurement for the Early Treatment of Diabetic Retinopathy Study (ETDRS). These charts are used in all subsequent clinical studies, and did much to familiarize the profession with the new layout and progression. Data from the ETDRS were used to select letter combinations that give each line the same average difficulty, without using all letters on each line.
The International Council of Ophthalmology approves a new 'Visual Acuity Measurement Standard', also incorporating the above features.
20/20 is normal (daylight) vision. In low light (i.e., scotopic) vision, spatial resolution is much lower. This is due to spatial summation of rods, i.e. a number of rods merge into a bipolar cell, in turn connecting to a ganglion cell, and the resulting unit for resolution is large (and acuity small). Visual acuity is much better in bright light than dim light, the former reaching 2 with a bright center and surrounding, the latter perhaps being 0.4 (25 arc minutes). In this case, the stimulus is 1.7 inches (4.3 cm) seen at a distance of 20 feet (6.1 m).
The maximum angular resolution of the human eye at a distance of 1 km is typically 30 to 60 cm. This gives an angular resolution of between 0.02 to 0.03 degrees, which is roughly 0.6 arc minutes per line pair, which implies a pixel spacing of 0.3 arc minutes. 20/20 vision is defined as the ability to resolve two points of light separated by a visual angle of one minute of arc, or about 600 pixels per inch for a display on a device held 10 to 12 inches from the eye (since by the Nyquist theorem two points are needed to resolve a space).
Thus, visual acuity, or resolving power (in daylight, central vision), is the property of cones. To resolve detail, the eye's optical system has to project a focused image on the fovea, a region inside the macula having the highest density of cone photoreceptor cells (the only kind of photoreceptors existing on the fovea), thus having the highest resolution and best color vision. Acuity and color vision, despite being mediated by the same cells, are different physiologic functions that do not interrelate except by position. Acuity and color vision can be affected independently.
The grain of a photographic mosaic has just as limited resolving power as the "grain" of the retinal mosaic. In order to see detail, two sets of receptors must be intervened by a middle set. The maximum resolution is that 30 seconds of arc, corresponding to the foveal cone diameter or the angle subtended at the nodal point of the eye. In order to get reception from each cone, as it would be if vision was on a mosaic basis, the "local sign" must be obtained from a single cone via a chain of one bipolar, ganglion, and lateral geniculate cell each. A key factor of obtaining detailed vision, however, is inhibition. This is mediated by neurons such as the amacrine and horizontal cells, which functionally render the spread or convergence of signals inactive. This tendency to one-to-one shuttle of signals is powered by brightening of the center and its surroundings, which triggers the inhibition leading to a one-to-one wiring. This scenario, however, is rare, as cones may connect to both midget and flat (diffuse) bipolars, and amacrine and horizontal cells can merge messages just as easily as inhibit them.
Light travels from the fixation object to the fovea through an imaginary path called the visual axis. The eye's tissues and structures that are in the visual axis (and also the tissues adjacent to it) affect the quality of the image. These structures are: tear film, cornea, anterior chamber, pupil, lens, vitreous, and finally the retina. The posterior part of the retina, called the retinal pigment epithelium (RPE) is responsible for, among many other things, absorbing light that crosses the retina so it cannot bounce to other parts of the retina. Interestingly, in many vertebrates, such as cats, where high visual acuity is not a priority, there is a reflecting tapetum layer that gives the photoreceptors a "second chance" to absorb the light, thus improving the ability to see in the dark. This is what causes an animal's eyes to seemingly glow in the dark when a light is shone on them. The RPE also has a vital function of recycling the chemicals used by the rods and cones in photon detection. If the RPE is damaged and does not clean up this "shed" blindness can result.
As in a photographic lens, visual acuity is affected by the size of the pupil. Optical aberrations of the eye that decrease visual acuity are at a maximum when the pupil is largest (about 8 mm), which occurs in low-light conditions. When the pupil is small (1–2 mm), image sharpness may be limited by diffraction of light by the pupil (see diffraction limit). Between these extremes is the pupil diameter that is generally best for visual acuity in normal, healthy eyes; this tends to be around 3 or 4 mm.
If the optics of the eye were otherwise perfect, theoretically, acuity would be limited by pupil diffraction, which would be a diffraction-limited acuity of 0.4 minutes of arc (minarc) or 20/8 acuity. The smallest cone cells in the fovea have sizes corresponding to 0.4 minarc of the visual field, which also places a lower limit on acuity. The optimal acuity of 0.4 minarc or 20/8 can be demonstrated using a laser interferometer that bypasses any defects in the eye's optics and projects a pattern of dark and light bands directly on the retina. Laser interferometers are now used routinely in patients with optical problems, such as cataracts, to assess the health of the retina before subjecting them to surgery.
The visual cortex is the part of the cerebral cortex in the posterior part of the brain responsible for processing visual stimuli, called the occipital lobe. The central 10° of field (approximately the extension of the macula) is represented by at least 60% of the visual cortex. Many of these neurons are believed to be involved directly in visual acuity processing.
Proper development of normal visual acuity depends on an animal having normal visual input when it is very young. Any visual deprivation, that is, anything interfering with such input over a prolonged period, such as a cataract, severe eye turn or strabismus, or covering or patching the eye during medical treatment, will usually result in a severe and permanent decrease in visual acuity in the affected eye if not treated early in life. The decreased acuity is reflected in various abnormalities in cell properties in the visual cortex. These changes include a marked decrease in the number of cells connected to the affected eye as well as few cells connected to both eyes, resulting in a loss of binocular vision and depth perception, or stereopsis. The period of time over which an animal is highly sensitive to such visual deprivation is referred to as the critical period.
The eye is connected to the visual cortex by the optic nerve coming out of the back of the eye. The two optic nerves come together behind the eyes at the optic chiasm, where about half of the fibers from each eye cross over to the opposite side and join fibers from the other eye representing the corresponding visual field, the combined nerve fibers from both eyes forming the optic tract. This ultimately forms the physiological basis of binocular vision. The tracts project to a relay station in the midbrain called the lateral geniculate nucleus, part of the thalamus, and then to the visual cortex along a collection of nerve fibers called the optic radiations.
Any pathological process in the visual system, even in older humans beyond the critical period, will often cause decreases in visual acuity. Thus measuring visual acuity is a simple test in accessing the health of the eyes, the visual brain, or pathway to the brain. Any relatively sudden decrease in visual acuity is always a cause for concern. Common causes of decreases in visual acuity are cataracts and scarred corneas, which affect the optical path, diseases that affect the retina, such as macular degeneration and diabetes, diseases affecting the optic pathway to the brain such as tumors and multiple sclerosis, and diseases affecting the visual cortex such as tumors and strokes.
Though the resolving power depends on size and packing density of the photoreceptors, the neural system of receptors must interpret this resolving power. As determined from various experiments on the cat, different ganglion cells are tuned to different frequencies of detail, as from a grating, so some ganglion cells have better acuity than others. In humans the results are the same, this time utilizing the same method as well as a device to read electrical changes in the scalp.
Besides the neural connections of the receptors, the optical system is an equally key player in retinal resolution. In the ideal eye, the image of a diffraction grating can subtend 0.5 micrometre on the retina. This is certainly not the case, however, and furthermore the pupil can cause diffraction of the light. Thus, black lines on a grating will be mixed with the intervening white lines to make a gray appearance. Defective optical issues (such as uncorrected myopia) can render it worse, but suitable lenses can help. Images (such as gratings) can be sharpened by lateral inhibition, i.e., more highly excited cells inhibiting the less excited cells. A similar reaction is in the case of chromatic aberrations, in which the color fringes around black-and-white objects are inhibited similarly.
Using the foot as a unit of measurement, (fractional) visual acuity is expressed relative to 20/20. Otherwise, using the metre, visual acuity is expressed relative to 6/6. For all practical purposes, 6/6 vision is equivalent to 20/20. In the decimal system, acuity is defined as the reciprocal value of the size of the gap (measured in arc minutes) of the smallest Landolt C, the orientation of which can be reliably identified. A value of 1.0 is equal to 20/20.
LogMAR is another commonly used scale, expressed as the (decadic) logarithm of the minimum angle of resolution. The LogMAR scale converts the geometric sequence of a traditional chart to a linear scale. It measures visual acuity loss: positive values indicate vision loss, while negative values denote normal or better visual acuity. This scale is rarely used clinically; it is more frequently used in statistical calculations because it provides a more scientific equivalent for the traditional clinical statement of “lines lost” or “lines gained”, which is valid only when all steps between lines are equal, which is not usually the case.
A visual acuity of 20/20 is frequently described as meaning that a person can see detail from 20 feet (6.1 m) away the same as a person with normal eyesight would see from 20 feet. If a person has a visual acuity of 20/40, he is said to see detail from 20 feet (6.1 m) away the same as a person with normal eyesight would see it from 40 feet (12 m) away.
Healthy young observers have a binocular acuity superior to 20/20; the limit of acuity in the unaided human eye is around 20/10–20/8 (6/3–6/2.4), although 20/8.9 was the highest score recorded in a study of some US professional athletes. Some birds of prey, such as hawks, are believed to have an acuity of around 20/2; in this respect, their vision is much better than human eyesight.
When visual acuity is below the largest optotype on the chart, the reading distance is reduced until the patient can read it. Once the patient is able to read the chart, the letter size and test distance are noted. If the patient is unable to read the chart at any distance, he or she is tested as follows:
|Counting Fingers||CF||Ability to count fingers at a given distance.|
|Hand Motion||HM||Ability to distinguish a hand if it is moving or not in front of the patient's face.|
|Light Perception||LP||Ability to perceive any light.|
|No Light Perception||NLP||Inability to see any light. Total blindness.|
Various countries have defined statutory limits for poor visual acuity that qualifies as a disability. For example, in Australia, the Social Security Act defines blindness as:
A person meets the criteria for permanent blindness under section 95 of the Social Security Act if the corrected visual acuity is less than 6/60 on the Snellen Scale in both eyes or there is a combination of visual defects resulting in the same degree of permanent visual loss.—Table 13, Schedule 1B, Social Security Act 1991
In the USA, the relevant federal statute defines blindness as follows:
[T]he term "blindness" means central visual acuity of 20/200 or less in the better eye with the use of a correcting lens. An eye that is accompanied by a limitation in the fields of vision such that the widest diameter of the visual field subtends an angle no greater than 20 degrees shall be considered for purposes in this paragraph as having a central visual acuity of 20/200 or less.
A person's visual acuity is registered documenting the following: whether the test was for distant or near vision, the eye(s) evaluated and whether corrective lenses (i.e. glasses or contact lenses) were used:
So, distant visual acuity of 20/60 and 20/25 with pinhole in the right eye will be: DscOD 20/60 PH 20/25. Distant visual acuity of count fingers and 20/50 with pinhole in the left eye will be: DscOS CF PH 20/50. Near visual acuity of 20/25 with pinhole remaining at 20/25 in both eyes with spectacles will be: NccOU 20/25 PH 20/25.
"Dynamic visual acuity" defines the ability of the eye to visually discern fine detail in a moving object.
Visual acuity measurement involves more than being able to see the optotypes. The patient should be cooperative, understand the optotypes, be able to communicate with the physician, and many more factors. If any of these factors is missing, then the measurement will not represent the patient's real visual acuity.
Visual acuity is a subjective test meaning that if the patient is unwilling or unable to cooperate, the test cannot be done. A patient being sleepy, intoxicated, or having any disease that can alter the patient's consciousness or his mental status can make the measured visual acuity worse than it actually is.
Illiterate patients who cannot read letters and/or numbers will be registered as having very low visual acuity if this is not known. Some of the patients will not tell the physician that they don't know the optotypes unless asked directly about it. Brain damage can result in a patient not being able to recognize printed letters, or being unable to spell them.
A motor inability can make a person respond incorrectly to the optotype shown and negatively affect the visual acuity measurement.
Variables such as pupil size, background adaptation luminance, duration of presentation, type of optotype used, interaction effects from adjacent visual contours (or “crowding") can all affect visual acuity measurement.
The measurement of visual acuity in infants, pre-verbal children and special populations (for instance, handicapped individuals) is not always possible with a letter chart. For these populations, specialised testing is necessary. As a basic examination step, one must check whether visual stimuli can be fixated, centered and followed.
More formal testing using preferential looking techniques use Teller acuity cards (presented by a technician from behind a window in the wall) to check whether the child is more visually attentive to a random presentation of vertical or horizontal gratings on one side compared with a blank page on the other side — the bars become progressively finer or closer together, and the endpoint is noted when the child in its adult carer's lap equally prefers the two sides.
Another popular technique is electro-physiologic testing using visual evoked (cortical) potentials (VEPs or VECPs), which can be used to estimate visual acuity in doubtful cases and expected severe vision loss cases like Leber's congenital amaurosis.
VEP testing of acuity is somewhat similar to preferential looking in using a series of black and white stripes (sine wave gratings) or checkerboard patterns (which produce larger responses than stripes). Behavioral responses are not required and brain waves created by the presentation of the patterns are recorded instead. The patterns become finer and finer until the evoked brain wave just disappears, which is considered to be the endpoint measure of visual acuity. In adults and older, verbal children capable of paying attention and following instructions, the endpoint provided by the VEP corresponds very well to the psychophysical measure in the standard measurement (i.e. the perceptual endpoint determined by asking the subject when they can no longer see the pattern). There is an assumption that this correspondence also applies to much younger children and infants, though this does not necessarily have to be the case. Studies do show the evoked brain waves, as well as derived acuities, are very adult-like by one year of age.
For reasons not totally understood, until a child is several years old, visual acuities from behavioral preferential looking techniques typically lag behind those determined using the VEP, a direct physiological measure of early visual processing in the brain. Possibly it takes longer for more complex behavioral and attentional responses, involving brain areas not directly involved in processing vision, to mature. Thus the visual brain may detect the presence of a finer pattern (reflected in the evoked brain wave), but the "behavioral brain" of a small child may not find it salient enough to pay special attention to.
A simple but less-used technique is checking oculomotor responses with an optokinetic nystagmus drum, where the subject is placed inside the drum and surrounded by rotating black and white stripes. This creates involuntary abrupt eye movements (nystagmus) as the brain attempts to track the moving stripes. There is a good correspondence between the optokinetic and usual eye-chart acuities in adults. A potentially serious problem with this technique is that the process is reflexive and mediated in the low-level brain stem, not in the visual cortex. Thus someone can have a normal optokinetic response and yet be cortically blind with no conscious visual sensation.
Visual acuity depends upon how accurately light is focused on the retina, the integrity of the eye's neural elements, and the interpretative faculty of the brain. Normal visual acuity (in central, i.e. foveal vision) is frequently considered to be what was defined by Hermann Snellen as the ability to recognize an optotype when it subtended 5 minutes of arc, that is Snellen's chart 20/20 feet, 6/6 meter, 1.00 decimal or 0.0 logMAR. In young humans, the average visual acuity of a healthy, emmetropic eye (or ametropic eye with correction) is approximately 20/16 to 20/12, so it is inaccurate to refer to 20/20 visual acuity as "perfect" vision. 20/20 is the visual acuity needed to discriminate two contours separated by 1 arc minute—about 1/16 of an inch at 20 feet. This is because a 20/20 letter, E for example, has three limbs and two spaces in between them, giving 5 different detailed areas. The ability to resolve this therefore requires 1/5 of the letter's total size, which in this case would be 1 minute (visual angle). The significance of the 20/20 standard can best be thought of as the lower limit of normal or as a screening cutoff. When used as a screening test, subjects that reach this level need no further investigation, even though the average visual acuity with a healthy visual system is typically better.
Some people may suffer from other visual problems, such as color blindness, reduced contrast, mild amblyopia, cerebral visual impairments, inability to track fast-moving objects, or one of many other visual impairments and still have normal visual acuity. Thus, normal visual acuity by no means implies normal vision. The reason visual acuity is very widely used is that it is easily measured, its reduction (after correction) often indicates some disturbance, and that it often corresponds with the normal daily activities a person can handle, and evaluates their impairment to do them (even though there is heavy debate on that).
Normally visual acuity refers to the ability to resolve two separated points or lines, but there are other measures of the ability of the visual system to discern spatial differences.
Vernier acuity measures the ability to align two line segments. Humans can do this with remarkable accuracy, it is a hyperacuity. Under optimal conditions of good illumination, high contrast, and long line segments, the limit to vernier acuity is about 8 arc seconds or 0.13 arc minutes, compared to about 0.6 arc minutes (20/12) for normal visual acuity or the 0.4 arc minute diameter of a foveal cone. Because the limit of vernier acuity is well below that imposed on regular visual acuity by the "retinal grain" or size of the foveal cones, it is thought to be a process of the visual cortex rather than the retina. Supporting this idea, vernier acuity seems to correspond very closely (and may have the same underlying mechanism) enabling one to discern very slight differences in the orientations of two lines, where orientation is known to be processed in the visual cortex.
The smallest detectable visual angle produced by a single fine dark line against a uniformly illuminated background is also much less than foveal cone size or regular visual acuity. In this case, under optimal conditions, the limit is about 0.5 arc seconds or only about 2% of the diameter of a foveal cone. This produces a contrast of about 1% with the illumination of surrounding cones. The mechanism of detection is the ability to detect such small differences in contrast or illumination, and does not depend on the angular width of the bar, which cannot be discerned. Thus as the line gets finer, it appears to get fainter but not thinner.
Stereoscopic acuity is the ability to detect tiny differences in depth with the two eyes. For more complex targets, stereoacuity is similar to normal monocular visual acuity, or around 0.6-1.0 arc minutes, but for much simpler targets, such as vertical rods, may be as low as only 2 arc seconds. Although stereoacuity normally corresponds very well with monocular acuity, it may be very poor or even absent even with normal monocular acuities. Such individuals typically have abnormal visual development when they are very young, such as an alternating strabismus or eye turn, where both eyes rarely or never point in the same direction and therefore do not function together.