Large Animal Neurology. Joe Mayhew

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Figure 2.9 Visual and light pathways.

The first observation of CN III function to be made is the size and symmetry of the pupillary apertures, considering the amount of ambient light and the emotional status of the patient. The response of the pupils to light directed into each eye, the pupillary light responses, can be noted after observing the eyeballs for any lesions that may interfere with the response of the pupil such as iritis, iris atrophy, or adhesions. The normal response to light directed into one eye is constriction of both pupils. This is referred to as a direct response in the same or ipsilateral eye in which the light is shone and a slightly less pronounced consensual (indirect) response in the other, contralateral eye. The incoming or afferent pathway for this reflex is similar to that for the menace response to the level of the brainstem. The pathway goes via the optic nerve with most axons crossing within the optic chiasm, then through the optic tracts lateral and dorsal to the thalamus, and finally passing ventrally into the midbrain. Interconnections between left and right sides occur via the caudal commissure so that impulses arrive at each parasympathetic oculomotor nucleus in the midbrain on both sides. The motor, efferent pathway is from these nuclei, via the oculomotor nerves to the ciliary ganglia behind the eyeball and to the constrictor muscles of the pupils.

      Because the observation of pupillary light responses in both eyes simultaneously is awkward to perform alone in large animals, the swinging light test is a useful alternative. The use of this test essentially removes the need to do consensual pupillary light reflex testing. The swinging light test is performed as follows. A bright focused source of light is shone into one eye, and after pupillary constriction is completed, the light is quickly transferred to the opposite eye in which further pupillary constriction is expected to occur if the eye is normal. This test is then performed in reverse and repeated with swinging movements of the light source, starting at say 30 cm from the eyes and moving step‐wise closer to say 5 cm from the eyeball. It is best to perform this test in dim light, and in performing the test in this manner the patient becomes accustomed to the swinging bright light so that it does not blink with a dazzle response when the light reaches the retina, which often obscures the initial fast pupillary response. If the pupil dilates when the light reaches the second eye in this test, there must be an afferent optic lesion involving that second eye.

The reason for further pupillary constriction occurring when the light reaches the second, normal eye is that the direct pupillary light reflex is stronger in its effect than the indirect or consensual pupillary light reflex. This fact should be recalled when interpreting some complex results of testing vision and pupillary responses, and two other issues are also worthy of iteration. First, the mydriatic effect of atropine can last for days if not weeks, producing confusion in evaluation and interpretation of pupillary responses to light. Second, it appears to take a more complete optic nerve or chiasmal lesion to cause observable mydriasis even with poor vision and a poor or even absent menace response, most particularly with bilateral lesions. Consider for example a yearling colt with obvious bilateral blindness when in its environment, that followed head trauma occurring after rearing and falling over backward onto the poll and suffering from bilateral, focal, traumatic optic neuropathy. The colt may still have essentially appropriate, mid‐sized pupils that even respond somewhat to a bright light. Evaluation of partial, especially asymmetric lesions such as this can be problematic unless this factor is appreciated.

      These pupillary light reflexes are within the brainstem and thus are not affected by lesions involving the cerebral visual cortex (Figure 2.9). A widely dilated, mydriatic pupil in an eye that has normal vision suggests an oculomotor nerve lesion; the pupil being unresponsive to light directed into either eye. The pupil in the contralateral eye, with normal oculomotor function, responds to light directed into both the ipsilateral eye (direct response) and the contralateral eye (consensual response). The oculomotor nerves are subject to damage following diffuse brain swelling and from space‐occupying lesions in the forebrain. Both processes can cause pressure to be exerted ventrally onto the brainstem and these nerves can be damaged as they lay between the midbrain and the basilar bones. With asymmetric swelling of cerebral tissue, greater pressure may be applied to one oculomotor nerve resulting in unequal pupils or anisocoria, which is usually evident as ipsilateral pupillary dilation. A severe brainstem contusion can produce various pupillary abnormalities in association with coma or semicoma, and these can change rapidly in the first few hours following injury. Progressive, bilateral, pupillary dilation following cranial injury warrants a grave prognosis.

      When reporting results of pupillary function and light responses, it removes considerable confusion to describe what happens to each pupil when light is shone in each eye in turn and not to use the terms direct and consensual or indirect responses. Thus, with a left‐sided retrobulbar abscess involving left CN III parasympathetic fibers or ciliary ganglion or nerve, as well as СКАЧАТЬ