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Third International Visual Field Symposium - Imaging and Perimetry ...

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field. A flicker attachment, originally designed by Dr. Nakabayashi (1967)<br />

was inserted in the optical pathway of Autoplot Tangent Screen made by<br />

Bausch <strong>and</strong> Lomb.<br />

Patients were chosen from those who visited the outpatient clinic <strong>and</strong><br />

neuro-ophthalmology clinic of our institutions during the past 8 years.<br />

RESULTS AND DISCUSSION<br />

Figure 2 is a typical case of optic neuritis in which kinetic Goldmann pe-<br />

rimetry failed to detect central scotoma. However, in central flicker field<br />

studies we detected central scotoma. The central vision was 0.3 <strong>and</strong> central<br />

CFF was 15 Hz. We could easily come to a diagnosis of optic neuritis.<br />

Figure 3 is a typical course of recovery of vision <strong>and</strong> CFF in optic neuritis.<br />

Following steroid therapy, vision was recovered first, followed by the recov-<br />

ery of CFF. After one month <strong>and</strong> a half, the patient complained of blurring<br />

of vision. Although there was very small reduction of visual acuity, CFF was<br />

reduced remarkably, indicating that there was recurrence of optic neuritis.<br />

As far as we rely on central vision <strong>and</strong> ordinary kinetic perimetry <strong>and</strong><br />

campimetry, it is not easy to detect very early changes of optic nerve lesion<br />

or recurrence of optic neuritis.<br />

Various types of recovery of central vision <strong>and</strong> central CFF are shown in<br />

figure 4. Figure 5 is a schematic drawing of the course of recovery of vision<br />

<strong>and</strong> central CFF in optic neuritis. Vertical lines indicates the time of obser-<br />

vation. If we see a patient in a very early stage, we can detect dissociation of<br />

vision <strong>and</strong> CFF as shown in type IV. If we see a patient at the time of<br />

lowest vision <strong>and</strong> CFF, the course of recovery <strong>and</strong> CFF may vary from case<br />

to case. This observation of dissociation of vision <strong>and</strong> CFF is most impor-<br />

tant in the diagnosis of optic nerve diseases in their early stages.<br />

Normal values ranges from 40 to 50 Hz <strong>and</strong> the lowest limit is 35 Hz. If<br />

central CFF is less than 25 Hz, we can definitely make a diagnosis of optic<br />

nerve disease even though vision is restored within a normal range. There-<br />

fore, the ‘flicker test’ is equally or even more important than the examina-<br />

tion of pupillary reflex.<br />

Based on our experience in the past 8 years, we can conclude that the<br />

‘flicker test’ is useful in the diagnosis of optic neuritis <strong>and</strong> papillits, toxic<br />

amblyopia, optic nerve injury, compression of the optic nerve by the tumor.<br />

This test is also useful in the differential diagnosis of atrophic stage of<br />

papilledema, optic atrophy <strong>and</strong> disc pallor only, amblyopia, refractive<br />

anomaly, disturbance of accommodation, hysteria <strong>and</strong> simulation.<br />

SUMMARY<br />

We developed an apparatus for the measurement of central CFF <strong>and</strong> used<br />

this on over 10,000 cases during the last 8 years. It was confirmed that CFF<br />

is remarkably decreased in optic nerve or 3rd neuron diseases <strong>and</strong> this<br />

‘flicker test’ is the most reliable test to be used in the diagnosis of optic<br />

nerve diseases in neuro-ophthalmological practice.<br />

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