Programs for diagnosis and therapy of visual field deficits in vision rehabilitation



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Spatial Vision, vol. 10, No.4, pp. 499-503 (1997) Programs for diagnosis and therapy of visual field deficits in vision rehabilitation Erich Kasten*, Hans Strasburger & Bernhard A. Sabel Institut für Medizinische Psychologie, Otto-von-Guericke Universität. Leipziger Str. 44, 39120 Magdeburg, Germany Reseived 20 June 1996; reseived 30 september 1996; accepted 30 September 1996 Abstract-A suite of computer ms is descibed for visual field-assessment of residual vision in neuropsychological rehabilitation. 1. INTRODUCTION Recent findings of higher plasticity and limited functional recovery from visual field defects (Zihl 1979; Zihl and Cramon, 1981; Schmielau, 1989; Kasten et al., 1994, Kasten and Sabel, 1995) suggest that training patients having certain types of visual field loss is beneficial. Hence, the availability of specialised, easy-to-use techniques for restoring some aspects of visual function is important. Here we describe a suite of computer s for the diagnosis and therapy of visual field deficits for use in neuropsychological rehabilitation. This set of s complements commercially available perimeters. The aim is to concentrate measurements to a certain, patientspecific subfield and to provide, through automation, in that limited field more detailed information about certain low-level visual functions. Of particular interest are those functions that are typically affected, or provide differential information, in the various kinds of visual field deficits. Furthermore, a derived, slightly modified version of the s allows the training of those same visual functions, with particular emphasis of the training in those parts of the visual field where residual function has been ascertained. The limitations of measurement when a computer monitor is used for perimetry purposes are a natural consequence of a number of physical and optical limitations. Minimum luminance of a black monitor screen is limited by phosphor characteristics and is often visible under dark adapted viewing conditions (e.g. Di Lollo et al., 1996). Visual field size is limited through the monitor s physical screen size, through the min- * erich.kasten@medizin.uni-magdeburg.de

500 E.Kasten et al. imal viewing distance that must be kept in order to limit the influence of screen resolution, accomodation, and also X-ray screen radiation. A further limitation stems from the fact that the screen is not concavely spherical such that eccentric field positions are seen with accomodative error. We use a viewing distance of 30 cm such that the field size is 40 horizontally and 25 vertically. Refractive correction to that distance is advisable for subjects over 45 years of age, specifically for form recognition (PeriForm) at small target size but this is at the border of the s intended use. When only a hemifield or a quadrant is of interest, that field can be shifted by using an appropriate eccentric fixation point. Tests are done in a darkened room; the head of the subjects is stabilized with a head-support. The stimulus is presented at random positions both in the blind and intact areas of the visual field. There is no acoustic signal prior to the visual stimulus to prevent anticipatory eye movements toward the stimulus. All s Tab. 1: Normative data obtained from a group of 19 healthy subjects (21 66 years age, mean 39.7) for the three diagnostic s. Stimulus size 0.25 (PeriMat), 1 (Peri- Form), 1.5 (PeriColor); black background (< 1 cd/m²), stimulus luminance 50 cd/m 2 (PeriMat), 50 cd/m 2 (PeriForm), 25-95 cd/m 2 (PeriColor); 150 ms stimulus duration. Monocular viewing, separately for the center and the four quadrants as shown by the five squares in part of the table (table position corresponds to field position). Bold font: median, plain font: lower und upper quartile. PeriMat (500 items) PeriForm (250 items) PeriColor (250 items) Left Eye Right Eye 487 (465.5-489.5) 488 (463.0-497.0) 487 (452.0-495.0) 488 (475.0-492.5) 489 (481.0-492.0) 488 (479.5-492.0) 487 (482.5-490.5) 488 (465.5-495.0) 488 (473.0-491.0) 489 (484.5-492.0) 220 (209.0-231.0) 221 (204.0-226.0) 213 (192.0-219.5) 227 (213.0-234.5) 238 (226.0-240.5) 229 (217.5-234.5) 220 (208.5-229.5) 206 (196.0-220.0) 194 (184.0-209.5) 227 (217.0-232.0) 204 (170.0-213.5) 187 (161.5-202.0) 183 (154.5-188.0) 209 (194.0-216.0) 225 (206.5-235.0) 222 (193.5-228.0) 203 (185.0-223.0) 186 (166.5-193.0) 168 (158.0-188.0) 219 (194.0-228.5)

Programs for vision rehabilitation 501 allow the use of different levels of stimulus and background luminance, in the range given by the monitor, and a range of stimulus sizes. The s further allow different levels of stimulus duration (e.g. 50, 100, 150 or 200 ms) and use of randomized intervals of stimuli. Each item is presented at a given screen position only once. Correct fixation is ascertained by having a 0.5 fixation point that changes its colour, e.g. from bright green to yellow, and instructing the patient to press a key upon change. The amount of colour change can be adjusted to the patient s capabilities and there is a warning message when a subject is unable to recognize the change. A first set of normative data was obtained from a group of 19 healthy subjects; the results are shown in Tab. 1. The measurements were done monocularly and separately for the central visual field and the four quadrants. The table shows medians (bold) and lower and upper quartiles. The has further been extensively used for examination of patients having visual field deficits (Kasten et al., 1994; Kasten and Sabel, 1995). Figure 1: Example of visual field as assessed by PeriMat. ASCII graphics are used to allow the s to run on the whole range of MS-DOS computers. Homonymous hemianopia in a 46 years old male after an accident. (+ = stimulus position, X = un position, * = fixation point).

502 E.Kasten et al. 2. Diagnostic s: PeriMat: This examines visual field defects; it measures the responses to small light spots (stimulus size 0.25 1, 15 100 cd/m²) which are presented at random positions on a monitor screen for a given duration (50, 100, 150, or 200 ms). While fixating, the patient is asked to press the space bar as soon as he or she perceives the stimulus. The stimulus is presented at 500 different positions within a period of about 20 minutes. In patients with cerebral blindness the shows the intact and defective areas (Fig. 1). PeriForm: The PeriForm examines the patient s ability to recognize simple forms in different areas of the visual field. The stimulus set consists of letters, figures, or small lines, with four alternatives in each group (smallest size: 1 ). A session consist of 250 presentations at different positions in randomized sequence. The examination needs 15 min. PeriColor: This assesses discrimination of broad colour categories in the visual field. PeriColor works similarly to PeriForm, except that coloured squares are used as stimuli. 3. Training s: For each task, a corresponding version of the is available for training of that particular function. Current evidence suggests that training is most promising in areas with residual function. For each patient these areas are first determined. The patients then receive a disk with the software adapted to their respective deficit and they are instructed to train for one hour each day in a darkened room at home. The results of every session are saved onto disk for subsequent analysis. Whenever the patient has reached a pre-determined level of performance (more than 90% correct responses), the advances to the next level where stimuli are presented further out in the blind visual field section. Visure: The Visure was developed to train at the border between the intact and the deficient sectors. A large white stimulus which rhythmically changes its size moves from the intact visual field into the borderline area. The patient is instructed to press a key upon detection of the stimulus. The stimulus then moves further into the direction of the blind area and continues to change its size to maximally activate residual function. If the patient is unable to see the stimulus at this position, the stimulus retracts back into the intact area and the procedure is repeated. SeeTrain: In this, the task is to detect a stimulus on a black screen. The

Programs for vision rehabilitation 503 brightness of the stimulus changes from dark gray to light white in the same position. A further training method is based on the detection of a growing black line on a gray screen. In both parts of the, task difficulty can be adjusted by changing the appropriate stimulus parameters such as size or brightness in order to adapt to the patient s specific deficit. FormTrain: This is the training variant of PeriForm, for training form discrimination. ColorTrain: This is the training variant of PeriColor, for training discrimination of broad colour categories. FixTrain: this fixation-training includes several procedures for patients having fixation deficits. The stimuli undergo small changes at random intervals that are not visible without proper fixation. The tests show high objectivity, retest reliability and validity (Kasten, 1993). We have encouraging results about the effectivity of the training with these s. In a first study the treatment group displayed a reliable enlargement of visual field size (Kasten et al., 1994; Kasten and Sabel, 1995). The study seems to indicate that the key to success is extended training. The s have therefore been explicitly designed to allow home training after the areas of residual vision have been determined by the clinician. The s use ASCII graphics in order to run on the whole range of MS- DOS computers. REFERENCES Di Lollo, V., Seiffert, A.E., Burchett, G., Rabeeh, R. and Ruman, T. A. (1996). Phosphor persistence of oscilloscopic displays: a comparison of four phosphors. Spatial Vision 10, 353 360. Kasten, E., Wiegmann, U. and Sabel, B.A. (1994). Rehabilitation cerebral bedingter Gesichtsfeldeinschränkungen Überblick. Z. Neuropsych. 5, 127-150. Kasten, E. and Sabel, B.A. (1995). Visual field enlargement after computer training in braindamaged patients with homonymous deficits: an open pilot trial. Rest. Neurol. Neurosci., 113-127. Schmielau, F. (1989). Restitution visueller Funktionen bei hirnverletzten Patienten: Effizienz lokalisationsspezifischer sensorischer und sensomotorischer Maßnahmen. In: Psychologie in der Neurologie. P. Jakobi (Ed.), Springer, Berlin, pp. 115-126. Zihl, J. (1981). Recovery of visual functions in patients with cerebral blindness: Effect of specific practice with saccadic localization. Exp. Brain Res. 44, 159-169. Zihl, J. and Cramon, D.Y. (1979). Restitution of visual field function in patients with cerebral blindness. J. Neurol. Neurosurg, Psychiat. 42, 312-32.