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INTRODUCTION
The digit repetition test is commonly used to assess verbal short term
memory and is included in both standard intelligence tests and mental status
examinations (Ruesch and Moore, 1943; Heilbrun, 1958). The supposition
underlying the use of this test is that it reflects an important area of intellec
tual functioning which is highly vulnerable to brain damage. There is, how
ever, research evidence which casts doubt upon the usefulness of the digit
span test in differentiating organic patients from normals. Sterne (1969) was
unable to demonstrate significant differences in digit repetition between brain
damaged and non-brain-damaged patients. As a specific clinical example, there
are patients with particular organic amnestic syndromes (Korsakoff's syndro
me) who have been shown to have normal digit span performance (Milner,
1962, Drachman and Arbit, 1966 ).
Recent research interest has focused upon the possibility of localizing
focal lesions from digit span performance. The currently available data regard
ing the digit repetition of patients with unilateral lesions is contradictory.
McFie (1969) and Newcombe (1969) reported that digit span performance
is impaired in patients with left hemisphere lesions, irrespective of the locus
of the lesion within the hemisphere. De Renzi and Nichelli (1975) stated
that verbal memory span (as tested by digit repetition) is directly dependent
upon the intactness of the left hemisphere, with impaired performance being
the result of aphasia. Digit repetition performance was not affected by damage
to the right hemisphere wherever localized. Weinberg, Diller, Gerstman
and Schulman ( 1972) found that patients with left hemisphere lesions per
form like poorly educated normals on both forward and backward digit
repetition. In their right hemisphere lesion patients, digit span forward was
superior to that of left hemisphere lesion patients, and did not differ
significantly from that of normal controls. The right hemisphere lesion pa
tients with visuospatial dysfunction (as assessed by a visual confrontation
Subjects
Clinical subject samples were composed of patients with discrete brain lesiom
secondary to high velocity small shrapnel fragments penetrating the skull and
dura. All injuries were war inflicted. For the purpose of this study, the brain
was divided into quadrants following the schema of Benson and Barton ( 1970 ),
with the fissure of Rolando designated as the anterior-posterior line of demarca
tion. Seventy-one subjects with lesions restricted to one of the four quadrants
were available from the population of all patients studied with war-related brain
injuries. Fourteen patients were assigned to the right frontal, 20 to the left
frontal, 19 to the right posterior, and 18 to the left posterior samples. The locus
and limitation of the lesions were documented by neurosurgical exploration in
all cases. Considerable care was exercised to exclude any patient with evidence
of bilateral or diffuse lesions. This was accomplished by the use of skull x-ray,
brain scan, EEG, and other neurodiagnostic procedures when deemed necessary
by the referring neurosurgeon. To preclude any contamination of results, poten
tial subjects with clinically significant vascular or infectious complications of the
initial brain lesion were also excluded from the subject pool. Patients with
significant wounds, infections, or other illness were not considered for selection.
As has been recommended (De Renzi and Nichelli, 1975), aphasia was not used
as an exclusion criterion. On clinical neurological examination, three of the left
frontal quadrant sample, two of the left posterior sample, and one of the right
posterior sample showed some evidence of aphasia. In all such cases, the aphasia
was mild and near-normal communication was possible. All aphasic patients were
easily able to meet Goodglass et al.'s criterion that the patient be able to ade
quately repeat at least one verbal item (digit) (Goodglass, Gleason and Hyde,
1970).
The diameter of entrance wounds in the four clinical samples was approxi
mately equal, with a total sample range from .5 to 4.2 em and a median dia
meter of 2 em. All selected subjects were right handed and were healthy prior
to injury without history of psychiatric or neurological problems.
For purpose of comparison, a 25 subject control sample was selected from
patients hospitalized because of war-related peripheral injuries. None of the con
trol sample had wounding of the head or upper extremities and showed no
evidence of brain lesions of any etiology.
The age of clinical and control subjects ranged from 18 to 31 years, with
a total sample mean of 21.5 years (SD. = 2.1). Variations in mean age for
the five samples was nonsignificant (F = 1.1). The mean educational level for
the total sample was 11.8 years (S.D. = 1.8), with no significant differences
among sample means (F = .86 ). The recency of injury (time in weeks between
dates of wounding and evaluation) in the five samples also did not differ appre
ciably (total sample mean= 1.2 months; S.D. = .9).
All patients were also administered the WAIS, Wechsler· Memory Scale
(Form II) and the Bender Gestalt Test under standard conditions.
Following the hypothesis that defective backward digit repetition may be
related to a difficulty in revisualization (Weinberg et al., 1972), the total brain
damaged sample was divided into a group with and a group without visual
constructional deficits. Bender Gesta,h protocols were scored for integration,
distortion, perseveration, and rotation errors according to the Koppitz ( 1964)
system. Twenty-two patients ·made more than one of the above errors and
were classified as demonstrating visual constructional deficits; while the remaining
49 patients made either no errors (N = 31) or only one scoreable error (N =
18) and were classified as not demonstrating visual constructional deficits.
RESULTS
Means and standard deviations for digit span forward and backward
in the four brain-damaged and the control samples appear in Tab~e I.
TABLE I
Digit span forward differed significantly from that of controls in the right
frontal (F = 19.75, p < .001), left frontal (F = 8.82, p < .001), and left
posterior (F = 28.41, p < .001) samples. The mean digit span forward scores
of controls and right posterior lesion samples did not differ significantly (F
= 3.65). The left and right hemisphere lesion samples did not differ appre
ciably on digit span forward (F = 1.03) nor were there significant differences
among the four quadrant brain-damaged samples (F = .87). Then mean digit
span forward scores of subjects with visual constructional deficits and those
without such deficits did not differ appreciably (F = .29).
The mean digit span backward scores of controls did not differ signifi
cantly from those of any of the brain-damaged samples (right frontal lesion
sample: F = 2.19; left frontal lesion sample: F = 3.73; right posterior
lesion sample: F = 3.39; and left posterior lesion sample: F = 3.00). The
16 F. W. Black and R. L. Strub
right and left hemisphere lesion samples also did not show significant differ
ences on digit span backward (F = .43). There were no significant differences
in digit span backward among the four quadrant samples (F = .31). Subjects
with visual constructional deficits did not differ appreciably from subjects
without such deficits (F = .98).
TABLE II
Incidence of Significantly Impaired DSF and DSB Performance (- 2 Standard Deviations)
Controls 0 0
Right frontal lesion 50 0
Left frontal lesion 55 6
Right posterior lesion 45 8
Left posterior lesion 67 5
All brain-damaged 57 5
of the right frontal lesion subjects, and 7% of the left posterior subjects.
The incidence of large discrepancies was significantly lower than that in the
control sample for the right frontal lesion sample (chi2 = 10.81, p < .01)
and left posterior lesion sample (chi2 = 23.62, p < .01). The incidence
of such discrepancies in the right posterior and left frontal lesion samples,
although less than that in the control sample, were not significantly different.
The right and left hemisphere lesion samples showed no significant differ
ence in the incidence of forward-backward discrepancies (chi2 = 1.42 ).
TABLE III
frontal lesion sample. WAIS Full Scale I.Q. was significantly related to
digit span forward in all samples and with digit span backward in the right
frontal and posterior lesion samples. Significant correlations among digit
repetition and other cognitive measures were much less consistent, tending
to predominate in the right posterior lesion sample.
DISCUSSION
span forward was impaired in many patients, there was a general narrowing
of the digit forward-backward discrepancy.
Our findings may in part be explained by the nature of the particular
sample studied. The patients examined were young, healthy prior to injury,
and without histories of neurological or psychiatric problems. They received
rather discrete brain lesions from small metallic fragments, and in general
suffered limited cognitive and neurological deficits. The cognitive effects seen
by others researching this topic are probably due to the more extensive lesions
and longstanding neurological disease suffered by their patients.
SuMMARY
REFERENCES
BENSON, D. F., ,and BARTON, M; (1970) Disturbances in constructional ability, "Cortex," 6, 19-46.
CosTA, L. D. (1975) The relation of visuospatial dysfunction to digit span performance on patients
with cerebral lesions, "Cortex," 11, 31-36.
DE RENZI, E., and NICHELLI, P. (1975) Verbal and non-verbal short-term memory impairment
following hemispheric damage, "Cortex," 11, 341-354.
DRACHMAN, D. A., and ABIT, J. (1966) Memory and the hippocampal complex, II, "Arch.
Neurol.," 15, 52-61.
GooDGLASS, H., GLEASON, ]. B., and HYDE, M. R. (1970) Some dimensions of auditory language
comprehension in aphasics, "J. Speech Hear. Res.," 13, 595-606.
HEILBRUN, A. B. (1958) The digit span test and the prediction of cerebral pathology, "Arch.
Neurol. Psychiat.," 80, 228-231. ·
KoPPITZ, E. M. (1964) The Bander Gestalt Test for Young Children, Grune and Stratton, New
York.
McFIE, J. (1969) The diagnostic significance of disorders of higher nervous activity, in Handbook
of Clinical Neurology, Vol. 4, ed. by P. J. Vinken and G. V. Bruyn, North Holland
Publishing Company, Amsterdam.
Digit repetition performance 21
F. William Black, Ph.D. & Richard L. Strub, M.D., Department of Neurology, LSU Medical Center, 1542
Tulane Avenue, New Orleans, Louisiana 70112.