The 3 subtests did not show sufficient divergent validity to warrant a conclusion of their domain specificity. Thus, when a more detailed diagnostic profile is required, a thorough neuropsychological evaluation will provide a more valid description of an individual's cognitive profile.
The London Psychogeriatric Rating Scale (LPRS) was administered to 76 probable Alzheimer's patients, 59 patients with dementia unrelated to Alzheimer's, 102 neurologically normal subjects, and 27 patients with symptoms of both Alzheimer's and dementia of other etiologies. By examining the relationships among the four subscales of the LPRS and conducting factor analyses, it was demonstrated that the four subscales were not measuring different phenomena. The internal consistency of the full 36-item scale was high (Cronbach's Alpha = 0.96) indicating the total LPRS score provided a reliable global index of behavioral function. The total LPRS scores correlated with the independently administered Goldfarb Mental Status Examination scores (r = -0.79). The LPRS differentiated between the normals and the combined demented groups and between inpatients and outpatients. The LPRS continues to have clinical value for functional assessments in a non-intrusive manner. The LPRS may be particularly useful in situations where direct assessment of mental status is not practical.
We undertook a longitudinal crossvalidation of the Ryan and Paolo (1992) equation's ability to postdict Wechsler Adult Intelligence Scale-Revised (WAIS-R) Verbal IQ (VIQ) from National Adult Reading Test (NART) performance measured 5 years after VIQ scores were obtained, for a sample of 49 elderly normal individuals (mean age 71 years). Five-year interval postdiction accuracy agreed very well with the results of the original, concurrent study. Clinical utility is still limited, however, as VIQ must decline by 16.3 points for 95%-detection sensitivity. A new regression equation that utilizes a combination of NART errors and WAIS-R Vocabulary age-scaled scores (measured 3 years earlier) provided slightly better expected clinical sensitivity and accounted for 49% of the variance in VIQ scores.
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