Reference
Lace, J. W., Merz, Z. C., Kennedy, E. E., Seitz, D. J., Austin, T. A., Ferguson, B. J., & Mohrland, M. D. (2022). Examination of five- and four-subtest short-form IQ estimations for the Wechsler Intelligence Scale for Children-Fifth edition (WISC-V) in a mixed clinical sample. Applied Neuropsychology: Child, 11(1), 50-61. https://doi.org/10.1080/21622965.2020.1747021
Review
Lace et al. (2022) investigated the efficacy of ten unique five-subtest (pentad) and four-subtest (tetrad) short-form (SF) combinations in estimating full-scale IQ (FSIQ) on the Wechsler Intelligence Scale for Children-Fifth Edition (WISC-V) in a mixed clinical sample. A total of 268 pediatric participants were included in the study, with mean scores falling in the low average-to-average ranges. Regression-based and prorated FSIQ estimates were calculated, and the accuracy of each SF combination was assessed by comparing the estimates to the true FSIQ. Results showed that both regression-based and prorated/adjusted methods provided FSIQ estimates that were accurate within five Standard Score points of true FSIQ for approximately 81-92% (pentad) and 65-76% (tetrads) of participants. Prorated/adjusted estimates appeared to provide somewhat better accuracy than regression-based estimates. The study provides clinicians with useful information when selecting abbreviated assessments of intelligence in clinical practice.
The study adds value to the existing literature by examining the efficacy of SF IQ estimations for the WISC-V in a mixed clinical sample. The authors' finding that both regression-based and prorated/adjusted methods provided accurate FSIQ estimates within five Standard Score points of true FSIQ for most participants is useful for clinicians who are seeking to administer abbreviated assessments of intelligence. The authors also provide useful information on the benefits, detriments, and other considerations of each SF combination. However, the authors acknowledge the limitations of the study, including the use of an archival sample and the lack of consideration for specific clinical populations, which may limit the generalizability of the findings.