Two Views of Invalid Response Set and Malingering Attributions in Forensic Assessment: Credibility and Non-Credibility.

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This article reviews two major sets of six articles on malingering and invalid response set, which have diametrically opposite conclusions on the value of performance and symptom validity tests (PVTs and SVTs) in forensic and related disability assessments (FDRA). First, we review the six-article series by the Leonhards, which takes the stance that PVTs and SVTs lack sufficient conceptual and empirical support to be utilized in FDRA. More specifically, the Leonhards criticize the circularity in using PVTs both as predictors and outcome criterion variables. Also, they argue that PVTs are highly correlated and collinear. However, we note that the Leonhards refer to PVTs as "malingering" tests, which they are not. Next, our article summarizes Young six-article series on invalid response sets, which (a) provides revised definitions of key terms; (b) proposes a new multivariate cutoff for invalid performance tied to the number of PVTs administered ("the 30% rule"); and (c) reviews research on the base rate of invalid response sets (generally below 30%). Finally, the present article reviews additional papers criticizing the Leonhards' approach, and introduces new data that support the standard approach. We recommend continued conceptual and empirical refinement, while re-affirming the utility of PVTs and SVTs in FDRA.

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Performance validity tests (PVTs) and symptom validity tests (SVTs) are essential to neuropsychological evaluations, helping ensure findings reflect true abilities or concerns. It is unclear how PVTs and SVTs perform in children who received radiotherapy for brain tumors. Accordingly, we investigated the rate of noncredible performance on validity indicators as well as associations with fatigue and lower intellectual functioning. Embedded PVTs and SVTs were investigated in 98 patients with pediatric craniopharyngioma undergoing proton radiotherapy (PRT). The contribution of fatigue, sleepiness, and lower intellectual functioning to embedded PVT performance was examined. Further, we investigated PVTs and SVTs in relation to cognitive performance at pre-PRT baseline and change over time. SVTs on parent measures were not an area of concern. PVTs identified 0-31% of the cohort as demonstrating possible noncredible performance at baseline, with stable findings 1 year following PRT. Reliable digit span (RDS) noted the highest PVT failure rate; RDS has been criticized for false positives in pediatric populations, especially children with neurological impairment. Objective sleepiness was strongly associated with PVT failure, stressing need to consider arousal level when interpreting cognitive performance in children with craniopharyngioma. Lower intellectual functioning also needs to be considered when interpreting task engagement indices as it was strongly associated with PVT failure. Embedded PVTs should be used with caution in pediatric craniopharyngioma patients who have received PRT. Future research should investigate different cut-off scores and validity indicator combinations to best differentiate noncredible performance due to task engagement versus variable arousal and/or lower intellectual functioning.

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