Lippa Sara M, Axelrod Bradley N, Lange Rael T
a Defense and Veterans Brain Injury Center , Silver Spring , MD , USA.
b Walter Reed National Military Medical Center , Bethesda , MD , USA.
J Clin Exp Neuropsychol. 2016 Sep;38(7):721-9. doi: 10.1080/13803395.2016.1161732. Epub 2016 May 9.
The Mild Brain Injury Atypical Symptoms (mBIAS) scale was developed as a symptom validity test (SVT) for use with patients following mild traumatic brain injury. This study was the first to examine the clinical utility of the mBIAS in a mixed clinical sample presenting to a Department of Veterans Affairs (VA) neuropsychology clinic.
Participants were 117 patients with mixed etiologies (85.5% male; age: M = 39.2 years, SD = 11.6) from a VA neuropsychology clinic. Participants were divided into pass/fail groups using two different SVT criteria, based on select validity scales from the Minnesota Multiphasic Personality Inventory-2 (MMPI-2): first, Infrequency Scale (F) scores: (a) MMPI-F-Fail (n = 21) and (b) MMPI-F-Pass (n = 96); and, second, Symptom Validity Scale (FBS) scores: (a) MMPI-FBS-Fail (n = 36) and (b) MMPI-FBS-Pass (n = 81).
The mBIAS demonstrated good internal consistency, and each item contributed meaningfully to the total score. At a symptom exaggeration base rate of 35%, an mBIAS cutoff of ≥11 was optimal for screening symptom exaggeration when groups were classified using both F and FBS scales. This cutoff score resulted in very high specificity (.89 to .94); moderate-high positive predictive power (.71 to .75) and negative predictive power (.72 to .79); and low-moderate sensitivity (.31 to .57). At all base rates of probable somatic exaggeration, a cutoff of ≥16 resulted in perfect specificity and positive predictive power, but very low sensitivity.
The mBIAS has potential for use in samples outside of mild traumatic brain injury. In settings where the symptom exaggeration base rate is 35%, a cutoff of ≥11 may be used as a "red flag" for further evaluation, but should not be relied on for clinical decision making. At all base rates of probable somatic exaggeration, psychologists with patients who score ≥16 can be confident that those patients were exaggerating. Importantly, however, this cutoff may fail to identify a large proportion of patients who are exaggerating.
轻度脑损伤非典型症状(mBIAS)量表是作为一种症状效度测试(SVT)开发的,用于轻度创伤性脑损伤后的患者。本研究首次在一家退伍军人事务部(VA)神经心理学诊所就诊的混合临床样本中检验了mBIAS的临床效用。
参与者为来自VA神经心理学诊所的117名病因混合的患者(85.5%为男性;年龄:M = 39.2岁,SD = 11.6)。根据明尼苏达多相人格调查表-2(MMPI-2)中的选定效度量表,使用两种不同的SVT标准将参与者分为通过/未通过组:第一,低频量表(F)得分:(a)MMPI-F-未通过(n = 21)和(b)MMPI-F-通过(n = 96);第二,症状效度量表(FBS)得分:(a)MMPI-FBS-未通过(n = 36)和(b)MMPI-FBS-通过(n = 81)。
mBIAS表现出良好的内部一致性,每个项目对总分都有显著贡献。在症状夸大基础率为35%时,当使用F量表和FBS量表对组进行分类时,mBIAS临界值≥11最适合筛查症状夸大。这个临界值分数导致非常高的特异性(0.89至0.94);中度偏高的阳性预测力(0.71至0.75)和阴性预测力(0.72至0.79);以及低中度敏感性(0.31至0.57)。在所有可能的躯体夸大基础率下,临界值≥16导致完美的特异性和阳性预测力,但敏感性非常低。
mBIAS在轻度创伤性脑损伤以外的样本中具有应用潜力。在症状夸大基础率为35%的情况下,临界值≥11可作为进一步评估的“警示信号”,但不应依赖其进行临床决策。在所有可能的躯体夸大基础率下,对于得分≥16的患者,心理学家可以确信这些患者在夸大症状。然而,重要的是,这个临界值可能无法识别很大一部分夸大症状的患者。