Neurocognitive parameters should be incorporated in the Minnesota Multiphasic Personality Inventory-2 assessment of patients with alcohol use disorders
Introduction and Aims. Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory‐2 (MMPI‐2). However, during periods of abstinence, cognitive impairments (e.g. attention, memo...
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| Published in: | Drug and alcohol review Vol. 31; no. 4; pp. 550 - 557 |
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| Language: | English |
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Blackwell Publishing Asia
01-06-2012
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| Abstract | Introduction and Aims. Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory‐2 (MMPI‐2). However, during periods of abstinence, cognitive impairments (e.g. attention, memory and executive dysfunctions) related to neurological and somatic pathology may affect level and pattern of MMPI‐2 scale scores, resulting in clinical misinterpretation.
Design and Methods. A re‐analysis of the data of the Egger et al. study is conducted in order to examine the clinical significance of the MMPI‐2 profiles of 222 AUD patients (mean age 42.2 ± 9.6 years; 76.6% men) by using neurologically relevant item correction procedures. Hierarchical cluster analyses of neurologically relevant item‐corrected solutions were compared to the original MMPI‐2 profile.
Results. Impulsiveness and psychopathic deviation were identified as a common denominator.
Discussion and Conclusions. Uncorrected MMPI‐2 assessment in AUD tends to overstress psychopathology and to overlook disinhibitory traits in early abstinence, caused by chronic alcoholism.[Walvoort SJW, Wester AJ, Egger JIM. Neurocognitive parameters should be incorporated in the Minnesota Multiphasic Personality Inventory‐2 assessment of patients with alcohol use disorders. Drug Alcohol Rev 2012;31:550–557] |
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| AbstractList | Introduction and Aims.Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory-2 (MMPI-2). However, during periods of abstinence, cognitive impairments (e.g. attention, memory and executive dysfunctions) related to neurological and somatic pathology may affect level and pattern of MMPI-2 scale scores, resulting in clinical misinterpretation. Design and Methods.A re-analysis of the data of the Egger et al. study is conducted in order to examine the clinical significance of the MMPI-2 profiles of 222 AUD patients (mean age 42.2 +/- 9.6 years; 76.6% men) by using neurologically relevant item correction procedures. Hierarchical cluster analyses of neurologically relevant item-corrected solutions were compared to the original MMPI-2 profile. Results.Impulsiveness and psychopathic deviation were identified as a common denominator. Discussion and Conclusions.Uncorrected MMPI-2 assessment in AUD tends to overstress psychopathology and to overlook disinhibitory traits in early abstinence, caused by chronic alcoholism. Adapted from the source document. INTRODUCTION AND AIMSTreatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory-2 (MMPI-2). However, during periods of abstinence, cognitive impairments (e.g. attention, memory and executive dysfunctions) related to neurological and somatic pathology may affect level and pattern of MMPI-2 scale scores, resulting in clinical misinterpretation.DESIGN AND METHODSA re-analysis of the data of the Egger et al. study is conducted in order to examine the clinical significance of the MMPI-2 profiles of 222 AUD patients (mean age 42.2 ± 9.6 years; 76.6% men) by using neurologically relevant item correction procedures. Hierarchical cluster analyses of neurologically relevant item-corrected solutions were compared to the original MMPI-2 profile.RESULTSImpulsiveness and psychopathic deviation were identified as a common denominator.DISCUSSION AND CONCLUSIONSUncorrected MMPI-2 assessment in AUD tends to overstress psychopathology and to overlook disinhibitory traits in early abstinence, caused by chronic alcoholism. Introduction and Aims. Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory‐2 (MMPI‐2). However, during periods of abstinence, cognitive impairments (e.g. attention, memory and executive dysfunctions) related to neurological and somatic pathology may affect level and pattern of MMPI‐2 scale scores, resulting in clinical misinterpretation. Design and Methods. A re‐analysis of the data of the Egger et al. study is conducted in order to examine the clinical significance of the MMPI‐2 profiles of 222 AUD patients (mean age 42.2 ± 9.6 years; 76.6% men) by using neurologically relevant item correction procedures. Hierarchical cluster analyses of neurologically relevant item‐corrected solutions were compared to the original MMPI‐2 profile. Results. Impulsiveness and psychopathic deviation were identified as a common denominator. Discussion and Conclusions. Uncorrected MMPI‐2 assessment in AUD tends to overstress psychopathology and to overlook disinhibitory traits in early abstinence, caused by chronic alcoholism.[Walvoort SJW, Wester AJ, Egger JIM. Neurocognitive parameters should be incorporated in the Minnesota Multiphasic Personality Inventory‐2 assessment of patients with alcohol use disorders. Drug Alcohol Rev 2012;31:550–557] Introduction and Aims. Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory‐2 (MMPI‐2). However, during periods of abstinence, cognitive impairments (e.g. attention, memory and executive dysfunctions) related to neurological and somatic pathology may affect level and pattern of MMPI‐2 scale scores, resulting in clinical misinterpretation. Design and Methods. A re‐analysis of the data of the Egger et al. study is conducted in order to examine the clinical significance of the MMPI‐2 profiles of 222 AUD patients (mean age 42.2 ± 9.6 years; 76.6% men) by using neurologically relevant item correction procedures. Hierarchical cluster analyses of neurologically relevant item‐corrected solutions were compared to the original MMPI‐2 profile. Results. Impulsiveness and psychopathic deviation were identified as a common denominator. Discussion and Conclusions. Uncorrected MMPI‐2 assessment in AUD tends to overstress psychopathology and to overlook disinhibitory traits in early abstinence, caused by chronic alcoholism. [Walvoort SJW, Wester AJ, Egger JIM. Neurocognitive parameters should be incorporated in the Minnesota Multiphasic Personality Inventory‐2 assessment of patients with alcohol use disorders. Drug Alcohol Rev 2012;31:550–557] Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota Multiphasic Personality Inventory-2 (MMPI-2). However, during periods of abstinence, cognitive impairments (e.g. attention, memory and executive dysfunctions) related to neurological and somatic pathology may affect level and pattern of MMPI-2 scale scores, resulting in clinical misinterpretation. A re-analysis of the data of the Egger et al. study is conducted in order to examine the clinical significance of the MMPI-2 profiles of 222 AUD patients (mean age 42.2 ± 9.6 years; 76.6% men) by using neurologically relevant item correction procedures. Hierarchical cluster analyses of neurologically relevant item-corrected solutions were compared to the original MMPI-2 profile. Impulsiveness and psychopathic deviation were identified as a common denominator. Uncorrected MMPI-2 assessment in AUD tends to overstress psychopathology and to overlook disinhibitory traits in early abstinence, caused by chronic alcoholism. |
| Author | WESTER, ARIE J. WALVOORT, SERGE J. W. EGGER, JOS I. M. |
| Author_xml | – sequence: 1 givenname: SERGE J. W. surname: WALVOORT fullname: WALVOORT, SERGE J. W. email: swalvoort@vvgi.nl organization: Vincent van Gogh Institute for Psychiatry, Venray, the Netherlands – sequence: 2 givenname: ARIE J. surname: WESTER fullname: WESTER, ARIE J. organization: Vincent van Gogh Institute for Psychiatry, Venray, the Netherlands – sequence: 3 givenname: JOS I. M. surname: EGGER fullname: EGGER, JOS I. M. organization: Vincent van Gogh Institute for Psychiatry, Venray, the Netherlands |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22176199$$D View this record in MEDLINE/PubMed |
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A 2002; 16 1982; 56 2009; 44 2006; 30 2006; 32 2002; 57 2002; 10 1992; 17 2003; 15 2008; 32 2003; 18 2008; 103 2008; 31 1988; 75 2005; 29 2003; 10 1997; 7 1978 1993; 6 1992; 7 1998; 171 2009; 13 1991; 47 2010; 29 1997; 12 2011; 20 1999; 13 2007; 4 2008; 22 2011; 23 2011; 69 2001; 12 1998; 121 1996; 20 1989 2007; 17 1995; 9 2007; 19 1995; 51 2010; 35 2006; 13 1997; 20 2008; 18 2005; 40 2008; 14 1988; 56 1999; 22 1996 2008; 57 2006 1993 1992 2009; 373 1995; 18 1991 2008; 90 2005; 162 2004; 16 1993; 10 1999; 34 2000; 81 2003; 27 2005; 1 2010; 92 2007; 42 2005; 17 2001; 36 2005; 18 1989; 17 2003; 22 1990; 4 e_1_2_6_51_2 e_1_2_6_72_2 e_1_2_6_53_2 e_1_2_6_74_2 e_1_2_6_30_2 e_1_2_6_70_2 Butcher JN (e_1_2_6_47_2) 1996 e_1_2_6_19_2 e_1_2_6_13_2 e_1_2_6_34_2 e_1_2_6_59_2 Alfano DP (e_1_2_6_35_2) 1993; 6 e_1_2_6_11_2 e_1_2_6_32_2 e_1_2_6_17_2 e_1_2_6_38_2 e_1_2_6_55_2 e_1_2_6_76_2 Oscar‐Berman M (e_1_2_6_18_2) 2003; 27 e_1_2_6_15_2 e_1_2_6_36_2 e_1_2_6_78_2 Lindboe CF (e_1_2_6_67_2) 1988; 75 e_1_2_6_62_2 e_1_2_6_64_2 e_1_2_6_20_2 e_1_2_6_60_2 e_1_2_6_7_2 Allen JP (e_1_2_6_25_2) 1996; 20 e_1_2_6_3_2 e_1_2_6_5_2 e_1_2_6_24_2 e_1_2_6_22_2 Sloore H (e_1_2_6_49_2) 1996 e_1_2_6_43_2 Morey LC (e_1_2_6_57_2) 1991 e_1_2_6_66_2 e_1_2_6_26_2 e_1_2_6_45_2 e_1_2_6_68_2 e_1_2_6_50_2 e_1_2_6_73_2 e_1_2_6_52_2 e_1_2_6_75_2 e_1_2_6_31_2 e_1_2_6_71_2 Graham JR (e_1_2_6_9_2) 2006 Åsberg M (e_1_2_6_44_2) 1978 e_1_2_6_12_2 e_1_2_6_58_2 e_1_2_6_10_2 e_1_2_6_33_2 e_1_2_6_16_2 e_1_2_6_39_2 Becker HC (e_1_2_6_41_2) 2008; 31 e_1_2_6_54_2 e_1_2_6_77_2 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_56_2 e_1_2_6_79_2 e_1_2_6_61_2 Derksen JLL (e_1_2_6_40_2) 2006 e_1_2_6_63_2 e_1_2_6_42_2 Martin PR (e_1_2_6_28_2) 2003; 27 Butcher JN (e_1_2_6_48_2) 1989 e_1_2_6_8_2 Derksen J (e_1_2_6_46_2) 1993 e_1_2_6_29_2 e_1_2_6_4_2 e_1_2_6_6_2 e_1_2_6_23_2 e_1_2_6_69_2 Arbisi PA (e_1_2_6_80_2) 1999; 13 e_1_2_6_2_2 e_1_2_6_21_2 e_1_2_6_65_2 e_1_2_6_27_2 |
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| Snippet | Introduction and Aims. Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with... Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the Minnesota... Introduction and Aims. Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with... INTRODUCTION AND AIMSTreatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with the... Introduction and Aims.Treatment planning for alcohol use disorder (AUD) patients is often preceded by the assessment of psychopathology and personality with... |
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| SubjectTerms | Abstinence Adult alcohol dependence Alcohol related disorders Alcohol-Related Disorders - diagnosis Alcohol-Related Disorders - psychology Assessment Cognition Dysfunction Female Humans Male Middle Aged Minnesota Multiphasic Personality Inventory-2 MMPI MMPI-2 neurobehavioural correction neurocognitive assessment Neuropsychological Tests Personality Disorders - diagnosis Personality Disorders - psychology Psychopathology |
| Title | Neurocognitive parameters should be incorporated in the Minnesota Multiphasic Personality Inventory-2 assessment of patients with alcohol use disorders |
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