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External validity study of a personality disorders screening test in a community sample

Abstract

Background

A screening test for personality disorders was recently developed in Brazil, the Dimensional Clinical Personality Inventory – screening version (IDCP-SV). However, no relationship between this screening measure and other scales or external criteria was tested.

Objective

To seek for validity evidence based on related criteria (e.g., other psychological tests) and external criteria (e.g., sample demographics).

Methods

Sample comprised 804 participants from São Paulo (Brazil), most female and college students, with mean age equal to 29.65 (SD = 10.73). They answered the IDCP-SV and another screening for personality disorders (IPDS), a depression measure (EBADEP-screening), a scale assessing reasoning for living (EMVIVER), and a self-report for personality disorders categories assessment (SCID-II-PQ).

Results

IDCP-SV identified 46.4% of community sample as positive for personality disorders. The positive group showed the great mean for almost all comparisions, including psychological tests and the demographics characteristics, including large expressive effect sizes.

Discussion

Data suggest that the IDCP-SV discriminates a similar percentage of people from the community to what was reported previously using other screening measures; besides, the mean comparisons between groups showed good discriminative capacity by IDCP-SV items.

Screening measure; personality test; diagnosis; personality disorders

Introduction

Personality disorders (PDs) are characterized as persistent and maladaptive patterns of thoughts, feelings, perceptions, and behaviors, deviant from the expectations of the sociocultural group of belonging11. American Psychiatry Association. Diagnostic and Statistical Manual of Mental Disorders – DSM-5. 5.ed. Washington: American Psychiatry Association, 2013.,22. Millon T. Disorders of personality: introducing a DSM/ICD spectrum from normal to abnormal. New Jersey: Wiley, 2011.. PDs’ prevalence in the general population (US) is from 5 to 10%33. Samuels J. Personality disorders: epidemiology and public health issues. Int Rev Psychiatry. 2011;23(3):223-33., with a mean of 13% in Western countries44. Germans S, Van Heck GL, Hodiamont PPG. Results of the search for personality disorder screening tools: clinical implications. J Clin Psychiatry. 2012;73(2):165-73., and even greater numbers in North and South America55. Huang B, Grant BF, Dawson DA, Stinson FS, Chou SP, Saha TD, et al. Race-ethnicity and the prevalence and co-occurrence of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, alcohol and drug use disorders and Axis I and II disorders: United States, 2001 to 2002. Compr Psychiatry. 2006;47(4):252-7.. They are linked to clinical diseases, difficulties in adhering to treatment, bad prognoses, risk suicide, and mortality33. Samuels J. Personality disorders: epidemiology and public health issues. Int Rev Psychiatry. 2011;23(3):223-33.,66. Cailhol L, Damsa C, Bui E, Klein R, Adam E, Schmitt L, et al. Is assessing for borderline personality disorder useful in the referral after a suicide attempt? Encephale. 2008;34(1):23-30.

7. Mergui J, Raveh D, Gropp C, Golmard JL, Jaworowski S. Prevalence and characteristics of cluster B personality disorder in a consultation–liaison psychiatry practice. Int J Psychiatry Clin Pract. 2015;19(1):65-70.

8. Moran P, Jenkins R, Tylee A, Blizard R, Mann A. The prevalence of personality disorder among UK primary care attenders. Acta Psychiatr Scand. 2000;102(1):52-7.

9. Newton-Howes G, Tyrer P, Johnsen T. Personality disorder and the outcome of depression: Meta-analyses of published studies. Br J Psychiatry. 2006;188:13-20.

10. Rodriguez OMAAS, Fernández JL, Lora CH, León SO, González MH, Huerta AA, et al. Personality disorders and suicide attempts. Eur Psychiatry. 2016;33:S506.
-1111. Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet. 2015;385(9969):717-26..

Despite the empirical correlations between PDs and harmful outcomes, data indicate that these conditions are underdiagnosed44. Germans S, Van Heck GL, Hodiamont PPG. Results of the search for personality disorder screening tools: clinical implications. J Clin Psychiatry. 2012;73(2):165-73.,1111. Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet. 2015;385(9969):717-26.,1212. Hengartner MP. The detrimental impact of maladaptive personality on public mental health: a challenge for psychiatric practice. Frontiers in psychiatry. 2015;6:87.. Among several factors, greater familiarity of professionals with other psychiatric disorders and limitations on the diagnosis of PDs are possible explanations44. Germans S, Van Heck GL, Hodiamont PPG. Results of the search for personality disorder screening tools: clinical implications. J Clin Psychiatry. 2012;73(2):165-73.,1313. Paris J. A conside guide to personality disorders. 2015; Washington: American Psychological Association, 2015.. In Brazil, where the present research took place, the lack of studies in the field and the tiny number of adapted or developed psychiatric and psychological exams for the assessment of personality disorders are indicators of potential underdiagnosis or even poorly stablishment of diagnosis.

The low number of personality assessment tools for PDs in Brasil is real for both, diagnostic and screening tests (e.g., Carvalho et al.1414. Carvalho LF, Bartholomeu D, Silva MCR. Instrumentos para avaliação dos transtornos da personalidade no Brasil. Avaliação Psicológica. 2010;9(2):289-98.), but also reflecting problems encountered at an international level (e.g., Tyrer et al.1111. Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet. 2015;385(9969):717-26.; Olssøn et al.1515. Olssøn I, Sørebø O, Dahl AA. A cross-sectional testing of The Iowa Personality Disorder Screen in a psychiatric outpatient setting. BMC Psychiatry. 2011;11:105.). The availability of screening tools for PDs are importante for a number of factors44. Germans S, Van Heck GL, Hodiamont PPG. Results of the search for personality disorder screening tools: clinical implications. J Clin Psychiatry. 2012;73(2):165-73.,1616. Gárriz M, Gutiérrez F. Personality disorder screenings: A meta-analysis. Actas Esp Psiquiatr. 2009;37(3):148-52., including help in the PDs diagnosis and lower costs of this process, providing clinicians with a rapid tool of measurement, and allowing investigations in clinical and community samples in relation to PDs occurrence. Not many studies have investigated the occurrence of PDs in community samples, but those who investigated found frequency above 40%, as 44% using the final best-estimate consensus from the IIP Personality Disorder Scales, Iowa Personality Disorder Screen, and Temperament and Character Inventory1717. Morse JQ, Pikonis PA. Screening for personality disorders. J Pers Disord. 2007;21(2):179-98., 54.4% using the IIP-PD 25 items version1818. Shkëmbi F, Melonashi E, Fanaj N. A brief screening for personality disorders: Comparisons between clinical and nonclinical samples. EpSBS. 2015;144-23., and 43% using the International Personality Disorder Examination – Screen1919. Lenzenweger MF, Loranger AW, Korfine L, Neff C. Detecting personality disorders in a nonclinical population: application of a 2-stage procedure for case identification. Arch Gen Psychiatry. 1997;54:345-51.. Schöttke et al.2020. Schöttke H, Lange J, Imholz M, Wiedl KH. Development of a screening measure for the assessment of personality disorders: the Personality Disorder Screening – Shor Version (PSS-K). Verhaltenstherapie. 2011;21:154-61. did not present percentages, but considering the cutoff proposed in the study (i.e., > 4) for the Personality Disorder Screening – Short Version (PSS-K) and the mean and standard deviation of the community sample (F = 3.92; SD = 2.8), one can assume occurrences exceeding 40% for personality disorders in the sample sample. We could not find published studies in Brazil concerning screenings tests for PDs.

Recently, a screening test for personality disorders developed in Brazil was proposed2121. Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted.. The Dimensional Clinical Personality Inventory (IDCP) screening version (SV) was builded using the full version IDCP items2222. Carvalho LF, Primi R. Development and Internal Structure Investigation of the Dimensional Clinical Personality Inventory (IDCP). Psicol Refle Crit. 2015;28:322-30. as a starting point. Multiple regression analyzes and item level comparisions were made for items set final composition following a similar empirical approach based on criteria2323. Gregory RJ. Psychological Testing: History, Principles, and Applications. 7. ed. Boston: Pearson, 2013. as the one adopted in the development of the Minnesota Multiphasic Personality Inventory (MMPI). Seeking to determine the ideal cutoff for the IDCP-SV, authors applyed the ROC curve reaching a sensitivity equal to 89.5% and a specificity of 67.2%.

The study of Carvalho et al.2121. Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted. described step by step the development process and diagnostic accuracy indicators of IDCP-SV. However, no relationship between screening measure and other scales or external criteria was tested. As testing for consentaneity of a measure with other variables is a welcome indication of the test score validity2424. American Educational Research Association, American Psychological Association, National Council on Measurement in Education. Standards for Educational and Psychological Testing. New York: American Educational Research Association, 2013., in the present study we seek for validity evidence based on related criteria (e.g., other psychological tests) and external criteria (e.g., sample demographics).

Methods

Sample

Using a cross-sectional design, a convenience sample from community was recruited. The total sample comprised 804 participants from São Paulo State, Brazil, most of whom were caucasian (64.9%), female (65.4%), not living in a marital relationship (66%), college students (83%; varying from complete high school to postgraduate). Age ranged from 18 to 69 (M = 29.65; SD = 10.73), and 60.3% reported having attended to psychotherapy and 14.8% reported have attended to psychiatric treatment.

Instruments

Dimensional Clinical Personality Inventory – Screening Version (IDCP-SV2121. Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted.)

The IDCP-SV was developed based on the full version of IDCP2222. Carvalho LF, Primi R. Development and Internal Structure Investigation of the Dimensional Clinical Personality Inventory (IDCP). Psicol Refle Crit. 2015;28:322-30., test for measurement of pathological personality traits. The instrument aims to conduct personality disorder screening, and consists of 15 items arranged in a Likert 4-point scale, where 1 equals “has nothing to do with me” and 4 “all about me”. It is an integrative part of the IDCP-SV’s instructions to respond to socio-demographic questions, which were used for analysis in this research. We tested for the Cronbach’s alpha internal consistency reliability of IDCP-SV, that was equal to 0.83.

Iowa Personality Disorder Screen2525. Langbehn DR, Pfohl BM, Reynolds S, Clark LA, Battaglia M, Bellodi L, et al. The Iowa Personality Screen Tool: development and preliminary validation of a brief screening interview. J Pers Disord. 1999;13:75-89.

IPDS consists of 11 items, some containing two questions, refering to the diagnostic criteria for personality disorders. The items are answered on a dichotomous scale, yes (1) or not (0). In the case of items containing two questions, the item is scored 1 when both questions are answered with “yes”. The authors present data suggesting psychometric adequacy of IPDS, which is corroborated by other studies (e.g., Germans et al.44. Germans S, Van Heck GL, Hodiamont PPG. Results of the search for personality disorder screening tools: clinical implications. J Clin Psychiatry. 2012;73(2):165-73.). In the present study, Cronbach’s alpha internal consistency reliability of IPDS was 0.77.

Baptista Depression Scale – Screening Version (EBADEP-screening2626. Baptista MN, Carvalho LF. Diagnostic accuracy of a Brazilian depression self-report measure: original and short versions. Avaliação Psicológica. Submitted.)

The EBADEP-screening was developed based on the adult version of EBADEP (EBADEP-A2727. Baptista MN. Manual técnico da Escala Baptista de Depressão em Adultos (EBADEP-A). São Paulo: Vetor, 2012.), and aims to track symptoms of depression. In the short version of EBADEP-A were selected 15 items, with the descriptors most commonly used in psychiatric manuals (core symptons), i.e., items related to the sad mood, anhedonia, guilt, fatigue, concentration, suicidal ideation and sleep. In the development study, EBADEP-screening was able to discriminate 40 patients diagnosed with depression by SCID-I 40 people without depression with sensitivity equal to 95.0 and specificity of 87.5. In this research, Cronbach’s alpha internal consistency reliability of EBADEP-screening was 0.88.

Reasons for Living Scale (EMVIVER2828. Gomes MA. Construção da Escala Motivos para Viver (EMVIVER). (Tese de doutorado não publicada. 2015. Universidade São Francisco.)

The EMVIVER is a scale developed in order to predict protective factors of risk behavior for life. The instrument has 55 items that show reasons for living divided into three categories: meaningful relationships; attraction for life; plans for the future; and virtues. The EMVIVER has satisfactory psychometric properties evaluated in previous studies2828. Gomes MA. Construção da Escala Motivos para Viver (EMVIVER). (Tese de doutorado não publicada. 2015. Universidade São Francisco.. Cronbach’s alpha internal consistency reliability of EMVIVER was 0.94.

Structured Clinical Interview for DSM-IV Personality Questionnaire2929. First MB, Gibbon M, Spitzer RL, Williams JBW, Benjamin LS. SCID-II Personality Questionnaire. Washington, DC: American Psychiatric Press, 1997.

SCID-PQ-II was developed to assess the 10 personality disorders of DSM-IV Axis II, besides the two personality disorders not included (depressive, passive-aggressive). The instrument is a self-report, consisting of 119 items that should be answered with yes or no. Psychometric properties demonstrated adequacy in the development study. Cronbach’s alpha internal consistency reliability of SCID-II-PQ was higher than or equal to 0.60 for some of the scales but varied from 0.06 to 0.52 for obsessive-compulsive, passive-aggressive, paranoid, schizotypal, schizoid, histrionic and narcissist.

Procedures and statistical analysis

This study was approved by an ethics committee. Following approval the data collection was conducted online (n = 546) and live (n = 256), the latter case in particular universities. All subjects read and agree to the Terms of Consent. For data analysis, using the SPSS statistical software, we use the previous cutoffs from the literature for IDCP-SV2121. Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted. e para o IPDS2525. Langbehn DR, Pfohl BM, Reynolds S, Clark LA, Battaglia M, Bellodi L, et al. The Iowa Personality Screen Tool: development and preliminary validation of a brief screening interview. J Pers Disord. 1999;13:75-89.. For the interpretation of data, we considered as significant levels equal or less than 0.01, to avoid Type II error. We first presented descriptive statistics, then the group mean comparisions.

Results

Applying the cutoff criteria for dichotomizing, i.e., up to 8 points as negative for PDs and from 9 points as positive for PDs, we found 46.4% as positive. Looking more carefully to the data, we observed a higher rate of people showing score equal to 9 (12.1%), to 7 or 10 (11.3%), to 8 (8.5%), and to 11 (8.3%), presenting 51.1% in total. As the IPDS is also a screening measure, the same procedures were proceed to it, and from the 203 people that responded the test, only 3.9% reached its cutoff, with the higher rate of people at score equal to 1 (32.5%), 0 (23.8%), 2 (18.3%), and 3 (10.3%), representing 85.6% of total.

As we find expressive differences related to people reaching the cutoff in IDCP-SV and IPDS, we verified the correlation btween them, and observed a small to moderate effect size (0.38; p < 0.001). The disagreement between the measures, as observed in Figure 1, is located at the high score level of IDCP-SV, ie, there is many people high in IDCP-SV but not in IPDS. In Table 1 comparisons between means are presented, using IDCP-SV classification as criterion for group establishment.

Figure 1
Scatterplot of IDCP and IPDS scores.

Table 1
t-test for group comparison in tests based on IDCP-SV classification

In all cases the IDCP-SV positive group showed the great mean but in Schizoid SCID-II-PQ factor. Together, Schizoid and Antisocial SCID-II-PQ factors were the exception presenting inexpressive effect size, less than 0.20. The highest scores were for depression (total score and almost all factors bur irritability), SCID-II-PQ Cluster C composition, Borderline and Depressive personality disorder factors. Figure 2 helps to observe the main differences between the two groups.

Figure 2
Profile of IDCP-SV groups in administered tests. IPDS scores not included in the figure since it was administered with other part of the sample.

The positive group is clearly distinguished from the negative group on the left side of the figure (F = 2.795; gl = 3.993; p = 0.001); and despite the positive group show almost all means higher than negative group on the right side of the figure, this distinction is a little less obvious, but equally significant (F = 173.398; gl = 4.208; p < 0.001). Table 2 presents again mean comparisons, but now using criteria variables.

Table 2
t-test for group comparison in criteria variables based on IDCP-SV classification

All comparisons were significant and the effect sizes were expressive. Current suicide ideation, history of suicide attempt, and participate on both, psychological and psychiatric treatment, were the criteria with the most visible differences between groups.

Discussion

Based on previous research2121. Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted. and in the requirement for knowing the strengths and weaknesses of a measure using external criteria2424. American Educational Research Association, American Psychological Association, National Council on Measurement in Education. Standards for Educational and Psychological Testing. New York: American Educational Research Association, 2013., this research reports validity evidence based psychological tests and relevant sample characteristics. Data suggest that the screening version of IDCP (IDCP-SV) discriminates a similar percentage of people from the community to what is found in other countries with similar tools for screening of personality disorders. In addition, mean comparisons between groups showed good discriminative capacity by IDCP-SV items.

The proportion of subjects identified as positive by IDCP-SV was higher compared to the expected prevalence in community samples, even considering the data found to America (e.g., Huang et al.55. Huang B, Grant BF, Dawson DA, Stinson FS, Chou SP, Saha TD, et al. Race-ethnicity and the prevalence and co-occurrence of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, alcohol and drug use disorders and Axis I and II disorders: United States, 2001 to 2002. Compr Psychiatry. 2006;47(4):252-7.). This is expected, since screening tests must have high sensitivity and low specificity1717. Morse JQ, Pikonis PA. Screening for personality disorders. J Pers Disord. 2007;21(2):179-98. to ensure that all individuals with particular psychiatric disorder are referred for diagnosis. Compared of the amount of individuals identified by other screening tests for personality disorders, we found very similar data to what is reported in the literature for community samples, ranging from 43% to 54.4%1717. Morse JQ, Pikonis PA. Screening for personality disorders. J Pers Disord. 2007;21(2):179-98.,1919. Lenzenweger MF, Loranger AW, Korfine L, Neff C. Detecting personality disorders in a nonclinical population: application of a 2-stage procedure for case identification. Arch Gen Psychiatry. 1997;54:345-51.,2020. Schöttke H, Lange J, Imholz M, Wiedl KH. Development of a screening measure for the assessment of personality disorders: the Personality Disorder Screening – Shor Version (PSS-K). Verhaltenstherapie. 2011;21:154-61.. This suggests that the IDCP screening version is comparable to screening for personality disorders used in the world, confirming the favorable data found previously2121. Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted..

Specifically regarding the observed discrepancy between IDCP-SV and IPDS, it raises questions about whether the IDCP-SV identifies an excessive number of false positives or IPDS identifies an excessive number of false negatives. However, it should be considered that for screening tests, is the most desirable identification of false positives than false negatives. In the study of Morse and Pikonis1717. Morse JQ, Pikonis PA. Screening for personality disorders. J Pers Disord. 2007;21(2):179-98., the authors did not show the percentage of cases identified as positive by the IPDS in the community sample for the score considering the 11 items, but only for subgroups of items, ranging from 17% to 26% cases identified as positive, which is below than observed in the studies with other instruments in community samples and in the study itself, in which consensus was 44% for this sample. The data obtained in the study of Morse and Pikonis seems to be comparable to from the present study in relation to IPDS, since the means obtained are similar (d = 0.04; p = 0.57). The data suggest that the IPDS for screening in community samples may have lower sensitivity than desired for screening tools, since the percentage of cases identified as positive, are smaller to what has presently found and what is reported in literature. However, future studies should implement an design for comparing the diagnostic accuracy of IDCP-SV and IPDS, also using a gold standard measure.

Furthermore, means comparisons with the different measures (i.e., IPDS, EBADEP, EMVIVER, and diagnostic categories for SCID-II-PQ) pointed to higher scores for the group identified as positive in the IDCP-SV, suggesting that this group tends to have more pathological functioning compared to the group identified as negative. This indicates the discriminative ability of the IDCP-SV for persons with pathological functioning in relation to people with healthier functionings. We observed that the largest discrepancies between groups happened for more general indicators of pathology (e.g., Eaton et al.3030. Eaton NR, Krueger RF, Keyes KM, Skodol AE, Markon KE, Grant BF, et al. Borderline personality disorder co-morbidity: relationship to the internalizing-externalizing structure of common mental disorders. Psychol Med. 2011;41(5):1041-50.) as the total score of depression and borderline factor of SCID-II-PQ. Along with this, the score on the Cluster C also presented salient difference, which needs to be further investigated, it may reflect a specific tendency of the sample. We also highlight that the groups (positive and negative) established based on the classification of the IDCP-SV were widely differentiated in criterion variables used, which is highly desirable for measurements with discriminative purpose2424. American Educational Research Association, American Psychological Association, National Council on Measurement in Education. Standards for Educational and Psychological Testing. New York: American Educational Research Association, 2013., demonstrating alarming differences for cases of suicide and psychiatric treatment, as would be expected.

The data currently reported must be observed as initial for a Brazilian screening tool for personality disorders. On one hand the data being found with the IDCP-SV seem to be promising, on the other, the limitations of the present research and the need for research with other study designs and samples should be carefully considered. Among the main limitations of this study, is the absence of a clinical sample diagnosed with personality disorders. Another extremely important limitation is the lack of a gold standard measure and the use of other screening tests used worldwide (e.g., IIP-PD). Future studies should seek to embrace these limitations, deepening the knowledge about the applications of IDCP-SV and, equally important, its limitations.

References

  • 1
    American Psychiatry Association. Diagnostic and Statistical Manual of Mental Disorders – DSM-5. 5.ed. Washington: American Psychiatry Association, 2013.
  • 2
    Millon T. Disorders of personality: introducing a DSM/ICD spectrum from normal to abnormal. New Jersey: Wiley, 2011.
  • 3
    Samuels J. Personality disorders: epidemiology and public health issues. Int Rev Psychiatry. 2011;23(3):223-33.
  • 4
    Germans S, Van Heck GL, Hodiamont PPG. Results of the search for personality disorder screening tools: clinical implications. J Clin Psychiatry. 2012;73(2):165-73.
  • 5
    Huang B, Grant BF, Dawson DA, Stinson FS, Chou SP, Saha TD, et al. Race-ethnicity and the prevalence and co-occurrence of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, alcohol and drug use disorders and Axis I and II disorders: United States, 2001 to 2002. Compr Psychiatry. 2006;47(4):252-7.
  • 6
    Cailhol L, Damsa C, Bui E, Klein R, Adam E, Schmitt L, et al. Is assessing for borderline personality disorder useful in the referral after a suicide attempt? Encephale. 2008;34(1):23-30.
  • 7
    Mergui J, Raveh D, Gropp C, Golmard JL, Jaworowski S. Prevalence and characteristics of cluster B personality disorder in a consultation–liaison psychiatry practice. Int J Psychiatry Clin Pract. 2015;19(1):65-70.
  • 8
    Moran P, Jenkins R, Tylee A, Blizard R, Mann A. The prevalence of personality disorder among UK primary care attenders. Acta Psychiatr Scand. 2000;102(1):52-7.
  • 9
    Newton-Howes G, Tyrer P, Johnsen T. Personality disorder and the outcome of depression: Meta-analyses of published studies. Br J Psychiatry. 2006;188:13-20.
  • 10
    Rodriguez OMAAS, Fernández JL, Lora CH, León SO, González MH, Huerta AA, et al. Personality disorders and suicide attempts. Eur Psychiatry. 2016;33:S506.
  • 11
    Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet. 2015;385(9969):717-26.
  • 12
    Hengartner MP. The detrimental impact of maladaptive personality on public mental health: a challenge for psychiatric practice. Frontiers in psychiatry. 2015;6:87.
  • 13
    Paris J. A conside guide to personality disorders. 2015; Washington: American Psychological Association, 2015.
  • 14
    Carvalho LF, Bartholomeu D, Silva MCR. Instrumentos para avaliação dos transtornos da personalidade no Brasil. Avaliação Psicológica. 2010;9(2):289-98.
  • 15
    Olssøn I, Sørebø O, Dahl AA. A cross-sectional testing of The Iowa Personality Disorder Screen in a psychiatric outpatient setting. BMC Psychiatry. 2011;11:105.
  • 16
    Gárriz M, Gutiérrez F. Personality disorder screenings: A meta-analysis. Actas Esp Psiquiatr. 2009;37(3):148-52.
  • 17
    Morse JQ, Pikonis PA. Screening for personality disorders. J Pers Disord. 2007;21(2):179-98.
  • 18
    Shkëmbi F, Melonashi E, Fanaj N. A brief screening for personality disorders: Comparisons between clinical and nonclinical samples. EpSBS. 2015;144-23.
  • 19
    Lenzenweger MF, Loranger AW, Korfine L, Neff C. Detecting personality disorders in a nonclinical population: application of a 2-stage procedure for case identification. Arch Gen Psychiatry. 1997;54:345-51.
  • 20
    Schöttke H, Lange J, Imholz M, Wiedl KH. Development of a screening measure for the assessment of personality disorders: the Personality Disorder Screening – Shor Version (PSS-K). Verhaltenstherapie. 2011;21:154-61.
  • 21
    Carvalho LF, Pianowski G, Reis AM. Development and diagnostic accuracy of the screening of the Dimensional Clinical Personality Inventory – Screening version. Psicologia Ciência e Profissão. Submitted.
  • 22
    Carvalho LF, Primi R. Development and Internal Structure Investigation of the Dimensional Clinical Personality Inventory (IDCP). Psicol Refle Crit. 2015;28:322-30.
  • 23
    Gregory RJ. Psychological Testing: History, Principles, and Applications. 7. ed. Boston: Pearson, 2013.
  • 24
    American Educational Research Association, American Psychological Association, National Council on Measurement in Education. Standards for Educational and Psychological Testing. New York: American Educational Research Association, 2013.
  • 25
    Langbehn DR, Pfohl BM, Reynolds S, Clark LA, Battaglia M, Bellodi L, et al. The Iowa Personality Screen Tool: development and preliminary validation of a brief screening interview. J Pers Disord. 1999;13:75-89.
  • 26
    Baptista MN, Carvalho LF. Diagnostic accuracy of a Brazilian depression self-report measure: original and short versions. Avaliação Psicológica. Submitted.
  • 27
    Baptista MN. Manual técnico da Escala Baptista de Depressão em Adultos (EBADEP-A). São Paulo: Vetor, 2012.
  • 28
    Gomes MA. Construção da Escala Motivos para Viver (EMVIVER). (Tese de doutorado não publicada. 2015. Universidade São Francisco.
  • 29
    First MB, Gibbon M, Spitzer RL, Williams JBW, Benjamin LS. SCID-II Personality Questionnaire. Washington, DC: American Psychiatric Press, 1997.
  • 30
    Eaton NR, Krueger RF, Keyes KM, Skodol AE, Markon KE, Grant BF, et al. Borderline personality disorder co-morbidity: relationship to the internalizing-externalizing structure of common mental disorders. Psychol Med. 2011;41(5):1041-50.

Publication Dates

  • Publication in this collection
    Mar-Apr 2017

History

  • Received
    9 Sept 2016
  • Accepted
    31 Jan 2017
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