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Personality disorder and substance related disorders: a six-month follow-up study with a Brazilian sample

Transtorno de personalidade e transtorno por uso de substâncias: experiência brasileira com seis meses de seguimento

ABSTRACT

Objectives

A few Brazilian researches correlate personality disorders (PD) and substance related disorders (SRD). The aim of the present study is to investigate the association between them, to evaluate the PD frequency among chemical dependents inpatients, this comorbidity association with social and demographic characteristics, used drug of choice, its impact on clinical evolution until the moment of their committal, the frequency of relapse, self-help group – and psychotherapic adherence among SRD patients six months following committal.

Methods

A 101 inpatients sample of chemical dependents was enrolled in 2 hospitals. The following instruments were applied: a questionnaire for social and demographic characteristics identification and drug use pattern, some questions from the sixth version of the Addiction Severity Index (ASI-6), the SCID-II questionnaire and specific questions concerning psychotherapic and self-help groups participation, and medication use.

Results

From these 101 patients, 55.4% were diagnosed with PD, being avoidant (14.9%), borderline (11.9%) and antisocial (8.9%) the more frequent ones found. PD patients had an earlier crack use in life (p = 0.038) and had also more previous treatments than the ones without PD (p = 0.005). Borderline PD patients were less worried to substance use problem (p = 0.003). After 6-months follow-up, no statistical significance was found between patients with and without PD regarding drug use or treatment adherence.

Conclusion

A high PD diagnosis was found in drug use inpatients. Patients diagnosed with SRD and PD need the identification of this comorbidity and of their personality characteristics in order to plan a more comprehensive and effective treatment.

Substance related disorders; personality disorder; comorbidity; dual diagnosis

RESUMO

Objetivos

Poucos estudos brasileiros correlacionam transtornos de personalidade (TP) com transtorno por uso de substâncias (TUS). O objetivo deste estudo é verificar a associação entre eles, avaliar a frequência dos TP na população de dependentes químicos internados, correlacionar com características sociodemográficas, drogas de escolha, frequência de recaída, aderência a grupos de autoajuda e psicoterapia em até seis meses após a alta hospitalar.

Métodos

Uma amostra de 101 pacientes internados em dois hospitais foi selecionada. Os seguintes instrumentos foram aplicados: um questionário para identificação de características sociodemográficas e padrão de uso de drogas, algumas questões da sexta versão do ASI-6 (Addiction Severity Index), o SCID-II e algumas questões específicas sobre participação em grupos de autoajuda e em psicoterapia, bem como o uso de medicações.

Resultados

Destes 101 pacientes, 55,4% foram diagnosticados com TP, sendo evitativa (14,9%), limítrofe (11,9%) e antissocial (8,9%) as mais frequentemente encontradas. Pacientes com TP demonstraram ter feito uso mais precoce de crack na vida (p = 0,038) e também tinham mais tratamentos anteriores do que aqueles sem TP (p = 0,005). Pacientes com TP limítrofe estavam menos preocupados com o problema de abuso de substâncias (p = 0,003). Após seis meses de seguimento, nenhuma diferença estatística significativa foi encontrada entre pacientes com e sem TP acerca do uso de drogas ou aderência ao tratamento.

Conclusão

Uma alta prevalência de TP foi encontrada em pacientes internados por TUS. Pacientes diagnosticados com TP e TUS necessitam a identificação da comorbidade e das características de sua personalidade, a fim de planejar um tratamento mais abrangente e eficaz.

Transtorno por uso de drogas; transtorno de personalidade; comodidade; patologia dual

INTRODUCTION

Several international studies have correlated substance related disorders (SRD) and personality disorders (PD)11. González JMM, García AV. Evolución de las crencias nucleares relacionadas con la adicción en drogodependientes con y sin trastornos de personalidad. Addicciones. 2012;24(3):229-38.

2. Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412-26.

3. Moran P, Coffey C, Mann A, Carlin JB, Patton GC. Personality and substance use disorders in young adults. Br J Psychiatry. 2006;188:374-9.

4. Khan AA, Jacobson KC, Gardner CO, Prescott CA, Kendler KS. Personality and comorbidity of common psychiatric disorders. Br J Psychiatry. 2005;186:190-6.

5. Grant BF, Stinson FS, Dawson DA, Chou SP, Ruan WJ, Pickering RP. Co-occurrence of 12-month alcohol and drug use disorders and personality disorders in the United States: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Arch Gen Psychiatry. 2004;61(4):361-8.
-66. Verheul R. Co-morbidity of personality disorders in individuals with substance use disorders. Eur Psychiatry. 2001;16(5):274-82.. In Brazil, however, we have few studies on this association. Besides that, major part of these studies focuses on a specific PD and its prevalence among substance abusers44. Khan AA, Jacobson KC, Gardner CO, Prescott CA, Kendler KS. Personality and comorbidity of common psychiatric disorders. Br J Psychiatry. 2005;186:190-6.,77. Schneider JA, Lisboa CM, Mallmann C. Relação entre dependência de cocaína e/ou crack, transtorno de personalidade antissocial e psicopatia em pacientes internados em uma instituição de reabilitação. Revista Debates em Psiquiatria. 2014;4(3):24-32.

8. Tull MT, Gratz KL. The impact of borderline personality disorder on residential substance abuse treatment dropout among men. Drug Alcohol Depend. 2012;121(1-2):97-102.
-99. Westermeyer J, Thuras P. Association of antisocial personality disorder and substance disorder morbidity in a clinical sample. Am J Drug Alcohol Abuse. 2005;31(1):93-110.. Then, little is known concerning the several Axis II diagnosis and its interference on SRD.

González and García11. González JMM, García AV. Evolución de las crencias nucleares relacionadas con la adicción en drogodependientes con y sin trastornos de personalidad. Addicciones. 2012;24(3):229-38. found a 56.4% prevalence of SRD and PD comorbidity. An American observational study showed that, among alcohol-abusers, 28.6% had at least one associated PD and that 47.7% of drug users (but alcohol) have one PD diagnosis either55. Grant BF, Stinson FS, Dawson DA, Chou SP, Ruan WJ, Pickering RP. Co-occurrence of 12-month alcohol and drug use disorders and personality disorders in the United States: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Arch Gen Psychiatry. 2004;61(4):361-8.. The prevalence of PD varies according the drug being studied22. Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412-26.,33. Moran P, Coffey C, Mann A, Carlin JB, Patton GC. Personality and substance use disorders in young adults. Br J Psychiatry. 2006;188:374-9.. The ones more frequently associated with PD are antisocial, hysterical and dependent22. Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412-26.,55. Grant BF, Stinson FS, Dawson DA, Chou SP, Ruan WJ, Pickering RP. Co-occurrence of 12-month alcohol and drug use disorders and personality disorders in the United States: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Arch Gen Psychiatry. 2004;61(4):361-8., also paranoid, avoidant and obsessive-compulsive1010. Langas AM, Matl UF, Opjordsmoen S. In-depth study of personality disorders in first-admission patients with substance use disorders. BMC Psychiatry. 2012;12:180.. The borderline PD was evaluated in several studies22. Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412-26.,1111. Fenton MC, Keyes K, Geier T, Greenstein E, Skodol A, Krueger B, et al. Psychiatric comorbidity and the persistence of drug use disorders in the United States. Addiction. 2012;107(3):599-609., leading to its association with treatment drop-out88. Tull MT, Gratz KL. The impact of borderline personality disorder on residential substance abuse treatment dropout among men. Drug Alcohol Depend. 2012;121(1-2):97-102. and with a worse long-term prognosis, as also antisocial and schizotype PD1111. Fenton MC, Keyes K, Geier T, Greenstein E, Skodol A, Krueger B, et al. Psychiatric comorbidity and the persistence of drug use disorders in the United States. Addiction. 2012;107(3):599-609.. Concerning specific drug types, a Brazilian study showed that crack users presented a higher rate of antisocial personality disorder (25%) than powder cocaine (9%) and non-cocaine psychoactive substances users (9%)1212. Paim Kessler FH, Barbosa Terra M, Faller S, Ravy Stolf A, Carolina Peuker A, Benzano D; Brazilian ASI Group, Pechansky F. Crack users show high rates of antisocial personality disorder, engagement in illegal activities and other psychosocial problems. Am J Addict. 2012;21(4):370-80..

In Brazil, in a study that evaluated how personality traits are associated with occasional use, abuse, and dependence of psychoactive drugs in a large sample of adults via online questionnaires, it was found that novelty seeking was the trait most associated with increased involvement with alcohol, cannabis, and cocaine. Persistence was lower in cannabis-, benzodiazepine-, and cocaine-dependent subjects, as well as in hallucinogen abusers and self-directedness was reduced in dependents of all drug classes1313. Schneider Jr. R, Ottoni GL, Carvalho HW, Elisabetsky E, Lara DR. Temperament and character traits associated with the use of alcohol, cannabis, cocaine, benzodiazepines, and hallucinogens: evidence from a large Brazilian web survey. Rev Bras Psiquiatr. 2015;37(1):31-9.. Another study evaluated the presence of mental disorders among prisoners in the Salvador City pointed to high rates for borderline personality disorder 19.7% and 34.8%; antisocial personality disorder 26.9% and 24.2%; alcohol addiction 26.6% and 35.3%; drug addiction 27.9% and 32.4% among those who were, respectively, in semi-opened or closed regime, reinforcing that disorders comorbid idea is related to psychoactive substances and personality disorders are quite frequent1414. Pondé MP, Freire AC, Mendonça MS. The prevalence of mental disorders in prisoners in the city of Salvador, Bahia, Brazil. J Forensic Sci. 2011;56(3):679-82..

This frequent association can increase drug prevalence consumption as well as jeopardize these patients to enroll treatment in order to avoid relapse11. González JMM, García AV. Evolución de las crencias nucleares relacionadas con la adicción en drogodependientes con y sin trastornos de personalidad. Addicciones. 2012;24(3):229-38.,22. Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412-26.. It is known that patients with this association have dysfunctional beliefs related to addiction and are, therefore, more treatment resistant by cognitive therapy for example1515. Beck J. Terapia cognitiva para la superación de retos. Barcelona: Gedisa; 2007.. A Brazilian trial emphasized the need for strengthening even more the therapeutic alliance in these two diseases diagnosed patients because they are more resistant for changing treatment stages, less adherent to treatment, have earlier and higher relapse rates1616. Zaleski M, Laranjeira RR, Marques ACPR, Ratto L, Romano M, Alves HNP, et al. Diretrizes da Associação Brasileira de Estudos do Álcool e outras Drogas (ABEAD) para o diagnóstico e tratamento de comorbidades psiquiátricas e dependência de álcool e outras substâncias. Rev Bras Psiquiatr. 2006;28(2):142-8..

Therefore, the identification of this comorbidity is fundamental as it greatly impacts on SRD patients. The aim of this trial is to investigate the association of psychoactive drug dependency and personality disorders, verifying PDs frequency among SRD patients in the studied hospitals, this comorbidity association with social and demographic variables, with identification of drug use pattern and type, the past impact of the SRD/PD comorbidity in patients clinical evolution until the moment of their hospitalization and, at last, to verify relapse rates and adherence adhesion to self-help groups (alcoholic/narcotics) and psychotherapic treatment in this population, with and without PDs associated six months following committal.

METHODS

The sample was composed by inpatients with substance related disorder in a unit for this at São José Clinic, with 90 beds for chemical dependency of the total 200 beds (private and health plans users), and in a psychiatric unit at Parque Belém Hospital, with 120 beds for chemical dependency from 242 beds in total (private and social health plan users). Both hospitals are located at Porto Alegre city, in Brazil. Data collection period was from march/2013 to december/2014. This was a 101 patients convenience sample with a 6-months follow-up period (cohort design).

Patients should be aged 18 years or older and fulfill DSM-IV-TR psychoactive dependency criteria. They should live in Porto Alegre and have a contact phone number for follow-up. Were included patients already interned for at least two weeks so their responses to questionnaires would suffer less interference of psychoactive substances use. Exclusion criteria were: age lower than 18, mental handicap, confusional and/or psychotic states or imbalanced clinical comorbidity. Initially 14 patients were excluded and 3 refused to participate in the study. Patients were excluded by psychiatric evaluation or medical records data. In the analysis of results, was also excluded one patient that did not want to answer SCID-II questions.

Patients were chosen by lot to avoid a possible selection bias in patients’ choice and rather than they were invited to participate on study and to them was explained the interview goals and procedures. In case of agreement, they signed the informed consent form. The Project was submitted to the Porto Alegre Health Science Federal University Institutional Review Board (IRB), opinion approval: 257.251 – and the two mentioned hospitals IRBs, having received approval.

On the first stage, inpatients were inquired by two medical doctors, specializing in psychiatry, with an interview with approximately 50 minutes of duration. On a second stage, six months following discharge, the patients were submitted to a new interview, phone collected, performed by psychology students. Interviewers were trained for the instruments application and periodic interviews evaluations were performed. There were no previous defined criteria for choosing an interviewer to each patient. On the second stage, interviewers were blinded to the presence or not of PDs. A kappa test was performed for instruments application agreement at the first stage with a 0.9 score1717. Gordis L. Epidemiology. Philadelphia: WB Saunders; 1996..

On the first stage, the following instruments were applied:

– A social and demographic features questionnaire;

– A Drug Use Pattern questionnaire to characterize quantity, frequency and consumption pattern;

– SCID-I (Semi-structured Clinical Interview based on APA-1994 DSM-IV)1818. First MB, Spitzer RL, Gibbon M, Williams JB. Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition. (SCID-I/P). New York: Biometrics Research, New York State Psychiatric Institute; 2002. to evaluate psychoactive substance dependency presence. The SCID-I, in its clinical version, was translated and adapted to Portuguese, and, in general, it presents good reliability. For treating the disorders related to substance use, the reliability, as the weighted kappa, was K = 0.761919. Del-Ben CM, Vilela JA,A Crippa, JAS, Hallak JEC, Labate CM, Zuardi AW. Confiabilidade da “Entrevista Clínica Estruturada para o DSM-IV – Versão Clínica” traduzida para o português. Rev Bras Psiquiatr. 2001;23(3):156-9..

– A questionnaire with some questions from ASI-6 – the Sixth Version of Addiction Severity Index. This is a semi-structured interview used to verify the seriousness of problems in many life aspects related to psychoactive substance consumption like physical and psychological health, job and finances, family and legal problems2020. McLellan AT, Cacciola JC, Alterman AI, Rikoon SH, Carise D. The Addiction Severity Index at 25: origins, contributions and transitions. Am J Addict. 2006;15(2):113-24.,2121. Kessler FH, Cacciola J, Faller S, Souza-FormigoniIII MS, Cruz M, Brasiliano S, et al. Multi-center transcultural adaptation of the sixth version of Addiction Severity Index (ASI6) for Brazil. Rev Psiquiatr Rio Gd Sul. 2007;29(3):335-6.. The psychometric properties’ analysis of the ASI-6 indicates good reliability and validity of this instrument for Brazilian culture, both in hospitalized patients as in outpatients treatment. The Cronbach’s alpha for subscales of the ASI-6 ranged from 0.64 to 0.95. Correlations between scores of Alcohol and Drugs ASI-6 area and concurrent instrument (ASSIST) were high (0.72 and 0.89, respectively)2222. Kessler F, Cacciola J, Alterman A, Faller S, Souza-Formigoni ML, Cruz MS, et al. Psychometric properties of the sixth version of the Addiction Severity Index (ASI-6) in Brazil. Rev Bras Psiquiatr. 2012;34(1):24-33..

– SCID-II (Semi-structured Clinical Interview based on APA-1994 DSM-IV)2323. First MB, Gibbon M, Spitzer RL, Williams JB, Benjamin LS. Structured Clinical Interview for DSM-IV Axis II Personality Disorders, (SCID-II). Washington DC: American Psychiatric Press, Inc.; 1997. to verify the PD presence. There are literature’s evidences about the consistency between the SCID-II and clinical observation, denoting good reliability and internal consistency of the instrument2424. Maffei C, Fossati A, Agostoni I, Barraco A, Bagnato M, Deborah D, et al. Interrater reliability and internal consistency of the structured clinical interview for DSM-IV axis II personality disorders (SCID-II), version 2.0. J Pers Disord. 1997;11(3):279-84..

On the second step, a questionnaire for Drug Abuse Consumption (adapted for 30-days and the last 3 months evaluations) was applied plus specific questions concerning psychotherapic and self-help groups participation and medication use.

Data were stored in Excel program and then exported to SPSS v. 18.0 for statistical analysis. Categorical values were described by absolute frequency and percentual relative frequency, and then compared between groups by Chi-Square or Fisher Exact test. Quantitative measures were described when they had symmetrical distribution, by mean and standard deviation and t Student test for independent random samples compared. In case of asymmetrical distribution, they were described by median and interquartile interval and were compared by Mann-Whitney test use. Prevalences were described with their own 95% confidence interval. A 5% significance level was considered. It was performed a logistic regression with the variables that had p < 0.20 when comparing patients with and without personality disorders.

RESULTS

A 101 patients sample was collected, 70 being male. In sample, 56 patients had PD (55.4%) (IC95%: 45.6-65.3). Following on table 1, frequencies of patients PDs are described.

Table 1
Personality disorders frequency in sample

There was no statistical difference for social and demographic patients characteristics with and without personality disorder (Table 2).

Table 2
Social and demographic characteristics of with and without PD patients

In sample, alcohol was consumed during life for 89.1% patients, tobacco 73.3%, cocaine 62.4%, cannabis 55.4%, crack 33.7%, stimulants 21.8%, solvents 18.8%, hallucinatory 15.8%, tranquilizers 6.9%, amphetamines 5.9%, feeding supplements 4.0% and opioids 2%. It was not found a significant statistical difference between groups with and without PD regarding psychoactive substance use.

During last year, alcohol was consumed by 77.2% patients, tobacco 67.3%, cocaine 48.5%, cannabis 35.6%, crack 32.7%, stimulants 16.8%, solvents 5.9%, tranquilizers 5.9%, hallucinatory 5.0%, anabolizer 4.0%, amphetamines 3.0%, feeding supplements 2.0% and opioids 1.0%. During last 30 days, 71.3% patients consumed alcohol, 64.5% tobacco, 40.7% cocaine, 30.7% crack, 28.7% cannabis, 11.9% stimulants, 4.0% tranquilizers, 3.0% hallucinatory and 2.0% solvents.

There were found no differences between groups with or without PD regarding last year/last month on alcohol, tobacco, cannabis, hallucinatory, cocaine, crack, solvents, tranquilizers, stimulants, anabolizer, amphetamines, feeding supplements or opioid use.

For both groups, there were found no differences either concerning age of onset of all drugs use but crack. Patients with PD used crack earlier than the ones without PD with a significant statistical difference (p = 0.038).

No significant statistical difference was verified among patients with or without PD that used alcohol only and/or tobacco and the ones that used illicit drugs but did not drank during last 30 days or last year before hospitalization. Also, no significant statistical difference between both groups was found regarding one or multiple drugs use.

When comparing individuals with most frequent PDs in sample (avoidant, borderline, antisocial) among their selves and with those without any PD, there was not found statistical significance neither in 12 months nor in 30 days before hospitalization concerning most used drugs consumption (alcohol, tobacco, cannabis, cocaine, crack).

The ASI scale variables used are described on table 3. Patients with PD had a greater number of previous treatments comparing to those without PD, showing a significant statistical difference (p = 0.005) (graphic 1). Patients with PD have presented a higher tendency on longer continuous treatments (p = 0.085) and used to consider that cocaine/crack was the most disturbing drug (p = 0.082).

Table 3
ASI Scale variables comparison between groups with and without PD

Graphic 1
Number of treatments comparison between groups with and without PD.

Comparing individuals with the most often PDs in sample among them and with those without PD was found that the ones with borderline PD were less worried to substance use problem than all others (p = 0.033).

It was performed a logistic regression, including some variables like: education, number of previous treatments, continuous treatment time, degree of treatment importance, the drug considered the leading problem and age of onset crack use. After adjusting the factors associated in bivariate analysis with p < 0.20, only the variable age of onset of crack use was significance (p = 0.03), been this use earliest precocious in patients with personality disorder.

During follow-up phase, after 6 months discharge, we could reach only 59.4% of patients, 31.9% were not localized and 8.7% refused to be interviewed. In the PDs group, there was 51.8% losses, while in the group without PDs, there was 26.7% losses, this finding demonstrating to have statistical significance (p = 0.019). Such losses were more frequent among men (p = 0.008), and these patients less frequently found important to reach/keep abstinence (p = 0.04). There were not found any others statistically significant differences regarding other social or demographical variables or to other ASI-6 Scale questions (psychoactive substance disorder, treatment importance and more troubling drug).

After discharge, 66.7% consumed drug (but tobacco), being 18.3% twice to ten times, 10.1% eleven to twenty times and 38.3% more than twenty times. Concerning used drug type, 51.6% had used alcohol, 68.3% tobacco, 18.3% cannabis, 25% cocaine, 25% crack, 10% stimulants (energy drink), 5% tranquilizers, 1.7% solvents during the three months before interview, 43.3% had used alcohol, 66.7% tobacco, 16.6% cannabis, 205 cocaine, 16.7% crack, 5% stimulants (energy drink), 3.3% tranquilizers and 1.7% opioids during the last 30 days before interview.

Only 11.7% patients were participating in self-help groups and 48.3% had psychotherapic treatment, and in this sample, 3.6% had twice a week sessions, 46.6% had a weekly one, 7.1% fortnightly, 39.3% monthly, 3.4% less than once a month ones, and 73.3% were using a psychiatric medication. In 85% of interviews, the interviewers considered to have reliable answers.

There were not found any statistical significant differences between patients with or without PDs regarding every drug use type or treatment adherence rates after 6-months follow-up.

DISCUSSION

A high frequency of PDs was found in patients hospitalized for drug use despite age, civil status, instruction, family earning and work status before admission. More than half patients presented these conditions. This high frequency is according to previous studies like found Langas et al.1010. Langas AM, Matl UF, Opjordsmoen S. In-depth study of personality disorders in first-admission patients with substance use disorders. BMC Psychiatry. 2012;12:180. and González and García11. González JMM, García AV. Evolución de las crencias nucleares relacionadas con la adicción en drogodependientes con y sin trastornos de personalidad. Addicciones. 2012;24(3):229-38., the former finding almost same results. It is a largely higher PD frequency than in general population that is about 9% to 13% according to Lenzenweger et al.2525. Lenzenweger MF, Lane MC, Loranger AW, Kessler RC. DSM-IV personality disorders in the National Comorbidity Survey Replication. Biol Psychiatry. 2007;62(6):553-64. and Verheul66. Verheul R. Co-morbidity of personality disorders in individuals with substance use disorders. Eur Psychiatry. 2001;16(5):274-82.. A systematic review of personality disorder and addiction show high comorbidity rates too2626. Euler S, Sollberger D, Bader K, Lang UE, Walter M. [A systematic review of personality disorders and addiction: epidemiology, course and treatment]. Fortschr Neurol Psychiatr. 2015;83(10):544-54.. Regarding social and demographic variables, previous trials show that PD patients are younger, have lower educational level and marry less either1010. Langas AM, Matl UF, Opjordsmoen S. In-depth study of personality disorders in first-admission patients with substance use disorders. BMC Psychiatry. 2012;12:180.,2727. Kokkevi A, Stefanis N, Anastasopoulou E, Kostogianni C. Personality disorders in drug abusers: prevalence and their association with AXIS I disorders as predictors of treatment retention. Addict Behav. 1998;23(6):841-53., what is not matching our study findings.

Most frequently found PDs were avoidant, borderline and antisocial, reinforcing literature findings22. Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412-26.,55. Grant BF, Stinson FS, Dawson DA, Chou SP, Ruan WJ, Pickering RP. Co-occurrence of 12-month alcohol and drug use disorders and personality disorders in the United States: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Arch Gen Psychiatry. 2004;61(4):361-8.,1010. Langas AM, Matl UF, Opjordsmoen S. In-depth study of personality disorders in first-admission patients with substance use disorders. BMC Psychiatry. 2012;12:180.,1111. Fenton MC, Keyes K, Geier T, Greenstein E, Skodol A, Krueger B, et al. Psychiatric comorbidity and the persistence of drug use disorders in the United States. Addiction. 2012;107(3):599-609.,2828. Skinstad AH, Swain A. Comorbidity in a clinical sample of substance abusers. Am J Drug Alcohol Abuse. 2001;27(1):45-64., although this last one shows a higher prevalence in these studies66. Verheul R. Co-morbidity of personality disorders in individuals with substance use disorders. Eur Psychiatry. 2001;16(5):274-82.,77. Schneider JA, Lisboa CM, Mallmann C. Relação entre dependência de cocaína e/ou crack, transtorno de personalidade antissocial e psicopatia em pacientes internados em uma instituição de reabilitação. Revista Debates em Psiquiatria. 2014;4(3):24-32.. The presenting authors figure that in Brazil, as in USA, these patients are often in jail or in forensic psychiatric units, which ones were not covered in this study. Regarding borderline PD, a main issue for its high frequency is emotional imbalance and impulsiveness (nuclear aspects), and the last one has been considered the most relevant factor for drug addiction66. Verheul R. Co-morbidity of personality disorders in individuals with substance use disorders. Eur Psychiatry. 2001;16(5):274-82.,2929. Cohen P, Chen H, Crawford TN, Brook JS, Gordon K. Personality disorders in early adolescence and the development of later substance use disorders in the general population. Drug Alcohol Depend. 2007;88 Suppl 1:S71-84.. Concerning avoidant PD, a study showed either a high frequency of individuals with phobic symptoms in drug dependents, mainly alcohol users3030. Terra MB, Barros HM, Stein AT, Figueira I, Jorge MR, Palermo LH, et al. Social anxiety disorder in 300 patients hospitalized for alcoholism in Brazil: high prevalence and undertreatment. Compr Psychiatry. 2006;47(6):463-7..

No significant statistical difference was found related to drugs type, what is not according to a previous study that pointed the fact that alcohol dependents present with less PDs when comparing to other psychoactive drug users55. Grant BF, Stinson FS, Dawson DA, Chou SP, Ruan WJ, Pickering RP. Co-occurrence of 12-month alcohol and drug use disorders and personality disorders in the United States: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Arch Gen Psychiatry. 2004;61(4):361-8.. The only significant statistical difference found was that patients with PD aged younger for crack first use that those without PD and had also a tendency to have more troubles with this drug use, maybe because a longer time of consumption. Including, the earliest age for beginning crack use in patients with PD was the only variable that remained with statistically significance, after logistic regression analysis, which presented slightly wider intervals.

PDs patients had a higher number of previous treatment episodes. This finding may suggest a more severe disease and less treatment adherence according to literature findings11. González JMM, García AV. Evolución de las crencias nucleares relacionadas con la adicción en drogodependientes con y sin trastornos de personalidad. Addicciones. 2012;24(3):229-38.,88. Tull MT, Gratz KL. The impact of borderline personality disorder on residential substance abuse treatment dropout among men. Drug Alcohol Depend. 2012;121(1-2):97-102., although opposing to this, these patients had a tendency to have a higher treatment time for drug related problems. Another study with substance related disorders patients showed that antisocial PD individuals had significantly higher treatment markers like hospitalization days and medical visits99. Westermeyer J, Thuras P. Association of antisocial personality disorder and substance disorder morbidity in a clinical sample. Am J Drug Alcohol Abuse. 2005;31(1):93-110.. Regarding borderline PD, the patients presenting with this condition had a lower concern level to psychoactive drug related troubles, what can decrease their treatment adherence and worsen evolution, a finding also found in a previous study88. Tull MT, Gratz KL. The impact of borderline personality disorder on residential substance abuse treatment dropout among men. Drug Alcohol Depend. 2012;121(1-2):97-102..

Our findings do not allow us to conclude that the comorbidity with PDs leads to worse results on substance related disorders treatment. The absence of difference between groups may be due to the high number of losses, bigger in the group with PDs. It’s possible to guess that this comorbidity leads to relapse and can explain such losses. Remarkable findings were the high relapse frequency and low adherence to treatment in both patients groups. A Brazilian study compared alcohol dependents during 6 months, and also found a high relapse frequency and little adherence to psychotherapic treatment or to anonymous alcoholics groups3131. Skodol AE, Oldham JM, Gallaher PE. Axis II comorbidity of substance use disorders among patients referred for treatment of personality disorders. Am J Psychiatry. 1999;156(5):733-8..

This study has some limitations like little sample size, what jeopardized comparison among different PDs types, and the fact that was performed in only two hospitals, something that may decrease generalizability. Besides that, the two week drug withdrawal interval can be a bias for proper PD diagnosis. Concerning this issue, PDs prevalence has been shown to be similar in currently drug users and in those with higher abstinence withdrawal. This finding indicates that these diagnosis are not only due to symptoms overlap or diagnostic methodology used3232. Terra MB, Barros HM, Stein AT, Figueira I, Athayde LD, Spanemberg L, et al. Does co-occurring social phobia interfere with alcoholism treatment adherence and relapse? J Subst Abuse Treat. 2006;31(4):403-9.. The high number of losses can be a limitation of our study, but can also reflect the challenge of performing follow-up studies in this population, that often change telephones and addresses and have a high relapse rate. Besides that, the data being phone collected could be seen as a potential bias in answers, but 85% of them seemed to be reliable ones to the interviewers. Another aspect that needs to be considered is that a categorical PD diagnosis, based on specific criteria number, has some limitations. The DSM-V personality disorder group has recommended a significant reformulation on psychological personality diagnostic evaluation, proposing a hybrid dimensional and categorical model3333. American Psychiatric Association Diagnostic and Statistical Manual on Mental Disorders: DSM-5. Porto Alegre: Artmed; 2014.. However, these recommendations were not available by the moment of our project design and starting data collection.

Patients with PD and psychoactive substance use need the dual diagnosis identification in order to achieve a better therapeutical relationship and treatment conduction, as well as an effective treatment that covers the personality characteristics in a psychoactive substance dependence approach. Integrative treatment represents therapy of choice for patients with this dual diagnoses. Since PD patients tend to start the crack use earlier in their life, it is important to make a prevention regarding the drug’s use among these patients. Further studies with a larger sample, using a more rigorous methodology in the attempting of reducing the number of losses in the longitudinal follow-up and focused more in PD more frequently are needed, mainly in Brazilian population to proper map and care this comorbidity as licit and illicit drug consumption is increasing, causing individual, family and social troubles as far as a PD diagnosis in this individuals can lead to a reserved prognosis.

CONCLUSION

A high PD diagnosis was found in drug use inpatients, in our sample, being avoidant, borderline and antisocial the more frequent ones found. PD patients had an earlier crack use in life and had also more previous treatments than the ones without PD. No statistical significance was found between patients with and without PD, after 6-months follow-up, regarding drug use or treatment adherence, however patients diagnosed with SRD and PD need the identification of this comorbidity for to be promoted an integrative treatment for patients with this dual diagnoses.

Table 4
Patients with and without personality disorders. Logistic regression of variables where p < 0.2

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Publication Dates

  • Publication in this collection
    Apr-Jun 2016

History

  • Received
    6 Feb 2016
  • Accepted
    9 May 2016
Instituto de Psiquiatria da Universidade Federal do Rio de Janeiro Av. Venceslau Brás, 71 Fundos, 22295-140 Rio de Janeiro - RJ Brasil, Tel./Fax: (55 21) 3873-5510 - Rio de Janeiro - RJ - Brazil
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