J Clin Med Res
Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
Journal website https://www.jocmr.org

Original Article

Volume 12, Number 12, December 2020, pages 803-808


Substance Use Patterns and Schizophrenia Spectrum Disorders: A Retrospective Study of Inpatients at a Community Teaching Hospital

Terence Tumentaa, c, Oluwatoyin Oladejia, Manpreet Gilla, Basim Ahmed Khanb, Olaniyi Olayinkaa, Chiedozie Ojimbaa, Tolulope Oluponaa

aDepartment of Psychiatry and Behavioral Sciences, Interfaith Medical Center, Brooklyn, NY, USA
bShifa College of Medicine, Islamabad, Pakistan
cCorresponding Author: Terence Tumenta, Department of Psychiatry and Behavioral Sciences, Interfaith Medical Center, Brooklyn, NY, USA

Manuscript submitted October 23, 2020, accepted December 8, 2020, published online December 18, 2020
Short title: Substance Use Patterns in Patients With SSD
doi: https://doi.org/10.14740/jocmr4380

Abstract▴Top 

Background: Schizophrenia is one of the chronic mental illnesses, characterized by delusions, hallucinations, disorganized speech, grossly disorganized or catatonic behavior, and cognitive decline. It frequently leads to a lifetime of impairment and disability that span the entire lifespan of the patients. Several epidemiologic studies have shown that schizophrenia spectrum disorders (SSDs) contribute significantly to years lived with disability. Additionally, substance use disorders have been reported to co-occur commonly among patients with SSD (a comorbidity also known as dual diagnosis), attracting notable attention over the past few decades. This dual diagnosis often requires treatment modifications to ensure for best patient outcomes.

Methods: This study was a retrospective review of the electronic medical charts. The patients included in the study were discharged from the psychiatric unit of our hospital between July 1, 2017 and October 31, 2017. Patients were included in the study using three inclusion criteria: 1) age ≥18 years; 2) had a diagnosis of SSD at discharge; and 3) had urine drug screen performed. Sociodemographic and clinical variables were abstracted. Univariate analysis and summary statistics were performed. Bivariate and multivariate analyses were done via logistic regression models to determine the odds ratios (ORs) and corresponding P values (P).

Results: A total of 365 (52.2%) patients had a diagnosis of SSD at discharge. Of these, 349 met the inclusion criteria. The age ranged from 19 to 79 years, with a mean age of 42.2 years, and 76.8% of the patients used substances. Out of the 269 patients who used substances, 199 (74%) used two or more substances. Tobacco use was most prevalent (62.3%), followed by cannabis use (41.5%), alcohol use (40.2%), and cocaine use (27.4%). Patients who reported using tobacco, were more likely to have comorbid alcohol use (OR = 7.24; P = 0.000), cannabis use (OR = 2.80; P = 0.000), cocaine use (OR = 5.00; P = 0.000), and synthetic cannabis (K2) use (OR = 4.62; P = 0.048). Results of the multivariate analyses supported the other findings.

Conclusions: Our study found a high association between schizophrenia spectrum disorders and substance use, with three out of four patients with SSD using a substance. This prevalence is higher than previously reported by other studies. Among those who use substances, about three in four use multiple substances. These point to some interaction between the substances and appear to be heavily influenced by significant social determinants of mental health that continue to plague the community. It is important to establish if a patient with schizophrenia has a comorbid substance use disorder, because addressing both generally leads to better patient outcomes.

Keywords: Substance use; Schizophrenia; Schizophrenia spectrum disorders; Mental health; Public health

Introduction▴Top 

Schizophrenia is one of the chronic mental illnesses. Patients commonly present with delusions, hallucinations, disorganized speech, grossly disorganized or catatonic behavior, and negative symptoms. It frequently leads to a lifetime of impairment, cognitive decline, and disability that span the entire lifespan of the patients. Several epidemiologic studies have shown that schizophrenia spectrum disorders (SSDs) contribute significantly to years lived with disability [1]. Additionally, substance use disorders (SUDs) have been reported to co-occur commonly among patients with SSD (a comorbidity also known as dual diagnosis), attracting notable attention over the past few decades [2-5]. For example, in one epidemiological study, 47% of patients with schizophrenia were reported to have a SUD [2]. Patients diagnosed with schizophrenia and other psychotic disorders usually have comorbid SUDs. This dual diagnosis often requires treatment modifications to ensure for best outcomes. This estimate is in-keeping with other studies reporting approximately half of schizophrenia patients have a comorbid SUD [4, 5].

Most patients with comorbid SSD and substance use are young males and have been shown to have a higher risk for medication noncompliance, multiple hospitalizations, unstable housing and homelessness, human immunodeficiency virus (HIV) infection, suicide, and violent behavior [3]. Regarding specific substances, those who use alcohol are reported to have higher hospital admissions, higher severity of positive symptoms, higher rates of extrapyramidal side effects including tardive dyskinesia, and “relative neuroleptic refractoriness” [2]. There have been studies about the exacerbation of psychotic symptoms, increased hospital admissions, and increased tardive dyskinesia with cannabis use [2, 5]; while cocaine use reportedly is associated with a higher risk of depression, milder negative symptoms, and a high rate of readmission [2]. Additionally, patients with dual diagnosis have been shown to have a link between current suicide risk, positive symptoms, insight, and first-degree relatives with SUD [6].

Although several studies show an association between SSD and substance use, with the attendant negative health effects, the direction of influence remains unclear. Furthermore, it is uncertain if it is more likely that patients with SSD would use one or a combination of substances (e.g., use of tobacco alone versus tobacco and cannabis). Hence, investigating the pattern of substance use among patients with SSD in different clinical/geographic settings is a crucial step. In this research study, we choose to evaluate the prevalence of substance use and the common combination of substances used by patients diagnosed with SSDs at a community teaching hospital.

Materials and Methods▴Top 

Study setting and population

The study was conducted at Interfaith Medical Center, a community teaching hospital in Central Brooklyn, NY. The hospital serves patients, representing every racial, ethnic, and national origin group in Central Brooklyn, with the majority being Caribbean-Americans and African Americans.

Study design and sample

This study was a retrospective review of the electronic medical charts. The patients included in the study were discharged from the psychiatric unit of our hospital between July 1, 2017 and October 31, 2017. Patients were included in the study using three inclusion criteria: 1) age ≥ 18 years old; 2) had a diagnosis of SSD at discharge; and 3) had urine drug screen performed.

Data collection and management

Data on discharges from the inpatient psychiatric unit were obtained from the director of quality assurance. Data on study variables were manually abstracted from the electronic medical record system and populated into an excel spreadsheet. The data were recoded and exported to STATA software for analysis. To maintain HIPAA compliance, no personal identifiable information was recorded.

Choice of variables and categorization

The variables chosen were hypothesized to influence substance use directly or indirectly in patients with SSD. Socio-demographic characteristics included age, gender, race, employment status, and living arrangement of the patients. The clinical variables included length of stay in the hospital, readmission to the hospital within 30 days, urine drug screen result, and self-reported tobacco use.

Some quantitative variables were recoded into categorical variables. As such, age was recoded into two categories (0 = patients aged 18 to 42 years; 1 = patients aged 43 years or older); readmission to the hospital within 30 days was recoded as “0” for no readmission within 30 days following discharge and “1” for patients that were readmitted within 30 days of discharge; given that the median length of stay was 12 days, length of hospital stay (LOS) was recoded as “0” for patients with a hospital stay of 12 days or less, and “1” for those with a hospital stay greater than 12 days.

Statistical methods

Statistical analysis was done using STATA software version 16. The Chi-square test and t-test for independent samples were used to compare groups at baseline. A total of 10 variables were included in the baseline analysis and data description. Frequencies were reported for the substances used by the study population.

In patients who reported using tobacco (62.3%), bivariate logistic regression analyses were run to determine the odds ratios (ORs) and corresponding P values of co-occurring substance use. We defined statistical significance using a two-tailed P value of less than or equal to 0.05, for all analyses. A multivariate logistic regression was then performed including all covariates in the unadjusted bivariate models, regardless of statistical significance.

We used the Hosmer-Lemeshow test to verify the goodness-of-fit of our model. The goodness-of-fit model shows that the model cannot be dismissed and therefore leads to the inference that the model fits well.

Ethical issues

For this study, institutional review board (IRB) approval was obtained. This research was carried out in accordance with the ethical principles of the organization responsible for human subjects, as well as with the Declaration of Helsinki.

Results▴Top 

We extracted 365 (52.2%) of records with a discharge diagnosis of SSD out of a total of 698 discharges. Of these, 16 patients were excluded as they did not have a urine drug screen and did not report on their tobacco use. There were 349 patients that were included in the study (Table 1), of which 77.4% were African American, 6.6% White, 13.2% Hispanic, and 2.8% identified as other race. Of the 349 patients, 76.8% used substances as evidenced by urine drug screen results and/or self-reported tobacco use. The mean age was 42.2 years, with the youngest being 19 years and the oldest being 79 years. The mean age was 41.7 years for those using substances as compared to 43.3 years in those who did not report any substance use. There was no statistical difference between the young (18 - 42 years) versus the older age group (> 42 years), irrespective of whether they used substances or not. The male gender was the most represented, with 69.3% of the study population, and it was also significantly associated substance use (P value = 0.001). African Americans used substances more than any other race, though the association was not statistically significant (P value = 0.008). Other factors such as being single, being unemployed, and being homeless, were also found to be nonsignificant in our study populations, with P values of 0.578, 0.688, and 0.984, respectively.

Table 1.
Click to view
Table 1. Characteristics of the Study Population
 

Among those with substance use, 74% (199/269) used two or more substances. In the frequency analyses (Table 2), tobacco use was most prevalent (62.3%), followed by cannabis use (41.5%), alcohol use (40.2%), and cocaine use (27.4%). In the bivariate analyses (Table 3), among patients who reported using tobacco, alcohol use (OR = 7.24; P value = 0.000), cannabis use (OR = 2.80; P value = 0.000), cocaine use (OR = 5.00; P value = 0.000), and synthetic cannabis (K2) use (OR = 4.62; P value = 0.048), were all found to be statistically significant. However, after adjusting for all covariates in the multivariate analysis, the only variables significantly associated with tobacco use in our study population were alcohol use, cannabis use, and cocaine use (Table 4).

Table 2.
Click to view
Table 2. Frequency Distribution of the Substances Used in the Study Population
 

Table 3.
Click to view
Table 3. Unadjusted Odds Ratios (ORs), 95% Confidence Intervals (CIs) and P Values From Bivariate Logistic Regression Models in Patients Using Tobacco
 

Table 4.
Click to view
Table 4. Adjusted Odds Ratios (ORs), 95% Confidence Intervals (CIs) and P values From Multivariate Logistic Regression Model in Patients Using Tobaccoa
 

The Hosmer-Lemeshow test was used to verify the goodness-of-fit of our model (number of groups = 7; χ2 = 6.64; P value = 0.248). The result shows that the model cannot be dismissed and therefore leads to the inference that the model fits well.

Discussion▴Top 

This study found that more than three quarters of the patients reported substance use. Of these, more than six out of 10 reported smoking tobacco. Patients with schizophrenia are three times more likely than the general population to start smoking and are five times less likely to stop smoking, with current prevalence rates of up to 80% [7].

In our study, we found that most patients used multiple substances as well as a significant link between tobacco use and other substances such as alcohol, cannabis, and cocaine. According to Canadian Schizophrenia Guidelines, in people who have schizophrenia and other psychotic disorders, substance use is common [8]. A possible explanation is that the ultimate shared influence of substances on the brain reward circuitry affects individuals who use several [9]. The findings in this research like those of other studies, indicate that persons with SSD use substances at a higher rate. In a prevalence study of patients with a psychiatric disorder conducted in Denmark in 2016, of the 53,035 patients with schizophrenia, 37% (19,623) reported using a substance [10]. Mueser et al reported in their study that alcohol was mostly likely to be abused by patients (47%), followed by cannabis (42%), stimulants (25%), and hallucinogens (18%). Sedatives (7%) or narcotics (4%) were abused by very few patients [11]. In severely mentally ill psychiatric patients, the most common type of SUD, followed by cannabis and cocaine use, was alcohol [12]. The misuse of both alcohol and cannabis has a negative effect on the clinical outcomes of schizophrenia. In the case of cannabis, it was also debated whether schizophrenia would actually be induced, on the basis of a three-to-six-fold dose-dependent rise in the risk of psychosis among cannabis users [7].

Large epidemiologic studies indicate that among people with schizophrenia, the rate of SUDs (excluding nicotine and caffeine use disorders) is 47% and 44.8%, respectively; with alcohol and cannabis being the most used substances. Moreover, in 60-90% of people with schizophrenia and other psychotic disorders, cigarette smoking has been documented [8]. Hunt et al conducted a meta-analysis and found that SUDs are extremely prevalent in schizophrenia, and rates over time have remained unchanged. They reported that the prevalence of any SUD was 41.7%. This was followed by illicit drugs with 27.5%, cannabis with 26.2%, alcohol with 24.3%, and stimulant use with 7.3% of the study population [4]. However, Margolese et al found that patients with ongoing depressive disorder compared to those with SSD (49.6%) were more likely to smoke cigarettes (88.9%) and they had significantly longer cigarette smoking histories (19.1 years for depressive disorders vs. 11.5 years for SSD) [13, 14]. Nesvag et al looked at the prevalence of SUD in patients diagnosed with schizophrenia, bipolar disorder, and depression. They reported that SUD was prevalent among 25.1% patients with schizophrenia, 20.1% patients with bipolar disorder, and 10.9% patients with depressive illness [10]. Looking at the number of patients using cocaine in our study, the results are in line with other studies which reported that beginning in 1988 and continuing to the present, cocaine use has risen significantly among urban schizophrenic patients. In addition, since the crack epidemic, cocaine appears to be the preferred substance of abuse for schizophrenic patients, surpassing amphetamines [9].

With respect to gender, our study found that males used more substances than females. This finding is similar to that of DeQuardo and colleagues who reported that the rate of substance abuse was much lower in female (20%) compared to male subjects (48%). The most widely abused drug, however, was cannabis (28%), followed closely by alcohol (21%), with slightly less patients abusing cocaine, hallucinogens, and stimulants [15]. For both substance abuse and schizophrenia, gender is an especially significant factor. For alcohol and cannabis in particular, males abused each class of drugs more than females [12]. Verma et al reported in their study of the Asian population looking at patients with a first episode of SSD, that alcohol was the substance most abused. They also stated that substance users were more likely to be males and were also more likely to have a criminal record than those who did not use substances [16].

Limitations

There are some drawbacks to this study, including those relating to the retrospective study design of medical charts. We were constrained, for instance, by the quality of information given in the charts. To assess whether the patients met criteria for SUD, we did not characterize the substance based on severity, such as mild, moderate, and severe. This was further compounded by using self-reports to determine tobacco use disorder, which is inherently subject to recall bias and underreporting. Another limitation of the study is that we did not look at medical comorbidities in these patients, factors that can also predispose to substance use.

The relatively large sample size is a strength of this analysis, which makes it possible that minor variations were observed between the study variables.

Conclusions

Patients diagnosed with schizophrenia and other psychotic disorders usually have comorbid SUDs. This dual diagnosis often requires treatment modifications to ensure for best outcomes. Our study found a high association between SSDs and substance use, with three out of four patients with SSD using a substance. This prevalence is higher than previously reported by other studies. Among those who use substances, about three in four use multiple substances. These points to some interaction between the substances and appears to be heavily influenced by significant social determinants of mental health that continue to plague the community. As previously reported by almost all studies if not all, there is a need to modify treatment to accommodate or address substance use comorbidity to achieve a favorable outcome in patients with SSD. This makes it important to establish if a patient with schizophrenia has a comorbid SUD. Psychiatric patients with comorbid SUD are frequently diagnosed later than those with no substance use, therefore delaying effective treatment. Identifying those at high risk so that care is initiated sooner would be of great interest.

Acknowledgments

For her guidance and insightful suggestions, the authors wish to thank Dr. Noela Co, Director of Quality Assurance, Interfaith Medical Center, Department of Psychiatry and Behavioral Sciences, Brooklyn, NY, USA.

Financial Disclosure

The authors did not receive any funding and have no financial disclosures.

Conflict of Interest

The authors have no conflict of interest.

Informed Consent

This was a retrospective review of patients’ charts. The patients were discharged from Interfaith Medical Center’s inpatient psychiatric unit. No personal identifiable information was obtained from study participants.

Author Contributions

As the primary author of the manuscript, TT has contributed to the study design, data collection, data analysis, helped to write the final draft of the manuscript, and has complete access to all the data in the study. O. Oladeji assisted with the gathering of data and the preparation of the final draft of the manuscript. MG assisted with the gathering of data and the writing of the final draft of the manuscript. BK assisted with gathering of data and writing of the final draft of the manuscript. O. Olayinka contributed to the study’s design, assisted with collection of data, and the writing of the final manuscript. CO helped with data collection and the final manuscript writing. TO contributed to the design of the report and supervised the writing of the manuscript’s final draft.

Data Availability

Any questions should be addressed to the corresponding author about the supporting data availability.


References▴Top 
  1. Volk DW, Lewis DA. Chapter 105 - Schizophrenia. In: Rosenberg RN, Pascual JM, editor(s). Pascual. Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease (Fifth Edition), Academic Press. 2015. p. 1293-1299. ISBN 9780124105294.
    doi
  2. Fowler IL, Carr VJ, Carter NT, Lewin TJ. Patterns of current and lifetime substance use in schizophrenia. Schizophr Bull. 1998;24(3):443-455.
    doi pubmed
  3. Kivimies K, Repo-Tiihonen E, Kautiainen H, Tiihonen J. Comorbid opioid use is undertreated among forensic patients with schizophrenia. Subst Abuse Treat Prev Policy. 2018;13(1):39.
    doi pubmed
  4. Hunt GE, Large MM, Cleary M, Lai HMX, Saunders JB. Prevalence of comorbid substance use in schizophrenia spectrum disorders in community and clinical settings, 1990-2017: Systematic review and meta-analysis. Drug Alcohol Depend. 2018;191:234-258.
    doi pubmed
  5. Olayinka O, Ojimba C, Alemu B, Olaolu O, Edomias D, Popoola O, Kallikkadan J, et al. Cannabis use in inpatients with schizophrenia spectrum disorders at a community hospital. J Clin Med Res. 2020;12(4):243-250.
    doi pubmed
  6. Adan A, Capella MD, Prat G, Forero DA, Lopez-Vera S, Navarro JF. Executive functioning in men with schizophrenia and substance use disorders. Influence of Lifetime Suicide Attempts. PLoS One. 2017;12(1):e0169943.
    doi pubmed
  7. Thoma P, Daum I. Comorbid substance use disorder in schizophrenia: a selective overview of neurobiological and cognitive underpinnings. Psychiatry Clin Neurosci. 2013;67(6):367-383.
    doi pubmed
  8. Crockford D, Addington D. Canadian Schizophrenia Guidelines: Schizophrenia and Other Psychotic Disorders with Coexisting Substance Use Disorders. Can J Psychiatry. 2017;62(9):624-634.
    doi pubmed
  9. Patkar AA, Alexander RC, Lundy A, Certa KM. Changing patterns of illicit substance use among schizophrenic patients: 1984-1996. Am J Addict. 1999;8(1):65-71.
    doi pubmed
  10. Nesvag R, Knudsen GP, Bakken IJ, Hoye A, Ystrom E, Suren P, Reneflot A, et al. Substance use disorders in schizophrenia, bipolar disorder, and depressive illness: a registry-based study. Soc Psychiatry Psychiatr Epidemiol. 2015;50(8):1267-1276.
    doi pubmed
  11. Mueser KT, Yarnold PR, Rosenberg SD, Swett C, Jr., Miles KM, Hill D. Substance use disorder in hospitalized severely mentally ill psychiatric patients: prevalence, correlates, and subgroups. Schizophr Bull. 2000;26(1):179-192.
    doi pubmed
  12. Mueser KT, Yarnold PR, Levinson DF, Singh H, Bellack AS, Kee K, Morrison RL, et al. Prevalence of substance abuse in schizophrenia: demographic and clinical correlates. Schizophr Bull. 1990;16(1):31-56.
    doi pubmed
  13. Margolese HC, Malchy L, Negrete JC, Tempier R, Gill K. Drug and alcohol use among patients with schizophrenia and related psychoses: levels and consequences. Schizophr Res. 2004;67(2-3):157-166.
    doi
  14. Margolese HC, Carlos Negrete J, Tempier R, Gill K. A 12-month prospective follow-up study of patients with schizophrenia-spectrum disorders and substance abuse: changes in psychiatric symptoms and substance use. Schizophr Res. 2006;83(1):65-75.
    doi pubmed
  15. DeQuardo JR, Carpenter CF, Tandon R. Patterns of substance abuse in schizophrenia: nature and significance. J Psychiatr Res. 1994;28(3):267-275.
    doi
  16. Verma SK, Subramaniam M, Chong SA, Kua EH. Substance abuse in schizophrenia. A Singapore perspective. Soc Psychiatry Psychiatr Epidemiol. 2002;37(7):326-328.
    doi pubmed


This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Journal of Clinical Medicine Research is published by Elmer Press Inc.

 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Journal of Clinical Medicine Research, monthly, ISSN 1918-3003 (print), 1918-3011 (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.jocmr.org   editorial contact: editor@jocmr.org
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.