Clinical characteristics of synthetic cannabinoid-induced psychosis in relation to schizophrenia: a single-center cross-sectional analysis of concurrently hospitalized patients
Authors Altintas M, Inanc L, Akcay Oruc G, Arpacioglu S, Gulec H
Received 2 March 2016
Accepted for publication 20 June 2016
Published 2 August 2016 Volume 2016:12 Pages 1893—1900
Checked for plagiarism Yes
Peer reviewer comments 3
Editor who approved publication: Dr Roger Pinder
Merih Altintas, 1 Leman Inanc, 2 Gamze Akcay Oruc, 1 Selim Arpacioglu, 1 Huseyin Gulec 1
1 Department of Psychiatry, Erenköy Mental and Neurological Diseases Training and Research Hospital, Istanbul, 2 Department of Psychiatry, Dr Cevdet Aykan Mental Health and Diseases Hospital, Tokat, Turkey
Background: This study aimed to evaluate synthetic cannabinoid (SC)-induced psychosis in terms of patient profile and clinical characteristics with reference to concurrently hospitalized schizophrenic patients.
Methods: A total of 81 male patients diagnosed with psychotic disorder induced by the use of SCs (n=50; mean (standard deviation [SD]) age: 25.9 (5.5) years) or with schizophrenia (n=31, mean (SD) age: 42.9 (11.6) years) based on the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, diagnosis criteria who were concurrently hospitalized at Erenköy Mental and Neurological Diseases Training and Research Hospital were included in this cross-sectional study. Data on sociodemographic characteristics, Brief Psychiatric Rating Scale (BPRS), Positive and Negative Syndrome Scale (PANSS), Frontal Assessment Battery (FAB), Hamilton Rating Scale for Depression (HRSD), and Hamilton Anxiety Rating Scale (HAM-A) were recorded in all the patients.
Results: Mean (SD) age at disease onset in SC-induced psychosis patients was 22.3 (5.6) years; 26.0% had suicidal ideation and 58.4% were hospitalized involuntarily. Marijuana was the most common first used substance (72.0%), and solitary use of SC was noted in 38.0% of patients. SC-induced psychosis patients had similar PANSS positive, BPRS, HRSD, and FAB scores and significantly lower PANSS negative scores (18.0 [6.5] vs 22.3 [6.0], P=0.004) than patients with schizophrenia, while they had similar HAM-A scores (17.8 [10.3] vs 21.6 [5.5], P=0.085) as young schizophrenics. Age at onset for SC (r=0.364, P=0.05) or substance (r=0.395, P=0.01) use was correlated positively with total FAB scores.
Conclusion: In conclusion, our findings revealed SC-induced psychosis to influence young individuals and be associated with remarkable rates of suicidal ideation and involuntary hospitalization as well as similar clinical picture with schizophrenia in terms of PANSS positive, BPRS, HRSD, HAM-A, and FAB scores. Younger age at onset was associated with poorer frontal lobe functions overall, regardless of the type of substance, and with poorer inhibitory control and programming performance in case of SC use.
Keywords: synthetic cannabinoid, psychosis, schizophrenia, frontal lobe, cognition, psychotogenic, bonzai
Consumption of synthetic cannabinoids (SCs), marketed under different names such as K2, Spice, Aroma, and Dream in different countries and named as Bonzai in Turkey, has been increasing worldwide. 1–5 Albeit no data are available on the exact prevalence of SC use in Turkey, a rapidly growing increase in SC consumption among young population has been noted in Turkey consistent with the global increase in the prevalence of SC use among adolescents and young adults with a male predominance. 5–9
Cannabidiol (CBD) and delta-9-tetrahydrocannabinol (THC) are the two principal ingredients of natural cannabis (marijuana) with counteracting functions. 10 Whilst purchased and perceived as risk-free marijuana-like herbal blends, 1 SCs are much more potent than natural cannabis, since they act as a more potent full agonist at the cannabinoid subtype 1 receptor than THC, and they also lack cannabinoids such as CBD that may otherwise counteract psychoactive properties of THC. 1,5,11,12 Hence, SCs may induce a more severe clinical presentation than the natural plants they are supposed to mimic, including agitation, anxiety, tachycardia, hallucinations, irritability, memory and cognitive impairment, violent behavior, unresponsiveness, and psychosis. 1,13,14
SCs are shown to trigger psychotic symptoms including paranoia, hallucinations, disorganized behavior, and suicidal thoughts among individuals with or without concomitant psychiatric disorders. 5,7,10,13–20 SCs were also reported to be associated with a wide range of positive and negative symptoms and cognitive impairment that resemble the phenomenology of schizophrenia. 21,22 However, being mainly based on case reports and laboratory studies, limited data are available on SC-induced psychosis.
The present study was therefore designed to evaluate SC-induced psychosis in terms of patient profile, clinical characteristics, and psychotogenic profile with reference to concurrently hospitalized schizophrenic patients.
A total of 81 male patients diagnosed with psychotic disorder induced by the use of SCs (n=50) or with schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, diagnosis criteria 23 (n=31) who were concurrently hospitalized at Erenköy Mental and Neurological Diseases Training and Research Hospital, Istanbul, were included in this cross-sectional study. Age 16–60 years, being literate, use of SC for at least 4 months, and lack of previous diagnosis of any psychiatric disorder were the inclusion criteria for SC-induced psychosis group, while patients at the intoxication stage of SCs, decided based on successive analysis of laboratory and clinical findings, and patients with mental retardation or any other neurological disease and past history of head trauma were excluded. Aged 16–60 years and no personal or family history of substance use were the eligibility criteria for the patients with schizophrenia.
Written informed consent was obtained from each subject following a detailed explanation of the objectives and protocol of the study, which was conducted in accordance with the ethical principles stated in the Declaration of Helsinki and approved by the Ethics Committee of Erenköy Mental and Neurological Diseases Training and Research Hospital.
Data on sociodemographic (age, marital status) and disease (family history, age at onset, duration of disease, hospitalizations) characteristics, urinalysis for SC metabolites, and psychometric assessments including Brief Psychiatric Rating Scale (BPRS), Positive and Negative Syndrome Scale (PANSS), Frontal Assessment Battery (FAB), Hamilton Rating Scale for Depression (HRSD), and Hamilton Anxiety Rating Scale (HAM-A) were recorded on the seventh day of hospitalization in all the patients. Detailed history of SC and substance use (type, usage pattern) was also recorded in the SC-induced psychosis group.
Laboratory analysis to confirm SC use included SC screening of urine samples via enzyme immunoassay method (K2 Enzyme Immunoassay; Immunalysis, Pomona, CA, USA) with the use of a commercially available kit enabling the detection of JWH-018, JWH-073, and AM-2201 metabolites in the urine with a cutoff value of 20 ng/mL for positivity.
Brief Psychiatric Rating Scale
This scale was developed by Overall and Gorham 24 to assess the severity and change of psychotic and some depressive symptoms in schizophrenia and other psychotic disorders. It consists of 18 items, each being rated for severity of symptom ranging from 1 (not present) to 7 (extremely severe). Factor analysis results signal different symptom clusters in this scale: the set of negative symptoms (emotional withdrawal, blunted affect, and motor retardation) and the set of positive symptoms (conceptual disorganization, hallucinations, and unusual though content). Scores obtained from the BPRS rating do not separate negative schizophrenia cases from positive schizophrenia cases; rather they are used to establish both negative and positive symptoms seen in a given case. 24 Preliminary data for the reliability of Turkish translation of BPRS were reported in our country. 25
Positive and Negative Syndrome Scale
It is a semi-structured interview form designed to assess positive and negative symptoms as well as general psychopathology and to measure the levels of these symptoms in case of schizophrenia or any other psychotic disorder. 26 The scale consists of 30 items rated from 0 (absent) to 7 (extreme) that represent increasing levels of psychopathology. Seven items are related to positive syndrome subscale, seven items are related to negative syndrome subscale, and the remaining 16 items are related to general psychopathology subscale. The study of validity and reliability of this scale (in Turkish) was conducted by Kostakoglu et al. 27
Frontal Assessment Battery
FAB is a short bedside cognitive and behavioral test to assess frontal lobe functions. It has six subscales, giving a total possible score of 0–18. The subscales are conceptualization, mental flexibility, programming, sensitivity to interference, inhibitory control, and environmental autonomy. Higher scores indicate better performance. This short battery was designed to assess executive functions at bedside. 28,29
Hamilton Rating Scale for Depression
This scale aims to assess severity of, and change in, depressive symptoms for a given patient. It was first introduced by Hamilton and then was transformed into a structured form by Williams under the supervision of Hamilton. 30 Validity and reliability of the Turkish questionnaire was conducted by Akdemir et al. 31 This scale consists of 17 questions and it is not utilizable in making diagnosis, while enables assessment of existing level of, and change in, depressive symptoms with higher scores indicating more severe depression.
Hamilton Anxiety Rating Scale
This scale consists of 14 items designed to establish anxiety states and distribution of symptoms, and to measure change in severity. 32 Each item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0–56, where 33
Statistical analysis was made using IBM SPSS Statistics (version 20.0; IBM Corporation, Armonk, NY, USA). Chi-square (χ 2 ) test was used for the comparison of categorical data, while Student’s t-test was used for normally distributed metric data. Mann–Whitney U-test for metric data with non-normal distribution was used for the analysis of numerical data. Spearman correlation test was used for correlation analysis. Data were expressed as “mean (standard deviation [SD])”, minimum–maximum, and percent (%) where appropriate. P # Mann–Whitney U-test, *Student’s t-test (compared to SC-induced psychosis). Values in bold indicate statistical significance (P 34 emphasizing the likelihood of SC-induced psychosis to emerge in a short span of time. 17
Consistent with the statement that the majority of first-time SC users are experienced marijuana smokers, 1,35,36 SC was used following other transitional substances rather than as a first substance in majority of our patients, with cannabis being the most popular antecedent substance. SC was not the first substance in the majority of our patients, and preceded by use of other transitional substances, such as cannabis in most cases. 7,35
SC-induced psychosis was shown to be associated with similar psychotogenic profile in terms of PANSS positive, BPRS, and HRSD scores as well as FAB scores in our cohort. Although lower PANSS negative scores and higher HAM-A scores were noted in SC-induced psychosis patients as compared with overall schizophrenia population, subgroup analysis with age-matched young schizophrenia patients revealed similar level of anxiety and still lower PANSS scores in SC-induced psychosis patients.
Paranoia, disorganized behavior, visual and auditory hallucinations, and suicidal thoughts are considered amongst the psychotic-like symptoms that can be triggered by SCs, not only in vulnerable individuals but also in subjects with no previous history of psychosis. 1,16
Indeed, the rarity of negative symptoms in SC-induced psychosis has been reported; the term “spiceophrenia” is used to refer the involvement of hallucinations, delusions, and increased positive psychotic symptoms in SC-induced psychosis. 34,37,38 Therefore, our findings are in line with the publications describing SC psychosis 34,37 and support that SCs may trigger new-onset psychosis in otherwise healthy young men with no previous history of psychosis. 1 This seems notable given that exposure to cannabis in adolescence is thought to contribute to an increased risk of psychosis later in life. 11
Accordingly, data from laboratory studies indicate that SCs are likely to produce a wide range of positive, negative, and cognitive symptoms in healthy human subjects that resemble the phenomenology of schizophrenia, along with a transient exacerbation of symptoms when used by individuals with schizophrenia. 21
Given that anxiety is considered amongst the acute psychoactive adverse effects associated with the consumption of SCs, 1,11,38 identification of mild-to-moderate levels of anxiety similarly among SC-induced psychosis and young schizophrenia patients seems to be associated with the assessment of HAM-A scale on the seventh day of hospitalization. This also emphasizes the risk for the persistence of psychotic symptoms well beyond acute intoxication as reported in otherwise healthy young men with SC-induced new-onset psychosis. 37
SC-induced psychosis is considered to be an acute onset psychosis lasting from 1–5 weeks with a need for an average 8.5 days of hospital stay in patients with severe psychotic symptoms. 16,39,40 Accordingly, shorter length of hospitalization was noted in patients with SC-induced psychosis than schizophrenia in our cohort, despite similar psychotogenic profile.
Verbal learning, short-term memory and working memory, executive functions, abstract ability, decision making, and attention functions were reported to be the particularly affected cognitive domains among SC users. 41 Overall frontal lobe functions were worsened with younger age at onset for SC or substance use in our cohort; while in line with the characteristic behavioral disinhibition and low impulse control resulting from reduced neural inhibition among substance users, 42 inhibitory control and programming seem to be the cognitive domains specifically affected by SC.
Altered composition of SCs, with an increase of the psychoactive compound THC and a decrease of the potentially therapeutic compound CBD, is considered likely to be associated with persistent and neuroanatomic alterations in the hippocampus, prefrontal cortex, amygdala, and cerebellum. 43 Association between poorer cognitive performance and younger age of onset for SC usage has also been reported. 22,43
Similarity of FAB scores in terms of conceptualization, mental flexibility, programming, sensitivity to interference, inhibitory control, and environmental autonomy between the SC-induced psychosis and schizophrenia groups in our cohort supports that there is a good degree of overlap in the profile of cognitive impairments arising in response to SC use and due to schizophrenia. 21,42,44
Notably, adolescent cannabinoid exposure was shown to be associated with impaired brain maturation and long-term cognitive impairment in specific components of learning and memory, alike to schizophrenia. Hence, adolescent cannabinoid exposure is considered likely to be a risk factor for developing psychosis symptoms in adulthood. 45
Hence, our findings support the evidence regarding the link between cannabis use and psychosis along with similarities between SC and schizophrenia-induced cognitive impairment. 22,42
Presence of suicidal ideation in one-third and involuntary hospitalizations in more than half of SC-induced psychosis patients in our cohort seems consistent with the nature of SC-induced psychosis and the fact that involuntary hospitalization is mostly caused by the circumstances where the patient has lost his/her insight and discernment, the severity of psychosis is relatively stronger, and suicidal or homicidal ideations or rejection of treatment are evident. Suicidal ideation is considered to be highly frequent among SC patients, 46 and suicide-related death is considered likely to occur after severe acute psychosis or panic attack induced by SC. 47
Hence, our findings emphasize the importance of observing patients with SC use referred to the hospital in terms of homicidal or suicidal behaviors and clinical picture characteristically comparable to psychosis in schizophrenia along with the likelihood of faster recovery and quicker discharge than schizophrenic patients despite an acute clinical presentation.
Certain limitations of this study should be considered. First, evaluating SC-induced psychosis seems challenging since it is relatively harder to have access to those patients who only use SC. Accordingly, in the present study, only 38% of the patients were using only SC and thus our findings may not represent clear clinical presentation specific to SC usage given the likely contribution of co-ingestion with multiple illicit drugs or alcohol to the clinical picture.
Second, since SC is composed of various additives and chemicals that may also cause a wide variety of physical signs and symptoms, it seems not possible to discriminate the exact content of SC responsible for the presenting clinical manifestations. 5 Third, due to difference among SC users with respect to usage patterns and inability to reach precisely declared quantities particularly in cases with collective use with bucket or through rolling method, we failed to analyze the effects of daily dose on psychotogenic profile and cognitive impairment, which otherwise would extend the knowledge achieved in the current study. Fourth, given that urinalysis for SC screening revealed negative results for all patients consistent with the ability of the available kit to cover only three SC types, confirmation of SC use was based on anamnesis taken from patients and their relatives, rather than urinalysis in our study. Nonetheless, despite these limitations, given the paucity of the solid information regarding SC use that poses a significant risk with an ever-increasing rate notably among the youth, our findings contribute to available data on patient profile and clinical impacts of SC usage.
Our findings revealed that SC-induced psychosis influences young individuals and is associated with remarkable rates of suicidal ideation and involuntary hospitalization as well as similar psychotogenic profile with schizophrenia in terms of PANSS positive, BPRS, HRSD, HAM-A, and FAB scores. While younger age at onset was associated with poorer frontal lobe functions overall, inhibitory control and programming seem to be the cognitive function domains specifically affected by SC use. Hence, our findings emphasize the role of appropriate psychiatric management of SC-induced psychosis to minimize the potential risk for suicide attempt and cognitive dysfunction, given the likelihood of faster recovery despite psychotogenic profile and cognitive dysfunction comparable to schizophrenia. Further investigations are needed to have a better understanding of specific and dose-dependent long-term effects of newly emerging SCs.
The authors report no conflicts of interest in this work.
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Clinical characteristics of synthetic cannabinoid-induced psychosis in relation to schizophrenia: a single-center cross-sectional analysis of concurrently hospitalized patients Merih Altintas,1 Leman Inanc,2 Gamze Akcay Oruc,1 Selim Arpacioglu,1 Huseyin Gulec1 1Department of Psychiatry, Erenköy Mental and Neurological Diseases Training and Research Hospital, Istanbul, 2Department of Psychiatry, Dr Cevdet Aykan Mental Health and Diseases Hospital, Tokat, Turkey Background: This study aimed to evaluate synthetic cannabinoid (SC)-induced psychosis in terms of patient profile and clinical characteristics with reference to concurrently hospitalized schizophrenic patients. Methods: A total of 81 male patients diagnosed with psychotic disorder induced by the use of SCs (n=50; mean (standard deviation [SD]) age: 25.9 (5.5) years) or with schizophrenia (n=31, mean (SD) age: 42.9 (11.6) years) based on the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, diagnosis criteria who were concurrently hospitalized at Erenköy Mental and Neurological Diseases Training and Research Hospital were included in this cross-sectional study. Data on sociodemographic characteristics, Brief Psychiatric Rating Scale (BPRS), Positive and Negative Syndrome Scale (PANSS), Frontal Assessment Battery (FAB), Hamilton Rating Scale for Depression (HRSD), and Hamilton Anxiety Rating Scale (HAM-A) were recorded in all the patients. Results: Mean (SD) age at disease onset in SC-induced psychosis patients was 22.3 (5.6) years; 26.0% had suicidal ideation and 58.4% were hospitalized involuntarily. Marijuana was the most common first used substance (72.0%), and solitary use of SC was noted in 38.0% of patients. SC-induced psychosis patients had similar PANSS positive, BPRS, HRSD, and FAB scores and significantly lower PANSS negative scores (18.0 [6.5] vs 22.3 [6.0], P=0.004) than patients with schizophrenia, while they had similar HAM-A scores (17.8 [10.3] vs 21.6 [5.5], P=0.085) as young schizophrenics. Age at onset for SC (r=0.364, P=0.05) or substance (r=0.395, P=0.01) use was correlated positively with total FAB scores.Conclusion: In conclusion, our findings revealed SC-induced psychosis to influence young individuals and be associated with remarkable rates of suicidal ideation and involuntary hospitalization as well as similar clinical picture with schizophrenia in terms of PANSS positive, BPRS, HRSD, HAM-A, and FAB scores. Younger age at onset was associated with poorer frontal lobe functions overall, regardless of the type of substance, and with poorer inhibitory control and programming performance in case of SC use. Keywords: synthetic cannabinoid, psychosis, schizophrenia, frontal lobe, cognition, psychotogenic, bonzai
Synthetic Cannabinoids—”Spice” Can Induce a Psychosis: A Brief Review
Synthetic cannabinoids, popularly called Spice, are common drugs of abuse in the United States. They are utilized as a substitute for marijuana, primarily for their psychoactive properties. Consumption has been rapidly increasing due to recreational effects, easy accessibility, and not being detectable by urine drug screening tests. The side effect profile of synthetic cannabinoids involves many organs and is not well known to the public. Psychoses are a common adverse result from their consumption. Primary care physicians and other medical professionals should consider synthetic cannabinoid consumption in the differential diagnoses of a patient presenting with psychosis.
Synthetic cannabinoids (SC) are a public health concern due to their adverse effect and limited safety profile research. Synthetic marijuana products first appeared as recreational drugs in Europe in 2006, and consumption has increased in the United States since 2009. 1 SC is added to various herbal products and marketed as marijuana alternatives. SC distribution is rising, readily available over the counter and via the internet. 2 The United States Drug Enforcement Administration (DEA) labeled SC products under Schedule 1; thus, SC is categorized as an illegal substance. 3 Various compositions of SC have been synthesized and distributed in the US, despite governmental restrictions. 4 Young people are the most frequent users, which has been attributed to the recreational effects of SC, as well as its easy accessibility and difficulty in being detected in the urine by drug screening. 5
SC was developed to study cannabinoid receptors but emerged as a substance of abuse. 6 Wrapped in foil packages, SC has been marketed as nail polish remover, deodorizers, incense, and potpourri, offering a “natural, legal high,” but “not for human consumption.” Collectively referred to as “Spice” or “K2,” SC typically contains a mixture of synthetic cannabinoids including CP-47, 497, CP-47,497-C8, JWH-018, JWH-073, JWH-081, JWH-122, JWH-210, JWH-250, HU-211, and RCS-4. 7 Although sold as a marijuana “alternative,” SC has been linked to more adverse health effects than natural cannabinoids. Adolescents, in particular those who are male and/or African-American, account for 40 percent of all users, and many first-time users of SC are reported to have previously smoked marijuana. 9 SC consumption is most frequent among people who are either single, divorced, separated, homeless, and/or unemployed. 9 Poison control centers receive thousands of reports of adverse health effects related to SC annually. Recently, the Illinois Department of Public Health reported cases of bleeding and deaths due to contamination of SC with rat poison. 10 They issued an alert not to use SC purchased since March 1, 2018.
SC binds to CB1 and CB2 cannabinoid G protein-coupled receptors with effects similar to tetrahydrocannabinol (THC). These receptors are widely distributed throughout the body—CB1 being predominant in the brain and CB2 in the immune system. 11 The CB1 receptor is primarily responsible for psychoactive effects, while the CB2 receptor is involved in immune function. THC acutely increases dopamine release and neuronal activity, while long-term exposure is associated with blunting of dopamine; THC can induce diverse, potentially long-term effects on this system. 4 In contrast to THC being a partial agonist at brain cannabinoid receptors, SC is a full agonist, with high potency at CB1 receptors. 12
Adverse outcomes associated with SC consumption are more prevalent and severe than those arising from natural cannabis use. 13 There has been an increase in emergency medical treatment due to ill effects secondary to synthetic cannabinoids. 14 High receptor binding affinity might be explanatory. Adverse events include the following:
- • Fatality: Death has been attributed directly to SC due to cardiac dysrhythmias, seizures, liver toxicity, and/or kidney failure; deaths have also been related indirectly to SC use due to hypothermia 15
- • Cardiovascular: Effects include tachycardia, hypertension, arrhythmia, myocardial infarction, and/or cardiac arrest. 15
- • Renal: Effects include acute tubular necrosis, interstitial nephritis, and/or rhabdomyolysis. 15
- • Gastrointestinal: Effects include nausea and vomiting. 15
- • Neurologic: Effects include agitation, irritability, catatonia, seizures, sedation, cognitive deficits, memory loss, sympathomimetic syndrome, and coma. Additionally, structural abnormalities including subarachnoid hemorrhage and cerebrovascular accidents have been linked to SC usage. 14 – 17
- • Psychiatric: Effects include altered mental status, anxiety, panic, and psychoses. Symptoms have been reported to persist for over one month following ingestion, with psychiatric hospitalizations reported due to suicidality, affective symptoms, self-injury, catatonic features, and/or Capgras syndrome.
- • Bleeding: Patients with SC poisoning evidence hemoptysis, hematuria, bloody noses, bleeding gums, and/or internal hemorrhage. Patients presenting with brodifacoum, a dangerous anticoagulant contained in some rat poisons, has also been reported. 10
Reported psychotic symptoms associated with SC ingestion include perceptual alterations, illusions, paranoia, catatonia, depersonalization, dissociation, and auditory and/or visual hallucinations. Psychoses are usually transient and resolve spontaneously; however, these reactions appear to be a frequent reason for individuals to seek emergency medical attention.
The psychoses associated with SC ingestion can impact the determination of long-term mental health prognoses. The degree of SC-associated dysfunction is related to age of exposure, familial aspects, psychiatric predispositions, childhood trauma, and genetic factors. 14 Younger male users using SC appear to experience more psychotic symptoms compared to those who use marijuana. 18 Psychosis can persist even without a history of mental illness and has been reported to develop into chronic schizophrenia. 12
Neurophysiology studies document similarities between disruptions of neuronal network oscillations in schizophrenia and psychosis and those conditions triggered by SC. 11 There are more psychotic symptoms and agitation among SC users than in those ingesting cannabis. SC use has been observed to result in diagnosable psychotic disorders requiring more pharmacotherapy with antipsychotic medications and/or longer psychiatric hospitalizations compared to marijuana or natural cannabis use. 9
Due to the potentially serious consequences that can occur with SC use, medical professionals, governmental agencies, and the general public should work together to mitigate these dangers. The increase in cases of acute SC poisoning underscores the need for targeted prevention and treatment interventions. The chemical composition of SC has been altered to avoid being detected on urine screening; thus, assays specific for SC detection should be considered when screening select populations for substance use. Educating the public on the potentially life-threatening consequences of SC exposure is important. Expanding services for chemical dependence treatment is in the public interest.
Acute SC intoxications are managed by hospitalization, close monitoring, and supportive therapies, such as hydration, airway protection, and/or oxygen. Agitation can be quickly managed by intravenous benzodiazepines infusions. Psychotic symptoms can be controlled with antipsychotic medications, with careful consideration of individual patient needs. 19
Synthetic Cannabinoids—”Spice” Can Induce a Psychosis: A Brief Review Abstract Synthetic cannabinoids, popularly called Spice, are common drugs of abuse in the United States. They are utilized