Abstract
Context: Synthetic cannabinoids (SCs) such as "Spice", "K2", etc. are widely available via the internet despite increasing legal restrictions. Currently, the prevalence of use is typically low in the general community (<1%) although it is higher among students and some niche groups subject to drug testing. Early evidence suggests that adverse outcomes associated with the use of SCs may be more prevalent and severe than those arising from cannabis consumption. Objectives: To identify systematically the scientific reports of adverse events associated with the consumption of SCs in the medical literature and poison centre data. Method: We searched online databases (Medline, PsycInfo, Embase, Google Scholar and Pubmed) and manually searched reference lists up to December 2014. To be eligible for inclusion, data had to be from hospital, emergency department, drug rehabilitation services or poison centre records of adverse events involving SCs and included both self-reported and/or analytically confirmed consumption. Results: From 256 reports, we identified 106 eligible studies including 37 conference abstracts on about 4000 cases involving at least 26 deaths. Major complications include cardiovascular events (myocardial infarction, ischemic stroke and emboli), acute kidney injury (AKI), generalized tonic-clonic seizures, psychiatric presentations (including first episode psychosis, paranoia, self-harm/suicide ideation) and hyperemesis. However, most presentations were not serious, typically involved young males with tachycardia (≈37-77%), agitation (≈16-41%) and nausea (≈13-94%) requiring only symptomatic care with a length of stay of less than 8 hours. Conclusions: SCs most frequently result in tachycardia, agitation and nausea. These symptoms typically resolve with symptomatic care, including intravenous fluids, benzodiazepines and anti-emetics, and may not require inpatient care. Severe adverse events (stroke, seizure, myocardial infarction, rhabdomyolysis, AKI, psychosis and hyperemesis) and associated deaths manifest less commonly. Precise estimates of their incidence are difficult to calculate due to the lack of widely available, rapid laboratory confirmation, the variety of SC compounds and the unknown number of exposed individuals. Long-term consequences of SCs use are currently unknown.
Original language | English |
---|---|
Pages (from-to) | 1-13 |
Number of pages | 13 |
Journal | Clinical Toxicology |
Volume | 54 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2 Jan 2016 |
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In: Clinical Toxicology, Vol. 54, No. 1, 02.01.2016, p. 1-13.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - A systematic review of adverse events arising from the use of synthetic cannabinoids and their associated treatment
AU - Tait, Robert J.
AU - Caldicott, D.
AU - Mountain, David
AU - Hill, Simon L.
AU - Lenton, Simon
N1 - Cited By :17 Export Date: 15 December 2016 Correspondence Address: Tait, R.J.; Faculty of Health Sciences, National Drug Research Institute, Curtin University, GPO Box U1987, Australia; email: [email protected] Chemicals/CAS: Cannabinoids; Psychotropic Drugs References: (2009) Understanding the Spice Phenomenon, , European Monitoring Centre for Drugs and Drug Addiction. 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PY - 2016/1/2
Y1 - 2016/1/2
N2 - Context: Synthetic cannabinoids (SCs) such as "Spice", "K2", etc. are widely available via the internet despite increasing legal restrictions. Currently, the prevalence of use is typically low in the general community (<1%) although it is higher among students and some niche groups subject to drug testing. Early evidence suggests that adverse outcomes associated with the use of SCs may be more prevalent and severe than those arising from cannabis consumption. Objectives: To identify systematically the scientific reports of adverse events associated with the consumption of SCs in the medical literature and poison centre data. Method: We searched online databases (Medline, PsycInfo, Embase, Google Scholar and Pubmed) and manually searched reference lists up to December 2014. To be eligible for inclusion, data had to be from hospital, emergency department, drug rehabilitation services or poison centre records of adverse events involving SCs and included both self-reported and/or analytically confirmed consumption. Results: From 256 reports, we identified 106 eligible studies including 37 conference abstracts on about 4000 cases involving at least 26 deaths. Major complications include cardiovascular events (myocardial infarction, ischemic stroke and emboli), acute kidney injury (AKI), generalized tonic-clonic seizures, psychiatric presentations (including first episode psychosis, paranoia, self-harm/suicide ideation) and hyperemesis. However, most presentations were not serious, typically involved young males with tachycardia (≈37-77%), agitation (≈16-41%) and nausea (≈13-94%) requiring only symptomatic care with a length of stay of less than 8 hours. Conclusions: SCs most frequently result in tachycardia, agitation and nausea. These symptoms typically resolve with symptomatic care, including intravenous fluids, benzodiazepines and anti-emetics, and may not require inpatient care. Severe adverse events (stroke, seizure, myocardial infarction, rhabdomyolysis, AKI, psychosis and hyperemesis) and associated deaths manifest less commonly. Precise estimates of their incidence are difficult to calculate due to the lack of widely available, rapid laboratory confirmation, the variety of SC compounds and the unknown number of exposed individuals. Long-term consequences of SCs use are currently unknown.
AB - Context: Synthetic cannabinoids (SCs) such as "Spice", "K2", etc. are widely available via the internet despite increasing legal restrictions. Currently, the prevalence of use is typically low in the general community (<1%) although it is higher among students and some niche groups subject to drug testing. Early evidence suggests that adverse outcomes associated with the use of SCs may be more prevalent and severe than those arising from cannabis consumption. Objectives: To identify systematically the scientific reports of adverse events associated with the consumption of SCs in the medical literature and poison centre data. Method: We searched online databases (Medline, PsycInfo, Embase, Google Scholar and Pubmed) and manually searched reference lists up to December 2014. To be eligible for inclusion, data had to be from hospital, emergency department, drug rehabilitation services or poison centre records of adverse events involving SCs and included both self-reported and/or analytically confirmed consumption. Results: From 256 reports, we identified 106 eligible studies including 37 conference abstracts on about 4000 cases involving at least 26 deaths. Major complications include cardiovascular events (myocardial infarction, ischemic stroke and emboli), acute kidney injury (AKI), generalized tonic-clonic seizures, psychiatric presentations (including first episode psychosis, paranoia, self-harm/suicide ideation) and hyperemesis. However, most presentations were not serious, typically involved young males with tachycardia (≈37-77%), agitation (≈16-41%) and nausea (≈13-94%) requiring only symptomatic care with a length of stay of less than 8 hours. Conclusions: SCs most frequently result in tachycardia, agitation and nausea. These symptoms typically resolve with symptomatic care, including intravenous fluids, benzodiazepines and anti-emetics, and may not require inpatient care. Severe adverse events (stroke, seizure, myocardial infarction, rhabdomyolysis, AKI, psychosis and hyperemesis) and associated deaths manifest less commonly. Precise estimates of their incidence are difficult to calculate due to the lack of widely available, rapid laboratory confirmation, the variety of SC compounds and the unknown number of exposed individuals. Long-term consequences of SCs use are currently unknown.
KW - drug overdose
KW - drugrelated side effects and adverse reactions
KW - Emergency medical services
KW - Mental disorders
KW - Street drugs
KW - cannabinoid derivative
KW - poison
KW - synthetic cannabinoid derivative
KW - unclassified drug
KW - cannabinoid
KW - psychotropic agent
KW - acute kidney failure
KW - agitation
KW - automutilation
KW - brain ischemia
KW - drug exposure
KW - drug use
KW - Embase
KW - embolism
KW - emergency ward
KW - heart infarction
KW - hospital department
KW - hospital management
KW - human
KW - hyperemesis
KW - intervention study
KW - length of stay
KW - medical literature
KW - Medline
KW - nausea
KW - paranoia
KW - psychosis
KW - PsycINFO
KW - rehabilitation center
KW - Review
KW - self report
KW - side effect
KW - suicidal ideation
KW - systematic review
KW - tachycardia
KW - tonic clonic seizure
KW - vomiting
KW - adverse effects
KW - cannabis smoking
KW - Marijuana Abuse
KW - mortality
KW - prognosis
KW - risk factor
KW - substance abuse
KW - synthesis
KW - time factor
KW - Cannabinoids
KW - Drug Overdose
KW - Humans
KW - Marijuana Smoking
KW - Prognosis
KW - Psychotropic Drugs
KW - Risk Factors
KW - Substance Abuse Detection
KW - Time Factors
KW - Cannabinoids/adverse effects
KW - Drug Overdose/diagnosis
KW - Marijuana Abuse/diagnosis
KW - Psychotropic Drugs/adverse effects
KW - Marijuana Smoking/adverse effects
KW - drug-related side effects and adverse reactions
KW - mental disorders
KW - street drugs
UR - http://www.scopus.com/inward/record.url?scp=84951567352&partnerID=8YFLogxK
U2 - 10.3109/15563650.2015.1110590
DO - 10.3109/15563650.2015.1110590
M3 - Article
C2 - 26567470
SN - 1556-3650
VL - 54
SP - 1
EP - 13
JO - Clinical Toxicology
JF - Clinical Toxicology
IS - 1
ER -