Cited by 266Substance Abuse Treatment and OutcomesSchizophrenia research and treatmentForensic Toxicology and Drug Analysis

Methamphetamine Psychosis: Epidemiology and Management

Open access
Glasner-Edwards, Suzette, Mooney, Larissa J.·2014·CNS Drugs

Abstract

Psychotic symptoms and syndromes are frequently experienced among individuals who use methamphetamine, with recent estimates of up to approximately 40 % of users affected. Although transient in a large proportion of users, acute symptoms can include agitation, violence, and delusions, and may require management in an inpatient psychiatric or other crisis intervention setting. In a subset of individuals, psychosis can recur and persist and may be difficult to distinguish from a primary psychotic disorder such as schizophrenia. Differential diagnosis of primary vs. substance-induced psychotic disorders among methamphetamine users is challenging; nevertheless, with careful assessment of the temporal relationship of symptoms to methamphetamine use, aided by state-of-the art psychodiagnostic assessment instruments and use of objective indicators of recent substance use (i.e., urine toxicology assays), coupled with collateral clinical data gathered from the family or others close to the individual, diagnostic accuracy can be optimized and the individual can be appropriately matched to a plan of treatment. The pharmacological treatment of acute methamphetamine-induced psychosis may include the use of antipsychotic medications as well as benzodiazepines, although symptoms may resolve without pharmacological treatment if the user is able to achieve a period of abstinence from methamphetamine. Importantly, psychosocial treatment for methamphetamine dependence has a strong evidence base and is the optimal first-line treatment approach to reducing rates of psychosis among individuals who use methamphetamines. Prevention of methamphetamine relapse is the most direct means of preventing recurrence of psychotic symptoms and syndromes. Long-term management of individuals presenting with recurrent and persistent psychosis, even in the absence of methamphetamine use, may include both behavioral treatment to prevent resumption of methamphetamine use and pharmacological treatment targeting psychotic symptoms. In addition, treatment of co-occurring psychiatric disorders including depression and anxiety is important as a means of preventing relapse to methamphetamine use, which is often triggered by associated symptoms.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s40263-014-0209-8

Cites

97 of 97 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • For psychostimulant-induced psychosis, psychotic symptoms resolve with abstinence by about 1 week.

    “For psychostimulant-induced psychosis, psychotic symptoms resolve with abstinence by about 1 week”

    From Clinical management of psychostimulant withdrawal: review of the evidence (2023) · cites this paper as [80]

    Section 5.1 reports remission within one week of methamphetamine abstinence for a large majority of people with psychotic symptoms. The claim broadens this to psychostimulants generally and implies that symptoms resolve in all cases; Section 3.2 describes a subset with persistent psychosis. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Primary psychosis requires continued care with antipsychotic medication.

    “whereas primary psychosis will require continued care with antipsychotic medication (80).”
  • The standard of care for adolescent and young adult SUD treatment is to use interventions specifically tailored or designed for their unique developmental stage.

    “the standard of care for adolescent-and young adult SUD treatment is to use interventions that are specifically tailored or designed for their unique developmental stage.177,178,179”

    From The ASAM/AAAP Clinical Practice Guideline on the Management of Stimulant Use Disorder (2024) · cites this paper as [178]

    Section 5.1 discusses extra caution when prescribing antipsychotics to children and adolescents with methamphetamine-induced psychosis; it does not describe developmentally tailored SUD interventions. Sections 5.2–5.3 discuss psychosocial treatments for methamphetamine use without identifying such tailoring as the standard of care for adolescents and young adults. Searches for developmental-stage and age-appropriate treatment found no passage addressing that claim. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 4

  1. [26]Connell PH Amphetamine psychosis Maudsley Monograph No. 5 London Oxford University Press 1958
  2. [28]Griffith JD Cavanaugh JH Oates JA Psychosis induced by the administration of d-amphetamine to human volunteers Efron DH Psychomimetic drugs: proceedings of a workshop organised by the Pharmacology Section, Psychopharmacology Research Branch, National Institute of Mental Health, held at the University of California Irvine Jan. 25, 1969 New York Raven Press 1970
  3. [52]Connell PH Amphetamine psychosis Maudsley Monograph No. 5 London Oxford University Press 1958
  4. [70]First MB Spitzer RL Williams JEW Structured Clinical Interview for DSM-IV-Clinician Version (SCID-CV) (User’s guide and interview) Washington, DC American Psychiatric Press 1997

Cited by

Sorted by citations

Authors
Glasner-Edwards, S., & Mooney, L. J.
Affiliations
University of California, Los Angeles (US)
Venue
CNS Drugs
Published
2014-11-06
Volume
28
Issue
12
Pages
1115-1126
ISSN
  • 1172-7047 (ISSN-L)
  • 1179-1934
OpenAlex
W2035893127
Cited by
266
References
97
Citations by year
2026: 26 · 2025: 28 · 2024: 29 · 2023: 34 · 2022: 31 · 2021: 31 · 2020: 18 · 2019: 19 · 2018: 26 · 2017: 9 · 2016: 12 · 2015: 2 · 2014: 1
FWCI
6.04
Type
journal article
Language
en
Open access
Locations
  • CNS Drugs (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institute on Drug Abuse (K23DA020085)
Topics
  • Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
  • Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Forensic Toxicology and Drug Analysis
Keywords
methamphetamine psychosis, drug-induced psychosis, differential diagnosis, schizophrenia, antipsychotic drugs, benzodiazepines, methamphetamine dependence, psychosocial interventions, relapse prevention, urine toxicology, crisis intervention
MeSH terms
Central Nervous System Stimulants, Humans, Methamphetamine, Psychoses, Substance-Induced

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review