Evidence map›Paper›PMID 38502289›Full record

ReviewCNS drugs2024

An Evidence-Based Update on Anticholinergic Use for Drug-Induced Movement Disorders.

Nora Vanegas-Arroyave, Stanley N Caroff, Leslie Citrome, Jovita Crasta, Roger S McIntyre, Jonathan M Meyer, Amita Patel, J Michael Smith, Khody Farahmand, Rachel Manahan and 2 more

Open access · hybridAbstract readReview
In one paragraph

Review in CNS drugs, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
10.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Review
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Organosulfur Compounds: Potential Therapeutics for Parkinson's Disease.CNS & neurological disorders drug targets · 2026
    Review
  14. Article
  15. Treatment of Parkinson's Disease-Related Psychosis.Clinical pharmacology : advances and applications · 2026
    Review
  16. Review
  17. Article
  18. Observational
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 2 countries.

Nora Vanegas-ArroyaveDepartment of Neurology, Baylor College of Medicine, 7200 Cambridge Street, Suite 9A, Houston, TX, 77030, USA. Nora.VanegasArroyave@bcm.edu.ORCID http://orcid.org/0000-0002-5073-4024
Stanley N CaroffCorporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
Leslie CitromeNew York Medical College, Valhalla, NY, USA.
Jovita CrastaSouth Nassau Communities Hospital, Baldwin, NY, USA.
Roger S McIntyreDepartment of Psychiatry and Pharmacology, University of Toronto, Toronto, ON, Canada.
Jonathan M MeyerDepartment of Psychiatry, University of California San Diego, La Jolla, CA, USA.
Amita PatelDayton Psychiatric Associations, Dayton, OH, USA.
J Michael SmithLifeSpring Behavioral Health, Spring, TX, USA.
Khody FarahmandNeurocrine Biosciences, Inc, San Diego, CA, USA.
Rachel ManahanNeurocrine Biosciences, Inc, San Diego, CA, USA.
Leslie LundtNeurocrine Biosciences, Inc, San Diego, CA, USA.
Samantha A CiceroNeurocrine Biosciences, Inc, San Diego, CA, USA.
Neurocrine Biosciences (United States) · USBaylor College of Medicine · USDayton Clinical Oncology Program · USNew York Medical College · USPhiladelphia VA Medical Center · USSouth Nassau Communities Hospital · USUniversity of California San Diego · USUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug-induced movement disorders (DIMDs) are associated with use of dopamine receptor blocking agents (DRBAs), including antipsychotics. The most common forms are drug-induced parkinsonism (DIP), dystonia, akathisia, and tardive dyskinesia (TD). Although rare, neuroleptic malignant syndrome (NMS) is a potentially life-threatening consequence of DRBA exposure. Recommendations for anticholinergic use in patients with DIMDs were developed on the basis of a roundtable discussion with healthcare professionals with extensive expertise in DIMD management, along with a comprehensive literature review. The roundtable agreed that "extrapyramidal symptoms" is a non-specific term that encompasses a range of abnormal movements. As such, it contributes to a misconception that all DIMDs can be treated in the same way, potentially leading to the misuse and overprescribing of anticholinergics. DIMDs are neurobiologically and clinically distinct, with different treatment paradigms and varying levels of evidence for anticholinergic use. Whereas evidence indicates anticholinergics can be effective for DIP and dystonia, they are not recommended for TD, akathisia, or NMS; nor are they supported for preventing DIMDs except in individuals at high risk for acute dystonia. Anticholinergics may induce serious peripheral adverse effects (e.g., urinary retention) and central effects (e.g., impaired cognition), all of which can be highly concerning especially in older adults. Appropriate use of anticholinergics therefore requires careful consideration of the evidence for efficacy (e.g., supportive for DIP but not TD) and the risks for serious adverse events. If used, anticholinergic medications should be prescribed at the lowest effective dose and for limited periods of time. When discontinued, they should be tapered gradually.

Indexed as

Antipsychotic AgentsDystoniaDystonic DisordersMovement DisordersNeuroleptic Malignant SyndromeTardive DyskinesiaAgedCholinergic AntagonistsHumansPsychomotor AgitationAntipsychotic AgentsCholinergic Antagonists

Identifiers

PMID38502289
PMCPMC10980662
OpenAlexW4392954175

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.