Evidence map›Paper›PMID 41210421›Full record

ArticleAME case reports2025

Bilateral temporomandibular joint dislocation secondary to acute dystonia induced by antipsychotic depot injection: a case report.

Harvey Stevenson, Daniele Ramsay, Waseem Jerjes

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In one paragraph

Article in AME case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Harvey StevensonDepartment of Trauma and Orthopaedic Surgery, James Cook University Hospital, Middlesbrough, UK.
Daniele RamsayDepartment of Primary Care and Public Health, Faculty of Medicine, Imperial College London, London, UK.
Waseem JerjesDepartment of Primary Care and Public Health, Faculty of Medicine, Imperial College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acute dystonia is a well-recognised extrapyramidal side effect of antipsychotic medications, often presenting within hours to days of administration. While orofacial involvement is common, bilateral temporomandibular joint (TMJ) dislocation as a direct consequence of drug-induced dystonia is exceedingly rare and may be misinterpreted as a primary psychiatric or dental issue. Case Description: A 39-year-old man with schizophrenia had been stable on regular intramuscular flupentixol decanoate (40 mg every four weeks). When his mental health deteriorated, the depot dose was increased. Three weeks later, his sister contacted the general practitioner (GP) about new slurred speech, drooling, and inability to close his mouth. During a home visit, the GP noted facial spasm, trismus, and an open-locked jaw, suggesting bilateral temporomandibular joint (TMJ) dislocation, and arranged urgent referral to the emergency department (ED). In the ED, the patient was distressed and unable to speak or close his mouth. Examination and radiography confirmed bilateral anterior TMJ dislocation. Intravenous diazepam provided little relief, and manual reduction under conscious sedation failed due to severe dystonia. Both joints were successfully reduced under general anaesthesia using the standard two-thumb technique. Symptoms resolved completely, and no recurrence was observed on follow-up. A diagnosis of acute drug-induced dystonia leading to bilateral TMJ dislocation was established, and his antipsychotic regimen was reviewed with the psychiatric team. Conclusions: This case highlights an uncommon mechanical complication of antipsychotic-induced dystonia. Timely recognition and management are essential to avoid airway risk, prolonged joint dysfunction, or misattribution to psychiatric pathology. It reinforces the need for multidisciplinary coordination between emergency medicine, psychiatry, and maxillofacial services.

Indexed as

acute dystoniaantipsychotic side effectscase reportextrapyramidal symptoms (EPS)Temporomandibular joint dislocation (TMJ)

Identifiers

PMID41210421
PMCPMC12593143

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