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Atypical neuroleptic malignant syndrome in an incarcerated patient: a demographic who may be at increased risk.
Zabel, Matthew; Kandukuri, Rajeev.
Affiliation
  • Zabel M; College of Osteopathic Medicine, Rocky Vista University College of Osteopathic Medicine, Parker, Colorado, USA matthew.zabel@rvu.edu.
  • Kandukuri R; Psychiatry, Parkview Medical Center, Pueblo, Colorado, USA.
BMJ Case Rep ; 17(2)2024 Feb 06.
Article in En | MEDLINE | ID: mdl-38320820
ABSTRACT
An incarcerated male patient with a psychiatric history of schizoaffective disorder presented to the emergency department with muscle rigidity and mutism after receiving a 150 mg haloperidol decanoate injection. At the peak of his illness, symptoms included muscular rigidity, mutism, excessive drooling, an altered level of consciousness, tachycardia, diaphoresis and tremors. Atypical neuroleptic malignant syndrome (NMS) was diagnosed after discrediting similar illnesses through clinical reasoning, laboratory and imaging studies. He was successfully treated during a 40-day hospitalisation with lorazepam, amantadine, methocarbamol and supportive care. This case represents an atypical presentation of NMS due to the patient's lack of fever development. Nonetheless, he satisfied many other criteria, most notably rapid symptom onset after receiving a first-generation antipsychotic medication. The case also provides an opportunity to discuss the prevalence of psychiatric illness among the US incarcerated population and incarceration as a risk factor for developing NMS.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prisoners / Antipsychotic Agents / Mutism / Neuroleptic Malignant Syndrome Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: BMJ Case Rep Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prisoners / Antipsychotic Agents / Mutism / Neuroleptic Malignant Syndrome Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: BMJ Case Rep Year: 2024 Document type: Article Affiliation country: Country of publication: