Neuroleptic malignant syndrome

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Neuroleptic malignant syndrome
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Fever, muscle rigidity, autonomic dysfunction, altered mental status
Complications Rhabdomyolysis, renal failure, seizures
Onset Hours to days after starting or increasing antipsychotic medication
Duration Days to weeks
Types N/A
Causes Antipsychotic medications, dopamine antagonists
Risks High doses of antipsychotics, rapid dose escalation, dehydration, agitation
Diagnosis Clinical evaluation, exclusion of other conditions
Differential diagnosis Serotonin syndrome, malignant hyperthermia, encephalitis, heat stroke
Prevention N/A
Treatment Discontinuation of causative agent, supportive care, dantrolene, bromocriptine, benzodiazepines
Medication N/A
Prognosis Variable; can be life-threatening if untreated
Frequency Rare
Deaths N/A


Definition[edit]

Neuroleptic malignant syndrome is a rare neurological condition that is caused by an adverse reaction to neuroleptic (tranquilizer) or antipsychotic drugs. These drugs are commonly prescribed for the treatment of schizophrenia and other neurological, mental, or emotional disorders. The syndrome can also occur in people taking anti-Parkinsonism drugs known as dopaminergics if those drugs are discontinued abruptly.

Cause[edit]

The exact underlying cause of neuroleptic malignant syndrome is unknown. In some cases, more than one family member can be affected which suggests there may be a genetic component.

Onset[edit]

In most cases, the disorder develops within the first 2 weeks of treatment with the drug; however, the disorder may develop any time during the therapy period.

Signs and symptoms[edit]

Symptoms include high fever, sweating, unstable blood pressure, stupor, muscular rigidity, and autonomic dysfunction.

Clinical presentation[edit]

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. 80%-99% of people have these symptoms

30%-79% of people have these symptoms

5%-29% of people have these symptoms

Diagnosis[edit]

  • The diagnosis of NMS is based on history and the presence of certain physical examination and laboratory findings.[1].
  • Patients typically develop NMS within hours or days after exposure to a causative drug, with most exhibiting symptoms within 2 weeks and nearly all within 30 days.
  • NMS has classically been characterized by the presence of the triad of fever, muscle rigidity, and altered mental status.

Treatment[edit]

Prognosis[edit]

  • Early identification of and treatment for individuals with neuroleptic malignant syndrome improves outcome.
  • If clinically indicated, a low potency neuroleptic can be reintroduced very slowly when the individual recovers, although there is a risk that the syndrome might recur.
  • Another alternative is to substitute another class of drugs for the neuroleptic.
  • Anesthesia may be a risk to individuals who have experienced neuroleptic malignant syndrome.

References[edit]

  1. Berman B. D. (2011). Neuroleptic malignant syndrome: a review for neurohospitalists. The Neurohospitalist, 1(1), 41–47. https://doi.org/10.1177/1941875210386491

NIH genetic and rare disease info[edit]

Neuroleptic malignant syndrome is a rare disease.



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