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Summary of the review “Neuroleptic Malignant Syndrome”

6 Oct, 2024 | 16:20h | UTC

In a comprehensive review published in the New England Journal of Medicine, Wijdicks and Ropper discuss neuroleptic malignant syndrome (NMS), a rare but potentially fatal complication of antipsychotic therapy characterized by fever, muscle rigidity, and autonomic dysfunction. Given the widespread use of dopamine-blocking agents across various medical specialties, it is crucial for practicing physicians to recognize and manage this syndrome promptly to improve patient outcomes.

Key Aspects Influencing Patient Care:

  • Epidemiology and Risk Factors:
    • NMS occurs in approximately 0.02 to 3% of patients exposed to dopamine-blocking agents.
    • Risk factors include dehydration, high doses of antipsychotics, rapid dose escalation, intramuscular administration, and prior episodes of NMS.
    • Both first-generation (typical) and second-generation (atypical) antipsychotics can cause NMS, though it may be less severe with atypical agents.
  • Clinical Presentation:
    • Hyperthermia: Elevated temperatures often exceeding 40°C.
    • Muscle Rigidity: Lead-pipe rigidity leading to rhabdomyolysis and elevated creatine kinase levels.
    • Autonomic Dysfunction: Tachycardia, fluctuating blood pressure, diaphoresis.
    • Altered Mental Status: Ranges from agitation to stupor or catatonia.
    • Laboratory Findings: Leukocytosis, electrolyte imbalances, and signs of renal impairment.
  • Diagnosis:
    • Based on clinical criteria including recent exposure to dopamine antagonists and presence of key symptoms.
    • Important to differentiate from serotonin syndrome, malignant hyperthermia, heat stroke, and severe catatonia.
  • Management:
    • Immediate Discontinuation of the offending agent.
    • Supportive Care in ICU:
      • Stabilize vital signs and manage autonomic instability.
      • Aggressive hydration to prevent renal failure from rhabdomyolysis.
      • Cooling measures for hyperthermia.
    • Pharmacologic Interventions:
      • Dantrolene: Reduces muscle rigidity and hyperthermia.
      • Dopamine Agonists: Bromocriptine or amantadine may reverse dopamine blockade.
      • Benzodiazepines: Lorazepam for sedation and muscle relaxation.
    • Monitoring for Complications:
      • Watch for respiratory failure, renal dysfunction, electrolyte disturbances, and cardiac arrhythmias.
    • Electroconvulsive Therapy (ECT):
      • Considered in refractory cases unresponsive to medical management.
  • Outcome and Prognosis:
    • Recovery typically occurs within 7 to 11 days with appropriate treatment.
    • Mortality rates have decreased but can reach up to 15% within one year due to complications.
    • Rechallenge with Antipsychotics:
      • If necessary, reintroduce antipsychotics cautiously after full recovery, using low doses and slow titration.
      • Prefer atypical agents and monitor closely for recurrence.

Clinical Implications:

  • Early Recognition: Timely identification of NMS is critical for initiating life-saving interventions.
  • Interdisciplinary Approach: Collaboration among psychiatrists, intensivists, neurologists, and other specialists enhances patient care.
  • Education and Prevention:
    • Educate healthcare providers about the signs and risk factors of NMS.
    • Monitor patients on antipsychotics closely, especially during dose changes or when using high-potency agents.

Reference: Wijdicks, E. F. M., & Ropper, A. H. (2024). Neuroleptic Malignant Syndrome. New England Journal of Medicine, 391(12), 1130–1138. DOI: 10.1056/NEJMra2404606

 


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