Neuroleptic malignant syndrome

Background

  • Life threatening neurologic emergency associated with the use of neuroleptic agents[1][2]
    • Can occur with single dose, increasing dose, or same dose as usual [3]
    • May also occur with withdrawal of anti-Parkinson medication or use of antiemetics
  • Develops over 1-3 days
  • Majority of deaths occur from complications of muscle rigidity

Clinical Features

  • Tetrad of:[4]
  • Altered mental status
    • Agitated delirium progressing to stupor/coma
  • Muscular Rigidity
    • Generalized, "lead pipe" rigidity
  • Hyperthermia
    • >38C (87%)
    • >40C (40%)
  • Autonomic Instability
    • Tachycardia
    • Hypertension
    • Diaphoresis

Differential Diagnosis

Altered mental status and fever

Diagnosis

Workup

  • Total CK
    • Typically >1000
    • Correlates with degree of rigidity
  • CBC
    • WBC >10K is typical
  • Chemistry
    • May show hypocalcemia, hypomagnesemia, hyperkalemia, metabolic acidosis
  • UA
    • Myoglobinuria (from rhabdo)
  • LFT
    • Transaminitis
  • CT/LP
    • CSF may have mildly elevated protein

Serotonin syndrome vs Neuroleptic malignant syndrome

  • History of a new serotonergic drug or a dose increase of a serotonergic drug are helpful
  • Serotonin syndrome is usually much more acute in onset than NMS which may develop over days or weeks
  • Presence of ‘lead pipe’ rigidity is typical of NMS, while serotonin syndrome typically manifests with tremor and hyperreflexia
  • Elevations in CK, LFTs, and WBC, coupled with a low iron level, distinguishes NMS from serotonin syndrome among patients taking both neuroleptic and serotonin agonist medications simultaneously

Treatment

  • The causative agent should be stopped
  • If precipitant is a dopaminergic therapy (L-dopa or Carbidopa) it can be restarted later at lower doses as an outpatient

Supportive Care

Directed Medical therapy[5]

  • Controversial with unclear and disputed efficacy
  • Dantrolene
    • Skeletal muscle relaxant; may cause hepatotoxicity in pts w/ liver disease
    • Consider only in pts with severe rigidity
    • Give 0.25-2mg/kg IV q6-12hr
  • Bromocriptine
    • Dopamine agonist
    • Give 2.5mg NG q6-8hr
  • Amantadine
    • Alternative to bromocriptine
    • Give 100mg PO/NG initially; titrate up as needed to max dose 200mg q12hr

Complications

References

  1. Su YP, Chang CK, Hayes RD, Harrison S, Lee W, Broadbent M, et al. Retrospective chart review on exposure to psychotropic medications associated with neuroleptic malignant syndrome. Acta Psychiatr Scand. Nov 15 2013
  2. Trollor JN, Chen X, Sachdev PS. Neuroleptic malignant syndrome associated with atypical antipsychotic drugs. CNS Drugs. 2009;23(6):477-92
  3. Dunkley, E. J. C., Isbister, G. K., Sibbritt, D., Dawson, A. H. and Whyte, I. M. (2003) ‘The Hunter Serotonin Toxicity Criteria: simple and accurate diagnostic decision rules for serotonin toxicity’, QJM, 96(9), pp. 635–642. doi: 10.1093/qjmed/hcg109
  4. Gurrera RJ, Velamoor V, Cernovsky ZZ. A Validation Study of the International Consensus Diagnostic Criteria for Neuroleptic Malignant Syndrome. J Clin Psychopharmacol. Aug 22 2013
  5. Addonizio G, Susman VL, Roth SD. Neuroleptic malignant syndrome: review and analysis of 115 cases. Biol Psychiatry. Aug 1987;22(8):1004-20