eMedicine Specialties > Emergency Medicine > Toxicology
Neuroleptic Malignant Syndrome: Follow-up
Updated: Aug 18, 2009
Follow-up
Further Inpatient Care
- Additional evaluation and treatment should be in an inpatient setting, preferably an ICU.
- The patient must be monitored closely to rule out underlying infection.
- Adequate hydration must be maintained.
- Rhabdomyolysis must be diagnosed and treated aggressively with alkalinization and hydration to prevent renal failure.
- The patient's psychiatric disease must be evaluated and treated during withdrawal of the neuroleptic medication.
- Challenge with an atypical antipsychotic may be appropriate since these drugs have a lower incidence of neuroleptic malignant syndrome (NMS).
- Treatment with ECT may be useful to treat the underlying psychiatric disease after an episode of NMS.
Further Outpatient Care
- NMS may be prolonged. If the patient is discharged, close follow-up care should be given to monitor residual symptoms. If neuroleptics are to be reinstituted, they should be administered at relatively low initial doses.
Transfer
- If NMS is diagnosed in a psychiatric facility, the patient should be transferred to an acute care medical facility where intensive monitoring and treatment is available.
Deterrence/Prevention
- Take a careful history before starting a new neuroleptic medication. NMS frequently recurs when medications are restarted.
- Monitor a patient carefully while administering neuroleptic medication to prevent excessive agitation and dehydration because these conditions may predispose a patient to NMS.
- Benzodiazepines and physical restraints may be useful.
Complications
- Rhabdomyolysis
- Renal failure
- Seizures
- Respiratory failure
- Aspiration pneumonia
- Decompensation of psychiatric disease with the withdrawal of neuroleptics
- Diffuse intravascular coagulation (DIC)
Prognosis
- Increased mortality, up to 50%, is seen in patients who develop renal failure during an episode of NMS.
- In the absence of rhabdomyolysis, renal failure, or aspiration pneumonia, and with good supportive care, the prognosis for recovery is good.
- The syndrome may last 7-10 days after discontinuing oral neuroleptics and up to 21 days after using depot neuroleptics (eg, fluphenazine).
Patient Education
- After an episode of NMS, the patient must be told that he or she is at risk for recurrence if rechallenged with a neuroleptic medication. The patient should report this reaction to all health care providers.
Miscellaneous
Medicolegal Pitfalls
- Failure to consider this diagnosis and to institute prompt therapies
- Failure to consider other non-NMS diagnoses as the cause of similar symptoms
- Failure to obtain a prior history of NMS before instituting medical therapies with any medications known to cause NMS
More on Neuroleptic Malignant Syndrome |
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| Differential Diagnoses & Workup: Neuroleptic Malignant Syndrome |
| Treatment & Medication: Neuroleptic Malignant Syndrome |
Follow-up: Neuroleptic Malignant Syndrome |
| References |
| « Previous Page |
References
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Further Reading
Keywords
neuroleptic malignant syndrome, neuroleptic medication, NMS, idiosyncratic reaction, muscular rigidity, autonomic dysfunction, haloperidol, fluphenazine, antipsychotic agents, prochlorperazine, promethazine, clozapine, risperidone, metoclopramide, amoxapine, lithium, dopamine D2-receptor antagonist, withdrawal of anti-Parkinson medication, respiratory failure, cardiovascular collapse, myoglobinuric renal failure, arrhythmias, diffuse intravascular coagulation, DIC, rhabdomyolysis, pneumonia, renal failure, seizures, hyperthermia, profuse diaphoresis, sialorrhea, metabolic acidosis, dopamine receptor blockade, impaired temperature regulation
Follow-up: Neuroleptic Malignant Syndrome