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Neuroleptic malignant syndrome

Neuroleptic malignant syndrome (NMS) is a life-threatening, neurological disorder most often caused by an adverse reaction to neuroleptic or antipsychotic drugs. It is considered to be a very serious neurological disorder. more...

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Causes

NMS is caused almost exclusively by antipsychotics, which includes all types of neuroleptic medicines along with newer antipsychotic drugs. The higher the dosage, the more common the occurrence. Rapid and large increases in dosage can also be attributed to the development of NMS. Other drugs, environmental or psychological factors, hereditary conditions, and specific demographics may be at greater risk, but to date no conclusive evidence has been found to support this. The disorder typically develops within two weeks of the initial treatment with the drug, but may develop at any time that the drug is being taken. NMS may also occur in people taking a class of drugs known as dopaminergics.

Symptoms

The first symptom to develop is usually muscular rigidity, followed by high fever and changes in cognitive functions. Other symptoms can vary, but may be unstable blood pressure, confusion, coma, delirium, muscle tremors, etc. Once symptoms do appear, they rapidly progress and can reach peak intensity in no more than three days. These symptoms can last as little as eight hours or as long as forty days.

Prognosis

As with most illnesses, the prognosis is best when identified early and treated aggressively. In these cases, NMS is usually not fatal, although there is currently no agreement on the exact mortality rate for the disorder. Studies have given the disorder a mortality rate as low as 5% and as high as 76%, although most studies agree that the correct percentage is in the lower spectrum, perhaps between 10% - 20%. Re-introduction to the drug that originally caused NMS to develop may also trigger a recurrence, although in most cases it does not.

Treatment

Although treatment is not always necessary, it will help to cure the disease and prevent fatal developments from occurring. The first step in treatment is generally to remove the patient from any neuroleptic or antipsychotic drugs being taken and to treat fever agressively. Many cases require intensive care, or some kind of supportive care at the minimum. Depending on the severity of the case, patients may require other treatments to contend with specific effects of the disorder. These include circulator and ventilatory support, the drugs dantrolene sodium, bromocriptine, apomorphine and electroconvulsive therapy (ECT) if medication fails.

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When antipsychotic drugs can be lethal - neuroleptic malignant syndrome
From Science News, 10/25/86 by Bruce Bower

When Antipsychotic Drugs Can Be Lethal

Neuroleptic drugs, also known as antipsychotic agents, are among the most commonly prescribed medications in the United States, used by up to 3 million people annually. Although in some cases neuroleptics lead to severe movement disorders and other side effects (SN: 7/20/85, p.45), psychiatrists have found that the drugs are often effective at moderating psychotic symptoms.

Yet, according to a report in the October AMERICAN JOURNAL OF PSYCHIATRY, a dangerous but little-known complication of antipsychotic drug use appears to be more common than previously thought. It often goes unrecognized in its early stages, add psychiatrist Harrison G. Pope Jr. and his colleagues of McLean Hospital in Belmont, Mass.

The complication is referred to as neuroleptic malignant syndrome, or NMS. Its cardinal signs are a fever, severe muscle rigidity, elevated blood pressure, elevated heart rate and clouded consciousness. The last feature can include delirium, stupor, mutism or coma. In some cases, a patient takes only a few hours to go from symptoms without serious illness to an inability to swallow, coma, kidney failure or brain damage. It is estimated that about 20 percent of the time, NMS is fatal. Death can result from respiratory, cardiovascular or kidney failure.

The researchers who first described the syndrome in 1968 estimated that it occurs among 0.5 to 1 percent of those taking neuroleptics, which are, among other things, powerful tranquilizers. Case reports of NMS have been published since then, but clinicians have considered the condition to be rare.

Pope and his co-workers, however, found seven definite or probable cases of NMS among an estimated 483 patients who received several types of neuroleptics at McLean Hospital over a recent one-year period. Another patient admitted during the study did not receive antipsychotic drugs because she had twice developed NMS during a previous admission. This prevalence rate of 1.4 percent is a conservative estimate, say the researchers; mild cases may have been missed, and some patients develop NMS years after going on the medication.

"In an extrapolation of our results,' note the psychiatrists, "even a conservative estimate would place the annual prevalence of [NMS] in the United States in the thousands of cases, a significant number of which may have fatal consequences.'

The good news, they say, is that many patients displaying symptoms of NMS recover fully when neuroleptic treatment is stopped. In addition, the muscle relaxant dantrolene and several medications that increase the transmission of the neurochemical dopamine in the brain (believed to be impeded by neuroleptics) have recently been shown to ease NMS. Low-dose neuroleptic treatment can begin again for some successfully treated patients.

Another encouraging trend is noted by Chester Pearlman of the Boston Veterans Administration Medical Center in the October JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY. He reviewed 320 reported cases of NMS since 1968 and found that "with wider recognition, mortality [from NMS] has decreased from about 22 percent of cases reported through 1980 to 4 percent of the last 50.'

But much is still unknown about the syndrome's underlying causes, frequency and possible treatments. Even with the McLean study, it is hard to draw a conclusion about the true prevalence of NMS, according to Shervert Frazier, director of the National Institute of Mental Health (NIMH). Diagnostic changes in only a few of the subjects would have significantly altered the final percentage, he points out.

NMS "has been more recognized in the past few years, but I don't think it's occurring more often than the originally estimated rate of about 1 percent,' Frazier told SCIENCE NEWS.

A problem with any piece of research on NMS, says psychiatrist Darrell Kirch of St. Elizabeths Hospital in Washington, D.C., is that the condition's early signs are still unclear. At first, a fever or muscle rigidity cannot be exclusively linked to neuroleptic use. Frazier says an NIMH research team is beginning to look for reliable early signs of NMS.

For the time being, says psychiatrist David E. Sternberg in an editorial accompanying the McLean report, regular monitoring of blood pressure and muscle tone may lead to early recognition of NMS. Furthermore, he says, the syndrome appears to be more common among those under 40 years of age, males and patients with psychiatric disorders that do not include schizophrenia. Sternberg, of Falkirk Hospital in Central Valley, N.Y., concurs with the researchers that the lifetime risk of NMS will probably prove to be higher than the 1.4 percent one-year rate uncovered at McLean Hospital.

COPYRIGHT 1986 Science Service, Inc.
COPYRIGHT 2004 Gale Group

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