Acute psychotic symptoms

Acute psychotic symptoms have been reported in two young women shortly after withdrawal of long-term phenelzine 90 mg/day (10). 

In a randomized, double-blind, multicenter comparison of amisulpride 1000 mg/day (n = 70) and flupenthixol 25 mg/day (n = 62) for 6 weeks, the two drugs significantly improved the acute psychotic symptoms to a similar extent (32). The total numbers of dropouts were 19 with amisulpride and 25 with flupenthixol. Adverse effects accounted for 8.6 and 18% respectively of the totals. Amisulpride caused significantly fewer extrapyramidal adverse effects. Apart from the extrapyramidal adverse effects, there were treatment-related adverse events in 87% of the patients given amisulpride and 92% of those given flupenthixol. Prolactin concentrations were higher with amisulpride. 

Khan A, Faught E, Gilliam F, Kuzniecky R. Acute psychotic symptoms induced by topiramate. Seizure 1999 8(4) 235-7. 

After reducing acute psychotic symptoms in mania, switch to a mood stabilizer and/or an atypical antipsychotic tor mood stabilization and maintenance... 

Miscellaneous Compounds - A benzodiazepine, SCH-12,041 ( , halazepam), showed evidence of efficacy against acute psychotic symptoms in an uncontrolled trial.28 CI-686 (10) was predicted to have major tranquilizer... 

Antipsychotic medications are indicated in the treatment of acute and chronic psychotic disorders. These include schizophrenia, schizoaffective disorder, and manic states occurring as part of a bipolar disorder or schizoaffective disorder. The co-adminstration of antipsychotic medication with antidepressants has also been shown to increase the remission rate of severe depressive episodes that are accompanied by psychotic symptoms. Antipsychotic medications are frequently used in the management of agitation associated with delirium, dementia, and toxic effects of both prescribed medications (e.g. L-dopa used in Parkinson s disease) and illicit dtugs (e.g. cocaine, amphetamines, andPCP). They are also indicated in the management of tics that result from Gilles de la Tourette s syndrome, and widely used to control the motor and behavioural manifestations of Huntington s disease. 

Delirium. Delirium is an abrupt change in mental status often accompanied by agitation and seemingly psychotic symptoms that may resemble mania. Unlike mania, however, delirium is commonly characterized by a fluctuating level of consciousness and disorientation. The chief precipitants of delirium include infections, medications, and metabolic disturbances. Therefore, all patients who present in an acutely agitated state should undergo a comprehensive yet expeditious medical evaluation to rule out potential causes of delirium. This evaluation must include a thorough physical examination and a battery of laboratory tests. 

In addition to the acute ingestion of these hallucinogenic drugs, the chronic use of alcohol, amphetamines, or cocaine can lead to paranoia that in many respects resembles the psychosis of schizophrenia. In these cases, the psychotic symptoms may persist long after the substance use has been stopped. 

The goals of treatment during the acute phase of illness are to reduce the positive symptoms of schizophrenia and to plan for extended treatment during the maintenance phase. Reducing the positive symptoms quickly is important for at least two reasons. First, the erratic behavior of an acutely psychotic patient can take a tremendous toll, risking arrest, loss of job, suicide, and the alienation of friends and family. Second, there is some evidence that psychosis itself is harmful to the brain. In other words, it may be that the longer the patient is actively psychotic, the worse the prognosis becomes. 

Delusions/Psychosis. Demented patients who are acutely psychotic and agitated should be treated in much the same manner as demented patients with delirium. Low doses of a high potency conventional antipsychotic like haloperidol were once preferred. This was mainly because it can be given both orally and by injection. In recent years, the atypical antipsychotic ziprasidone, which is now also available in oral and injectable forms, has superseded haloperidol as the preferred agent when treating the acutely psychotic and agitated patient with dementia. As previously noted, ziprasidone affords the same tranquilizing benefit as haloperidol, it can now be administered via injection when necessary, and it avoids the problematic extrapyramidal symptoms of haloperidol to which patients with dementia are often keenly sensitive. 

Glutamate was initially implicated in schizophrenia by studies of the behavioral effects of N-methyl-D-aspartate (NMDA) receptor antagonists (e.g., PCP, ketamine), which produce psychotic symptoms and cognitive dysfunction in healthy subjects and exacerbate psychotic, negative, and cognitive symptoms in patients with schizophrenia. Studies show that acute administration of NMDA antagonists causes NMDA receptor dysfunction, resulting in decreased inhibition of subcortical dopamine neurons and consequent increased mesolimbic dopamine release. Chronic administration produces decreased release, or hypoactivity, of dopamine in the prefrontal cortex (Davis and Lieberman, 2000). 

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