General Resources / Legal Resources / Medical Resources / Briefing Papers / State Activity    
Hospital Closures / Preventable Tragedies / Press Room / Search Our Site / Home

Prolonged recovery in first-episode psychosis.

 

Edwards J, Maude D, McGorry PD, Harrigan SM, and Cocks JT (1998).

British Journal of Psychiatry (Supplement) 172 (Suppl 33): 107-116.

IMPORTANCE FOR EARLY INTERVENTION

This study found that 6.6% of a sample of individuals experiencing their first episode of psychosis were treatment resistant, and that between 9 and 17% of individuals with schizophrenia, schizophreniform, and schizoaffective disorder were treatment resistant. These rates are much lower than the 30% reported in more chronic samples. In assessing differences between treatment resistant individuals and those who responded to treatment, it was found that the duration of psychotic symptoms before treatment approached significance, which suggests that untreated psychosis may lead to treatment resistance, and supports the argument for early intervention as soon as possible following the onset of positive symptoms. The lack of a difference between the groups on a scale assessing premorbid functioning further suggests that premorbid factors are less important than duration of untreated psychosis in preventing treatment refractoriness.

SUMMARY

The aim of this study was to identify individuals experiencing treatment resistance early in the course of their psychotic disorder. It has been suggested that approximately 30% of individuals with schizophrenia have a less than adequate response to antipsychotic medications; however, it is not clear how many of these individuals are treatment refractory at the beginning of their illness and how many become so subsequently. Studies have suggested that the critical period for the development of chronic impairment is approximately one year.

The sample in this study consisted of 227 individuals experiencing their first psychotic episode, assessed at three time points (at admission, at stabilization of symptoms, at three or six months after stabilization, and at 12 months after stabilization) over a 12 month period. Thirty-six percent had schizophrenia, 22.5% had schizophreniform disorder, 11% had schizoaffective disorder, 2.2% had delusional disorder, 12.8% had bipolar disorder, 8.4% had depression with psychotic features, 0.4% had brief reactive psychosis, and 6.6% had psychotic disorder NOS. Individuals were identified as treatment resistant when they attained threshold on at least one positive symptom item of the Brief Psychiatric Rating Scale (BPRS) at stabilization, at the second time point (three or six months after stabilization), and at 12 months after stabilization.

The authors found that 6.6% of all the individuals with first-episode psychosis experienced psychotic symptoms at these three time points. When the analysis was restricted to people initially diagnosed with schizophrenia, schizophreniform, or schizoaffective disorder, the percentage of treatment-refractory individuals was 8.9%. When only schizophrenia and schizophreniform disorder were considered, the total rose to 11.4%. These numbers are much lower than the estimated 30% of treatment resistant schizophrenics in the larger schizophrenic population.

Treatment refractory individuals were found to have a significantly longer duration of psychotic symptoms during their first hospitalization, a greater severity of depressive symptoms 12 months after stabilization, and poor psychosocial functioning 12 months after stabilization. Interestingly, the treatment-refractory patients did not differ from the treatment responders on measures of premorbid functioning. However, the duration of psychotic symptoms before treatment also approached statistical significance, which suggests that untreated psychosis may lead to treatment resistance. The authors conclude that, in order to shorten the duration of active psychosis, there is a need to shorten not only the duration of untreated psychosis prior to entering treatment, but also to reduce the duration of psychosis after treatment has begun; the global aim can thus be seen as shortening the duration of active psychosis.


General Resources / Legal Resources / Medical Resources / Briefing Papers / State Activity   
Hospital Closures / Preventable Tragedies / Press Room / Search Our Site / Home

FootnoteImage2.jpg (1088 bytes)
Treatment Advocacy Center

The contents of all material available on the Center's website are copyrighted by the Treatment Advocacy Center unless otherwise indicated.  All rights reserved and content may be reproduced, downloaded, disseminated, or transferred, for single use, or by nonprofit organizations for educational purposes only, if correct attribution is made to the Treatment Advocacy Center.  Please feel free to call with questions on mental illness, treatment laws or the benefits of medication compliance at 703.294.6001 or send questions via email to [email protected].    Write to us at:  The Treatment Advocacy Center; 3300 N. Fairfax Drive; Suite 220; Arlington, VA  22201.  Technical comments on the Center's website (www.psychlaws.org) can be sent to [email protected]. The Treatment Advocacy Center is an I.R.C. � 501(c)(3) tax-exempt corporation.  Donations are appreciated and are eligible for the charitable contribution deduction under the provisions of I.R.C. � 170.