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Brief Report
Published Online: 1 January 2002

Pharmacologic Treatment of Hospitalized Patients With Schizoaffective Disorder

Abstract

This study examined changes in the pharmacologic treatment of 70 patients who were hospitalized with a diagnosis of schizoaffective disorder at some time during a six-year period. An increasing use of divalproex sodium and atypical antipsychotics instead of lithium and conventional antipsychotics was observed. The use of a combination of an antipsychotic and a thymoleptic medication was more common than monotherapy, and physicians tended to continue antidepressants if patients had a history of depression. Patients with a new diagnosis of schizoaffective disorder were stabilized less quickly than those with a previous diagnosis. The use of divalproex sodium and newer antipsychotics did not reduce the time to stabilization in routine clinical practice.
The essential feature of schizoaffective disorder is an uninterrupted period of illness during which, at some time, there is a major depressive, manic, or mixed episode concurrent with the symptoms that meet criterion A for schizophrenia. During the same period of illness, there must be delusions or hallucinations for at least two weeks in the absence of prominent mood symptoms. In addition, the mood symptoms are present for a substantial proportion of the period of illness (1).
Schizoaffective disorder is often chronic (2). Treatment may include multiple hospitalizations and multiple psychotropic medications (3,4). For patients who present with exacerbations of illness, the extent to which clinicians select medications on the basis of current presentation rather than historical information is unclear. It is also unclear whether the duration of illness, the number of previous hospitalizations, or a change in diagnosis to schizoaffective disorder during a hospital admission influences the clinician's choice of medication or the time to stabilization.
In recent years, valproic acid has shown efficacy similar to that of lithium in the treatment of bipolar disorder (5,6) and has been used in the treatment of schizoaffective disorder (7). Newer—atypical—antipsychotics are also being used (8). One study showed a decline in the use of lithium and an increase in the use of valproic acid between 1989 and 1994 (9). It is unclear whether this trend has continued and whether the use of newer agents has substantially affected stabilization rates in routine clinical practice. Also, it has been suggested that the thymoleptic properties of the atypical antipsychotics may result in their use as monotherapy for patients who have schizoaffective disorder (3,10), but it is unclear whether this proposed method of treatment has been adopted by clinicians. This study examined whether pharmacologic treatment of patients with schizoaffective disorder changed over a six-year period and whether these changes led to improved rates of stabilization.

Methods

The first two authors retrospectively reviewed all available inpatient hospitalization records of patients who received a discharge diagnosis of schizoaffective disorder between September 1993 and October 1999. If both researchers did not agree that a particular record documented symptoms consistent with DSM-IV criteria for schizoaffective disorder, that record was excluded from further analysis. To avoid overrepresentation of patients with refractory illness, data for patients who had had multiple hospitalizations during the study period were obtained only for the first hospitalization.
Demographic data, diagnosis, age at onset of psychiatric illness, number of previous admissions, presence or absence of psychosis, and data on primary mood symptoms at admission, recent drug or alcohol use, and psychotropic medications at discharge were extracted from the medical charts.
The time to stabilization was determined by counting the number of days from admission to the attainment of ward and hospital status. Ward status was assigned when the patient was no longer imminently dangerous and could participate in group treatment activities. Hospital status was assigned when the patient was deemed ready for transfer to a noninpatient level of care. Throughout hospitalization, ward or hospital status was determined by the multidisciplinary treatment team's assessments of dangerousness, cognitive processes, and ability to conform behavior to the unit and hospital norms.
For the statistical analyses, the Mantel-Haenszel chi square test was used for linear by linear analysis. Comparisons of continuous variables between groups were made with the nonparametric Mann-Whitney U test, because group data were not normally distributed.
The research protocol was reviewed by the research review service and approved by the department of clinical investigation of the Walter Reed Army Medical Center.

Results

During the study period, 114 hospitalized patients were discharged with a diagnosis of schizoaffective disorder. On the basis of chart data, 70 patients met the inclusion criteria, which represented 1.6 percent of all patients admitted to the psychiatric inpatient units during the study period.
The sample comprised 29 men and 41 women. The mean±SD age of the men at admission was 30.1±11.4 years, compared with 43±15.1 years for the women (z=−3.437, p<.001). Twenty-eight patients (40 percent) reported use of alcohol or illicit drugs in the month preceding admission. Sixty-six (94 percent) presented with psychotic symptoms, 37 (53 percent) with depressive symptoms, 11 (16 percent) with mania, and seven (10 percent) with mixed mood symptoms; 15 patients (21 percent) had no active mood symptoms on admission.
Sixty-three patients (90 percent) were treated with either a conventional or an atypical antipsychotic; 55 of these (87 percent) were also treated with a thymoleptic (antimanic or antidepressant) medication. No significant difference was found in the proportion of patients who were treated with monotherapy—four (6 percent) were treated with an atypical antipsychotic and four (6 percent) with a conventional antipsychotic. Of the 15 patients who presented without mood symptoms, 12 were discharged with a prescription for the same thymoleptic medication that had been prescribed before admission.
Patients who had a previous diagnosis of schizoaffective disorder were compared with those who had a new diagnosis. Those with a new diagnosis were younger (32.6±11.7 years compared with 41.2±16.2 years; z=−2.07, p<.01), had a shorter duration of illness (7.5±10 years compared with 14.1±11.1 years; z=−3.2, p<.01), and had had fewer previous admissions (1.6±2.1 compared with 5.3±3.9; z=−4.1, p<.01). The patients with a previous diagnosis of schizoaffective disorder were more rapidly stabilized: 5.2±6.4 days compared with 9.6±10.3 days to ward status (z=−2.02, p=.044) and 10±9.2 days compared with 17.6±12.6 days to hospital status (z=−3.49, p<.001). No significant differences were found between the two diagnostic groups in the use of lithium as opposed to divalproex sodium or in the use of conventional as opposed to atypical antipsychotic medications.
Year-by-year examination of data revealed a statistically significant shift toward discharging patients with a prescription for atypical rather than conventional antipsychotic medications (linear-by-linear association [LL]=15.6, df=1, p<.001) and toward discharging patients with a prescription for divalproex instead of lithium (LL=4.67, df=1, p=.031). No significant differences were found in time to ward status or time to hospital status associated with treatment with conventional versus atypical antipsychotic medications or lithium versus divalproex sodium. No associations were found between substance abuse and the medication selected or the time to stabilization.

Discussion and conclusions

On admission to the hospital, a larger proportion of patients had psychotic symptoms than had mood symptoms. It was evident that in selecting a medication, clinicians relied on a history of mood symptoms rather than basing their decision on current mood symptoms; they maintained patients on their prehospitalization antidepressant or antimanic agents, even when significant mood symptoms were not present. Despite the theoretical advantage of using atypical antipsychotics for monotherapy, the data indicate that clinicians had not adopted that practice during the study.
To a large extent, atypical antipsychotics and divalproex sodium replaced conventional antipsychotics and lithium for the treatment of patients hospitalized with schizoaffective disorder during the study period. Although specific aspects of treatment were not controlled, there was no evidence of a decrease in the time to stabilization with the use of the newer medications.
The patients in this study had experienced a chronic course of psychiatric illness before receiving a diagnosis of schizoaffective disorder. Those who already had a diagnosis of schizoaffective disorder on admission to the hospital were more rapidly stabilized, even though this group of patients had a longer history of psychiatric illness and a greater number of previous hospitalizations. Thus a history of multiple hospitalizations and long-term outpatient management may provide some clarity in the management of patients with this disorder.
The results of this study also point to several aspects of schizoaffective disorder that require further study. Because the rate of stabilization does not appear to change with newer medications, further analysis of changes in patients' adherence to regimens of the newer medications compared with the old ones may clarify the value of using the newer agents. Also, although the patients who had a diagnosis of schizoaffective disorder before hospitalization were stabilized more rapidly than those who received the diagnosis during admission, factors that affect the rate of stabilization—other than clarity of diagnosis—are areas for future study.

Acknowledgment

The work outlined in this article was performed under Walter Reed research protocol WU-00-7201.

Footnote

The authors are affiliated with the department of psychiatry of the Walter Reed Army Medical Center in Washington, D.C., and with the department of psychiatry of the Uniformed Services University of the Health Sciences in Bethesda, Maryland. Send correspondence to Dr. Grieger at the Uniformed Services University of the Health Sciences, Department of Psychiatry, 4301 Jones Bridge Road, Bethesda, Maryland 20814 (e-mail, [email protected]). A version of this paper was presented at the annual meeting of the American Psychiatric Association held May 14-18, 2000, in Chicago.

References

1.
Diagnostic and Statistical Manual of Mental Disorders, 4th ed. Washington, DC, American Psychiatric Association, 1994
2.
Strakowski SM, Keck PE, Sax KW, et al: Twelve month outcome of patients with DSM-III-R schizoaffective disorder: comparisons to matched patients with bipolar disorder. Schizophrenia Research 35:167-174, 1999
3.
McElroy SL, Keck PE, Strakowski SM, et al: An overview of the treatment of schizoaffective disorder. Journal of Clinical Psychiatry 60(suppl 5):16-21, 1999
4.
Levinson DF, Umapathy C, Musthaq M: Treatment of schizoaffective disorder and schizophrenia with mood symptoms. American Journal of Psychiatry 8:1138-1148, 1999
5.
Bowden CL, Brugger AM, Swann AC, et al: Efficacy of divalproex vs lithium and placebo in the treatment of mania. JAMA 271:918-924, 1994
6.
McElroy SL, Keck PE, Stanton SP, et al: A randomized comparison of divalproex oral loading versus haloperidol in the initial treatment of acute psychotic mania. Journal of Clinical Psychiatry 57:142-146, 1996
7.
Keck PE, McElroy SL, Strakowski SM, et al: Pharmacologic treatment of schizoaffective disorder. Psychopharmacology 114:529-538, 1994
8.
Keck PE, Wilson DR, Strakowski SM, et al: Clinical predictors of acute risperidone response in schizophrenia, schizoaffective disorder, and psychotic mood disorder. Journal of Clinical Psychiatry 56:466-470, 1995
9.
Fenn HH, Robinson D, Luby V, et al: Trends in pharmacotherapy of schizoaffective and bipolar affective disorders: a 5-year naturalistic study. American Journal of Psychiatry 153:711-713, 1996
10.
Tollefson GD, Beasley CM, Tran PV, et al: Olanzapine versus haloperidol in the treatment of schizophrenia and schizoaffective and schizophreniform disorders: results of an international collaborative trial. American Journal of Psychiatry 154:457-465, 1997

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Go to Psychiatric Services
Go to Psychiatric Services
Psychiatric Services
Pages: 94 - 96
PubMed: 11773657

History

Published online: 1 January 2002
Published in print: January 2002

Authors

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Thomas A. Grieger, M.D.
David M. Benedek, M.D.

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