Brief reportDelirious mania: Clinical features and treatment response
Introduction
A severe psychiatric syndrome characterized by acute onset of delirium, excitement and psychosis was initially described by Calmeil in 1832, as an uncommon but life-threatening psychosis with extreme hyperactivity and mounting fear fading to stuporous exhaustion (Calmeil, 1832). A subsequent case series published by Luther Bell in 1849 described 40 patients with the condition among 1700 admissions to McLean Hospital (Bell, 1849). He reported a mortality rate of 75% in these patients.
The modern literature pertaining to clinical characteristics and treatment outcomes of delirous mania is sparse, consisting mainly of case series (Bond, 1980). There is also debate about proper nomenclature, with terms such as “lethal catatonia” and “malignant catatonia” proposed along with delirious mania (Fink, 1999, Mann et al., 1986). It is thought of as an uncommon syndrome, although it may be under-recognized since several authors have suggested that as many as 15–20% of all acutely manic patients show signs of delirium (reviewed in Fink, 1999). Patients with this syndrome experience significant morbidity (Friedman et al., 2003) and a high mortality rate without treatment.
There is no clear consensus on which clinical features are associated with delirous mania or which treatments are effective. Recognition of this syndrome is further hampered by the fact that many delirium cases in psychiatric patients are precipitated by medical or neurological conditions or the use of psychoactive substances. Guidelines for the rapid and accurate recognition as well as proper treatment are needed to improve the care of patients with this serious condition. We undertook a chart review of patients presenting with symptoms of delirium and mania admitted to an inpatient unit specializing in schizophrenia and bipolar disorder in an academic psychiatric hospital. We focused on clinical presentation and hospital course, with the aim of delineating clinical characteristics and treatment responses.
Section snippets
Method
Following approval from the Institutional Review Board, we carried out a retrospective chart review of patients who had been admitted to McLean Hospital with symptoms of delirium and mania between 2003 and 2007, with one additional case from the previous decade. Systematic examination of all patient records with diagnoses of delirium and mania during the selected time period was not possible because delirium was not always recorded among admission or discharge diagnoses. Thus, patients were
Demographics
We evaluated 16 cases of delirium and mania. The median age of these patients was 21, with two outlier cases at age 43 and 64. Thirteen (81.25%) were women. Ten patients (62.5%) carried a prior diagnosis of bipolar disorder. Two others had been previously diagnosed with depression, one with an anxiety disorder, one with posttraumatic stress disorder, and one with a psychotic episode; one patient had no previous psychiatric history. There were no patients with previous diagnoses of schizophrenia
Discussion
The incidence of co-occurring symptoms of mania and delirium is unknown, and thought to be low in the general psychiatric population. However, in our psychiatric inpatient unit specializing in bipolar disorder and schizophrenia, we see several such cases every year. As with any patient presenting with delirium, the initial evaluation of patients with delirious mania should focus on medical and neurological etiologies, including the effects of illicit substances. We propose that, if such
Role of funding source
Funding for this study, in the form of salary support, was provided by the Adam Corneel Young Investigator Award at McLean Hospital, the American Psychiatric Association/Pfizer Research Fellowship, the Ethel DuPont-Warren Fellowship and Peter B. Livingston Fellowship from Harvard Medical School and the Harvard-MIT Clinical Investigator Program. The funding agencies had no role in the study design, in the collection, analysis and interpretation of data, in the writing of the report, and in the
Conflict of Interest
The authors of this paper do not have any commercial associations that might pose a conflict of interest in connection with this manuscript.
Acknowledgements
R.K. was supported by the Adam Corneel Young Investigator Award from McLean Hospital, the American Psychiatric Association/Pfizer Research Fellowship, the Ethel DuPont-Warren Fellowship and Peter B. Livingston Fellowship from Harvard Medical School. D.O. was supported by the Harvard-MIT Clinical Investigator Training Program.
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