The American Psychiatric Association (APA) has updated its Privacy Policy and Terms of Use, including with new information specifically addressed to individuals in the European Economic Area. As described in the Privacy Policy and Terms of Use, this website utilizes cookies, including for the purpose of offering an optimal online experience and services tailored to your preferences.

Please read the entire Privacy Policy and Terms of Use. By closing this message, browsing this website, continuing the navigation, or otherwise continuing to use the APA's websites, you confirm that you understand and accept the terms of the Privacy Policy and Terms of Use, including the utilization of cookies.

×
Letter to the EditorFull Access

Dr. Sachdev Replies

Published Online:https://doi.org/10.1176/ajp.155.11.1626x

To the Editor: I thank Dr. Rasmussen and Dr. Francis and his colleagues for raising important issues in relation to our study. For the diagnosis of catatonia, we needed the presence of one of the following: mutism, extreme negativism, peculiarities of voluntary movement (posturing, waxy flexibility, and so forth) or echophenomena. Excessive and purposeless motor activity was in itself not sufficient for this purpose, since we considered establishing “purposelessness” to be an unreliable exercise and excessive motor activity to be a common feature of many psychiatric disorders. Such an approach would underdiagnose catatonic excitement, which we accepted as a limitation of a retrospective study. Catatonia was diagnosed in 11 subjects (44%) with neuroleptic malignant syndrome but in only two comparison subjects (4%) in our study. Catatonia was, however, present before the onset of neuroleptic malignant syndrome in only one subject from the neuroleptic malignant syndrome group.Our data, therefore, do not permit us to comment on catatonia as a possible risk factor for the development of neuroleptic malignant syndrome as has been suggested elsewhere (1). We acknowledge that catatonia is an important manifestation of neuroleptic malignant syndrome, and lethal catatonia (2) may be indistinguishable from a severe case of neuroleptic malignant syndrome. The overlap does suggest some common features in the pathophysiology, but until we understand the pathogenesis of catatonic withdrawal and how that may differ from excitement, this similarity will not yield new insights. That the presence of catatonia may be a risk factor for neuroleptic malignant syndrome is worth examining further, however, as it may urge us to use alternative treatments such as ECT.

The finding of previous ECT as a risk factor for neuroleptic malignant syndrome has excited comment from both groups. In our article, we resisted the temptation to speculate on this finding until it had been confirmed independently. We agree with Dr. Rasmussen that it is, at best, an association that possibly flags the characteristics of the primary psychiatric disorder that prompted treatment with ECT. A prominence of affective symptoms (manic or depressive) or catatonia in the histories of these individuals is distinctly possible, but we cannot present satisfactory data to examine either. Future studies should pay attention to these possibilities.

References

1. White DAC: Catatonia and the neuroleptic malignant syndrome—a single entity? Br J Psychiatry 1992; 161:558–560Google Scholar

2. Mann SC, Caroff SN, Bleier HR, Welz WKR, Kling MA, Hayashida M: Lethal catatonia. Am J Psychiatry 1986; 143:1374–1381LinkGoogle Scholar