Is There a Real Difference in Severity of Tardive Dyskinesia Between Risperidone and Olanzapine?

Is There a Real Difference in Severity of Tardive Dyskinesia Between Risperidone and Olanzapine?

To the Editor: We read with great interest an important contribution by Chan and colleagues1 of a randomized, modestly dosed comparison of risperidone and olanzapine in patients with schizophrenia/schizoaffective disorder and tardive dyskinesia (TD). They found a lower severity of TD with risperidone than olanzapine, but there are several caveats in the interpretation of their findings.

First, their use of a washout period, although short in duration, may pose a problem because it is well known that TD temporarily worsens upon discontinuation of antipsychotics (known as withdrawal dyskinesia).2 In fact, scores on the Abnormal Involuntary Movement Scale (AIMS) deteriorated by about 2 points in both groups as a result of termination of previous antipsychotic treatment. This would have acutely afforded more room for later improvement but could complicate interpretation of pure medication effects in the chronic condition of TD. As the authors’ main concern was TD, the necessity of antipsychotic withdrawal may be questioned.

Second, the baseline AIMS score of about 18 (after antipsychotic withdrawal) in this study appears to be rather high compared with those in similar studies of TD. Therefore, the finding may be applicable only to patients with severe TD loading. In other words, generalizability of their results to more commonly encountered patients remains unknown.

Third, in addition to the fact that TD shows fluctuation in severity,3,4 it is occasionally challenging to disentangle extrapyramidal complications5 (in this instance, to separate TD from parkinsonism6). In this context, their finding appears complex in that, although parkinsonism improved with olanzapine, TD improved more with risperidone. In contrast, significantly more frequent use of anticholinergics, which could be detrimental to TD,5 was noted among risperidone-treated patients. To avoid confounding, the doses of both antipsychotics may need to have been adjusted so that use of anticholinergics would be counterbalanced between the groups. Our view is that most of the patients indeed could have been treated in the absence of anticholinergics.7

Finally and most critically, the sole presentation of last-observation-carried-forward data for the AIMS scores appears to be a concern in this particular case. As readers, we would like to know the results for completers only, so as to be sure that improvements in severity were consistent and not largely biased by those who prematurely dropped out (26.7% of the total sample). This would have made a real differential, if any existed, between the 2 antipsychotics more distinct. As such, completers-only data should have been presented as well.

The first 2 issues we list do not necessarily provide the basis of the authors’ observation of differential improvements in TD severity for both antipsychotics under investigation. They may, however, explain a contradiction between the result found in this study and a recent negative result from a longer study,8 in which a more benign effect of newer versus older antipsychotics in general was not found. Our last point, though, regarding the need for a completers-only analysis, needs to be addressed, since the data would be available, in order to be certain of true differential effects. When these limitations are taken together, the authors’ conclusion may be considered tentative, calling for more work on this highly pertinent topic.

References

1. Chan HY, Chiang SC, Chang CJ, et al. A randomized controlled trial of risperidone and olanzapine for schizophrenic patients with neuroleptic-induced tardive dyskinesia. J Clin Psychiatry. 2010;71(9):1226-1233. PubMed doi:10.4088/JCP.09m05155yel

2. Tranter R, Healy D. Neuroleptic discontinuation syndromes. J Psychopharmacol. 1998;12(4):401-406. PubMed doi:10.1177/026988119801200412

3. Caligiuri MP, Lohr JB, Vaughan RM, et al. Fluctuation of tardive dyskinesia. Biol Psychiatry. 1995;38(5):336-339. PubMed doi:10.1016/0006-3223(95)00228-9

4. Baca-Garcia E, Stanilla JK, Büchel C, et al. Diurnal variability of orofacial dyskinetic movements. Pharmacopsychiatry. 1999;32(2):73-75. PubMed doi:10.1055/s-2007-979195

5. Marsálek M. Tardive drug-induced extrapyramidal syndromes. Pharmacopsychiatry. 2000;33(suppl 1):14-33. PubMed doi:10.1055/s-2000-7672

6. Brown KW, White T. The psychological consequences of tardive dyskinesia: the effect of drug-induced parkinsonism and the topography of the dyskinetic movements. Br J Psychiatry. 1991;159(3):399-403. PubMed doi:10.1192/bjp.159.3.399

7. Suzuki T, Uchida H, Watanabe K, et al. How effective is it to sequentially switch among olanzapine, quetiapine and risperidone? a randomized, open-label study of algorithm-based antipsychotic treatment to patients with symptomatic schizophrenia in the real-world clinical setting. Psychopharmacology (Berl). 2007;195(2):285-295. PubMed doi:10.1007/s00213-007-0872-2

8. Woods SW, Morgenstern H, Saksa JR, et al. Incidence of tardive dyskinesia with atypical versus conventional antipsychotic medications: a prospective cohort study. J Clin Psychiatry. 2010;71(4):463-474. PubMed doi:10.4088/JCP.07m03890yel

Takefumi Suzuki, MD, PhD

[email protected]

Hiroyoshi Takeuchi, MD

Koichiro Watanabe, MD, PhD

Author affiliations: Department of Neuropsychiatry, School of Medicine, Keio University, Tokyo, Japan. Potential conflicts of interest: Within the last 5 years, Dr Suzuki has received grants from the Government of Canada Post-Doctoral Research Fellowships, Japanese Society of Clinical Neuropsychopharmacology, Kanae Foundation, and Mochida Memorial Foundation. Dr Takeuchi has received speaker’s honoraria or manuscript fees from Dainippon Sumitomo, Eli Lilly, GlaxoSmithKline, Janssen, and Otsuka. Dr Watanabe has received grants or consultant fees from Dainippon Sumitomo, Eli Lilly, GlaxoSmithKline, Janssen, and Pfizer and has received speaker’s honoraria from Astellas, Dainippon Sumitomo, Eli Lilly, GlaxoSmithKline, Janssen, Meiji, Otsuka, Pfizer, and Yoshitomiyakuhin. Funding/support: None reported.

doi:10.4088/JCP.10lr06261yel

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