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A comparison of risperidone and olanzapine in the acute treatment of persistent delusional disorder: Data from a retrospective chart review

Published online by Cambridge University Press:  23 March 2020

K. Kulkarni*
Affiliation:
National Institute of Mental Health & Neurosciences, Psychiatry, Bangalore, India
R. Arasappa
Affiliation:
National Institute of Mental Health & Neurosciences, Psychiatry, Bangalore, India
K. Prasad
Affiliation:
National Institute of Mental Health & Neurosciences, Psychiatry, Bangalore, India
A. Zutshi
Affiliation:
Epworth Hospital, Psychiatry, Melbourne, Australia
P. Chand
Affiliation:
National Institute of Mental Health & Neurosciences, Psychiatry, Bangalore, India
K. Muralidharan
Affiliation:
National Institute of Mental Health & Neurosciences, Psychiatry, Bangalore, India
P. Murthy
Affiliation:
National Institute of Mental Health & Neurosciences, Psychiatry, Bangalore, India
*
*Corresponding author.

Abstract

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Introduction

There is a lack of pharmacological trials studying drug response in Persistent Delusional Disorder (PDD) to guide clinical practice. Available reviews of retrospective data indicate good response to second-generation antipsychotics, but even such data from India is sparse.

Objectives and aims

We aimed to compare the response of acute PDD to risperidone and olanzapine in our retrospective review.

Methods

We conducted a retrospective chart review of patients diagnosed with PDD (ICD-10) from 2000 to 2014 (n = 455) at our Center. We selected the data of patients prescribed either olanzapine or risperidone for the purpose of this analysis. We extracted data about dose, drug compliance and response, adverse effects, number of follow-up visits and hospitalizations. The study was approved by the Institute Ethics Committee.

Results

A total of 280/455 (61%) were prescribed risperidone and 86/455 (19%) olanzapine. The remaining (n = 89; 20%) had received other antipsychotics. The two groups were comparable in socio-demographic and clinical characteristics of PDD. Compliance was good and comparable in both groups (> 80%, P = 0.2). Response to treatment was comparable in both groups (85% partial response and > 52% good response, all P > 0.3). Olanzapine was effective at lower mean chlorpromazine equivalents than risperidone (240 vs. 391, P < 0.05).

Conclusion

Our study indicates a good response to both risperidone and olanzapine, if compliance to treatment can be ensured. In the absence of specific treatment guidelines for PDD, second-generation antipsychotics like risperidone and olanzapine offer good treatment options for this infrequently encountered and difficult to treat psychiatric disorder.

Disclosure of interest

The authors have not supplied their declaration of competing interest.

Type
EV1026
Copyright
Copyright © European Psychiatric Association 2016
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