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Combined therapy with low-potency neuroleptic levomepromazine as an adjunct to haloperidol for agitated patients with acute exacerbation of schizophrenia

Published online by Cambridge University Press:  16 April 2020

Masato Higashima*
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Tsutomu Takeda
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Tatsuya Nagasawa
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Naohisa Hirao
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Takashi Oka
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Mitsuhiko Nakamura
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Maki Kitamura
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
Yoshifumi Koshino
Affiliation:
Department of Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa920-8641, Japan
*
*Corresponding author. Email address: [email protected] (M. Higashima).
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Extract

As a practical strategy for reducing agitation in schizophrenia, low-potency neuroleptics have been commonly used as an adjunct in combination with high-potency neuroleptics that seem superior in reducing positive symptoms. There is no evidence, however, that giving more than one antipsychotics at a time enhances therapeutic effects. Antipsychotic polypharmacy has been rather considered an unproven and potentially harmful practice [4].

The low-potency neuroleptic levomepromazine has been in common use for agitated patients with schizophrenia in Europe and Japan [2,3], because of its markedly sedative property. In order to clarify whether levomepromazine as an adjunct to high-potency neuroleptics are beneficial or harmful, therefore, we compared the efficacy of the combined therapy with levomepromazine and high-potency neuroleptic haloperidol with the monotherapy with haloperidol for patients with acute exacerbation of schizophrenia.

Type
Short communication
Copyright
Copyright © 2004 European Psychiatric Association

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References

Hayashi, OMiyoshi, SHigashimura, TMiyoshi, CNakata, SOhya, F, et al. Blood concentration and clinical effects of haloperidol therapy in combination with levomepromazine. Jpn J Neuropsychop-harmacol 1983;5:41–7.Google Scholar
Ito, CKubota, YSato, M. A prospective survey on drug choice for prescriptions for admitted patients with schizophrenia. Psychiatry Clin Neurosci 1999;53(Suppl):35–40.Google ScholarPubMed
Lal, SNair, NPVCecyre, DQuirion, R. Levomepromazine receptor binding profile in human brain—implications for treatment-resistant schizophrenia. Acta Psychiatr Scand 1993;87:380–3.Google ScholarPubMed
Miller, ALCraig, CS. Combination antipsychotics: pros, cons, and questions. Schizophr Bull 2002;28:105–9.CrossRefGoogle ScholarPubMed
Overall, JEGorham, DR. The brief psychiatric rating scale. Psychol Rep 1962;10:799–812.CrossRefGoogle Scholar
Peroutka, SJU’Prichard, DCGreenberg, DASnyder, SH. Neuroleptic drug interactions with norepinephrine alpha receptor binding sites in rat brain. Neuropharmacology 1977;16:549–56.Google ScholarPubMed
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