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   <subfield code="a">10.1007/s002280050123</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s002280050123</subfield>
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   <subfield code="a">Neuroleptic monitoring: relation between antipsychotic efficiency and radioreceptor assay of serum haloperidol</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[P. Odou, G. Vaiva, M. Luyckx, C. Brunet, T. Dine, B. Gressier, M. Cazin, J. C. Cazin]</subfield>
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   <subfield code="a">Objective: We report preliminary results from use of a radioreceptor assay (RRA) to measure serum haloperidol levels and their relation to clinical response and adverse effects in 19 psychotic patients with positive symptoms treated with haloperidol. Methods: Blood samples were taken on Days 7, 14 and 21. Clinical evaluation was based on the PANSS, and UKU scales. The D2 antidopaminergic RRA was used to measure haloperidol serum levels. Results: Our results show a correlation between psychosis with positive symptoms assessed by positive scores in the PANSS and the serum drug level measured by RRA concentrations. The observed relationship made it possible to establish a therapeutic serum range of haloperidol equivalents 15-30 ng/ml−1. This range contained no &quot;non-responders”. Analysis of the correlation between each item on the positive subscale of the PANSS and the RRA concentration suggested that there was no specific symptom of psychosis closely related to RRA concentration during the first 15 days of treatment. In the third week, however, certain specific symptoms were closely connected to the RRA concentration. Conclusion: From these results, it can be concluded that antipsychotic activity can be related to blockade of serum D2 dopamine receptors. In future would be desirable to monitor neuroleptic treatment in this way. The study also showed that the antipsychotic treatment did not correct any specific component of the psychosis during the first stage of the treatment but that it did so at later times.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 1996</subfield>
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   <subfield code="a">Key words Schizophrenia</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Haloperidol</subfield>
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   <subfield code="a">Odou</subfield>
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   <subfield code="u">Laboratoire de Pharmacologie, Pharmacocinétique, Pharmacie clinique (EA 1051), Faculté des Sciences Pharmaceutiques et Biologiques, 3 rue du Professeur Laguesse, Université de Lille II, F-59006, Lille Cedex, France</subfield>
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   <subfield code="a">Vaiva</subfield>
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   <subfield code="u">Department of General Psychiatry, School of Medecine, 6, rue du Professeur Laguesse, F-59037, Lille Cedex, France</subfield>
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