Zusammenfassung
Die Einbeziehung der therapeutischen Serumspiegelüberwachung als Teil der rationalen Behandlung mit Neuroleptika wird seit den sechziger Jahren gefordert (Brodie 1967); sie hat jedoch noch keinen Eingang in den Klinikalltag gefunden. Dies gilt auch für die therapeutische Neuroleptika-Serumspiegelüberwachung bei Nonresponse. Die Gründe hierfür sind vielschichtig:
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1.
Da die Serumspiegel von einigen Neuroleptika sehr niedrig sind, erfordert ihre Quantifizierung komplizierte Verfahren. Geräte und Personal stehen hierfür nur in seltenen Fällen zur Verfügung.
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2.
Neuroleptika weisen ein hohes Verteilungsvolumen auf, und daher sind die zu postulierenden therapeutischen Fenster breit.
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3.
Neuroleptika werden zu aktiven und inaktiven Metaboliten verstoffwechselt, d.h. einige der Neuroleptika-Metaboliten sind ebenso aktiv wie oder aktiver als die Mutterverbindung, andere weisen keine Dopamin-D2-Rezeptor-blockierende Wirkung auf; es ergibt sich außerdem das Problem, daß sie unterschiedlich gehirngängig sind, wie beispielsweise die Metaboliten des Thioridazins.
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4.
Zur Behandlung einer akuten psychotischen Exazerbation sind höhere Serumspiegel notwendig als zur Erhaltungstherapie.
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Rao, M.L. (1993). Zur Bedeutung der therapeutischen Serumspiegelüberwachung von Neuroleptika bei Nonresponse. In: Möller, HJ. (eds) Therapieresistenz unter Neuroleptikabehandlung. Springer, Vienna. https://doi.org/10.1007/978-3-7091-9292-4_8
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