Outcomes in Treatment-resistant Schizophrenia: Symptoms, Function and Clozapine Plasma Concentrations
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Background: Clozapine is the only medication licenced for treating patients with treatment-refractory schizophrenia. However, there are no evidence-based guidelines as to the optimal plasma level of clozapine to aim for, and their association with clinical and functional outcome.
Objective: We assessed the relationship between clinical and functional outcome measures and blood concentrations of clozapine among patients with treatment-refractory psychosis.
Methods: Data were reviewed in 82 patients with treatment-refractory psychosis admitted to a specialised tertiary-level service and treated with clozapine. Analysis focussed on the relationship between clozapine and norclozapine plasma concentrations and the patient's clinical symptoms and functional status.
Results: Clinical symptom improvement was positively correlated with norclozapine plasma concentrations and inversely correlated with clozapine to norclozapine plasma concentrations ratio. Clozapine concentrations showed a bimodal association with clinical improvement (peaks around 350 and 660 ng/ml). Clinical symptom improvement correlated with functional outcomes, although there was no significant correlation between the latter and clozapine or norclozapine plasma concentrations.
Conclusion: Clozapine treatment was associated with optimal clinical improvement at two different peak plasma concentrations around 350 and 650 ng/ml. Clinical improvement was associated with functional outcome; however, functionality was not directly associated with clozapine concentrations. A subset of patients may require higher clozapine plasma concentrations to achieve clinical improvement.
Kitajima K, Tamura S, Sasabayashi D, Nakajima S, Iwata Y, Ueno F Psychiatry Clin Neurosci. 2022; 77(1):2-11.
PMID: 36165228 PMC: 10092309. DOI: 10.1111/pcn.13482.
Underuse of recommended treatments among people living with treatment-resistant psychosis.
Lappin J, Davies K, ODonnell M, Walpola I Front Psychiatry. 2022; 13:987468.
PMID: 36147973 PMC: 9485552. DOI: 10.3389/fpsyt.2022.987468.