Key points are not available for this paper at this time.
In numerous countries, including Serbia, therapeutic drug monitoring (TDM) for clozapine is unavailable, leaving dose adjustments based solely on clinical judgment, could increase risk of therapeutic failure or adverse outcomes. The present study aimed to assess associations between clozapine and norclozapine serum concentrations, measured via Dried Blood Spot (DBS), and symptom severity, functioning, disability, and side effects in Serbian inpatients with treatment-resistant schizophrenia (TRS). In a cross-sectional design, patients with TRS with ongoing clozapine treatment and who did not meet exclusion criteria, were to be included. For clinical assessments of symptom severity, functionality, disability and side effects, were used: Simplified Interview for Negative and Positive Symptoms (SNAPSI), Clinical Global Impression (CGI), Global Assessment of Functioning (GAF), WHO Disability Assessment Schedule (WHODAS) and the Clozapine Adverse Effects Scale (GASS-C). Spearman's analysis showed no significant correlation between GASS-C scores and clozapine dose or plasma levels. WHODAS scores showed significant positive correlations with clozapine dose (ρ=0.409, P=0.006), clozapine (ρ=0.333, P=0.038) and norclozapine (ρ=0.481, P=0.002) levels. GAF scores negatively correlated with clozapine (ρ=-0.354, P=0.027) and norclozapine (ρ=-0.370, P=0.020). GASS-C scores were significantly associated with female sex (P=0.003), body mass index (BMI; ρ=-0.678, P<0.0005) and WHODAS scores (ρ=0.372, P=0.014). Regression analysis identified clozapine dose, clozapine level, BMI, SNAPSI and CGI scores as significantly associated with GASS-C (P=0.045). Norclozapine, BMI and CGI scores significantly associated with WHODAS (P=0.018). In the present study, it was found that clozapine and norclozapine concentrations are significantly associated with functioning, disability and side effects in patients with TRS treated without TDM. DBS-based monitoring may offer a valuable alternative for optimizing treatment. Further longitudinal studies are needed to clarify the clinical utility of (nor) clozapine level-guided care in such settings.
Petrovic et al. (Tue,) studied this question.