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Department

Toxicology

Preferred Sample Type

Clozapine (Clozaril)

Suitable Specimen Types

  • Serum
  • EDTA Whole Blood
  • EDTA Plasma
50 ul of plasma or serum.

Sample Processing in Laboratory

Usual

Sample Preparation

Centrifuge. Place in toxicology box in cold room.

Turnaround Time

1-5 working days

Sample Stability

4 ºC

Clozapine (Clozaril)

General Information

Clozapine is an atypical antipsychotic used to treat schizophrenia resistant to conventional therapy. Because of the risk of agranulocytosis, white blood cell counts (WBC) are monitored weekly in the early stages of therapy and monthly thereafter. It is recommended that therapy is withheld if the WBC is less than 3,500 mm-3 and abandoned if the WBC falls below 3000 mm-3 or the granulocyte count below 1,500 mm-3. Side-effects of clozapine include lethargy, hypersalivation, constipation and somnolence. There is a risk of hypo-tension and seizure at higher doses. A single dose of 300-400 mg may be life-threatening in a clozapine-naïve subject. Clozapine is metabolised by N-demethylation, hydroxylation and N-oxidation. The N-demethylated metabolite, nor-clozapine, is present in plasma at similar concentrations to the parent compound, but has a longer plasma half-life. Plasma clozapine concentrations of 350 ug/L and above have been associated with a good response, with the risk of convulsions increasing above 600 ug/L.

Patient Preparation

Take the sample before a morning dose, or in the morning after an evening dose (“trough sample”). Sampling less than 6 h post-dose may make the results difficult to interpret.

Notes

Clozapine should only be measured via the Heart of England Pathology Service in acute cases of suspected overdose/poisoning OR if the patient is taking a generic formulation of clozapine (i.e. not clozaril)

Clozapine will not be measured for monitoring on patients prescribed clozaril. Patients should be registered with CPMS (Clozaril Patient Monitoring Service): special request forms are available via the CPMS.

Reference Range

350 - 600 ug/L (Schulz et al. Critical Care 2012, 16:R136).

Specifications

  • EQA Scheme?: Yes
  • EQA Status: LGC TDM