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Monitoring
Table 2.6 summarises suggested monitoring for those receiving antipsychotics. More
detail and background is provided in specific sections in this chapter.
Table 2.6 Monitoring of metabolic parameters for patients receiving antipsychotic drugs
CHAPTER 2
Parameter/ Suggested ifresults outside Drugs with special monitoring
test frequency reference range precautions is not required
Urea and Baseline and yearly Investigate all Amisulpride and None
electrolytes as part of aroutine abnormalities detected sulpiride renally
(including physical health check excreted consider
creatinine or reducing dose if
estimated GFR) GFR reduced
Full blood count Baseline and yearly Stop suspect drug if Clozapine FBC None
(FBC)16 as part of aroutine neutrophils fallbelow weekly for
physical health check 1.5 109/L 18weeks, then
and to detect Refer to specialist fortnightly up to
chronic bone medical care ifneutro- one year, then
marrow suppression phils below 0.5 109/L monthly (schedule
(small riskassociated Note high frequency of varies from country
with some benign ethnicneutro- to country)
antipsychotics) penia in certain ethnic
groups
Blood lipids7,8 Baseline, at 3 Offer lifestyle advice Clozapine, Some antipsychotics
(cholesterol; months then yearly Consider changing olanzapine, (e.g. aripiprazole) not
triglycerides) to detect antipsychotic and/or quetiapine, clearly associated
Fasting sample, if antipsychotic initiating statin therapy phenothiazines with dyslipidaemia
possible induced changes, 3monthly for first but prevalence is
and generally year, thenyearly high inthis patient
monitor physical group911 so all
health patients should be
monitored
Continued
46 The Maudsley Prescribing Guidelines in Psychiatry
Liver function Baseline, then yearly Stop suspect drug if Clozapine and Amisulpride, sulpiride
tests (LFTs)1618 as part of aroutine LFTs indicate hepatitis chlorpromazine
physical health check (transaminases 3 associated with
and to detect chronic normal) orfunctional hepatic failure
antipsychoticinduced damage (PT/albumin
changes (rare) change)
Other tests:
Patients on clozapine may benefit from an EEG19,20 as this may help determine the need for valproate (although
interpretation is obviously complex). Those on quetiapine should have thyroid function tests yearly although the
risk of abnormality is very small.21,22
BMI, body mass index; DEXA, dualenergy Xray absorptiometry; ECG, electrocardiogram; EEG, electrocephalogram;
GFR, glomerular filtration rate; IFG, impaired fasting glucose; PT, prothrombin time.
48 The Maudsley Prescribing Guidelines in Psychiatry
Amisulpride + + + +++
Aripiprazole +
Asenapine + + + +
Flupentixol + ++ ++ ++ ++ + +++
Iloperidone ++ + + +
Lurasidone + + + +
Olanzapine ++ +++ + + + +
Paliperidone + ++ + + + ++ +++
Pimozide + + + + + + +++
Pipothiazine ++ ++ + ++ ++ ++ +++
Promazine +++ ++ + + ++ ++ ++
Quetiapine ++ ++ + ++
Risperidone + ++ + + + ++ +++
Sertindole + +++
Sulpiride + + + +++
Ziprasidone + + + +
Zuclopenthixol ++ ++ ++ ++ ++ + +++
Either:
Agree choice of antipsychotic with patient and/or carer
Or, if not possible:
Start second-generation antipsychotic
CHAPTER 2
Titrate, if necessary, to minimum effective dose
(See section on Minimum effective dose in this chapter)
Change drug and follow above If poor compliance related to poor tolerability,
Continue at dose established as effective process. Consider use of either a discuss with patient and change drug
SGA or a FGA
If poor compliance related to other factors,
consider early use of depot
Not effective
Clozapine**
* Any improvement is likely to be apparent within 23 weeks of receiving an effective dose. Most improvement occurs during this period.1
If no effect at 23 weeks, change dose or drug. If some response detected, continue for a total of at least 4 weeks before
abandoning treatment.
** Early use of clozapine much more likely than anything else to be successful.2
Treatment ineffective
Switch to clozapine
Figure 2.2 Treatment of relapse or acute exacerbation of schizophrenia (full adherence to medication confirmed).
Lack of insight
or support Poorly tolerated treatment
*Compliance aids (e.g. Medidose system in the UK) are not a substitute for patient
education. The ultimate aim should be to promote independent living, perhaps with
patients filling their own compliance aid, having first been given support and training.
Note that such compliance aids are of little use unless the patient is clearly motivated
to adhere to prescribed treatment. Note also that some medicines are not suitable for
storage in compliance aids
Figure 2.3 Treatment of relapse or acute exacerbation of schizophrenia (adherence doubtful or known to be poor).