Do the New
Antipsychotics
Make A Difference?
British Medical Journal - Oct 16, 1999
Although most individuals with psychosis show a moderate to substantial
reduction in their positive symptoms after treatment with antipsychotic drugs,
about 30% of patients do not respond to psychopharmacology. The negative
symptoms of schizophrenia are even less responsive to drug treatment. Once an
individual is in remission, antipsychotic drugs substantially reduce the risk
of relapse. During one year, 55% of those on placebo have a relapse compared
with 20-25% of those on antipsychotic drugs.
The greatest limitation of treatment with traditional antipsychotic drugs
has been their side effects. In particular, people with schizophrenia have had
to tolerate disabling and distressing extrapyramidal side effects such as
parkinsonism, akathisia (restlessness in the legs and body), acute dystonia,
and tardive dyskinesia (involuntary movements, often of the tongue and face but
also of the fingers, hands, legs, and trunk).
The recommended doses for acute and maintenance treatment with traditional
antipsychotics can be found in guidelines such as those published by the
Patient Outcomes Research Team. [4] Several new antipsychotic drugs have been
introduced recently. Of these, risperidone, olanzapine, and clozapine are available in most countries. At the time of
writing,
aripiprazole (Abilify) has been approved in the U.S.,
quetiapine was available in some
countries but sertindole has been withdrawn pending review of data on cardiac
safety. Ziprasidone is awaiting
approval in many countries, but may be introduced in the next year or so. These
drugs are sometimes called atypical antipsychotics.
There is a substantial body of evidence that shows that the new
antipsychotic drugs are effective in treating positive symptoms.[9] Data from
trials and clinical experience also suggest that they are effective in reducing
the risk of relapse during maintenance treatment, although the evidence is less
extensive. In the past it was commonly thought that all traditional
antipsychotics were equally effective.[10] A recently published Cochrane review
comparing clozapine with traditional antipsychotics has shown that clozapine
has greater clinical efficacy than traditional antipsychotics.[11] It has been
claimed that some of the other new antipsychotics have statistically
significant advantages on various measures of clinical outcome when compared
with traditional antipsychotics; however, it remains to be seen whether these
differences are clinically relevant in daily practice. There is evidence to
suggest that patients on the new antipsychotic drugs have superior performance
on neurocognitive measures (for example, working memory) compared with patients
on traditional antipsychotics.[12 13]
The table summarises selected data on the efficacy and side effects of the
new antipsychotics. Clozapine, olanzapine, and quetiapine have a wide range of
receptor affinities and the other products have more selective dopamine and
serotonergic properties. Because of the increased risk of agranulocytosis
associated with clozapine, it should not be the first choice treatment. Updated
sources of evidence based recommendations should be consulted regularly. Some
of these sources are given in the box.
The greatest limitation of treatment with traditional antipsychotic drugs
has been their side effects. In particular, people with schizophrenia have had
to tolerate disabling and distressing extrapyramidal side effects such as
parkinsonism, akathisia (restlessness in the legs and body), acute dystonia,
and tardive dyskinesia (involuntary movements, often of the tongue and face but
also of the fingers, hands, legs, and trunk).
The recommended doses for acute and maintenance treatment with traditional
antipsychotics can be found in guidelines such as those published by the
Patient Outcomes Research Team.[4] Several new antipsychotic drugs have been
introduced recently. Of these, risperidone, olanzapine, and clozapine are
available in most countries. At the time of writing quetiapine was available in
some countries but sertindole has been withdrawn pending review of data on
cardiac safety. Ziprasidone is awaiting approval in many countries, but may be
introduced in the next year or so. These drugs are sometimes called atypical
antipsychotics.
There is a substantial body of evidence that shows that the new
antipsychotic drugs are effective in treating positive symptoms.[9] Data from
trials and clinical experience also suggest that they are effective in reducing
the risk of relapse during maintenance treatment, although the evidence is less
extensive. In the past it was commonly thought that all traditional
antipsychotics were equally effective.[10] A recently published Cochrane review
comparing clozapine with traditional antipsychotics has shown that clozapine
has greater clinical efficacy than traditional antipsychotics.[11] It has been
claimed that some of the other new antipsychotics have statistically
significant advantages on various measures of clinical outcome when compared
with traditional antipsychotics; however, it remains to be seen whether these
differences are clinically relevant in daily practice. There is evidence to
suggest that patients on the new antipsychotic drugs have superior performance
on neurocognitive measures (for example, working memory) compared with patients
on traditional antipsychotics.[12 13]
The table summarises selected data on the efficacy and side effects of the
new antipsychotics. Clozapine, olanzapine, and quetiapine have a wide range of
receptor affinities and the other products have more selective dopamine and
serotonergic properties. Because of the increased risk of agranulocytosis
associated with clozapine, it should not be the first choice treatment. Updated
sources of evidence based recommendations should be consulted regularly. Some
of these sources are given in the box.
Selected features of new antipsychotic drugs
Drug (dose) Study Findings
Clozapine (200-800mg/day) Cochrane Effective
versus traditional review[11] antipsychotic, fewer
antipsychotic drugs 29 studies relapses, greater
based 2490 reduction in
participants symptoms, fewer
drop-outs greater
patient satisfaction
satisfaction
Risperidone (2-6mg/day) Cochrane Effective
versus traditional review[14] antipsychotic,
antipsychotic drugs 14 studies greater clinical
based on 3401 improvement little
participants no additional effect
positive or negative
symptoms, fewer
drop-outs
Olanzapine (10-20mg/day) Cochrane Effective
versus traditional review[17] 5 antipsychotic, fewer
antipsychotic drugs studies based drop-outs, lower
on 2911 depression scores,
participants less sedation,
fewer extrapyramidal
side effects
Sertindole (12-20mg/day) Randomised Effective
versus traditional controlled antipsychotic, fewer
antipsychotic drugs trials[9] extrapyramidal side
effects
Ziprasidone (80-160mg/day) Randomised Effective
versus traditional controlled antipsychotic, fewer
antipsychotic drugs trials[6] extrapyramidal side
effects
Quetiapine (300-450mg/day) Cochrane Effective
versus traditional review[17] antipsychotic, fewer
antipsychotic drugs 6 trials extrapyramidal side
based on 1417 effects
participants
Drug (dose) Selected side effects
Clozapine (200-800mg/day) Sedation, hypersalivation, weight
versus traditional gain, increased risk of
antipsychotic drugs convulsions at higher doses, 1%
risk of agranulocytosis
Risperidone (2-6mg/day) Weight gain, hyperprolactinaemia
versus traditional (leading to amenorrhoea,
antipsychotic drugs galactorrhea, impotence),
postural hypotension
Olanzapine (10-20mg/day) Sedation, weight gain, dizziness
versus traditional
antipsychotic drugs
Sertindole (12-20mg/day) Increased risk of QT interval
versus traditional prolongation (1.7% of patients)
antipsychotic drugs
Ziprasidone (80-160mg/day) Sedation
versus traditional
antipsychotic drugs
Quetiapine (300-450mg/day) Dizziness, dry mouth, sedation
versus traditional
antipsychotic drugs
Drug (dose) Comments
Clozapine (200-800mg/day) Patients require regular
versus traditional haematological monitoring, 31% of
antipsychotic drugs patients with schizophrenia
previously resistant to drug
treatment have clinical improvement
Risperidone (2-6mg/day) Lacks anticholinergic properties,
versus traditional patients switched from older
antipsychotic drugs antipsychotics (which often required
the coprescription of
anticholinergics to reduce
extrapyramidal side effects to
risperidone can undergo cholinergic
rebound (flu-like symptoms)
Olanzapine (10-20mg/day) Transient elevation of hepatic
versus traditional transaminases, lower incidence of
antipsychotic drugs tardive dyskinesia compared with
haloperidol
Sertindole (12-20mg/day) Baseline and regular ECG monitoring
versus traditional recommended, should be avoided in
antipsychotic drugs patients taking drugs known to
prolong the QT interval,
contraindicated in patients with
clinically significant
cardiovascular disease, now under
review because ECG changes noted in
some patients
Ziprasidone (80-160mg/day) Weight gain has not been a prominent
versus traditional feature of treatment with
antipsychotic drugs ziprasidone as compared with
clozapine, risperidone, and
olanzapine
Quetiapine (300-450mg/day) High drop-out rates in the trials
versus traditional limit interpretation
antipsychotic drugs
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