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BioMed Central Page 1 of 2 (page number not for citation purposes) Annals of General Psychiatry Open Access Oral presentation Comparison of second generation antipsychotics: are there any differences in efficacy? George Papageorgiou* Address: Department of Psychiatry, Evangelismos General Hospital, Athens, Greece * Corresponding author Since the re-introduction of clozapine in 1988, the so- called atypical or second generation antipsychotics (SGAs) have contributed considerably to the treatment of schizophrenia. The term "atypical" was at first given to clozapine because of its low propensity to cause extrapy- ramidal symptoms. This term has been applied uncriti- cally to a series of drugs despite their striking differences in chemistry, pharmacology and specific clinical action profile. Their use also may be limited because of various existing controversies. At first, there is the question whether SGAs have to be preferred over the older, conven- tional first generation antipsychotics (FGAs). Secondly, there has been an ongoing debate to differentiate between them in terms of efficacy and safety. The initial enthusiasm that most of the second generation antipsychotics (SGAs) showed a better efficacy and tolera- bility profile over the FGAs was subsided over the publica- tion of a series of meta-analyses, the most recent being the first results of the CATIE study. These showed that there was no clear evidence of the advantage of SGAs compared to the FGAs. Treatment guidelines from various institu- tions issued analogous and equivocating recommenda- tions between the two antipsychotic groups. Therefore, the clinician has remained free to make his own choice. There have been many publications comparing SGAs with FGAs, in the regulatory process of the drugs. For example, a meta-analysis comparing SGAs over FGAs found reduced dropout and treatment failure rates with risperi- done in comparison with haloperidol. Other efficacy trials have tried to find differences in efficacy between the SGAs but with conflicting results. In one study, clozapine proved more effective than risperidone in treatment resist- ant schizophrenia but methodological flaws prompt for cautiouness for the interpretation of the results A big issue was raised with two studies comparing the efficacy of ris- peridone versus olanzapine. The first showed an advan- tage of olanzapine over risperidone and the second showed the opposite. Two studies comparing ziprasidone with olanzapine and ziprasidone with risperidone didn't disclose any advantage in efficacy of either agent over the other. A better tolerability profile was found with ziprasi- done. Studies involving quetiapine showed that this agent had similar efficacy to risperidone and olanzapine. Switch studies showed that the use of aripiprazole maintained the clinical effect acquired by the previous agent. in another study, aripiprazole showed similar efficacy with risperidone. Amisulpride, an atypical antipsychotic with a different mechanism of action than the other SGAs, is an effective agent for the treatment of acute exacerbations as well as for the chronic treatment of positive and especially negative symptoms of schizophrenia. Compared with haloperidol in two studies, showed at least the same rate of improvement in positive symptoms and a clear advan- tage in long term over haloperidol in negative, suggested no efficacy differences between them, when the haloperi- dol equivalent didn't exceed 12 mg/day. In the light of most recent evidence comparing the relative efficacy of the SGAs, there are no clear-cut differences between them. It is up to the clinician to weigh the risks, the benefits and the cost of each drug and choose the most appropriate therapy for the individual patient. References 1. Davis JM, Chen N, Glick ID: A Meta-analysis of the Efficacy of Second Generation Antipsychotics. Arch Gen Psychiatry 2003, 60:553-4. 2. McKeage K, Plosker GL: Amisulpride: A Review of its Use in the Management of Schizophrenia. CNS Drugs 2004, 18:933-56. 3. Gardner DM, Baldessarini RJ, Waraich P: Modern Antipsychotic Drugs:a Critical Review. CMAJ 2005, 172:1703-9. from International Society on Brain and Behaviour: 2nd International Congress on Brain and Behaviour Thessaloniki, Greece. 17–20 November 2005 Published: 28 February 2006 Annals of General Psychiatry 2006, 5(Suppl 1):S37 doi:10.1186/1744-859X-5-S1-S37 <supplement> <title> <p>International Society on Brain and Behaviour: 2nd International Congress on Brain and Behaviour</p> </title> <note>Meeting abstracts – A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcen- tral.com/content/files/pdf/1744-859X-5-S1-full.pdf">here</a>.</note> </supplement>

Comparison of second generation antipsychotics: are there any differences in efficacy?

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Open AcceOral presentationComparison of second generation antipsychotics: are there any differences in efficacy?George Papageorgiou*

Address: Department of Psychiatry, Evangelismos General Hospital, Athens, Greece

* Corresponding author

Since the re-introduction of clozapine in 1988, the so-called atypical or second generation antipsychotics(SGAs) have contributed considerably to the treatment ofschizophrenia. The term "atypical" was at first given toclozapine because of its low propensity to cause extrapy-ramidal symptoms. This term has been applied uncriti-cally to a series of drugs despite their striking differencesin chemistry, pharmacology and specific clinical actionprofile. Their use also may be limited because of variousexisting controversies. At first, there is the questionwhether SGAs have to be preferred over the older, conven-tional first generation antipsychotics (FGAs). Secondly,there has been an ongoing debate to differentiate betweenthem in terms of efficacy and safety.

The initial enthusiasm that most of the second generationantipsychotics (SGAs) showed a better efficacy and tolera-bility profile over the FGAs was subsided over the publica-tion of a series of meta-analyses, the most recent being thefirst results of the CATIE study. These showed that therewas no clear evidence of the advantage of SGAs comparedto the FGAs. Treatment guidelines from various institu-tions issued analogous and equivocating recommenda-tions between the two antipsychotic groups. Therefore,the clinician has remained free to make his own choice.

There have been many publications comparing SGAs withFGAs, in the regulatory process of the drugs. For example,a meta-analysis comparing SGAs over FGAs foundreduced dropout and treatment failure rates with risperi-done in comparison with haloperidol. Other efficacy trialshave tried to find differences in efficacy between the SGAsbut with conflicting results. In one study, clozapineproved more effective than risperidone in treatment resist-ant schizophrenia but methodological flaws prompt forcautiouness for the interpretation of the results A big issue

was raised with two studies comparing the efficacy of ris-peridone versus olanzapine. The first showed an advan-tage of olanzapine over risperidone and the secondshowed the opposite. Two studies comparing ziprasidonewith olanzapine and ziprasidone with risperidone didn'tdisclose any advantage in efficacy of either agent over theother. A better tolerability profile was found with ziprasi-done. Studies involving quetiapine showed that this agenthad similar efficacy to risperidone and olanzapine. Switchstudies showed that the use of aripiprazole maintainedthe clinical effect acquired by the previous agent. inanother study, aripiprazole showed similar efficacy withrisperidone. Amisulpride, an atypical antipsychotic with adifferent mechanism of action than the other SGAs, is aneffective agent for the treatment of acute exacerbations aswell as for the chronic treatment of positive and especiallynegative symptoms of schizophrenia. Compared withhaloperidol in two studies, showed at least the same rateof improvement in positive symptoms and a clear advan-tage in long term over haloperidol in negative, suggestedno efficacy differences between them, when the haloperi-dol equivalent didn't exceed 12 mg/day. In the light ofmost recent evidence comparing the relative efficacy of theSGAs, there are no clear-cut differences between them. Itis up to the clinician to weigh the risks, the benefits andthe cost of each drug and choose the most appropriatetherapy for the individual patient.

References1. Davis JM, Chen N, Glick ID: A Meta-analysis of the Efficacy of

Second Generation Antipsychotics. Arch Gen Psychiatry 2003,60:553-4.

2. McKeage K, Plosker GL: Amisulpride: A Review of its Use in theManagement of Schizophrenia. CNS Drugs 2004, 18:933-56.

3. Gardner DM, Baldessarini RJ, Waraich P: Modern AntipsychoticDrugs:a Critical Review. CMAJ 2005, 172:1703-9.

from International Society on Brain and Behaviour: 2nd International Congress on Brain and BehaviourThessaloniki, Greece. 17–20 November 2005

Published: 28 February 2006

Annals of General Psychiatry 2006, 5(Suppl 1):S37 doi:10.1186/1744-859X-5-S1-S37<supplement> <title> <p>International Society on Brain and Behaviour: 2nd International Congress on Brain and Behaviour</p> </title> <note>Meeting abstracts – A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcen-tral.com/content/files/pdf/1744-859X-5-S1-full.pdf">here</a>.</note> </supplement>

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Annals of General Psychiatry 2006, 5:S37

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4. Lieberman JA, et al.: Effectiveness of Antipsychotic Drugs inPatients with Chronic Schizophrenia. N Engl J Med 2005,353:1209-23.

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