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Published in: BMC Psychiatry 1/2008

Open Access 01-12-2008 | Research article

Evaluation of patients on sertindole treatment after failure of other antipsychotics: A retrospective analysis

Authors: Jean-Michel Azorin, Susana Murteira, Karina Hansen, Mondher Toumi

Published in: BMC Psychiatry | Issue 1/2008

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Abstract

Background

Use of the atypical antipsychotic sertindole was suspended for four years due to safety concerns. During the suspension, the regulatory authorities required further studies, including this one, to be conducted. The purpose of this study was to determine if a subset of patients with psychotic illness exists which particularly benefits from sertindole treatment after failure of other antipsychotic drugs, including atypical antipsychotics.

Methods

This was a retrospective single-arm observational crossover study of 344 patients, who served as their own controls. Patients mainly from the Sertindole Safety Study who had shown good response to sertindole, and who had followed up to four alternating six month periods of treatment with sertindole and other antipsychotics, were included. (In Period 1 patients took non-sertindole treatment, in Period 2, sertindole was taken, in Period 3, patients reverted to non-sertindole treatment, and in Period 4, sertindole was taken again.) Patient records for each period of treatment were assessed for objective data: number and duration of hospitalizations due to worsening of psychotic symptoms; the amount of self-harming behaviour; indicators of social status. Retrospective evaluation of changes in clinical symptoms from the patients' records was also conducted. Dates and reasons for stopping and/or switching medication were also recorded.

Results

There was improvement in all objective measured parameters during the periods of sertindole treatment. In particular, the average number of hospitalizations per year due to worsening of psychotic symptoms was reduced in the following way in the group studied over four treatment periods: Period 1 (non-sertindole treatment) 3.4; Period 2 (sertindole treatment) 1.0; Period 3 (non-sertindole treatment) 2.0; Period 4 (sertindole treatment) 1.8. The duration of hospitalizations also decreased significantly during the periods of sertindole treatment. Results showed that patients improved in objective social parameters when switched to sertindole treatment; assessment of the patients' affective lives showed a significant increase in the number of patients having a stable relationship during sertindole treatment; and assessment of the number of patients employed showed an increase after the first and second switch to sertindole treatment (from Period 1 to Period 2 and from Period 3 to Period 4, respectively).
Adverse events and lack of efficacy were the main reasons for switching to sertindole.

Conclusion

A group of patients benefited from sertindole after other antipsychotic treatments, including that with atypical antipsychotics, had failed. Further studies are needed to investigate if there is a specific patient profile that corresponds to these responders.
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Literature
2.
go back to reference Janca A, Kastrup M, Katschnig H, Lopez-Ibor JJ, Mezzich JE, Sartorius N: The World Health Organization Short Disability Assessment Schedule (WHO DAS-S): a tool for the assessment of difficulties in selected areas of functioning of patients with mental disorders. Soc Psychiatry Psychiatr Epidemiol. 1996, 31: 349-354. 10.1007/BF00783424.CrossRefPubMed Janca A, Kastrup M, Katschnig H, Lopez-Ibor JJ, Mezzich JE, Sartorius N: The World Health Organization Short Disability Assessment Schedule (WHO DAS-S): a tool for the assessment of difficulties in selected areas of functioning of patients with mental disorders. Soc Psychiatry Psychiatr Epidemiol. 1996, 31: 349-354. 10.1007/BF00783424.CrossRefPubMed
3.
go back to reference Marwaha S, Johnson S: Schizophrenia and employment - a review. Soc Psychiatry Psychiatr Epidemiol. 2004, 39: 337-349. 10.1007/s00127-004-0762-4.CrossRefPubMed Marwaha S, Johnson S: Schizophrenia and employment - a review. Soc Psychiatry Psychiatr Epidemiol. 2004, 39: 337-349. 10.1007/s00127-004-0762-4.CrossRefPubMed
4.
go back to reference Gilbert PL, Harris MJ, McAdams LA, Jeste DV: Neuroleptic withdrawal in schizophrenic patients. A review of the literature. Arch Gen Psychiatry. 1995, 52: 173-188.CrossRefPubMed Gilbert PL, Harris MJ, McAdams LA, Jeste DV: Neuroleptic withdrawal in schizophrenic patients. A review of the literature. Arch Gen Psychiatry. 1995, 52: 173-188.CrossRefPubMed
5.
6.
go back to reference Crow TJ, MacMillan JF, Johnson AL, Johnstone EC: A randomised controlled trial of prophylactic neuroleptic treatment. Br J Psychiatry. 1986, 148: 120-127.CrossRefPubMed Crow TJ, MacMillan JF, Johnson AL, Johnstone EC: A randomised controlled trial of prophylactic neuroleptic treatment. Br J Psychiatry. 1986, 148: 120-127.CrossRefPubMed
7.
go back to reference Edlinger M, Baumgartner S, Eltanaihi-Furtmuller N, Hummer M, Fleischhacker WW: Switching between second-generation antipsychotics: why and how?. CNS Drugs. 2005, 19: 27-42. 10.2165/00023210-200519010-00003.CrossRefPubMed Edlinger M, Baumgartner S, Eltanaihi-Furtmuller N, Hummer M, Fleischhacker WW: Switching between second-generation antipsychotics: why and how?. CNS Drugs. 2005, 19: 27-42. 10.2165/00023210-200519010-00003.CrossRefPubMed
8.
go back to reference Dossenbach M, rango-Davila C, Silva IH, Landa E, Aguilar J, Caro O, Leadbetter J, Assuncao S: Response and relapse in patients with schizophrenia treated with olanzapine, risperidone, quetiapine, or haloperidol: 12-month follow-up of the Intercontinental Schizophrenia Outpatient Health Outcomes (IC-SOHO) study. J Clin Psychiatry. 2005, 66: 1021-1030.CrossRefPubMed Dossenbach M, rango-Davila C, Silva IH, Landa E, Aguilar J, Caro O, Leadbetter J, Assuncao S: Response and relapse in patients with schizophrenia treated with olanzapine, risperidone, quetiapine, or haloperidol: 12-month follow-up of the Intercontinental Schizophrenia Outpatient Health Outcomes (IC-SOHO) study. J Clin Psychiatry. 2005, 66: 1021-1030.CrossRefPubMed
9.
go back to reference de Oliveira IR, Juruena MF: Treatment of psychosis: 30 years of progress. J Clin Pharm Ther. 2006, 31: 523-534. 10.1111/j.1365-2710.2006.00784.x.CrossRefPubMed de Oliveira IR, Juruena MF: Treatment of psychosis: 30 years of progress. J Clin Pharm Ther. 2006, 31: 523-534. 10.1111/j.1365-2710.2006.00784.x.CrossRefPubMed
10.
go back to reference Leucht S, Heres S: Epidemiology, clinical consequences, and psychosocial treatment of nonadherence in schizophrenia. J Clin Psychiatry. 2006, 67 Suppl 5: 3-8.PubMed Leucht S, Heres S: Epidemiology, clinical consequences, and psychosocial treatment of nonadherence in schizophrenia. J Clin Psychiatry. 2006, 67 Suppl 5: 3-8.PubMed
11.
go back to reference Moore N, Hall G, Sturkenboom M, Mann R, Lagnaoui R, Begaud B: Biases affecting the proportional reporting ratio (PPR) in spontaneous reports pharmacovigilance databases: the example of sertindole. Pharmacoepidemiol Drug Saf. 2003, 12: 271-281. 10.1002/pds.848.CrossRefPubMed Moore N, Hall G, Sturkenboom M, Mann R, Lagnaoui R, Begaud B: Biases affecting the proportional reporting ratio (PPR) in spontaneous reports pharmacovigilance databases: the example of sertindole. Pharmacoepidemiol Drug Saf. 2003, 12: 271-281. 10.1002/pds.848.CrossRefPubMed
13.
go back to reference Toumi M, Auquier P, Francois C: The safety and tolerability of sertindole in a named patient program. Schizophr Res. 2003, 60: 368-368. 10.1016/S0920-9964(03)80203-7.CrossRef Toumi M, Auquier P, Francois C: The safety and tolerability of sertindole in a named patient program. Schizophr Res. 2003, 60: 368-368. 10.1016/S0920-9964(03)80203-7.CrossRef
14.
go back to reference Misdrahi D, Llorca PM, Lancon C, Bayle FJ: [Compliance in schizophrenia: predictive factors, therapeutical considerations and research implications]. Encephale. 2002, 28: 266-272.PubMed Misdrahi D, Llorca PM, Lancon C, Bayle FJ: [Compliance in schizophrenia: predictive factors, therapeutical considerations and research implications]. Encephale. 2002, 28: 266-272.PubMed
15.
go back to reference Arnt J: Pharmacological differentiation of classical and novel antipsychotics. Int Clin Psychopharmacol. 1998, 13 Suppl 3: S7-14.CrossRefPubMed Arnt J: Pharmacological differentiation of classical and novel antipsychotics. Int Clin Psychopharmacol. 1998, 13 Suppl 3: S7-14.CrossRefPubMed
16.
go back to reference Hyttel J, Nielsen JB, Nowak G: The acute effect of sertindole on brain 5-HT2, D2 and alpha 1 receptors (ex vivo radioreceptor binding studies). J Neural Transm Gen Sect. 1992, 89: 61-69. 10.1007/BF01245352.CrossRefPubMed Hyttel J, Nielsen JB, Nowak G: The acute effect of sertindole on brain 5-HT2, D2 and alpha 1 receptors (ex vivo radioreceptor binding studies). J Neural Transm Gen Sect. 1992, 89: 61-69. 10.1007/BF01245352.CrossRefPubMed
17.
go back to reference Hyttel J, Arnt J, Costall B, Domeney A, Dragsted N, Lembol HL, Meier E, Naylor RJ, Nowak G, Sanchez C, .: Pharmacological profile of the atypical neuroleptic sertindole. Clin Neuropharmacol. 1992, 15 Suppl 1 Pt A: 267A-268A.CrossRefPubMed Hyttel J, Arnt J, Costall B, Domeney A, Dragsted N, Lembol HL, Meier E, Naylor RJ, Nowak G, Sanchez C, .: Pharmacological profile of the atypical neuroleptic sertindole. Clin Neuropharmacol. 1992, 15 Suppl 1 Pt A: 267A-268A.CrossRefPubMed
18.
go back to reference van Kammen DP, McEvoy JP, Targum SD, Kardatzke D, Sebree TB: A randomized, controlled, dose-ranging trial of sertindole in patients with schizophrenia. Psychopharmacology (Berl). 1996, 124: 168-175. 10.1007/BF02245618.CrossRef van Kammen DP, McEvoy JP, Targum SD, Kardatzke D, Sebree TB: A randomized, controlled, dose-ranging trial of sertindole in patients with schizophrenia. Psychopharmacology (Berl). 1996, 124: 168-175. 10.1007/BF02245618.CrossRef
Metadata
Title
Evaluation of patients on sertindole treatment after failure of other antipsychotics: A retrospective analysis
Authors
Jean-Michel Azorin
Susana Murteira
Karina Hansen
Mondher Toumi
Publication date
01-12-2008
Publisher
BioMed Central
Published in
BMC Psychiatry / Issue 1/2008
Electronic ISSN: 1471-244X
DOI
https://doi.org/10.1186/1471-244X-8-16

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