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Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses
BACKGROUND: A considerable proportion of patients suffering from schizophrenia show suboptimal responses to oral antipsychotics due to inadequate adherence. Hence, they are likely to benefit from switching to a long-acting injectable formulation. These post hoc analyses assessed the clinical effects...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825698/ https://www.ncbi.nlm.nih.gov/pubmed/24235837 http://dx.doi.org/10.2147/NDT.S50635 |
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author | Ciudad, Antonio Anand, Ernie Berggren, Lovisa Casillas, Marta Schacht, Alexander Perrin, Elena |
author_facet | Ciudad, Antonio Anand, Ernie Berggren, Lovisa Casillas, Marta Schacht, Alexander Perrin, Elena |
author_sort | Ciudad, Antonio |
collection | PubMed |
description | BACKGROUND: A considerable proportion of patients suffering from schizophrenia show suboptimal responses to oral antipsychotics due to inadequate adherence. Hence, they are likely to benefit from switching to a long-acting injectable formulation. These post hoc analyses assessed the clinical effects of switching to olanzapine long-acting injection (OLAI) from either oral olanzapine (OLZ) or other antipsychotics (non-OLZ). METHODS: Post hoc analyses were done based on two randomized studies (one short-term, one long-term) conducted in patients suffering from schizophrenia and treated with OLAI. The short-term study was an 8-week placebo-controlled, double-blind trial in acute patients, and the long-term study was a 2-year, oral olanzapine-controlled, open-label, follow-up of stabilized outpatients. RESULTS: These analyses used data from 62 OLAI-treated patients (12 switched from OLZ, 50 from non-OLZ) from the short-term study and 190 OLAI-treated patients (56 switched from OLZ, 134 from non-OLZ) from the long-term study. Kaplan–Meier survival analyses of time to all-cause discontinuation of OLAI treatment did not differ significantly between OLZ and non-OLZ patients in the short-term study (P=0.209) or long-term study (P=0.448). Similarly, the proportions of OLZ and non-OLZ patients that discontinued OLAI were not statistically different in the short-term (16.7% versus 36.0%, respectively; P=0.198) or long-term (57.1% versus 47.8% respectively; P=0.238) studies. In the short-term study, no significant differences were detected between the patient groups in mean change in Positive and Negative Syndrome Scale (PANSS) total score (−13.4 OLZ versus −20.8 non-OLZ; P=0.166). In the long-term study, mean change in PANSS total score (3.9 OLZ versus −3.6 non-OLZ; P=0.008) was significantly different between the non-OLZ and OLZ groups. Rates of treatment-emergent adverse events were similar in OLZ and non-OLZ groups per study. CONCLUSION: These post hoc analyses suggest that no significant differences in clinical effectiveness were seen after switching from non-OLZ or OLZ to OLAI. However, these findings should be interpreted with care, due to small sample sizes and differences in patients’ clinical profiles. |
format | Online Article Text |
id | pubmed-3825698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38256982013-11-14 Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses Ciudad, Antonio Anand, Ernie Berggren, Lovisa Casillas, Marta Schacht, Alexander Perrin, Elena Neuropsychiatr Dis Treat Original Research BACKGROUND: A considerable proportion of patients suffering from schizophrenia show suboptimal responses to oral antipsychotics due to inadequate adherence. Hence, they are likely to benefit from switching to a long-acting injectable formulation. These post hoc analyses assessed the clinical effects of switching to olanzapine long-acting injection (OLAI) from either oral olanzapine (OLZ) or other antipsychotics (non-OLZ). METHODS: Post hoc analyses were done based on two randomized studies (one short-term, one long-term) conducted in patients suffering from schizophrenia and treated with OLAI. The short-term study was an 8-week placebo-controlled, double-blind trial in acute patients, and the long-term study was a 2-year, oral olanzapine-controlled, open-label, follow-up of stabilized outpatients. RESULTS: These analyses used data from 62 OLAI-treated patients (12 switched from OLZ, 50 from non-OLZ) from the short-term study and 190 OLAI-treated patients (56 switched from OLZ, 134 from non-OLZ) from the long-term study. Kaplan–Meier survival analyses of time to all-cause discontinuation of OLAI treatment did not differ significantly between OLZ and non-OLZ patients in the short-term study (P=0.209) or long-term study (P=0.448). Similarly, the proportions of OLZ and non-OLZ patients that discontinued OLAI were not statistically different in the short-term (16.7% versus 36.0%, respectively; P=0.198) or long-term (57.1% versus 47.8% respectively; P=0.238) studies. In the short-term study, no significant differences were detected between the patient groups in mean change in Positive and Negative Syndrome Scale (PANSS) total score (−13.4 OLZ versus −20.8 non-OLZ; P=0.166). In the long-term study, mean change in PANSS total score (3.9 OLZ versus −3.6 non-OLZ; P=0.008) was significantly different between the non-OLZ and OLZ groups. Rates of treatment-emergent adverse events were similar in OLZ and non-OLZ groups per study. CONCLUSION: These post hoc analyses suggest that no significant differences in clinical effectiveness were seen after switching from non-OLZ or OLZ to OLAI. However, these findings should be interpreted with care, due to small sample sizes and differences in patients’ clinical profiles. Dove Medical Press 2013 2013-11-08 /pmc/articles/PMC3825698/ /pubmed/24235837 http://dx.doi.org/10.2147/NDT.S50635 Text en © 2013 Ciudad et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed. |
spellingShingle | Original Research Ciudad, Antonio Anand, Ernie Berggren, Lovisa Casillas, Marta Schacht, Alexander Perrin, Elena Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
title | Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
title_full | Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
title_fullStr | Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
title_full_unstemmed | Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
title_short | Switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
title_sort | switching to olanzapine long-acting injection from either oral olanzapine or any other antipsychotic: comparative post hoc analyses |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825698/ https://www.ncbi.nlm.nih.gov/pubmed/24235837 http://dx.doi.org/10.2147/NDT.S50635 |
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