TY - JOUR
T1 - Comparative effectiveness and safety of antipsychotic drugs in patients with schizophrenia initiating or reinitiating treatment
T2 - A Real-World Observational Study
AU - Brodeur, Sébastien
AU - Vanasse, Alain
AU - Courteau, Josiane
AU - Stip, Emmanuel
AU - Lesage, Alain
AU - Fleury, Marie Josée
AU - Courteau, Mireille
AU - Roy, Marc André
N1 - Funding Information:
This study was supported by the Centre de recherche du CHUS (CRCHUS) and the Département de Médecine de Famille et de Médecine d'urgence at the Université de Sherbrooke. This work was also partly supported by a Quebec Health Research Fund (FRQS) peer-reviewed and unrestricted grant from Janssen (division of Johnson & Johnson) and the Ministère de l'Économie et de l'Innovation (MEI), within the framework of Données de recherche en contexte réel—Partenariat Innovation-Québec-Janssen (PIQJ).
Funding Information:
This study was supported by the Centre de recherche du CHUS (CRCHUS) and the Département de Médecine de Famille et de Médecine d'urgence at the Université de Sherbrooke. This work was also partly supported by a Quebec Health Research Fund (FRQS) peer‐reviewed and unrestricted grant from Janssen (division of Johnson & Johnson) and the Ministère de l'Économie et de l'Innovation (MEI), within the framework of Données de recherche en contexte réel—Partenariat Innovation‐Québec‐Janssen (PIQJ).
Funding Information:
E.S. received funding from Lundbeck Canada Inc. and Otsuka Canada Pharmaceutical Inc. He has served on the advisory boards and been a lecturer for Lundbeck Canada Inc, Otsuka Canada Pharmaceutical Inc, and Janssen. M.‐A. R. reports grants from Mylan Canada, Janssen Canada, Mylan Canada and Otsuka‐Lundbeck Alliance Canada during the conduct of the study. Outside the submitted work, he has also received personal fees from Boehringer Canada (research contracts), Lundbeck Canada (research contracts), Otsuka‐Lundbeck Alliance (advisory honoraria; speaker honoraria), HLS Canada (advisory honoraria), Mylan Canada (advisory honoraria; speaker honoraria), and Janssen Canada (speaker honoraria). Except for the grant mentioned above, the authors declare no other competing interests.
Publisher Copyright:
© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2022/5
Y1 - 2022/5
N2 - Objective: To compare the effectiveness and safety of various second-generation antipsychotics (SGAs), newer oral and long-acting injectable (LAI) SGAs, and first-generation antipsychotics (FGAs) treatments in patients with schizophrenia or schizoaffective disorder (SCZ). Methods: This retrospective cohort study included medical administrative information for patients with a diagnosis of SCZ living in Quebec (Canada), initiating or reinitiating at least one antipsychotic (AP) drug (with a clearance baseline period of 12 months without any APs). Effectiveness was defined by a reduced risk of hospitalization for mental disorder and discontinuation, and safety by a reduced risk of all-cause death and hospitalization for non-mental disorder, 2 years after AP initiation or reinitiation. Cox proportional hazard models were used to estimate the events associated with different antipsychotics compared with oral olanzapine. Results: The study cohort included 19,615 patients initiating or reinitiating an antipsychotic drug between January 2006 and December 2015. Results showed better effectiveness of clozapine (adjusted HR 0.36, 95% CI 0.30–0.42, p < 0.0001) and LAI SGAs (adjusted HR 0.56, 95% CI 0.51–0.61, p < 0.0001) compared with oral olanzapine when adding discontinuation to hospitalizations for mental disorder as a composite measure of effectiveness, as opposed to oral FGAs (adjusted HR 1.36, 95% CI 1.27–1.46, p < 0.0001) and LAI FGAs (adjusted HR 1.22, 95% CI 1.12–1.32, p < 0.0001). Most APs were as safe as oral olanzapine. Conclusion: The effectiveness of LAI SGAs and clozapine appears to justify their use and are as safe as a recognized treatment (oral olanzapine) in Quebec (Canada).
AB - Objective: To compare the effectiveness and safety of various second-generation antipsychotics (SGAs), newer oral and long-acting injectable (LAI) SGAs, and first-generation antipsychotics (FGAs) treatments in patients with schizophrenia or schizoaffective disorder (SCZ). Methods: This retrospective cohort study included medical administrative information for patients with a diagnosis of SCZ living in Quebec (Canada), initiating or reinitiating at least one antipsychotic (AP) drug (with a clearance baseline period of 12 months without any APs). Effectiveness was defined by a reduced risk of hospitalization for mental disorder and discontinuation, and safety by a reduced risk of all-cause death and hospitalization for non-mental disorder, 2 years after AP initiation or reinitiation. Cox proportional hazard models were used to estimate the events associated with different antipsychotics compared with oral olanzapine. Results: The study cohort included 19,615 patients initiating or reinitiating an antipsychotic drug between January 2006 and December 2015. Results showed better effectiveness of clozapine (adjusted HR 0.36, 95% CI 0.30–0.42, p < 0.0001) and LAI SGAs (adjusted HR 0.56, 95% CI 0.51–0.61, p < 0.0001) compared with oral olanzapine when adding discontinuation to hospitalizations for mental disorder as a composite measure of effectiveness, as opposed to oral FGAs (adjusted HR 1.36, 95% CI 1.27–1.46, p < 0.0001) and LAI FGAs (adjusted HR 1.22, 95% CI 1.12–1.32, p < 0.0001). Most APs were as safe as oral olanzapine. Conclusion: The effectiveness of LAI SGAs and clozapine appears to justify their use and are as safe as a recognized treatment (oral olanzapine) in Quebec (Canada).
KW - antipsychotic
KW - effectiveness
KW - observational studies
KW - safety
KW - schizophrenia
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UR - http://www.scopus.com/inward/citedby.url?scp=85125497249&partnerID=8YFLogxK
U2 - 10.1111/acps.13413
DO - 10.1111/acps.13413
M3 - Article
C2 - 35158404
AN - SCOPUS:85125497249
SN - 0001-690X
VL - 145
SP - 456
EP - 468
JO - Acta Psychiatrica Scandinavica
JF - Acta Psychiatrica Scandinavica
IS - 5
ER -