TY - JOUR
T1 - Antipsychotic polypharmacy and corrected QT interval
T2 - A systematic review
AU - Takeuchi, Hiroyoshi
AU - Suzuki, Takefumi
AU - Remington, Gary
AU - Uchida, Hiroyuki
N1 - Funding Information:
Dr Takeuchi is supported by a Canadian Institutes of Health Research Fellowship. This funding source had no role in this study’s design, statistical analysis, interpretation of findings, manuscript preparation, or submission. Dr Takeuchi has received fellowship grants from the Centre for Addiction and Mental Health Foundation, the Japanese Society of Clinical Neuropsychopharmacology, and Astellas Foundation for Research on Metabolic Disorders, and manuscript fees from Dainippon Sumitomo Pharma.
Funding Information:
Dr Takeuchi is supported by a Canadian Institutes of Health Research Fellowship. This funding source had no role in this study's design, statistical analysis, interpretation of findings, manuscript preparation, or submission. Dr Takeuchi has received fellowship grants from the Centre for Addiction and Mental Health Foundation, the Japanese Society of Clinical Neuropsychopharmacology, and Astellas Foundation for Research on Metabolic Disorders, and manuscript fees from Dainippon Sumitomo Pharma. Dr Suzuki has received speaker or manuscript fees from Astellas, Dainippon Sumitomo, Eli Lilly, Elsevier Japan, Janssen, Novartis, Meiji Seika, Otsuka, and Weily Japan. Dr Remington has received research support from Novartis, Medicure, and Neurocrine Bioscience, consultant fees from Laboratorios Farmac?uticos Rovi, Synchroneuron, Novartis, and Roche, and speaker's fees from Novartis. Dr Uchida has received grants from Astellas Pharmaceutical, Eisai, Otsuka Pharmaceutical, GlaxoSmithKline, Shionogi, Dainippon-Sumitomo Pharma, Eli Lilly, Mochida Pharmaceutical, Meiji-Seika Pharma, and Yoshitomi Yakuhin, and speaker's honoraria from Otsuka Pharmaceutical, Eli Lilly, Shionogi, GlaxoSmithKline, Yoshitomi Yakuhin, Dainippon-Sumitomo Pharma, Meiji-Seika Pharma, Abbvie, MSD, and Janssen Pharmaceutical.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Objective: It remains unclear whether antipsychotic polypharmacy, a common clinical practice, is related to an increased risk of corrected time between start of Q wave and end of T wave (QTc) interval prolongation. We conducted a systematic review of the literature to address this important issue. Method: A systematic literature search was conducted in October 2014, using MEDLINE, Embase, and PsycINFO. Studies and case reports were included if they reported QTc intervals or QTc interval changes before and after antipsychotic polypharmacy or QTc intervals in both antipsychotic polypharmacy and monotherapy groups. Results: A total of 21 articles (10 clinical trials, 4 observational studies, and 7 case reports) met inclusion criteria. The clinical trials have shown that a combination treatment with risperidone or pimozide is not obviously related to an increase in QTc interval, whereas ziprasidone or sertindole combined with clozapine may prolong QTc interval. Among the 4 observational studies, antipsychotic polypharmacy was not clearly associated with QTc prolongation in 3 studies, each cross-sectional. In contrast, one prospective study showed a significant increase in QTc interval following antipsychotic coadministration. The case reports indicated an increased risk of QTc prolongation in at least some patients receiving antipsychotic polypharmacy. Conclusions: Currently available evidence fails to confirm that antipsychotic polypharmacy worsens QTc prolongation in general, although the evidence is scarce and inconsistent. Clinicians are advised to remain conservative in resorting to antipsychotic polypharmacy, as a combination of some QTc-prolongation liable antipsychotics may further prolong QTc interval, and efficacy supporting the clinical benefits of antipsychotic polypharmacy is equivocal, at best.
AB - Objective: It remains unclear whether antipsychotic polypharmacy, a common clinical practice, is related to an increased risk of corrected time between start of Q wave and end of T wave (QTc) interval prolongation. We conducted a systematic review of the literature to address this important issue. Method: A systematic literature search was conducted in October 2014, using MEDLINE, Embase, and PsycINFO. Studies and case reports were included if they reported QTc intervals or QTc interval changes before and after antipsychotic polypharmacy or QTc intervals in both antipsychotic polypharmacy and monotherapy groups. Results: A total of 21 articles (10 clinical trials, 4 observational studies, and 7 case reports) met inclusion criteria. The clinical trials have shown that a combination treatment with risperidone or pimozide is not obviously related to an increase in QTc interval, whereas ziprasidone or sertindole combined with clozapine may prolong QTc interval. Among the 4 observational studies, antipsychotic polypharmacy was not clearly associated with QTc prolongation in 3 studies, each cross-sectional. In contrast, one prospective study showed a significant increase in QTc interval following antipsychotic coadministration. The case reports indicated an increased risk of QTc prolongation in at least some patients receiving antipsychotic polypharmacy. Conclusions: Currently available evidence fails to confirm that antipsychotic polypharmacy worsens QTc prolongation in general, although the evidence is scarce and inconsistent. Clinicians are advised to remain conservative in resorting to antipsychotic polypharmacy, as a combination of some QTc-prolongation liable antipsychotics may further prolong QTc interval, and efficacy supporting the clinical benefits of antipsychotic polypharmacy is equivocal, at best.
KW - Antipsychotic
KW - Augmentation
KW - Cardiac sudden death
KW - Combination
KW - Corrected QT interval
KW - Polypharmacy
KW - Systematic review
UR - http://www.scopus.com/inward/record.url?scp=84964695739&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84964695739&partnerID=8YFLogxK
U2 - 10.1177/070674371506000503
DO - 10.1177/070674371506000503
M3 - Review article
C2 - 26174525
AN - SCOPUS:84964695739
SN - 0706-7437
VL - 60
SP - 215
EP - 222
JO - Canadian Journal of Psychiatry
JF - Canadian Journal of Psychiatry
IS - 5
ER -