TY - JOUR
T1 - Clozapine Use for Bipolar Disorder
T2 - An Asian Psychotropic Prescription Patterns Consortium Study
AU - Loo, Lek Wei Javier
AU - Chew, Qian Hui
AU - Lin, Shih Ku
AU - Yang, Su Yu
AU - Ouyang, Wen Chen
AU - Chen, Chih Ken
AU - Park, Seon Cheol
AU - Jang, Ok Jin
AU - Park, Jun Hyuk
AU - Chee, Kok Yoon
AU - Ding, Kwong Sen
AU - Chong, Jamaline
AU - Zhang, Ling
AU - Li, Keqing
AU - Zhu, Xiaomin
AU - Jatchavala, Chonnakarn
AU - Pariwatcharakul, Pornjira
AU - Kallivayalil, Roy A.
AU - Grover, Sandeep
AU - Avasthi, Ajit
AU - Ansari, Moin
AU - Maramis, Margarita M.
AU - Aung, Paing Phyo
AU - Sartorius, Norman
AU - Xiang, Yu Tao
AU - Tan, Chay Hoon
AU - Chong, Mian Yoon
AU - Park, Yong Chon
AU - Kato, Takahiro A.
AU - Shinfuku, Naotaka
AU - Baldessarini, Ross J.
AU - Sim, Kang
N1 - Publisher Copyright:
© Wolters Kluwer Health, Inc. All rights reserved.
PY - 2023/5/1
Y1 - 2023/5/1
N2 - Background Pharmacoepidemiological studies of clozapine use to treat bipolar disorder (BD), especially in Asia, are rare, although they can provide insights into associated clinical characteristics and support international comparisons of indications and drug dosing. Methods We examined the prevalence and clinical correlates of clozapine treatment for BD in 13 Asian countries and regions (China, Hong Kong SAR, India, Indonesia, Japan, Korea, Malaysia, Myanmar, Pakistan, Singapore, Sri Lanka, Taiwan, and Thailand) within an Asian Prescription Patterns Research Consortium. We compared BD patients treated with clozapine or not in initial bivariate comparisons followed by multivariable logistic regression modeling. Results Clozapine was given to 2.13% of BD patients overall, at a mean daily dose of 275 (confidence interval, 267-282) chlorpromazine-equivalent mg/day. Patients receiving clozapine were older, more likely males, hospitalized, currently manic, and given greater numbers of mood-stabilizing and antipsychotic drugs in addition to clozapine. Logistic regression revealed that older age, male sex, current mania, and greater number of other antipsychotics remained significantly associated with clozapine treatment. Clozapine use was not associated with depressed mood, remission of illness, suicidal risk, or electroconvulsive treatment within the previous 12 months. Conclusions The identified associations of clozapine use with particular clinical features call for vigilance in personalized clinical monitoring so as to optimize clinical outcomes of BD patients and to limit risks of adverse effects of polytherapy.
AB - Background Pharmacoepidemiological studies of clozapine use to treat bipolar disorder (BD), especially in Asia, are rare, although they can provide insights into associated clinical characteristics and support international comparisons of indications and drug dosing. Methods We examined the prevalence and clinical correlates of clozapine treatment for BD in 13 Asian countries and regions (China, Hong Kong SAR, India, Indonesia, Japan, Korea, Malaysia, Myanmar, Pakistan, Singapore, Sri Lanka, Taiwan, and Thailand) within an Asian Prescription Patterns Research Consortium. We compared BD patients treated with clozapine or not in initial bivariate comparisons followed by multivariable logistic regression modeling. Results Clozapine was given to 2.13% of BD patients overall, at a mean daily dose of 275 (confidence interval, 267-282) chlorpromazine-equivalent mg/day. Patients receiving clozapine were older, more likely males, hospitalized, currently manic, and given greater numbers of mood-stabilizing and antipsychotic drugs in addition to clozapine. Logistic regression revealed that older age, male sex, current mania, and greater number of other antipsychotics remained significantly associated with clozapine treatment. Clozapine use was not associated with depressed mood, remission of illness, suicidal risk, or electroconvulsive treatment within the previous 12 months. Conclusions The identified associations of clozapine use with particular clinical features call for vigilance in personalized clinical monitoring so as to optimize clinical outcomes of BD patients and to limit risks of adverse effects of polytherapy.
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U2 - 10.1097/JCP.0000000000001693
DO - 10.1097/JCP.0000000000001693
M3 - Article
C2 - 37068038
AN - SCOPUS:85158894715
SN - 0271-0749
VL - 43
SP - 278
EP - 282
JO - Journal of Clinical Psychopharmacology
JF - Journal of Clinical Psychopharmacology
IS - 3
ER -