Safety and tolerability of antipsychotic-mood stabilizer co-treatment in the management of acute bipolar disorder: results from a systematic review and exploratory meta-analysis

被引:10
|
作者
Galling, Britta [1 ]
Garcia, Maryam A. [2 ]
Osuchukwu, Uzoma [1 ]
Hagi, Katsuhiko [1 ,3 ]
Correll, Christoph U. [1 ,4 ,5 ,6 ]
机构
[1] Zucker Hillside Hosp, Psychiat Res, North Shore Long Isl Jewish Hlth Syst, Glen Oaks, NY USA
[2] Hosp Santa Caterina, Inst Assistencia Sanitaria, Salt, Spain
[3] Dainippon Sumitomo Pharma Co Ltd, Osaka, Japan
[4] Hofstra North Shore LIJ Sch Med, Hempstead, NY USA
[5] Feinstein Inst Med Res, Manhasset, NY USA
[6] Albert Einstein Coll Med, Bronx, NY 10467 USA
关键词
adverse effects; antipsychotic; augmentation; bipolar disorder; combination; co-treatment; meta-analysis; mood stabilizer; safety; tolerability; ADJUNCTIVE ORAL ZIPRASIDONE; DOUBLE-BLIND; ACUTE MANIA; ADD-ON; PSYCHIATRIC COMORBIDITY; DRUG-INTERACTIONS; I DISORDER; PLACEBO; LITHIUM; EFFICACY;
D O I
10.1517/14740338.2015.1053457
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Mood stabilizer (MS) plus antipsychotic (AP) co-treatment is common in patients with acute bipolar disorder (BD), but adverse effects (AEs) of this strategy have not been systematically reviewed. Areas covered: We conducted a systematic review searching PubMed/MEDLINE and PsycINFO on April 1, 2015 for randomized trials in >= 20 adults with acute manic/mixed or depressed BD comparing MS or AP monotherapy with their combination that reported quantitative AE data. Pooled together, MS+AP versus MS monotherapy (studies = 18, n = 4419) was associated with significantly higher burden regarding 21/53 (39.6%) individual AEs, particularly weight gain-related (5/5 = 100%), extrapyramidal (5/12 = 41.7%) and glucose/lipid-related AEs (3/8 = 37.5%). AP+MS versus AP monotherapy (studies = 3, n = 397) was associated with significantly higher burden regarding 4/21 (19.0%) individual AEs (>= 1 AE, tremor, sedation/somnolence, vomiting). Expert opinion: Efficacy advantages of AP+MS co-treatment versus monotherapy should be balanced with its greater AE burden. AE risk is higher for adding AP to MS (17 additional AEs) than adding MS to an AP, including the particularly concerning cardiometabolic AEs. More data are needed, as only one or two studies provided data for 21/21 (100%) AEs of MS augmentation of AP, and 13/53 (24.5%) AEs of AP augmentation of MS, and as sparse data suggest clinically relevant AE differences across individual AP+MS combinations.
引用
收藏
页码:1181 / 1199
页数:19
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