Treatment of Early-Age Mania: Outcomes for Partial and Non responders to Initial Treatment

被引:14
作者
Walkup, John T. [1 ]
Wagner, Karen Dineen [2 ]
Miller, Leslie [3 ]
Yenokyan, Gayane [4 ]
Luby, Joan L. [5 ]
Joshi, Paramjit T. [6 ]
Axelson, David A. [7 ,8 ]
Robb, Adelaide [6 ]
Salpekar, Jay A. [6 ]
Wolf, Dwight [2 ]
Sanyal, Abanti [4 ]
Birmaher, Boris [9 ]
Vitiello, Benedetto [10 ]
Riddle, Mark A. [3 ]
机构
[1] Weill Cornell Med Coll, New York Presbyterian Hosp, New York, NY USA
[2] Univ Texas Med Branch, Galveston, TX 77555 USA
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[4] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[5] Washington Univ, St Louis, MO USA
[6] George Washington Univ, Childrens Natl Med Ctr, Sch Med, Washington, DC USA
[7] Nationwide Childrens Hosp, Columbus, OH USA
[8] Ohio State Univ, Wexner Med Ctr, Columbus, OH USA
[9] Univ Pittsburgh, Med Ctr, Western Psychiat Inst & Clin, Pittsburgh, PA USA
[10] NIMH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
mania; bipolar; treatment; pharmacology; nonresponders; BIPOLAR-I DISORDER; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; DIVALPROEX SODIUM; KIDDIE SCHEDULE; ADOLESCENTS; CHILDREN; RISPERIDONE; PREDICTORS; EFFICACY;
D O I
10.1016/j.jaac.2015.09.015
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Objective: The Treatment of Early Age Mania (TEAM) study evaluated lithium, risperidone, and divalproex sodium (divalproex) in children with bipolar I disorder who were naive to antimanic medication, or were partial or nonresponders to 1 of 3 study medications. This report evaluates the benefit of either an add-on or a switch of antimanic medications for an 8-week trial period in partial responders and nonresponders, respectively. Method: TEAM is a randomized, controlled trial of individuals (N = 379) aged 6 to 15 years (mean +/- SD = 10.2 +/- 2.7 years) with DSM-IV bipolar I disorder (mixed or manic phase). Participants (n = 154) in this report were either nonresponders or partial responders to 1 of the 3 study medications. Nonresponders (n = 89) were randomly assigned to 1 of the other 2 antimanic medications and cross-tapered. Partial responders (n = 65) were randomly assigned to 1 of 2 other antimanic medications as an add-on to their initial medication. Adverse event (AE) rates are reported only for the add-on group. Results: Response rate for children switched to risperidone (47.6%) was higher than for those switched to either lithium (12.8%; p = .005; number needed to treat [NNT] = 3; 95% CI = 1.71-9.09) or divalproex (17.2%; p = .03; NNT = 3; 95% CI = 1.79-20.10); response rate for partial responders who added risperidone (53.3%) was higher than for those who added divalproex (0%; p = .0002; NNT = 2; 95% CI = 1.27-3.56) and trended higher for lithium (26.7%; p = .07; NNT = 4). Reported AEs in the add-on group were largely consistent with the known AE profile for the second medication. Weight gain (kg) was observed for all add-on medications: lithium add-on (n = 29 of 30) = 1.66 +/- 1.97; risperidone add-on (n = 15 of 15) = 2.8 +/- 1.34; divalproex add-on (n = 19 of 20) = 1.42 +/- 1.96. There was no evidence at the 5% significance level that the average weight gain was different by study medication for partial responders (p = .07, 1-way analysis of variance). Conclusion: Risperidone appears to be more useful than lithium or divalproex for children with bipolar I disorder and other comorbid conditions who are nonresponders or partial responders to an initial antimanic medication trial.
引用
收藏
页码:1008 / 1019
页数:12
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