Management of bipolar I depression: clinical utility of lurasidone

被引:11
|
作者
Findlay, Lillian Jan [1 ]
El-Mallakh, Peggy [1 ]
El-Mallakh, Rif S. [2 ]
机构
[1] Univ Kentucky, Coll Nursing, Lexington, KY USA
[2] Univ Louisville, Sch Med, Dept Psychiat & Behav Sci, Louisville, KY 40202 USA
关键词
lurasidone; bipolar disorder; bipolar depression; adjunctive therapy; WEEKLY SYMPTOMATIC STATUS; EYE-MOVEMENT SLEEP; DOUBLE-BLIND; 2ND-GENERATION ANTIPSYCHOTICS; RECEPTOR ANTAGONIST; NATURAL-HISTORY; OPEN-LABEL; DISORDER; 5-HT7; SCHIZOPHRENIA;
D O I
10.2147/TCRM.S57695
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Lurasidone is a benzisothiazol derivative second-generation antipsychotic. It has been approved in the United States and Europe for treatment of acute schizophrenia and bipolar depression. In type I bipolar subjects, treatment with lurasidone monotherapy of adjunctive therapy to lithium or valproic acid with doses of 20 to 120 mg once daily with food, results in statistically and clinically significant reduction of depressive symptoms. Patients experience relatively few side effects, which include somnolence, akathisia, nausea, and other gastrointestinal upset. Dopamine related side effects, such as Parkinsonism and elevated prolactin, are rare and mild. Longer term safety data obtained in 6 months long, open continuation observation periods, suggest that metabolic related elevations in weight, glucose, and lipids are absent or minimal. The mechanism of action of lurasidone is not known, but the data are compatible with antagonism of the serotonin 7 receptor. Lurasidone is a new option for the treatment of bipolar depression with relatively few side effects.
引用
收藏
页码:75 / 81
页数:7
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