Current strategies for predicting side effects from second generation antipsychotics in youth

被引:3
作者
Brown, Jacob T. [1 ]
Campo-Soria, Claudia [2 ]
Bishop, Jeffrey R. [3 ,4 ]
机构
[1] Univ Minnesota, Coll Pharm, Dept Pharm Practice & Pharmaceut Sci, Duluth, MN USA
[2] Childrens Hosp & Clin Minnesota, Dept Psychiat, Minneapolis, MN USA
[3] Univ Minnesota, Coll Pharm, Dept Expt & Clin Pharmacol, 308 Harvard St SE,Rm 7-115 Weaver Densford Hall, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Sch Med, Dept Psychiat & Behav Sci, Minneapolis, MN 55455 USA
关键词
Antipsychotics; children; pediatrics; adverse events; side effects; toxicity; movement disorders; weight gain; prolactin; pharmacogenetics; INDUCED WEIGHT-GAIN; NEUROLEPTIC MALIGNANT SYNDROME; AUTISM SPECTRUM DISORDERS; RECEPTOR GENE; ADVERSE EVENTS; RISPERIDONE TREATMENT; PEDIATRIC-PATIENTS; CHILDREN; OBESITY; ADOLESCENTS;
D O I
10.1080/17425255.2021.1922668
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Antipsychotic medications are used to treat a number of conditions in children and adolescents. While side effect profiles from second generation antipsychotics (SGAs) may differ from older antipsychotics, they do not come without risk. Knowing which children may be at higher risk for specific outcomes is important clinical information for prescribers. Common side effects and toxicities of SGAs in children include movement disorders, weight gain, and hormonal changes. There are also rare, but potentially dangerous adverse events including neuroleptic malignant syndrome, hypersensitivity and suicidal ideation. Areas covered: This review will summarize and comment on clinical, pharmacological, and genetic factors having evidence as predictors of SGA-associated side effects and toxicities in children. Expert opinion: Observations across studies note that older children and those that do not respond early in treatment may be more at risk for movement disorders, while younger, antipsychotic naive children are at increased risk for weight gain. Relatively fewer studies have looked at pharmacogenetic relationships, although variations in pharmacokinetic and pharmacodynamic genes hold promise to advance drug dosing or selection strategies. Future efforts to assimilate multiple clinical, pharmacological, and genetic factors to facilitate predictive analytics and clinical decision support for prescribers will advance precision care to patients.
引用
收藏
页码:655 / 664
页数:10
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