Kant Ravi, Chalansani Ranjit, Chengappa K N Roy, Dieringer Mary F
Head Injury Clinic, Pittsburgh, Pennsylvania, USA.
J Child Adolesc Psychopharmacol. 2004 Spring;14(1):57-63. doi: 10.1089/104454604773840490.
There are limited data in the literature regarding clozapine use in adolescents with diagnoses other than schizophrenia. This report describes the use of clozapine in adolescents with diagnoses of bipolar disorder, intermittent explosive disorder (IED), and posttraumatic stress disorder (PTSD).
A chart review of 39 adolescents treated with clozapine at two residential facilities was undertaken. Data extraction included demography, illness variables, medication information, and clinical outcomes. Categorical outcomes were analyzed using contingency statistics, and continuous variables were analyzed using a paired t test.
The cohort included 26 females and 13 males with a mean age of 14 years. Clozapine was titrated slowly, and the mean daily dose was 102 mg. The diagnoses included bipolar disorder (n = 7), IED (n = 9), and PTSD (n = 19). There were significant reductions in polypharmacy once the clozapine dosage was stabilized. Prior to clozapine treatment, nearly 70% of the subjects were receiving either mood-stabilizing or antidepressant agents in combination with the previous antipsychotic drug. Once the clozapine dosage was stabilized, only 24% of the subjects required concomitant mood stabilizers (p < 0.001), and only 21% of the subjects required concomitant antidepressants (p < 0.001). Anxiolytic medication use was also significantly reduced during clozapine treatment. Most patients were discharged to a less restrictive setting. Eight subjects discontinued clozapine due to agranulocytosis (n = 1), neutropenia (n = 2), excessive weight gain (n = 2), or not requiring it long term (n = 1), and data were unavailable in 2 subjects. Significant weight gain (5% or greater change from baseline) was noted in 20 subjects.
Clozapine, in relatively modest doses, appears to have clinical benefits for adolescent with bipolar disorder, IED, and PTSD. There is no labeled indication for clozapine use in these disorders. Clozapine is also associated with serious side effects in subsets of individuals. Therefore, a very careful evaluation of the risk-to-benefit ratio in each individual subject being considered for clozapine is highly recommended.
关于氯氮平在精神分裂症以外诊断的青少年中的使用,文献中的数据有限。本报告描述了氯氮平在诊断为双相情感障碍、间歇性爆发性障碍(IED)和创伤后应激障碍(PTSD)的青少年中的使用情况。
对两家住院机构中39例接受氯氮平治疗的青少年进行病历回顾。数据提取包括人口统计学、疾病变量、用药信息和临床结果。分类结果采用列联统计分析,连续变量采用配对t检验分析。
该队列包括26名女性和13名男性,平均年龄为14岁。氯氮平缓慢滴定,平均每日剂量为102毫克。诊断包括双相情感障碍(n = 7)、间歇性爆发性障碍(n = 9)和创伤后应激障碍(n = 19)。氯氮平剂量稳定后,联合用药显著减少。在氯氮平治疗前,近70%的受试者正在接受心境稳定剂或抗抑郁药与先前抗精神病药物的联合使用。氯氮平剂量稳定后,只有24%的受试者需要同时使用心境稳定剂(p < 0.001),只有21%的受试者需要同时使用抗抑郁药(p < 0.001)。在氯氮平治疗期间,抗焦虑药物的使用也显著减少。大多数患者出院后限制较少。8名受试者因粒细胞缺乏症(n = 1)、中性粒细胞减少症(n = 2)、体重过度增加(n = 2)或长期不需要(n = 1)而停用氯氮平,2名受试者的数据不可用。20名受试者出现显著体重增加(较基线变化5%或更大)。
相对中等剂量的氯氮平似乎对患有双相情感障碍、间歇性爆发性障碍和创伤后应激障碍的青少年有临床益处。氯氮平在这些疾病中的使用尚无标签适应证。氯氮平在部分个体中也与严重副作用相关。因此,强烈建议对每一位考虑使用氯氮平的个体进行非常仔细的风险效益比评估。