Schneck Christopher D, Chang Kiki D, Singh Manpreet K, DelBello Melissa P, Miklowitz David J
1 Department of Psychiatry, Helen and Arthur E. Johnson Depression Center, University of Colorado School of Medicine , Aurora, Colorado.
2 Department of Psychiatry, Stanford University School of Medicine , Stanford, California.
J Child Adolesc Psychopharmacol. 2017 Nov;27(9):796-805. doi: 10.1089/cap.2017.0035. Epub 2017 Jul 21.
Depression and brief periods of manic symptoms are linked to a significant risk of progression to bipolar disorder (BD) in children who have a first-degree relative with BD I or II. However, little evidence exists to guide the pharmacologic management of children with these high-risk phenotypes. We propose a pharmacological treatment algorithm for high-risk youth and present results on its use in a study of children with a first-degree relative with BD.
Subjects were 40 youth (mean 12.7 years, range 9-17 years) who had (1) a first-degree relative with lifetime history of BD I or II, (2) DSM-IV-TR diagnoses of BD not otherwise specified, major depressive disorder or cyclothymic disorder, and (3) active symptoms of depression, mania, or hypomania. Participants and their families were enrolled in a randomized trial examining the effects of two psychosocial interventions on the 1-year course of mood disorder. At study intake, participants received a psychiatric evaluation and were offered medications or had existing medications optimized to decrease symptom severity. During the 1-year study, psychiatrists treated participants using a medication algorithm to treat depressive or manic symptoms as well as comorbid anxiety and/or attention-deficit/hyperactivity disorder.
At study entry, 25 of 40 (62.5%) of the participants were taking at least one psychiatric medication. At 1 year, nearly an identical proportion were taking medications (22 of 35, 63%). Independent ratings indicated that in 84.7% of the study visits, physicians maintained adherence to the algorithm. No patients experienced antidepressant- or stimulant-induced mania during the study.
An algorithmic approach to pharmacologic interventions may aid in the management of youth (i.e., age <18) at high risk for BD. Future studies should compare outcomes in high-risk patients receiving algorithm-prescribed treatment versus those receiving treatment as usual.
Early Family-Focused Treatment for Youth at Risk for Bipolar Disorder; www.clinicaltrials.gov/ ; NCT00943085.
抑郁和短暂的躁狂症状与双相情感障碍(BD)I型或II型一级亲属的儿童发展为双相情感障碍的显著风险相关。然而,几乎没有证据可指导对具有这些高危表型的儿童进行药物治疗。我们提出了一种针对高危青少年的药物治疗方案,并展示了其在一项针对双相情感障碍一级亲属儿童的研究中的使用结果。
研究对象为40名青少年(平均年龄12.7岁,范围9 - 17岁),他们(1)有双相情感障碍I型或II型终身病史的一级亲属,(2)根据《精神疾病诊断与统计手册》第四版修订版(DSM-IV-TR)诊断为未另行规定的双相情感障碍、重度抑郁症或环性心境障碍,以及(3)存在抑郁、躁狂或轻躁狂的活跃症状。参与者及其家庭被纳入一项随机试验,该试验考察两种心理社会干预对心境障碍1年病程的影响。在研究入组时,参与者接受了精神科评估,并被给予药物治疗或对现有药物进行优化以减轻症状严重程度。在为期1年的研究期间,精神科医生使用药物治疗方案来治疗抑郁或躁狂症状以及共病的焦虑和/或注意力缺陷多动障碍。
在研究开始时,40名参与者中有25名(62.5%)正在服用至少一种精神科药物。在1年时,服用药物的比例几乎相同(35名中的22名,63%)。独立评级表明,在84.7%的研究访视中,医生坚持遵循治疗方案。在研究期间,没有患者经历抗抑郁药或兴奋剂诱发的躁狂。
药物干预的方案方法可能有助于管理双相情感障碍高危的青少年(即年龄<18岁)。未来的研究应比较接受方案规定治疗的高危患者与接受常规治疗的患者的结局。
针对双相情感障碍高危青少年的早期家庭聚焦治疗;www.clinicaltrials.gov/ ;NCT00943085。