Duffy A, Patten S, Goodday S, Weir A, Heffer N, Cipriani A
Mood Disorders Centre of Ottawa, University of Ottawa Health Services, 100 Marie Curie Private, Suite 300, Ottawa, ON, K1N 6N5, Canada.
Department of Psychiatry, Hotel Dieu Hospital, Queen's University, 166 Brock Street, Kingston, ON, K7L 5G2, Canada.
Int J Bipolar Disord. 2017 Dec;5(1):22. doi: 10.1186/s40345-017-0092-6. Epub 2017 Jun 13.
Epidemiological, clinical, and high-risk studies have provided evidence that the peak period for onset of diagnosable episodes of mania and hypomania starts in mid-to-late adolescence. Moreover, clinically significant manic symptoms may occur even earlier, especially in children at familial risk. Lithium is the gold standard treatment for acute mania in adults, yet to our knowledge, there is no published systematic review assessing lithium treatment of mania in children or adolescents. This is a major gap in knowledge needed to inform clinical practice.
As a working group within the ISBD Task Force on Lithium Treatment ( http://www.isbd.org/active-task-forces ), our aim is to complete a systematic review of the efficacy, tolerability, and acceptability of lithium compared with placebo and other active drugs in treating mania in children and adolescents diagnosed with bipolar disorder.
We will include double- or single-blind randomized controlled trials in patients aged less than 18 years. No restrictions will be made by study publication date or language. Several electronic databases will be searched along with secondary sources such as bibliographies and trial registry websites for published and unpublished studies. Response rates to lithium compared with placebo or other active drugs will be the primary efficacy outcome. Primary tolerability and acceptability outcomes will be rates of serious adverse events and dropouts, respectively. Secondary outcomes will include rates of remission, severity of manic symptoms at different time points, and incidence of specific adverse events.
Findings from this systematic review are critically needed to inform clinical practice. We should not generalize findings from adult studies, as children and adolescents are undergoing accelerated physiological and brain development. Therefore, efficacy, tolerability, and acceptability of lithium treatment of acute mania in children compared to adults may be very different. This systematic review has been registered in PROSPERO (CRD42017055675).
流行病学、临床及高危研究已提供证据表明,可诊断的躁狂和轻躁狂发作高峰期始于青春期中后期。此外,具有临床意义的躁狂症状甚至可能更早出现,尤其是在有家族风险的儿童中。锂盐是成人急性躁狂的金标准治疗药物,但据我们所知,尚无已发表的系统评价评估锂盐对儿童或青少年躁狂的治疗效果。这是指导临床实践所需知识的一个重大空白。
作为国际双相障碍学会锂盐治疗特别工作组(http://www.isbd.org/active-task-forces)的一个工作小组,我们的目的是完成一项系统评价,比较锂盐与安慰剂及其他活性药物在治疗双相情感障碍儿童和青少年躁狂方面的疗效、耐受性和可接受性。
我们将纳入年龄小于18岁患者的双盲或单盲随机对照试验。研究发表日期或语言不受限制。将检索多个电子数据库以及诸如参考文献和试验注册网站等二级来源,以查找已发表和未发表的研究。锂盐与安慰剂或其他活性药物相比的有效率将作为主要疗效指标。主要耐受性和可接受性指标将分别为严重不良事件发生率和脱落率。次要指标将包括缓解率、不同时间点的躁狂症状严重程度以及特定不良事件的发生率。
这一系统评价的结果对于指导临床实践至关重要。我们不应将成人研究的结果一概而论,因为儿童和青少年正处于生理和大脑快速发育阶段。因此,与成人相比,锂盐治疗儿童急性躁狂的疗效、耐受性和可接受性可能非常不同。本系统评价已在国际系统评价注册库(PROSPERO)注册(注册号:CRD42017055675)。