Department of Neurology, School of Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
J Neurol. 2011 May;258(5):874-81. doi: 10.1007/s00415-010-5861-4. Epub 2010 Dec 16.
The cause of idiopathic intracranial hypertension (IIH) remains unknown, and no consensus exists on how patients should be monitored and treated. Acetazolamide is a common treatment but has never been examined in a randomised controlled trial. The objectives of this pilot trial are to prospectively evaluate the use of acetazolamide, to explore various outcome measures and to inform the design of a definitive trial in IIH. Fifty patients were recruited from six centres over 23 months and randomised to receive acetazolamide (n = 25) or no acetazolamide (n = 25). Symptoms, body weight, visual function and health-related quality-of-life measures were recorded over a 12-month period. Recruited patients had typical features of mild IIH and most showed improvement, with 44% judged to have IIH in remission at the end of the trial. Difficulties with recruitment were highlighted as well as poor compliance with acetazolamide therapy (12 patients). A composite measure of IIH status was tested, and the strongest concordance with final disease status was seen with perimetry (Somers' D = 0.66) and optic disc appearance (D = 0.59). Based on the study data, a sample size of 320 would be required to demonstrate a 20% treatment effect in a substantive trial. Clinical trials in IIH require pragmatic design to involve sufficiently large numbers of patients. Future studies should incorporate weighted composite scores to reflect the relative importance of common outcome measures in IIH.
特发性颅内高压(IIH)的病因仍不清楚,如何监测和治疗患者也没有共识。乙酰唑胺是一种常见的治疗方法,但从未在随机对照试验中进行过检查。本试验的目的是前瞻性评估乙酰唑胺的使用,探索各种结局指标,并为 IIH 的确定性试验提供设计信息。在 23 个月内,从 6 个中心招募了 50 名患者,并随机分为乙酰唑胺组(n = 25)和无乙酰唑胺组(n = 25)。在 12 个月的时间里,记录了症状、体重、视觉功能和健康相关生活质量的测量结果。入组患者具有典型的轻度 IIH 特征,大多数患者有所改善,44%的患者在试验结束时被判定为 IIH 缓解。强调了招募的困难以及乙酰唑胺治疗的依从性差(12 名患者)。对 IIH 状态的综合衡量标准进行了测试,与最终疾病状态最一致的是视野计(Somers'D = 0.66)和视盘外观(D = 0.59)。根据研究数据,在实质性试验中,需要 320 名患者的样本量才能显示出 20%的治疗效果。IIH 的临床试验需要采用实用设计,以纳入足够数量的患者。未来的研究应纳入加权综合评分,以反映 IIH 中常见结局指标的相对重要性。