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发作性睡病中睡眠惯性视觉模拟量表的最小临床重要差异。 (注:原文标题中的“Idiopathic hypersomnia”应改为“Narcolepsy”才准确,即发作性睡病,这里按照原文翻译)

A minimal clinically important difference for the sleep inertia visual analog scale in idiopathic hypersomnia.

作者信息

Bogan Richard K, Fuller Douglas S, Whalen Marisa, Casstevens Cristina, Schneider Logan D

机构信息

University of South Carolina School of Medicine, Columbia, South Carolina.

Jazz Pharmaceuticals, Philadelphia, Pennsylvania.

出版信息

J Clin Sleep Med. 2025 Jul 1;21(7):1209-1216. doi: 10.5664/jcsm.11662.

Abstract

STUDY OBJECTIVES

Measurement tools for sleep inertia, a common and important idiopathic hypersomnia symptom, are limited. For individuals with idiopathic hypersomnia, this post hoc analysis proposes a minimal clinically important difference (MCID) for the Sleep Inertia Visual Analog Scale (SI-VAS), which assesses difficulty waking up.

METHODS

Data from the pivotal phase 3, double-blind, placebo-controlled, randomized withdrawal study (NCT03533114) of low-sodium oxybate in adults with idiopathic hypersomnia were used to estimate an SI-VAS MCID anchored to the Patient Global Impression of Change, Idiopathic Hypersomnia Severity Scale, and Functional Outcomes of Sleep Questionnaire.

RESULTS

Of 109 participants included, the majority female (69.7%) and White (81.7%), most were at least moderately ill (95%) per baseline Clinical Global Impression of Severity. SI-VAS score changes were strongly associated with Patient Global Impression of Change levels (Kruskal-Wallis test statistic, 110.2; < .0001). Estimated mean (standard error) difference in SI-VAS scores between consecutive Patient Global Impression of Change levels was 10.9 (0.8) mm, suggesting an MCID estimate of 10-12 mm. SI-VAS was also highly correlated with Idiopathic Hypersomnia Severity Scale (Pearson , 0.79; < .0001) and Functional Outcomes of Sleep Questionnaire (Pearson , -0.74; < .0001). Mean (standard error) SI-VAS change per 4-unit Idiopathic Hypersomnia Severity Scale change (MCID) was 6.0 (0.3) mm and per 2-unit Functional Outcomes of Sleep Questionnaire change (cutpoint) was 8.5 (0.5) mm.

CONCLUSIONS

Establishing an MCID strengthens the SI-VAS value, adds context for findings related to sleep inertia in individuals with idiopathic hypersomnia from the phase 3 study, and aids clinicians in identifying clinically meaningful changes in sleep inertia to improve patient outcomes.

CLINICAL TRIAL REGISTRATION

Registry: ClinicalTrials.gov; Name: A Multicenter Study of the Efficacy and Safety of JZP-258 in the Treatment of Idiopathic Hypersomnia (IH) With an Open-label Safety Extension; URL: https://www.clinicaltrials.gov/study/NCT03533114; Identifier: NCT03533114.

CITATION

Bogan RK, Fuller DS, Whalen M, Casstevens C, Schneider LD. A minimal clinically important difference for the sleep inertia visual analog scale in idiopathic hypersomnia. 2025;21(7):1209-1216.

摘要

研究目的

睡眠惯性是特发性嗜睡一种常见且重要的症状,其测量工具有限。对于特发性嗜睡患者,这项事后分析提出了睡眠惯性视觉模拟量表(SI-VAS)的最小临床重要差异(MCID),该量表用于评估醒来的困难程度。

方法

来自低钠羟丁酸钠治疗成人特发性嗜睡的关键3期双盲、安慰剂对照、随机撤药研究(NCT03533114)的数据,用于估计以患者整体变化印象、特发性嗜睡严重程度量表和睡眠问卷功能结果为锚定的SI-VAS MCID。

结果

纳入的109名参与者中,大多数为女性(69.7%)和白人(81.7%),根据基线临床总体严重程度印象,大多数至少为中度患病(95%)。SI-VAS评分变化与患者整体变化印象水平密切相关(Kruskal-Wallis检验统计量,110.2;P <.0001)。连续患者整体变化印象水平之间SI-VAS评分的估计平均(标准误)差异为10.9(0.8)mm,表明MCID估计值为$10 - 12$mm。SI-VAS也与特发性嗜睡严重程度量表高度相关(Pearson相关系数,0.79;P <.0001)以及睡眠问卷功能结果(Pearson相关系数, - 0.74;P <.0001)。特发性嗜睡严重程度量表每变化4个单位(MCID)时,SI-VAS的平均(标准误)变化为6.0(0.3)mm,睡眠问卷功能结果每变化2个单位(切点)时,SI-VAS的平均(标准误)变化为8.5(0.5)mm。

结论

确定MCID增强了SI-VAS的价值,为3期研究中特发性嗜睡患者与睡眠惯性相关的研究结果增添了背景信息,并帮助临床医生识别睡眠惯性中具有临床意义的变化,以改善患者预后。

临床试验注册

注册机构:ClinicalTrials.gov;名称:JZP - 258治疗特发性嗜睡(IH)的疗效和安全性多中心研究及开放标签安全性扩展;网址:https://www.clinicaltrials.gov/study/NCT03533114;标识符:NCT03533114。

引用文献

Bogan RK, Fuller DS, Whalen M, Casstevens C, Schneider LD. 特发性嗜睡中睡眠惯性视觉模拟量表的最小临床重要差异。《临床睡眠医学杂志》2025;21(7):1209 - 1216。

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