预测小儿轻中度阻塞性睡眠呼吸暂停的治疗成功:基于多导睡眠图参数的模型的真实世界证据。

IF 2
Yuanming Wang, Chen Cheng
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引用次数: 0

摘要

背景:小儿轻至中度阻塞性睡眠呼吸暂停(OSA)通常使用鼻内皮质类固醇(INCS)治疗,但反应率各不相同。确定治疗成功的早期预测因素可能有助于个体化治疗。方法:我们进行了一项单中心、两期观察性研究,以建立和验证3-12岁轻度至中度OSA儿童INCS反应的预测模型,该模型的基线呼吸暂停-低通气指数(AHI)为1.0-10.0事件/小时。衍生队列(n = 175)在2019年至2023年间回顾性入组。采用相同的诊断和治疗方案,在2024年至2025年间招募了前瞻性验证队列(n = 60)。所有患者均接受标准化的INCS治疗。治疗反应定义为6-9个月随访时AHI降低≥50%,临床症状改善。结果:从基线临床和多导睡眠图(PSG)参数中提取候选预测因子。采用多变量逻辑回归识别独立预测因子。基于这些变量构建了预测nomogram模型,并在前瞻性队列中进行了外部验证。该模型具有良好的标定和判别能力。结论:本研究提出了一种基于PSG和临床参数的有效nomogram模型来预测儿童OSA患者对INCS的治疗反应,为早期决策和个性化治疗策略提供支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting treatment success in pediatric mild-to-moderate OSA: real-world evidence from a model based on polysomnographic parameters.

Background: Pediatric mild-to-moderate obstructive sleep apnea (OSA) is often treated with intranasal corticosteroids (INCS), but response rates vary. Identifying early predictors of treatment success may facilitate individualized therapy.

Methods: We conducted a single-center, two-phase observational study to develop and validate a predictive model for INCS response in children aged 3-12 years with mild-to-moderate OSA, defined by a baseline apnea-hypopnea index (AHI) of 1.0-10.0 events/hour. The derivation cohort (n = 175) was retrospectively enrolled between 2019 and 2023. A prospective validation cohort (n = 60) was recruited between 2024 and 2025 using identical diagnostic and treatment protocols. All patients received standardized INCS therapy. Treatment response was defined as a ≥ 50% reduction in AHI along with improvement in clinical symptoms at 6-9 months follow-up.

Results: Candidate predictors were extracted from baseline clinical and polysomnographic (PSG) parameters. Multivariable logistic regression was used to identify independent predictors. A predictive nomogram model was constructed based on these variables and externally validated in the prospective cohort. The model demonstrated good calibration and discrimination.

Conclusion: This study presents a validated nomogram model based on PSG and clinical parameters to predict treatment response to INCS in pediatric OSA, supporting early decision-making and personalized treatment strategies.

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