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儿童睡眠呼吸障碍临床评估评分的验证。

Validation of a clinical assessment score for pediatric sleep-disordered breathing.

机构信息

Division of Pediatric Otolaryngology, State University of New York Downstate Medical Center, Brooklyn, New York, USA.

出版信息

Laryngoscope. 2012 Sep;122(9):2096-104. doi: 10.1002/lary.23455. Epub 2012 Aug 13.

Abstract

OBJECTIVES/HYPOTHESIS: To validate a clinical assessment score for pediatric sleep-disordered breathing.

STUDY DESIGN

Prospective instrument validation.

METHODS

One hundred children scheduled for overnight polysomnography were evaluated by a standardized history and physical examination and assigned a clinical assessment score. Parents completed the Obstructive Sleep Apnea (OSA)-18, the Pediatric Quality of Life Inventory (PedsQL) 4.0, and the Child Behavior Checklist questionnaires. Children with positive polysomnography underwent adenotonsillectomy or adenoidectomy. The identical assessments were performed at a mean follow-up of 8 months.

RESULTS

Item reduction yielded a score of 15 items (Clinical Assessment Score-15 [CAS-15]) that demonstrated the best internal consistency and predictive utility (Cronbach α = .80). Intraclass correlation (ICC) demonstrated good intrarater (ICC, 0.78; 95% confidence interval [CI], 0.58 to 0.89) and inter-rater agreement (ICC, 0.65; 95% CI, 0.26 to 0.84). All change scores were significantly improved after surgery. Effect sizes were large for the CAS-15 (2.6), OSA-18 (2.4), and apnea-hypopnea index (1.4), and moderate for the Child Behavior Checklist (0.7) and PedsQL 4.0 (-0.5). Moderate to strong correlation was found between the initial CAS-15 scores and the external measures (|r| between 0.32 and 0.65). Receiver operating characteristic curves were constructed to determine the optimal initial CAS-15 score for predicting positive polysomnography. The area under the curve was 0.77 (95% CI, 0.67 to 0.87); and a score ≥32 yielded a sensitivity of 77.3% (95% CI, 65.3 to 86.7) and a specificity of 60.7% (95% CI, 40.6 to 78.5).

CONCLUSIONS

The CAS-15 proved useful in an office setting and correctly diagnosed 72% of referred children when compared to polysomnography. It correlated well with external measures and demonstrated a good response to clinical change.

摘要

目的/假设:验证一种用于儿童睡眠呼吸障碍的临床评估评分。

研究设计

前瞻性仪器验证。

方法

100 名计划接受过夜多导睡眠图检查的儿童接受了标准化的病史和体格检查,并进行了临床评估评分。父母完成了阻塞性睡眠呼吸暂停(OSA)-18、儿科生活质量量表(PedsQL)4.0 和儿童行为检查表问卷。经多导睡眠图检查阳性的儿童行腺样体扁桃体切除术或腺样体切除术。在平均 8 个月的随访时进行相同的评估。

结果

项目减少得到了 15 项的评分(临床评估评分-15 [CAS-15]),该评分表现出最佳的内部一致性和预测实用性(Cronbach α=0.80)。组内相关(ICC)显示良好的组内(ICC,0.78;95%置信区间[CI],0.58 至 0.89)和组间一致性(ICC,0.65;95%CI,0.26 至 0.84)。所有的变化评分在手术后均显著改善。CAS-15(2.6)、OSA-18(2.4)和呼吸暂停低通气指数(1.4)的效应量较大,而儿童行为检查表(0.7)和 PedsQL 4.0(-0.5)的效应量中等。初始 CAS-15 评分与外部测量之间存在中度至高度相关性(|r|在 0.32 至 0.65 之间)。构建了受试者工作特征曲线以确定预测多导睡眠图阳性的初始 CAS-15 最佳评分。曲线下面积为 0.77(95%CI,0.67 至 0.87);评分≥32 时,灵敏度为 77.3%(95%CI,65.3%至 86.7%),特异性为 60.7%(95%CI,40.6%至 78.5%)。

结论

CAS-15 在办公室环境中证明是有用的,与多导睡眠图相比,正确诊断了 72%的转诊儿童。它与外部测量很好地相关,并表现出对临床变化的良好反应。

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