更新的韩国特应性皮炎诊断标准在韩国医院的临床验证。

IF 1.3
Seungah Yoo, Jaeeun Song, Jung Eun Kim, Ji Hae Lee, Hyun Ji Lee, Kyung Ho Lee, Yu Ri Woo, Young Bok Lee, Ji Hyun Lee, Sang Hyun Cho
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引用次数: 0

摘要

背景:特应性皮炎(AD)是一种常见的慢性炎症性皮肤病,由于缺乏明确的诊断试验或生物标志物,其诊断依赖于临床表现和病史。韩国特应性皮炎协会(KADA)最近更新了其诊断标准,以提高准确性和适用性。目的:本研究通过评估更新的KADA标准在临床环境中的诊断性能,并将其与以前的KADA和日本皮肤病协会(JDA)标准进行比较,验证了更新的KADA标准。方法:对231例AD患者和81例非AD对照组进行多中心横断面研究。分析入选标准和个体临床特征的敏感性、特异性、阳性预测值(PPV)、阴性预测值(NPV)、约登指数(Youden's index)和错误率。结果:与之前的KADA(61.04%)和JDA标准(47.62%)相比,更新后的KADA标准显示出最高的灵敏度(63.20%),能够更好地识别更广泛的AD表型。虽然其特异性(82.72%)略低于以前的KADA标准(88.89%)和JDA标准(95.06%),但更新后的标准保持了91.01%的PPV和44.10%的NPV。更新标准的约登指数为0.459,表明敏感性和特异性之间的平衡权衡,错误率最低(31.41%),强调其整体诊断准确性提高。结论:更新后的KADA标准提供了一种实用、直观的诊断工具,有效地解决了以往标准的局限性,提高了对AD的高效、全面诊断,特别是对表现多样的AD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical Validation of the Updated Korean Atopic Dermatitis Diagnostic Criteria in a Hospital Setting in South Korea.

Clinical Validation of the Updated Korean Atopic Dermatitis Diagnostic Criteria in a Hospital Setting in South Korea.

Clinical Validation of the Updated Korean Atopic Dermatitis Diagnostic Criteria in a Hospital Setting in South Korea.

Clinical Validation of the Updated Korean Atopic Dermatitis Diagnostic Criteria in a Hospital Setting in South Korea.

Background: Atopic dermatitis (AD) is a common chronic inflammatory skin disease whose diagnosis relies on clinical presentation and history due to the absence of definitive diagnostic tests or biomarkers. The Korean Atopic Dermatitis Association (KADA) recently updated its diagnostic criteria to enhance accuracy and applicability.

Objective: This study validates the updated KADA criteria by assessing their diagnostic performance in a clinical setting and comparing them with the previous KADA and Japanese Dermatological Association (JDA) criteria.

Methods: A multicenter, cross-sectional study was conducted with 231 AD patients and 81 non-AD controls. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), Youden's index, and error rates for the criteria and individual clinical features included were analyzed.

Results: The updated KADA criteria demonstrated the highest sensitivity (63.20%) compared to the previous KADA (61.04%) and JDA criteria (47.62%), enabling better identification of a broader range of AD phenotypes. While its specificity (82.72%) was slightly lower than that of the previous KADA (88.89%) and JDA criteria (95.06%), the updated criteria maintained a strong PPV of 91.01% and a comparable NPV of 44.10%. The Youden's index for the updated criteria was 0.459, indicating a balanced trade-off between sensitivity and specificity, and the error rate was the lowest (31.41%), underscoring its enhanced overall diagnostic accuracy.

Conclusion: The updated KADA criteria provide a practical and intuitive diagnostic tool, effectively addressing the limitations of previous criteria and improving the efficient and comprehensive diagnosis of AD, especially in those with diverse presentations.

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