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中文译文:《SNOT-22 中文版的翻译、跨文化调适及验证-针对立陶宛患者》。

Translation, cross-cultural adaptation, and validation of the sino-nasal outcome test (SNOT)-22 for Lithuanian patients.

机构信息

Department of Otorhinolaryngology, Medical Academy, Lithuanian University of Health Sciences, Eivenių 2, 50009 Kaunas, Lithuania.

出版信息

Eur Arch Otorhinolaryngol. 2013 May;270(6):1843-8. doi: 10.1007/s00405-012-2282-2. Epub 2012 Dec 1.

Abstract

The objective of this study was to perform translation, cross-cultural adaptation, and validation of the SNOT-22 in the Lithuanian language. This is a prospective case-control study. The study was conducted at the University clinic. The sino-nasal outcome test 22 (SNOT-22) was translated into the Lithuanian language; the pilot study involved 34 patients, the test-retest group consisted of 34 patients with chronic rhinosinusitis (CRS), and the control group of 115 patients with no CRS complaints; 36 patients were evaluated before surgery and 3 months after surgery. The results showed a good internal correlation with Cronbach's alpha-0.89 in the initial test, and 0.93 in the retest; both values suggesting good internal consistency within the SNOT-22. Pearson's correlation coefficient was 0.72 (p < 0.001), revealing good correlation between the initial scores and the retests scores. Our sample of healthy individuals had a median score of 12 points, and the instrument was capable of differentiating between the healthy and the patient group, demonstrating its validity (p < 0.0001). The statistically significant reduction in the post-operative scores, vis-à-vis pre-operative values, demonstrates the responsiveness of the instrument. The minimally important difference was 13 points in the SNOT-22 score. The Lithuanian version of the SNOT-22 is a valid instrument for assessing patients with CRS. It demonstrated good internal consistency, reproducibility, validity, and responsiveness.

摘要

本研究旨在将 SNOT-22 翻译成立陶宛语,并对其进行跨文化调适和验证。这是一项前瞻性病例对照研究。该研究在大学诊所进行。将鼻-鼻窦炎结局测试 22 项(SNOT-22)翻译成立陶宛语;初步研究涉及 34 例患者,重测组由 34 例慢性鼻-鼻窦炎(CRS)患者组成,对照组由 115 例无 CRS 症状的患者组成;36 例患者在术前和术后 3 个月进行评估。结果显示,初始测试的 Cronbach's alpha 值为 0.89,重测的 Cronbach's alpha 值为 0.93,均显示出 SNOT-22 内部一致性良好。Pearson 相关系数为 0.72(p < 0.001),表明初始评分与重测评分之间具有良好的相关性。我们的健康个体样本中位数得分为 12 分,该工具能够区分健康组和患者组,证明其具有有效性(p < 0.0001)。与术前相比,术后评分显著降低,表明该工具具有反应性。SNOT-22 评分的最小临床重要差异为 13 分。立陶宛语版 SNOT-22 是评估 CRS 患者的有效工具。它表现出良好的内部一致性、可重复性、有效性和反应性。

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