Olfactory testing with Sniffin' Sticks and University of Pennsylvania Smell Identification Test in Singapore.

IF 1.9
Margaret Ru Xiang Zhang, Yew Kwang Ong, Xinni Xu
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Abstract

Introduction: Sniffin' sticks (SS) and the University of Pennsylvania smell identification test (UPSIT) are widely used olfactory tests, but have not yet been validated in Singapore. The primary objective of our study was to compare the performance of the unmodified SS and UPSIT in healthy adults in Singapore. The clinical implication was illustrated with a group of patients with olfactory impairment.

Methods: The SS and UPSIT were prospectively administered to healthy adults at a tertiary otolaryngology clinic from 15 May 2023 to 31 July 2023. Primary outcome measures were identification scores, 10th percentile scores, diagnosed olfactory function, and number of unfamiliar test odours. A retrospective review of patients with olfactory impairment was then performed. We compare their diagnosed olfactory function before and after benchmarking against heathy participants' scores.

Results: Fifty healthy participants (mean age 34 ± 9.4 years) were recruited. With SS, the mean score was 12 ± 2.5 (out of 16) and the 10th percentile score was 10. With UPSIT, the mean score was 29.6 ± 5.8 (out of 40) and the 10th percentile score was 25.5. The SS and UPSIT categorised 22 (44.0%) and 46 (92.0%) healthy participants as having hyposmia/anosmia, respectively. Agreement between both tests was minimal (weighted Cohen's kappa -0.020, 95% CI -0.240 to 0.101, P = 0.626). Many test odours were unfamiliar (43.8% in SS vs. 47.5% in UPSIT). Seventy-one patients with olfactory impairment were then analysed. After adjustment, 13.9% (5/36) and 25.7% (9/35) of patients who underwent SS and UPSIT, respectively, had changes in diagnosed olfactory function.

Conclusion: Our findings show that olfactory identification tests must be adapted and validated for the Singapore population to ensure meaningful interpretation of results.

嗅探棒嗅觉测试和新加坡宾夕法尼亚大学嗅觉识别测试。
简介:嗅探棒(SS)和宾夕法尼亚大学气味识别测试(UPSIT)是广泛使用的嗅觉测试,但尚未在新加坡得到验证。我们研究的主要目的是比较未经改良的SS和UPSIT在新加坡健康成人中的表现。临床意义是通过一组嗅觉障碍患者来说明的。方法:于2023年5月15日至2023年7月31日在某三级耳鼻喉科门诊前瞻性地对健康成人进行SS和UPSIT。主要结果测量是识别分数、第10百分位分数、诊断嗅觉功能和不熟悉的测试气味的数量。然后对嗅觉障碍患者进行回顾性审查。我们将他们诊断出的嗅觉功能与健康参与者的得分进行比较。结果:招募50名健康受试者(平均年龄34±9.4岁)。SS的平均得分为12±2.5分(满分16分),第10百分位得分为10分。UPSIT的平均得分为29.6±5.8分(满分40分),第10百分位得分为25.5分。SS和UPSIT分别将22名(44.0%)和46名(92.0%)健康参与者归类为低嗅觉/嗅觉缺失。两个试验之间的一致性最小(加权Cohen’s kappa -0.020, 95% CI -0.240 ~ 0.101, P = 0.626)。许多测试气味是不熟悉的(在SS中为43.8%,在UPSIT中为47.5%)。然后对71例嗅觉障碍患者进行分析。调整后,分别有13.9%(5/36)和25.7%(9/35)接受SS和UPSIT的患者诊断嗅觉功能发生改变。结论:我们的研究结果表明,嗅觉识别测试必须适应和验证新加坡人口,以确保有意义的解释结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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