Topical Anesthesia and Olfactory Capability: A Pilot Study

IF 1.7 4区 医学 Q2 OTORHINOLARYNGOLOGY
Maxime Fieux, Esther Wang, David T. Liu, Zara M. Patel
{"title":"Topical Anesthesia and Olfactory Capability: A Pilot Study","authors":"Maxime Fieux,&nbsp;Esther Wang,&nbsp;David T. Liu,&nbsp;Zara M. Patel","doi":"10.1002/lio2.70250","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Introduction</h3>\n \n <p>Topical anesthesia (TA) of the nasal fossa has been shown to be sufficient for patient comfort during nasal endoscopy. However, investigators need to know how soon after the administration of TA they can accurately evaluate olfactory capability. Thus, the main aim of this study was to assess, in healthy volunteers (HV), when the effects of TA wear off to accurately measure olfactory capability after its administration.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A prospective, single-center, pilot study was conducted to evaluate the duration of the effect of TA on olfactory capability, using the UPSIT. Thirty healthy volunteers were recruited and analyzed. Following baseline testing (UPSIT), TA was administered intranasally (lidocaine + oxymetazoline). Then, participants underwent three additional UPSIT evaluations at distinct time points: immediately post-application (T0), 10 min (T + 10), and 30 min post-application (T + 30). The primary outcome was the change in UPSIT score from baseline to each subsequent time point. Paired <i>t</i>-tests were applied to compare within-subject score differences across time points. Significance was defined as <i>p</i> &lt; 0.05, and the R software was used.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>For the 30 HV included, the mean UPSIT at T0 was 32.8 ± 3.1. At T1, the mean UPSIT (29.6 ± 4.0) was significantly lower than at T0 (3.13 ± 3.7-point, <i>p</i> &lt; 0.0001). At T2, the mean UPSIT was 31.7 ± 4.2, without any significant difference from T0 (−1.03 ± 3.5-point, <i>p</i> = 0.350). At T3, the mean UPSIT was 31.7 ± 3.1, without any significant difference compared to T0 (−1.07 ± 2.6-point, <i>p</i> = 0.067). Regarding subgroup analysis between healthy volunteers with or without ITH, their own perception of smell and UPSIT were significantly different.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Immediately after receiving 4 sprays per nostril, the mean UPSIT—with testing begun directly after the spray was administered—was significantly lower than baseline, dropping under the threshold for normal olfactory function. It was fully recovered by ten min.</p>\n </section>\n \n <section>\n \n <h3> Level of Evidence</h3>\n \n <p>3.</p>\n </section>\n </div>","PeriodicalId":48529,"journal":{"name":"Laryngoscope Investigative Otolaryngology","volume":"10 5","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.70250","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laryngoscope Investigative Otolaryngology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/lio2.70250","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Topical anesthesia (TA) of the nasal fossa has been shown to be sufficient for patient comfort during nasal endoscopy. However, investigators need to know how soon after the administration of TA they can accurately evaluate olfactory capability. Thus, the main aim of this study was to assess, in healthy volunteers (HV), when the effects of TA wear off to accurately measure olfactory capability after its administration.

Methods

A prospective, single-center, pilot study was conducted to evaluate the duration of the effect of TA on olfactory capability, using the UPSIT. Thirty healthy volunteers were recruited and analyzed. Following baseline testing (UPSIT), TA was administered intranasally (lidocaine + oxymetazoline). Then, participants underwent three additional UPSIT evaluations at distinct time points: immediately post-application (T0), 10 min (T + 10), and 30 min post-application (T + 30). The primary outcome was the change in UPSIT score from baseline to each subsequent time point. Paired t-tests were applied to compare within-subject score differences across time points. Significance was defined as p < 0.05, and the R software was used.

Results

For the 30 HV included, the mean UPSIT at T0 was 32.8 ± 3.1. At T1, the mean UPSIT (29.6 ± 4.0) was significantly lower than at T0 (3.13 ± 3.7-point, p < 0.0001). At T2, the mean UPSIT was 31.7 ± 4.2, without any significant difference from T0 (−1.03 ± 3.5-point, p = 0.350). At T3, the mean UPSIT was 31.7 ± 3.1, without any significant difference compared to T0 (−1.07 ± 2.6-point, p = 0.067). Regarding subgroup analysis between healthy volunteers with or without ITH, their own perception of smell and UPSIT were significantly different.

Conclusion

Immediately after receiving 4 sprays per nostril, the mean UPSIT—with testing begun directly after the spray was administered—was significantly lower than baseline, dropping under the threshold for normal olfactory function. It was fully recovered by ten min.

Level of Evidence

3.

Abstract Image

局部麻醉与嗅觉能力:一项初步研究
鼻窝表面麻醉(TA)已被证明足以使患者在鼻内窥镜检查时感到舒适。然而,研究人员需要知道在给予TA多长时间后,他们可以准确地评估嗅觉能力。因此,本研究的主要目的是在健康志愿者(HV)中评估TA的作用何时消退,以准确测量其给药后的嗅觉能力。方法采用前瞻性、单中心、先导研究,采用UPSIT评估TA对嗅觉能力影响的持续时间。招募并分析了30名健康志愿者。在基线测试(UPSIT)之后,TA经鼻给药(利多卡因+ oxymetazoline)。然后,参与者在不同的时间点进行了三次额外的UPSIT评估:应用后立即(T0), 10分钟(T + 10)和应用后30分钟(T + 30)。主要结果是UPSIT评分从基线到每个后续时间点的变化。采用配对t检验比较各时间点受试者内得分差异。显著性定义为p <; 0.05,采用R软件。结果30 HV患者T0时的平均UPSIT为32.8±3.1。T1时,平均UPSIT(29.6±4.0)显著低于T0时(3.13±3.7点,p < 0.0001)。T2时,平均UPSIT为31.7±4.2,与T0无显著差异(- 1.03±3.5点,p = 0.350)。T3时,平均UPSIT为31.7±3.1,与T0相比无显著差异(- 1.07±2.6点,p = 0.067)。在亚组分析中,有或没有ITH的健康志愿者自身的嗅觉和UPSIT有显著差异。结论每鼻孔喷4次后,平均upsit(喷药后立即开始测试)显著低于基线,降至正常嗅觉功能阈值以下。十分钟后就完全恢复了,证据等级三级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.00
自引率
0.00%
发文量
245
审稿时长
11 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信