Paxlovid Is Associated With Lower Rates of Long COVID-19 Smell and Taste Disorders.

IF 7.2 2区 医学 Q1 OTORHINOLARYNGOLOGY
Esther Wang, Zara M Patel
{"title":"Paxlovid Is Associated With Lower Rates of Long COVID-19 Smell and Taste Disorders.","authors":"Esther Wang, Zara M Patel","doi":"10.1002/alr.23612","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Research is needed on treatments that prevent progression to long COVID-19 olfactory and gustatory dysfunction, which millions continue to suffer from. We sought to explore the utility of Paxlovid in decreasing rates of long COVID-19 smell and taste loss.</p><p><strong>Design: </strong>This case-control study at a single tertiary medical center examined patients who were acutely infected with COVID-19 and received Paxlovid from December 2021 to September 2023 and age-matched infected patients who did not receive Paxlovid. Occurrence of nasal congestion, rhinorrhea, facial pain/pressure and smell/taste loss were recorded both in the acute (<30 days for nasal congestion, rhinorrhea, facial pain/pressure; <90 days for smell/taste loss) and the long-term settings for both groups. Chi-square and t-tests were used to compare the two groups.</p><p><strong>Results: </strong>A total of 846 individuals had complete data (Paxlovid: 423, non-Paxlovid: 423). Significantly more individuals in the Paxlovid group experienced nasal congestion (p < 0.001) and rhinorrhea (p = 0.006) in the acute setting. However, resolution of these symptoms after 30 days did not differ between the Paxlovid and non-Paxlovid groups (p = 0.375 and p = 0.316, respectively). Facial pressure did not differ between the two groups in either the acute or long-term setting (p = 0.077 and p = 0.315). In the acute setting, there was no significant difference between groups in the number of patients experiencing olfactory/gustatory changes (p = 0.487). After taking Paxlovid however, individuals were less likely to experience long-term olfactory/gustatory changes (p < 0.001).</p><p><strong>Conclusions: </strong>Early intervention with Paxlovid may decrease the risk of long COVID-19 smell/taste changes. Further study with a randomized controlled trial would help providers know more definitively if they should consider this utility in preventing long-term smell and taste loss.</p>","PeriodicalId":13716,"journal":{"name":"International Forum of Allergy & Rhinology","volume":" ","pages":"e23612"},"PeriodicalIF":7.2000,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Forum of Allergy & Rhinology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/alr.23612","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Research is needed on treatments that prevent progression to long COVID-19 olfactory and gustatory dysfunction, which millions continue to suffer from. We sought to explore the utility of Paxlovid in decreasing rates of long COVID-19 smell and taste loss.

Design: This case-control study at a single tertiary medical center examined patients who were acutely infected with COVID-19 and received Paxlovid from December 2021 to September 2023 and age-matched infected patients who did not receive Paxlovid. Occurrence of nasal congestion, rhinorrhea, facial pain/pressure and smell/taste loss were recorded both in the acute (<30 days for nasal congestion, rhinorrhea, facial pain/pressure; <90 days for smell/taste loss) and the long-term settings for both groups. Chi-square and t-tests were used to compare the two groups.

Results: A total of 846 individuals had complete data (Paxlovid: 423, non-Paxlovid: 423). Significantly more individuals in the Paxlovid group experienced nasal congestion (p < 0.001) and rhinorrhea (p = 0.006) in the acute setting. However, resolution of these symptoms after 30 days did not differ between the Paxlovid and non-Paxlovid groups (p = 0.375 and p = 0.316, respectively). Facial pressure did not differ between the two groups in either the acute or long-term setting (p = 0.077 and p = 0.315). In the acute setting, there was no significant difference between groups in the number of patients experiencing olfactory/gustatory changes (p = 0.487). After taking Paxlovid however, individuals were less likely to experience long-term olfactory/gustatory changes (p < 0.001).

Conclusions: Early intervention with Paxlovid may decrease the risk of long COVID-19 smell/taste changes. Further study with a randomized controlled trial would help providers know more definitively if they should consider this utility in preventing long-term smell and taste loss.

Paxlovid与较低的COVID-19嗅觉和味觉障碍有关。
背景:需要研究预防进展为长期COVID-19嗅觉和味觉功能障碍的治疗方法,数百万人仍然患有这种疾病。我们试图探索Paxlovid在降低长期COVID-19嗅觉和味觉丧失率方面的效用。设计:该病例对照研究在单一三级医疗中心进行,检查了2021年12月至2023年9月期间急性感染COVID-19并接受Paxlovid治疗的患者以及未接受Paxlovid治疗的年龄匹配的感染患者。结果:846例患者资料完整(Paxlovid: 423例,非Paxlovid: 423例)。Paxlovid组在急性情况下出现鼻塞(p < 0.001)和鼻漏(p = 0.006)的个体明显更多。然而,30天后这些症状的缓解在Paxlovid组和非Paxlovid组之间没有差异(p = 0.375和p = 0.316)。两组的面部压力在急性和长期情况下均无差异(p = 0.077和p = 0.315)。在急性情况下,两组患者出现嗅觉/味觉变化的人数无显著差异(p = 0.487)。然而,服用Paxlovid后,个体不太可能经历长期的嗅觉/味觉变化(p < 0.001)。结论:Paxlovid早期干预可降低COVID-19长时间嗅觉/味觉改变的风险。通过一项随机对照试验进行的进一步研究将帮助提供者更明确地知道,他们是否应该考虑这种效用,以防止长期的嗅觉和味觉丧失。
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
11.70
自引率
10.90%
发文量
185
审稿时长
6-12 weeks
期刊介绍: International Forum of Allergy & Rhinologyis a peer-reviewed scientific journal, and the Official Journal of the American Rhinologic Society and the American Academy of Otolaryngic Allergy. International Forum of Allergy Rhinology provides a forum for clinical researchers, basic scientists, clinicians, and others to publish original research and explore controversies in the medical and surgical treatment of patients with otolaryngic allergy, rhinologic, and skull base conditions. The application of current research to the management of otolaryngic allergy, rhinologic, and skull base diseases and the need for further investigation will be highlighted.
×
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:481959085
Book学术官方微信