• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

成人囊性纤维化患者高效调节剂治疗后鼻腔鼻窦改善的预测因素。

Predictors of Sinonasal Improvement After Highly Effective Modulator Therapy in Adults with Cystic Fibrosis.

机构信息

Department of Otolaryngology-Head and Neck Surgery, University of California, Los Angeles, California, U.S.A.

Department of Otolaryngology-Head and Neck Surgery, Columbia University, New York, New York, U.S.A.

出版信息

Laryngoscope. 2024 Sep;134(9):3965-3973. doi: 10.1002/lary.31438. Epub 2024 Apr 18.

DOI:10.1002/lary.31438
PMID:38634358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11305934/
Abstract

OBJECTIVES

The 22-question SinoNasal Outcome Test (SNOT-22) assesses chronic rhinosinusitis (CRS) severity. We aimed to identify predictors of SNOT-22 score improvement following highly effective modulator therapy (HEMT) initiation and to corroborate the SNOT-22 minimal clinically important difference (MCID) in adults with cystic fibrosis (CF).

METHODS

Prospective observational data was pooled from four studies across 10 US centers investigating people with CF (PwCF) and CRS. Three studies evaluated HEMT's impact on CRS. For participants enrolled prior to HEMT initiation, SNOT-22 scores were obtained at baseline and after 3-6 months of HEMT. Multivariate regression identified predictors of improvement. Cronbach's alpha and four distribution-based methods were used to assess internal consistency and calculate the MCID of the SNOT-22.

RESULTS

A total of 184 PwCF participated with mean baseline SNOT-22 scores ranging from 18.1 to 56.7. Cronbach's alpha was ≥0.90 across sites. Participants at sites with pre- and post-HEMT data reported improvement in SNOT-22 scores after initiating HEMT (all p < 0.05). Worse baseline SNOT-22 score (odds ratio (OR): 1.05, p < 0.001, 95% CI: 1.02-1.08), F508del homozygosity (OR: 4.30, p = 0.040, 95% CI: 1.14-18.99), and absence of prior modulator therapy (OR: 4.99, p = 0.017, 95% CI: 1.39-20.11) were associated with greater SNOT-22 improvement. The mean MCID calculated via distribution-based methods was 8.5.

CONCLUSION

Worse baseline sinonasal symptoms, F508del homozygosity, and absence of prior modulator therapy predicted greater improvement after HEMT initiation. The mean MCID for SNOT-22 in PwCF is 8.5 points, similar to non-CF individuals with CRS, and provides a threshold specifically for PwCF. The SNOT-22 has strong internal consistency in PwCF.

LEVEL OF EVIDENCE

3 Laryngoscope, 134:3965-3973, 2024.

摘要

目的

22 项鼻鼻窦结局测试(SNOT-22)评估慢性鼻-鼻窦炎(CRS)的严重程度。我们旨在确定在开始高效调节剂治疗(HEMT)后 SNOT-22 评分改善的预测因素,并在囊性纤维化(CF)成人中证实 SNOT-22 的最小临床重要差异(MCID)。

方法

前瞻性观察性数据来自四个研究,这些研究在美国 10 个中心调查了囊性纤维化患者(PwCF)和 CRS。三项研究评估了 HEMT 对 CRS 的影响。对于在 HEMT 开始前入组的参与者,在基线和 HEMT 开始后 3-6 个月时获得 SNOT-22 评分。多变量回归确定了改善的预测因素。克朗巴赫的 α和四种基于分布的方法用于评估内部一致性并计算 SNOT-22 的 MCID。

结果

共有 184 名 PwCF 参与,平均基线 SNOT-22 评分范围为 18.1 至 56.7。在各个站点,克朗巴赫的α值均≥0.90。在有 HEMT 前后数据的参与者中,在开始 HEMT 后报告 SNOT-22 评分改善(均 p<0.05)。更差的基线 SNOT-22 评分(比值比(OR):1.05,p<0.001,95%CI:1.02-1.08)、F508del 纯合性(OR:4.30,p=0.040,95%CI:1.14-18.99)和缺乏先前的调节剂治疗(OR:4.99,p=0.017,95%CI:1.39-20.11)与更大的 SNOT-22 改善相关。通过分布基础方法计算的平均 MCID 为 8.5。

结论

更差的基线鼻-鼻窦症状、F508del 纯合性和缺乏先前的调节剂治疗预测了 HEMT 启动后更大的改善。SNOT-22 在 PwCF 中的平均 MCID 为 8.5 分,与患有 CRS 的非 CF 个体相似,为 PwCF 提供了一个特定的阈值。SNOT-22 在 PwCF 中具有很强的内部一致性。

证据水平

3 级喉镜,134:3965-3973,2024。

相似文献

1
Predictors of Sinonasal Improvement After Highly Effective Modulator Therapy in Adults with Cystic Fibrosis.成人囊性纤维化患者高效调节剂治疗后鼻腔鼻窦改善的预测因素。
Laryngoscope. 2024 Sep;134(9):3965-3973. doi: 10.1002/lary.31438. Epub 2024 Apr 18.
2
Corrector therapies (with or without potentiators) for people with cystic fibrosis with class II CFTR gene variants (most commonly F508del).针对携带 II 类 CFTR 基因突变(最常见的是 F508del)的囊性纤维化患者的校正治疗(有或没有增效剂)。
Cochrane Database Syst Rev. 2023 Nov 20;11(11):CD010966. doi: 10.1002/14651858.CD010966.pub4.
3
Determining the minimal clinically important difference for the questionnaire of olfactory disorders in people with cystic fibrosis and factors associated with improvement after highly effective modulator therapy.确定囊性纤维化患者嗅觉障碍问卷的最小临床重要差异,以及与高效调节剂治疗后改善相关的因素。
Int Forum Allergy Rhinol. 2024 Jun;14(6):1079-1087. doi: 10.1002/alr.23312. Epub 2023 Dec 25.
4
Vanzacaftor-tezacaftor-deutivacaftor versus elexacaftor-tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years and older (SKYLINE Trials VX20-121-102 and VX20-121-103): results from two randomised, active-controlled, phase 3 trials.12岁及以上囊性纤维化患者使用万扎卡托-替扎卡托-地替瓦卡托与依列卡托-替扎卡托-艾伐卡托的对比研究(SKYLINE试验VX20 - 121 - 102和VX20 - 121 - 103):两项随机、活性对照3期试验的结果
Lancet Respir Med. 2025 Mar;13(3):256-271. doi: 10.1016/S2213-2600(24)00411-9. Epub 2025 Jan 2.
5
Olfaction, Eating Preference, and Quality of Life in Cystic Fibrosis Chronic Rhinosinusitis.囊性纤维化慢性鼻-鼻窦炎患者的嗅觉、饮食偏好及生活质量
Laryngoscope. 2025 Jul;135(7):2476-2488. doi: 10.1002/lary.32155. Epub 2025 Mar 29.
6
Potentiators (specific therapies for class III and IV mutations) for cystic fibrosis.囊性纤维化的增效剂(针对III类和IV类突变的特定疗法)。
Cochrane Database Syst Rev. 2015 Mar 26(3):CD009841. doi: 10.1002/14651858.CD009841.pub2.
7
Beyond the Lung. Impact of Elexacaftor/Tezacaftor/Ivacaftor on Sinonasal Disease in Children With Cystic Fibrosis.肺部之外。依列卡福妥/替扎卡福妥/依伐卡托对囊性纤维化儿童鼻窦疾病的影响。
Int Forum Allergy Rhinol. 2025 Jul;15(7):715-723. doi: 10.1002/alr.23557. Epub 2025 Mar 6.
8
Evaluation of elexacaftor-tezacaftor-ivacaftor treatment in individuals with cystic fibrosis and CFTR in the USA: a prospective, multicentre, open-label, single-arm trial.在美国对患有囊性纤维化和CFTR的个体进行的依列卡福托-替扎卡福托-依伐卡托治疗评估:一项前瞻性、多中心、开放标签、单臂试验。
Lancet Respir Med. 2024 Dec;12(12):947-957. doi: 10.1016/S2213-2600(24)00205-4. Epub 2024 Aug 26.
9
Elexacaftor-Tezacaftor-Ivacaftor Improves Sinonasal Outcomes in Young Children With Cystic Fibrosis.依列卡福妥-替扎卡福妥-依伐卡福妥改善了患有囊性纤维化的幼儿的鼻窦结局。
Int Forum Allergy Rhinol. 2025 Jul;15(7):706-714. doi: 10.1002/alr.23555. Epub 2025 Mar 2.
10
Impact of Cystic Fibrosis Transmembrane Conductance Regulator Modulators on Maternal Outcomes During and After Pregnancy.囊性纤维化跨膜传导调节因子调节剂对孕期及产后母体结局的影响。
Chest. 2025 Feb;167(2):348-361. doi: 10.1016/j.chest.2024.09.019. Epub 2024 Sep 27.

引用本文的文献

1
Evaluation of Elexacafor/Tezacaftor/Ivacaftor therapy after lung transplantation in Cystic Fibrosis: The Dutch National KOALA study.囊性纤维化患者肺移植后使用依列卡福/替扎卡福/依伐卡托治疗的评估:荷兰全国性考拉研究
JHLT Open. 2025 Jan 17;7:100210. doi: 10.1016/j.jhlto.2025.100210. eCollection 2025 Feb.
2
Elexacaftor-Tezacaftor-Ivacaftor Improves Sinonasal Outcomes in Young Children With Cystic Fibrosis.依列卡福妥-替扎卡福妥-依伐卡福妥改善了患有囊性纤维化的幼儿的鼻窦结局。
Int Forum Allergy Rhinol. 2025 Jul;15(7):706-714. doi: 10.1002/alr.23555. Epub 2025 Mar 2.

本文引用的文献

1
Factors that predict pursuing sinus surgery in the era of highly effective modulator therapy.预测在高效调节剂治疗时代行鼻窦手术的因素。
Int Forum Allergy Rhinol. 2024 Apr;14(4):807-818. doi: 10.1002/alr.23270. Epub 2023 Sep 19.
2
Chronic rhinosinusitis in the era of CFTR modulator therapy.囊性纤维化跨膜传导调节因子(CFTR)调节剂治疗时代的慢性鼻-鼻窦炎。
J Cyst Fibros. 2024 Mar;23(2):208-213. doi: 10.1016/j.jcf.2023.08.009. Epub 2023 Sep 9.
3
Elexacaftor-Tezacaftor- Ivacaftor improves sinonasal outcomes in cystic fibrosis.依伐卡托与泰他卡托和艾美卡替联合治疗可改善囊性纤维化患者的鼻窦结局。
J Cyst Fibros. 2022 Sep;21(5):792-799. doi: 10.1016/j.jcf.2022.03.002. Epub 2022 Mar 14.
4
Cystic Fibrosis Foundation otolaryngology care multidisciplinary consensus recommendations.囊性纤维化基金会耳鼻喉科多学科护理共识建议。
Int Forum Allergy Rhinol. 2022 Sep;12(9):1089-1103. doi: 10.1002/alr.22974. Epub 2022 Feb 22.
5
Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical Trial.依伐卡托/泰它卡托/艾氟卡托治疗囊性纤维化的临床疗效:一项临床试验。
Am J Respir Crit Care Med. 2022 Mar 1;205(5):529-539. doi: 10.1164/rccm.202108-1986OC.
6
Multi-institutional minimal clinically important difference of the 22-item Sinonasal Outcome Test in medically managed chronic rhinosinusitis.多机构医学管理下慢性鼻-鼻窦炎 22 项鼻鼻窦结局测试的最小临床重要差异。
Rhinology. 2021 Dec 1;59(6):552-559. doi: 10.4193/Rhin21.253.
7
Impact of Cystic Fibrosis Transmembrane Conductance Regulator Therapy on Chronic Rhinosinusitis and Health Status: Deep Learning CT Analysis and Patient-reported Outcomes.囊性纤维化跨膜电导调节因子治疗对慢性鼻-鼻窦炎及健康状况的影响:深度学习 CT 分析与患者报告结局。
Ann Am Thorac Soc. 2022 Jan;19(1):12-19. doi: 10.1513/AnnalsATS.202101-057OC.
8
Inflammatory cytokines TNF-α and IL-17 enhance the efficacy of cystic fibrosis transmembrane conductance regulator modulators.炎性细胞因子 TNF-α 和 IL-17 增强囊性纤维化跨膜电导调节剂调节剂的疗效。
J Clin Invest. 2021 Aug 16;131(16). doi: 10.1172/JCI150398.
9
Airway Epithelial Inflammation Augments the Rescue of Mutant CFTR by Current CFTR Modulator Therapies.气道上皮炎症增强了当前CFTR调节剂疗法对突变型CFTR的挽救作用。
Front Pharmacol. 2021 Mar 30;12:628722. doi: 10.3389/fphar.2021.628722. eCollection 2021.
10
Effect of highly effective modulator therapy on quality of life in adults with cystic fibrosis.高效调节剂治疗对囊性纤维化成人生活质量的影响。
Int Forum Allergy Rhinol. 2021 Jan;11(1):75-78. doi: 10.1002/alr.22700. Epub 2020 Sep 28.