Suppr超能文献

肺功能与囊性纤维化呼吸道症状日记-慢性呼吸道感染症状评分(CFRSD-CRISS)中症状测量的相关性。

Correspondence between lung function and symptom measures from the Cystic Fibrosis Respiratory Symptom Diary-Chronic Respiratory Infection Symptom Score (CFRSD-CRISS).

机构信息

Department of Radiology, University of Washington, Seattle, Washington, United States.

Department of Health Services, University of Washington, Seattle, Washington, United States.

出版信息

J Cyst Fibros. 2019 Nov;18(6):886-893. doi: 10.1016/j.jcf.2019.05.009. Epub 2019 May 22.

Abstract

BACKGROUND

Pulmonary exacerbations (PEx) in cystic fibrosis (CF) patients reduce quality of life. Lung function, measured by the percent predicted forced expiratory volume in 1 s (ppFEV1), is widely used to evaluate PEx treatments. We analyzed the correspondence of ppFEV1 with 8 patient-reported symptom-based questions from the Cystic Fibrosis Respiratory Symptom Diary-Chronic Respiratory Infection Symptom Score (CFRSD-CRISS).

METHODS

Data were derived from the observational Standardized Treatment of Pulmonary Exacerbations (STOP) study. CF patients who had CFRSD-CRISS and ppFEV1 measurements on ≥2 timepoints were included: 1) day of initial PEx, 2) 7 days later, and/or 3) end of PEx. We calculated age-stratified Spearman correlation coefficients and 95% confidence intervals (95% CIs) between the change in ppFEV1 and change in CFRSD-CRISS items from index to day 7 and from index to the end of PEx treatment.

RESULTS

Lung function and symptom scores improved by the end of treatment; however, correlations between ppFEV1 and the specific CFRSD-CRISS measures were mostly weak to moderate. An exception was that among patients <18, we observed moderately strong correlations between changes in ppFEV1 and cough severity (r = -0.58 (95% CI: -0.80, -0.21)), mucus quantity (r = -0.51 (-0.77, -0.11)), and wheezing (r = -0.53 (-0.78, -0.14)) from index until end of treatment.

CONCLUSIONS

As novel treatments are developed for PEx, it is important to ensure that improvement is measured meaningfully. The generally weak associations between patient-reported symptoms and ppFEV1 that we found suggest that these measures capture different aspects of the disease and both metrics are important when evaluating new treatments.

摘要

背景

囊性纤维化(CF)患者的肺部恶化(PEx)会降低生活质量。通过测量预计用力呼气量的百分比(ppFEV1)来评估肺功能,这是广泛用于评估 PEx 治疗的方法。我们分析了 ppFEV1 与来自囊性纤维化呼吸症状日记-慢性呼吸道感染症状评分(CFRSD-CRISS)的 8 个基于患者报告的症状问题之间的对应关系。

方法

数据来自观察性标准化治疗肺部恶化(STOP)研究。纳入了在至少 2 个时间点有 CFRSD-CRISS 和 ppFEV1 测量值的 CF 患者:1)初始 PEx 当天,2)7 天后,和/或 3)PEx 结束时。我们计算了 ppFEV1 变化与从指数到第 7 天以及从指数到 PEx 治疗结束时的 CFRSD-CRISS 项目变化之间的年龄分层 Spearman 相关系数和 95%置信区间(95%CI)。

结果

在治疗结束时,肺功能和症状评分均有所改善;然而,ppFEV1 与特定 CFRSD-CRISS 测量值之间的相关性大多较弱至中度。一个例外是,在年龄<18 岁的患者中,我们观察到 ppFEV1 的变化与咳嗽严重程度(r = -0.58(95%CI:-0.80,-0.21))、黏液量(r = -0.51(-0.77,-0.11))和喘息(r = -0.53(-0.78,-0.14))之间存在较强的相关性,从指数开始直至治疗结束。

结论

随着针对 PEx 的新疗法的开发,重要的是确保改善得到有意义的衡量。我们发现,患者报告的症状与 ppFEV1 之间的关联普遍较弱,这表明这些测量方法捕捉到了疾病的不同方面,在评估新疗法时这两种方法都很重要。

相似文献

2
Correspondence between symptoms and preference-based health status measures in the STOP study.
J Cyst Fibros. 2019 Mar;18(2):251-264. doi: 10.1016/j.jcf.2018.08.001. Epub 2018 Aug 29.
4
The effect of oral and intravenous antimicrobials on pulmonary exacerbation recovery in cystic fibrosis.
J Cyst Fibros. 2021 Nov;20(6):932-936. doi: 10.1016/j.jcf.2021.02.012. Epub 2021 Mar 5.
5
Association between elevated peripheral blood eosinophil count and respiratory outcomes in adults with cystic fibrosis.
J Cyst Fibros. 2022 Nov;21(6):1048-1052. doi: 10.1016/j.jcf.2022.03.009. Epub 2022 Mar 31.
8
Lung function changes before and after pulmonary exacerbation antimicrobial treatment in cystic fibrosis.
Pediatr Pulmonol. 2020 Mar;55(3):828-834. doi: 10.1002/ppul.24577. Epub 2019 Nov 20.

引用本文的文献

1
Symptom factors and their clinical correlates among adults with cystic fibrosis.
J Cyst Fibros. 2025 Jul 8. doi: 10.1016/j.jcf.2025.07.001.
6
Adjunctive Systemic Corticosteroids for Pulmonary Exacerbations of Cystic Fibrosis.
Ann Am Thorac Soc. 2024 May;21(5):716-726. doi: 10.1513/AnnalsATS.202308-673OC.
8
Pulmonary Function and Quality of Life in Adults with Cystic Fibrosis.
Lung. 2023 Dec;201(6):635-639. doi: 10.1007/s00408-023-00658-y. Epub 2023 Nov 16.
10
Health care costs related to home spirometry in the eICE randomized trial.
J Cyst Fibros. 2022 Jan;21(1):61-69. doi: 10.1016/j.jcf.2021.02.014. Epub 2021 Mar 12.

本文引用的文献

1
2
Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis-A Cross Sectional Study.
Front Pediatr. 2018 Sep 4;6:244. doi: 10.3389/fped.2018.00244. eCollection 2018.
3
Dornase alfa for cystic fibrosis.
Cochrane Database Syst Rev. 2018 Sep 6;9(9):CD001127. doi: 10.1002/14651858.CD001127.pub4.
4
Correspondence between symptoms and preference-based health status measures in the STOP study.
J Cyst Fibros. 2019 Mar;18(2):251-264. doi: 10.1016/j.jcf.2018.08.001. Epub 2018 Aug 29.
5
"Thrust out of normality"-How adults living with cystic fibrosis experience pulmonary exacerbations: A qualitative study.
J Clin Nurs. 2019 Jan;28(1-2):190-200. doi: 10.1111/jocn.14646. Epub 2018 Aug 29.
6
Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del.
N Engl J Med. 2017 Nov 23;377(21):2013-2023. doi: 10.1056/NEJMoa1709846. Epub 2017 Nov 3.
9
Rationalizing endpoints for prospective studies of pulmonary exacerbation treatment response in cystic fibrosis.
J Cyst Fibros. 2017 Sep;16(5):607-615. doi: 10.1016/j.jcf.2017.04.004. Epub 2017 Apr 21.
10
Frequency and costs of pulmonary exacerbations in patients with cystic fibrosis in the United States.
Curr Med Res Opin. 2017 Apr;33(4):667-674. doi: 10.1080/03007995.2016.1277196. Epub 2017 Feb 9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验