• 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

修订后的囊性纤维化问卷 (CFQ-R Teen/Adult) 的开发和电子验证:监测 CF 患者心理健康的新工具。

Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult): New tool for monitoring psychosocial health in CF.

机构信息

Adult CF and Lung Transplant Unit, University Hospital la Fe, University of Valencia, Valencia, Spain.

UGC de Enfermedades Respiratorias, Hospital Regional Universitario / Universidad de Málaga, Instituto de Investigación Biomédica de Málaga, Spain.

出版信息

J Cyst Fibros. 2018 Sep;17(5):672-679. doi: 10.1016/j.jcf.2017.10.015. Epub 2017 Nov 20.

DOI:10.1016/j.jcf.2017.10.015
PMID:29157922
Abstract

BACKGROUND

The Cystic Fibrosis Questionnaire-Revised (CFQ-R+14) is a disease-specific, health-related quality of life instrument for cystic fibrosis (CF) patients ≥14years. We have developed a Spanish electronic version of the CFQ-R (e-CFQ-R+14 Spain). Our aim was to compare the paper and electronic versions and to validate the electronic version.

METHODS

Fifty CF patients completed the study. All answered the paper and electronic versions on day 1 and repeated the e-CFQR version 15days later.

RESULTS

Concordance between the electronic and paper copy versions was high, with correlations above 0.9 in all domains. Test-retest reliability of the e-CFQ-R results was strong, with coefficients ranging from 0.8 to 0.9.

CONCLUSIONS

The e-CFQ-R version is reliable and valid and can replace the paper copy, thus simplifying the assessment of quality of life. It also provides immediate results with no errors in scoring. It is a useful new tool in CF care.

摘要

背景

囊性纤维化问卷修订版(CFQ-R+14)是一种针对囊性纤维化(CF)患者≥14 岁的特定疾病、与健康相关的生活质量工具。我们已经开发了 CFQ-R 的西班牙语电子版本(e-CFQ-R+14 西班牙)。我们的目的是比较纸质版和电子版,并验证电子版的有效性。

方法

50 名 CF 患者完成了这项研究。所有患者在第 1 天同时回答纸质版和电子版问卷,并在 15 天后再次重复回答电子版 CFQ-R 问卷。

结果

电子版本和纸质副本之间的一致性很高,所有领域的相关性均高于 0.9。e-CFQ-R 结果的重测信度很强,系数范围为 0.8 至 0.9。

结论

e-CFQ-R 版本可靠且有效,可以替代纸质副本,从而简化生活质量评估。它还提供即时结果,不存在评分错误。它是 CF 护理中的一种有用的新工具。

相似文献

1
Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult): New tool for monitoring psychosocial health in CF.修订后的囊性纤维化问卷 (CFQ-R Teen/Adult) 的开发和电子验证:监测 CF 患者心理健康的新工具。
J Cyst Fibros. 2018 Sep;17(5):672-679. doi: 10.1016/j.jcf.2017.10.015. Epub 2017 Nov 20.
2
Development and validation of The Cystic Fibrosis Questionnaire in the United States: a health-related quality-of-life measure for cystic fibrosis.美国囊性纤维化问卷的编制与验证:一项针对囊性纤维化的健康相关生活质量测量工具
Chest. 2005 Oct;128(4):2347-54. doi: 10.1378/chest.128.4.2347.
3
[Validation of the Spanish version of the Revised Cystic Fibrosis Quality of Life Questionnaire in adolescents and adults (CFQR 14+ Spain)].[《修订版囊性纤维化青少年及成人生活质量问卷(CFQR 14+西班牙版)》的验证]
Arch Bronconeumol. 2010 Apr;46(4):165-75. doi: 10.1016/j.arbres.2010.01.006. Epub 2010 Mar 20.
4
Validation of the Danish version of the revised cystic fibrosis quality of life questionnaire in adolescents and adults (CFQ-R14+).丹麦版修订的青少年及成人囊性纤维化生活质量问卷(CFQ-R14+)的验证
J Cyst Fibros. 2008 Nov;7(6):531-6. doi: 10.1016/j.jcf.2008.06.006. Epub 2008 Aug 9.
5
Spanish adaptation and validation of the child- and parent-report cystic fibrosis questionnaire-revised (CFQ-R).西班牙语版儿童和家长报告囊性纤维化问卷修订版(CFQ-R)的适应和验证。
Pediatr Pulmonol. 2023 Dec;58(12):3447-3457. doi: 10.1002/ppul.26671. Epub 2023 Sep 13.
6
Psychometric evaluation of the Swedish translation of the revised Cystic Fibrosis Questionnaire in adults.成人版修订囊性纤维化问卷瑞典语翻译的心理测量学评估
Ups J Med Sci. 2017 Mar;122(1):61-66. doi: 10.1080/03009734.2016.1225871. Epub 2016 Sep 15.
7
Impact of bronchiectasis and trapped air on quality of life and exacerbations in cystic fibrosis.支气管扩张症和空气潴留对囊性纤维化患者生活质量和加重的影响。
Eur Respir J. 2013 Aug;42(2):371-9. doi: 10.1183/09031936.00137612. Epub 2013 Jan 11.
8
Easy measurement of health related quality of life in patients with cystic fibrosis by the COPD assessment test (CAT) - A pilot study.通过 COPD 评估测试 (CAT) 对囊性纤维化患者的健康相关生活质量进行简单测量 - 一项初步研究。
Respir Med. 2020 Jul;168:105992. doi: 10.1016/j.rmed.2020.105992. Epub 2020 Apr 30.
9
Longitudinal trends in health-related quality of life in adults with cystic fibrosis.成人囊性纤维化患者健康相关生活质量的纵向趋势。
Chest. 2013 Sep;144(3):981-989. doi: 10.1378/chest.12-1404.
10
Development of the Cystic Fibrosis Questionnaire-Revised-8 Dimensions: Estimating Utilities From the Cystic Fibrosis Questionnaire-Revised.囊性纤维化问卷修订版 - 8维度的开发:从囊性纤维化问卷修订版估计效用值
Value Health. 2023 Apr;26(4):567-578. doi: 10.1016/j.jval.2022.12.002. Epub 2022 Dec 9.

引用本文的文献

1
The Validity and Reliability of the Turkish Version of the AWESCORE Test.AWESCORE测试土耳其语版本的有效性和可靠性。
Turk Arch Pediatr. 2025 Mar 3;60(2):147-152. doi: 10.5152/TurkArchPediatr.2025.24199.
2
Tools used to measure quality of life in adults with cystic fibrosis- a systematic review.用于测量成年囊性纤维化患者生活质量的工具——一项系统综述。
Health Qual Life Outcomes. 2025 Feb 4;23(1):10. doi: 10.1186/s12955-025-02338-2.
3
Development of a Miniaturized Mechanoacoustic Sensor for Continuous, Objective Cough Detection, Characterization and Physiologic Monitoring in Children With Cystic Fibrosis.
用于囊性纤维化儿童连续、客观咳嗽检测、特征描述和生理监测的微型机械声传感器的研制。
IEEE J Biomed Health Inform. 2024 Oct;28(10):5941-5952. doi: 10.1109/JBHI.2024.3415479. Epub 2024 Oct 3.
4
Implementing Remote Patient Monitoring of Physical Activity in Clinical Practice.在临床实践中实施远程患者体力活动监测。
Rehabil Nurs. 2023;48(6):209-215. doi: 10.1097/RNJ.0000000000000435. Epub 2023 Sep 19.
5
Prospective evaluation of nontuberculous mycobacteria disease in cystic fibrosis: The design of the PREDICT study.前瞻性评估囊性纤维化中非结核分枝杆菌病:PREDICT 研究的设计。
J Cyst Fibros. 2024 Jan;23(1):50-57. doi: 10.1016/j.jcf.2023.08.007. Epub 2023 Sep 4.
6
Patient and Caregiver Perceptions of Airway Clearance Methods Used for Cystic Fibrosis.患者和照护者对囊性纤维化使用的气道清除方法的看法。
Can Respir J. 2023 Jul 28;2023:1422319. doi: 10.1155/2023/1422319. eCollection 2023.
7
Chronic cough in cystic fibrosis: the effect of modulator therapy on objective 24-h cough monitoring.囊性纤维化中的慢性咳嗽:调节剂治疗对24小时客观咳嗽监测的影响
ERJ Open Res. 2022 May 3;8(2). doi: 10.1183/23120541.00031-2022. eCollection 2022 Apr.
8
Long-term amikacin liposome inhalation suspension in cystic fibrosis patients with chronic P. aeruginosa infection.囊性纤维化患者慢性铜绿假单胞菌感染时使用长疗程阿米卡星脂质体吸入混悬液。
J Cyst Fibros. 2021 Nov;20(6):1010-1017. doi: 10.1016/j.jcf.2021.05.013. Epub 2021 Jun 16.
9
A Prospective Study of the Effects of Sex Hormones on Lung Function and Inflammation in Women with Cystic Fibrosis.一项关于性激素对女性囊性纤维化患者肺功能和炎症影响的前瞻性研究。
Ann Am Thorac Soc. 2021 Jul;18(7):1158-1166. doi: 10.1513/AnnalsATS.202008-1064OC.
10
Intravenous versus oral antibiotics for eradication of Pseudomonas aeruginosa in cystic fibrosis (TORPEDO-CF): a randomised controlled trial.静脉注射与口服抗生素治疗囊性纤维化患者铜绿假单胞菌感染的疗效比较(TORPEDO-CF):一项随机对照试验。
Lancet Respir Med. 2020 Oct;8(10):975-986. doi: 10.1016/S2213-2600(20)30331-3.