• 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

静脉注射抗生素治疗肺部加重期后囊性纤维化患儿健康相关生活质量的变化。

Changes in pediatric health-related quality of life in cystic fibrosis after IV antibiotic treatment for pulmonary exacerbations.

作者信息

Modi Avani C, Lim Crystal S, Driscoll Kimberly A, Piazza-Waggoner Carrie, Quittner Alexandra L, Wooldridge Jamie

机构信息

Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA.

出版信息

J Clin Psychol Med Settings. 2010 Mar;17(1):49-55. doi: 10.1007/s10880-009-9179-2.

DOI:10.1007/s10880-009-9179-2
PMID:20157799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2847844/
Abstract

Intravenous (IV) antibiotic therapy for pulmonary exacerbations (PE) has been shown to improve pulmonary functioning for patients with cystic fibrosis (CF); however, little is known about its effects on pediatric health-related quality of life (HRQOL). This prospective study assessed the impact of IV treatment of a PE on generic and CF-specific HRQOL for children and adolescents with CF. Participants included 52 children and adolescents with CF experiencing a PE (M (age) = 13.6 years; 54% males; M(FEV(1%)) predicted = 58.8%). HRQOL, pulmonary functioning, and body mass index were assessed before and after IV antibiotic treatment. Results of this prospective, observational study indicated significant improvements on CFQ-R Respiratory (M (change score) = 11.7; 95% CI = 6.3-17.1; p < .0001) and Weight (M (change score) = 15.9; 95% CI = 7.9-23.8; p < .0001) scales. The CF-specific measure was more sensitive to changes in HRQOL than the generic instrument. These data suggest that CF-specific HRQOL improves with treatment for a PE with IV antibiotics. The noted statistically and clinically significant changes in the CFQ-respiratory scale indicate that the measure may be beneficial to pulmonary health care teams.

摘要

静脉注射抗生素治疗肺部加重期(PE)已被证明可改善囊性纤维化(CF)患者的肺功能;然而,对于其对儿童健康相关生活质量(HRQOL)的影响知之甚少。这项前瞻性研究评估了静脉注射治疗PE对CF儿童和青少年的一般及CF特异性HRQOL的影响。参与者包括52名经历PE的CF儿童和青少年(平均年龄 = 13.6岁;54%为男性;预计平均第1秒用力呼气容积占预计值百分比(FEV(1%)) = 58.8%)。在静脉注射抗生素治疗前后评估了HRQOL、肺功能和体重指数。这项前瞻性观察性研究的结果表明,CFQ-R呼吸量表(平均变化得分 = 11.7;95%置信区间 = 6.3 - 17.1;p <.0001)和体重量表(平均变化得分 = 15.9;95%置信区间 = 7.9 - 23.8;p <.0001)有显著改善。CF特异性测量方法比一般测量工具对HRQOL变化更敏感。这些数据表明,静脉注射抗生素治疗PE可改善CF特异性HRQOL。CFQ-呼吸量表中 noted的统计学和临床显著变化表明该测量方法可能对肺部医疗团队有益。 (注:原文中“noted”翻译为“ noted”可能有误,推测可能是“notable”,译为“显著的” )

相似文献

1
Changes in pediatric health-related quality of life in cystic fibrosis after IV antibiotic treatment for pulmonary exacerbations.静脉注射抗生素治疗肺部加重期后囊性纤维化患儿健康相关生活质量的变化。
J Clin Psychol Med Settings. 2010 Mar;17(1):49-55. doi: 10.1007/s10880-009-9179-2.
2
Health-related quality-of-life in children with cystic fibrosis aged 5-years and associations with health outcomes.儿童囊性纤维化患者的健康相关生活质量及其与健康结果的关联。
J Cyst Fibros. 2020 May;19(3):483-491. doi: 10.1016/j.jcf.2020.02.022. Epub 2020 Mar 9.
3
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.
4
Characteristics and outcomes of oral antibiotic treated pulmonary exacerbations in children with cystic fibrosis.囊性纤维化患儿口服抗生素治疗肺部恶化的特征和结局。
J Cyst Fibros. 2018 Nov;17(6):760-768. doi: 10.1016/j.jcf.2018.05.015. Epub 2018 Jun 18.
5
A systematic review of factors associated with health-related quality of life in adolescents and adults with cystic fibrosis.对患有囊性纤维化的青少年和成年人中与健康相关生活质量相关因素的系统评价。
Ann Am Thorac Soc. 2015 Mar;12(3):420-8. doi: 10.1513/AnnalsATS.201408-393OC.
6
Rationale and design of a randomized trial of home electronic symptom and lung function monitoring to detect cystic fibrosis pulmonary exacerbations: the early intervention in cystic fibrosis exacerbation (eICE) trial.家用电子症状和肺功能监测以检测囊性纤维化肺部恶化的随机试验的原理和设计:囊性纤维化恶化早期干预(eICE)试验。
Contemp Clin Trials. 2013 Nov;36(2):460-9. doi: 10.1016/j.cct.2013.09.004. Epub 2013 Sep 19.
7
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.
8
Impact of acute antibiotic therapy on the pulmonary exacerbation endpoint in cystic fibrosis clinical trials.急性抗生素治疗对囊性纤维化临床试验中肺部恶化终点的影响。
Contemp Clin Trials. 2013 Sep;36(1):99-105. doi: 10.1016/j.cct.2013.06.004. Epub 2013 Jun 14.
9
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.
10
Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis.用于囊性纤维化患者肺部加重期的静脉用抗生素
Cochrane Database Syst Rev. 2025 Jan 20;1(1):CD009730. doi: 10.1002/14651858.CD009730.pub3.

引用本文的文献

1
The Effect of a High-Intensity PrO2Fit Inspiratory Muscle Training Intervention on Physiological and Psychological Health in Adults with Bronchiectasis: A Mixed-Methods Study.高强度PrO2Fit吸气肌训练干预对支气管扩张症成人患者生理和心理健康的影响:一项混合方法研究
Int J Environ Res Public Health. 2021 Mar 16;18(6):3051. doi: 10.3390/ijerph18063051.
2
A systematic review of patient-reported outcome measures (PROMs) in cystic fibrosis.一项关于囊性纤维化患者报告结局指标(PROMs)的系统评价。
BMJ Open. 2020 Oct 1;10(10):e033867. doi: 10.1136/bmjopen-2019-033867.
3
The Cystic Fibrosis Impact Questionnaire: qualitative development and cognitive evaluation of a new patient-reported outcome instrument to assess the life impacts of cystic fibrosis.

本文引用的文献

1
Determination of the minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with cystic fibrosis and chronic Pseudomonas aeruginosa airway infection.确定囊性纤维化问卷修订版呼吸症状量表在两组囊性纤维化合并慢性铜绿假单胞菌气道感染患者中的最小临床重要差异分数。
Chest. 2009 Jun;135(6):1610-1618. doi: 10.1378/chest.08-1190. Epub 2009 May 15.
2
Patient-reported outcomes in cystic fibrosis.囊性纤维化患者报告的结局
Proc Am Thorac Soc. 2007 Aug 1;4(4):378-86. doi: 10.1513/pats.200703-039BR.
3
Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis.
囊性纤维化影响问卷:一种用于评估囊性纤维化对生活影响的新型患者报告结局工具的定性开发与认知评估
J Patient Rep Outcomes. 2020 May 13;4(1):36. doi: 10.1186/s41687-020-00199-5.
4
Health-related quality of life in children after laparoscopic gastrostomy placement.腹腔镜胃造口术后儿童的健康相关生活质量。
Qual Life Res. 2020 Jan;29(1):171-178. doi: 10.1007/s11136-019-02272-z. Epub 2019 Aug 16.
5
Use of a Multiplex Transcript Method for Analysis of Pseudomonas aeruginosa Gene Expression Profiles in the Cystic Fibrosis Lung.使用多重转录本方法分析囊性纤维化肺中铜绿假单胞菌的基因表达谱。
Infect Immun. 2016 Sep 19;84(10):2995-3006. doi: 10.1128/IAI.00437-16. Print 2016 Oct.
6
Nutritional status is associated with health-related quality of life in children with cystic fibrosis aged 9-19 years.营养状况与 9-19 岁囊性纤维化患儿的健康相关生活质量有关。
J Cyst Fibros. 2013 Dec;12(6):746-53. doi: 10.1016/j.jcf.2013.01.006. Epub 2013 Feb 12.
7
Iron homeostasis during cystic fibrosis pulmonary exacerbation.囊性纤维化肺部恶化期间的铁稳态。
Clin Transl Sci. 2012 Aug;5(4):368-73. doi: 10.1111/j.1752-8062.2012.00417.x. Epub 2012 Jun 1.
8
Application of dyadic data analysis in pediatric psychology: cystic fibrosis health-related quality of life and anxiety in child-caregiver dyads.对偶数据分析在儿科心理学中的应用:囊性纤维化健康相关生活质量和儿童-照顾者对偶体中的焦虑。
J Pediatr Psychol. 2012 Jul;37(6):605-11. doi: 10.1093/jpepsy/jss063. Epub 2012 Apr 19.
9
Relationships among health-related quality of life, pulmonary health, and newborn screening for cystic fibrosis.健康相关生活质量、肺部健康与囊性纤维化新生儿筛查之间的关系。
Chest. 2011 Jul;140(1):170-177. doi: 10.1378/chest.10-1504. Epub 2010 Nov 24.
10
Quality of life in clinical trials for children.儿童临床试验中的生活质量。
Eur J Clin Pharmacol. 2011 May;67 Suppl 1:41-7. doi: 10.1007/s00228-010-0924-0. Epub 2010 Nov 21.
囊性纤维化的病情加重。1:流行病学与发病机制。
Thorax. 2007 Apr;62(4):360-7. doi: 10.1136/thx.2006.060889.
4
Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance.行业指南:患者报告的结局指标:用于医疗产品开发以支持标签声明:指南草案
Health Qual Life Outcomes. 2006 Oct 11;4:79. doi: 10.1186/1477-7525-4-79.
5
Effect of disease-related pain on the health-related quality of life of children and adolescents with cystic fibrosis.疾病相关性疼痛对囊性纤维化儿童及青少年健康相关生活质量的影响。
Clin J Pain. 2006 Jul-Aug;22(6):532-7. doi: 10.1097/01.ajp.0000210996.45459.76.
6
Comparison of hospital and home intravenous antibiotic therapy in adults with cystic fibrosis.成人囊性纤维化患者住院与居家静脉注射抗生素治疗的比较。
J Clin Nurs. 2006 Jan;15(1):52-60. doi: 10.1111/j.1365-2702.2005.01236.x.
7
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.
8
Overview of published evidence on outcomes with early diagnosis from large US observational studies.美国大型观察性研究中关于早期诊断结果的已发表证据概述。
J Pediatr. 2005 Sep;147(3 Suppl):S11-4. doi: 10.1016/j.jpeds.2005.08.010.
9
The impact of treatment of pulmonary exacerbations on the health-related quality of life of patients with cystic fibrosis: does hospitalization make a difference?肺部加重期治疗对囊性纤维化患者健康相关生活质量的影响:住院治疗有影响吗?
J Pediatr. 2004 Jun;144(6):711-8. doi: 10.1016/j.jpeds.2004.02.032.
10
Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis.囊性纤维化患儿健康相关生活质量疾病特异性测量方法的验证
J Pediatr Psychol. 2003 Dec;28(8):535-45. doi: 10.1093/jpepsy/jsg044.