• 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

家庭肺量计在儿童囊性纤维化患者中的应用:一项可行性研究的结果

The Use of Home Spirometry in Pediatric Cystic Fibrosis Patients: Results of a Feasibility Study.

作者信息

Shakkottai Aarti, Nasr Samya Z

机构信息

University of Michigan Health System, Ann Arbor, MI, USA.

出版信息

Glob Pediatr Health. 2017 Feb 2;4:2333794X17690315. doi: 10.1177/2333794X17690315. eCollection 2017.

DOI:10.1177/2333794X17690315
PMID:28229102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5308520/
Abstract

Medication adherence is poor among pediatric cystic fibrosis (CF) patients, with adolescents having one of the lowest adherence rates. We wanted to identify an adherence intervention that would be acceptable to CF adolescents and assess its feasibility. We surveyed 40 adolescents with CF and asked about barriers to and motivators for their own adherence and to generate ideas for potential adherence interventions. Since most of the respondents chose frequent spirometry at home and medication reminders for interventions, we selected 5 subjects, 10 to 14 years of age, with CF to test the feasibility of home spirometry and medication reminders in pediatric CF patients. This article summarizes the results of both the survey and the feasibility pilot study.

摘要

儿科囊性纤维化(CF)患者的药物依从性较差,青少年的依从率是最低的之一。我们希望确定一种CF青少年能够接受的依从性干预措施,并评估其可行性。我们对40名CF青少年进行了调查,询问他们自身依从性的障碍和动机,并征集潜在依从性干预措施的想法。由于大多数受访者选择在家中频繁进行肺活量测定和药物提醒作为干预措施,我们挑选了5名年龄在10至14岁的CF受试者,来测试在家中进行肺活量测定和药物提醒对儿科CF患者的可行性。本文总结了调查结果和可行性初步研究的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/945266a5dd10/10.1177_2333794X17690315-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/1c3508551905/10.1177_2333794X17690315-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/16bd40fb0148/10.1177_2333794X17690315-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/142856c0903c/10.1177_2333794X17690315-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/945266a5dd10/10.1177_2333794X17690315-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/1c3508551905/10.1177_2333794X17690315-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/16bd40fb0148/10.1177_2333794X17690315-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/142856c0903c/10.1177_2333794X17690315-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/5308520/945266a5dd10/10.1177_2333794X17690315-fig4.jpg

相似文献

1
The Use of Home Spirometry in Pediatric Cystic Fibrosis Patients: Results of a Feasibility Study.家庭肺量计在儿童囊性纤维化患者中的应用:一项可行性研究的结果
Glob Pediatr Health. 2017 Feb 2;4:2333794X17690315. doi: 10.1177/2333794X17690315. eCollection 2017.
2
Impact of home spirometry on medication adherence among adolescents with cystic fibrosis.家庭肺功能测定对青少年囊性纤维化患者药物依从性的影响。
Pediatr Pulmonol. 2018 Apr;53(4):431-436. doi: 10.1002/ppul.23950. Epub 2018 Feb 19.
3
Investigating the feasibility of text message reminders to improve adherence to nebulized medication in children and adolescents with cystic fibrosis.研究短信提醒对提高囊性纤维化儿童和青少年雾化药物治疗依从性的可行性。
Patient Prefer Adherence. 2017 May 8;11:861-869. doi: 10.2147/PPA.S123723. eCollection 2017.
4
Education and implementation of home spirometry in an adolescent cystic fibrosis population.青少年囊性纤维化患者家庭肺活量测定的教育与实施
Respir Med Res. 2023 Nov;84:101040. doi: 10.1016/j.resmer.2023.101040. Epub 2023 Jun 30.
5
Real-world feasibility of short-term, unsupervised home spirometry in CF.囊性纤维化患者短期、无监督家庭肺功能测定的真实世界可行性
Pediatr Pulmonol. 2022 Dec;57(12):3129-3135. doi: 10.1002/ppul.26147. Epub 2022 Sep 27.
6
The use of telehealth (text messaging and video communications) in patients with cystic fibrosis: A pilot study.远程医疗(短信和视频通信)在囊性纤维化患者中的应用:一项试点研究。
J Telemed Telecare. 2017 May;23(4):489-493. doi: 10.1177/1357633X16649532. Epub 2016 May 13.
7
Barriers to adherence to cystic fibrosis infection control guidelines.遵守囊性纤维化感染控制指南的障碍。
Pediatr Pulmonol. 2008 Sep;43(9):900-7. doi: 10.1002/ppul.20876.
8
Assessment of a Mobile App by Adolescents and Young Adults With Cystic Fibrosis: Pilot Evaluation.青少年和年轻成人囊性纤维化患者使用移动应用程序的评估:初步评估。
JMIR Mhealth Uhealth. 2019 Nov 21;7(11):e12442. doi: 10.2196/12442.
9
Identifying barriers to treatment adherence and related attitudinal patterns in adolescents with cystic fibrosis.识别青少年囊性纤维化患者治疗依从性的障碍及相关态度模式。
Pediatr Pulmonol. 2010 May;45(5):450-8. doi: 10.1002/ppul.21195.
10
Pharmacists' perspectives on monitoring adherence to treatment in Cystic Fibrosis.药剂师对囊性纤维化治疗依从性监测的看法。
Int J Clin Pharm. 2016 Apr;38(2):296-302. doi: 10.1007/s11096-015-0239-4. Epub 2015 Dec 29.

引用本文的文献

1
The Long-Term Uptake of Home Spirometry in Regular Cystic Fibrosis Care: Retrospective Multicenter Observational Study.常规囊性纤维化护理中家庭肺活量测定法的长期应用:回顾性多中心观察性研究。
J Med Internet Res. 2025 Jan 9;27:e60689. doi: 10.2196/60689.
2
Digital technology for early identification of exacerbations in people with cystic fibrosis.数字技术用于早期识别囊性纤维化患者的恶化情况。
Cochrane Database Syst Rev. 2023 Apr 14;4(4):CD014606. doi: 10.1002/14651858.CD014606.pub2.
3
Psychological interventions for improving adherence to inhaled therapies in people with cystic fibrosis.

本文引用的文献

1
A five-year retrospective analysis of adherence in cystic fibrosis.一项关于囊性纤维化患者依从性的五年回顾性分析。
Pediatr Pulmonol. 2015 Dec;50(12):1224-9. doi: 10.1002/ppul.23307. Epub 2015 Sep 7.
2
Tackling the increasing complexity of CF care.应对囊性纤维化护理日益增长的复杂性。
Pediatr Pulmonol. 2015 Oct;50 Suppl 40(0 40):S74-9. doi: 10.1002/ppul.23244.
3
Decline in lung function does not predict future decline in lung function in cystic fibrosis patients.肺功能下降并不能预测囊性纤维化患者未来的肺功能下降情况。
心理干预对改善囊性纤维化患者吸入治疗依从性的作用。
Cochrane Database Syst Rev. 2023 Mar 29;3(3):CD013766. doi: 10.1002/14651858.CD013766.pub2.
4
Adherence, reliability, and variability of home spirometry telemonitoring in cystic fibrosis.囊性纤维化患者家庭肺功能仪远程监测的依从性、可靠性和变异性
Front Pediatr. 2023 Feb 23;11:1111088. doi: 10.3389/fped.2023.1111088. eCollection 2023.
5
Home Spirometry in Children with Cystic Fibrosis.囊性纤维化患儿的家庭肺功能测定
Bioengineering (Basel). 2023 Feb 11;10(2):242. doi: 10.3390/bioengineering10020242.
6
Feasibility and acceptability of home monitoring with portable spirometry in young adults with asthma.便携式肺功能仪家庭监测在哮喘青年中的可行性和可接受性。
J Asthma. 2023 Jul;60(7):1474-1479. doi: 10.1080/02770903.2022.2160345. Epub 2023 Jan 2.
7
Proactive Electronic Visits for Smoking Cessation and Chronic Obstructive Pulmonary Disease Screening in Primary Care: Randomized Controlled Trial of Feasibility, Acceptability, and Efficacy.主动式电子访视用于初级保健中的戒烟和慢性阻塞性肺疾病筛查:可行性、可接受性和疗效的随机对照试验。
J Med Internet Res. 2022 Aug 30;24(8):e38663. doi: 10.2196/38663.
8
Exploring the 175-year history of spirometry and the vital lessons it can teach us today.探索肺量计 175 年的历史,以及它今天能给我们带来的重要启示。
Eur Respir Rev. 2021 Oct 5;30(162). doi: 10.1183/16000617.0081-2021. Print 2021 Dec 31.
9
Challenges of evaluating lung function as part of cancer care during the COVID-19 pandemic.评估 COVID-19 大流行期间癌症治疗中肺功能所面临的挑战。
Eur Respir J. 2020 Aug 13;56(2). doi: 10.1183/13993003.01621-2020. Print 2020 Aug.
Pediatr Pulmonol. 2015 Sep;50(9):856-62. doi: 10.1002/ppul.23227. Epub 2015 Jun 18.
4
Does the FEF25-75 or the FEF75 have any value in assessing lung disease in children with cystic fibrosis or asthma?用力呼气流量25%-75%(FEF25-75)或用力呼气流量75%(FEF75)在评估囊性纤维化或哮喘儿童的肺部疾病时是否有任何价值?
Pediatr Pulmonol. 2015 Sep;50(9):863-8. doi: 10.1002/ppul.23234. Epub 2015 Jun 16.
5
Risk factors for lung function decline in a large cohort of young cystic fibrosis patients.一大群年轻囊性纤维化患者肺功能下降的危险因素。
Pediatr Pulmonol. 2015 Aug;50(8):763-70. doi: 10.1002/ppul.23217. Epub 2015 Jun 9.
6
Adherence to treatment in children and adolescents with cystic fibrosis: a cross-sectional, multi-method study investigating the influence of beliefs about treatment and parental depressive symptoms.囊性纤维化儿童和青少年的治疗依从性:一项横断面多方法研究,调查治疗信念和父母抑郁症状的影响。
BMC Pulm Med. 2015 Apr 26;15:43. doi: 10.1186/s12890-015-0038-7.
7
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.
8
Motivating adherence among adolescents with cystic fibrosis: youth and parent perspectives.激励囊性纤维化青少年坚持治疗:青少年及其父母的观点
Pediatr Pulmonol. 2015 Feb;50(2):127-36. doi: 10.1002/ppul.23017. Epub 2014 Mar 10.
9
Pulmonary medication adherence and health-care use in cystic fibrosis.囊性纤维化患者的肺部药物治疗依从性和医疗保健使用情况。
Chest. 2014 Jul;146(1):142-151. doi: 10.1378/chest.13-1926.
10
Measurement of FEF25-75% and FEF75% does not contribute to clinical decision making.用力呼出量 25%-75%(FEF25-75%)和 75%用力呼出量(FEF75%)的测量对临床决策无帮助。
Eur Respir J. 2014 Apr;43(4):1051-8. doi: 10.1183/09031936.00128113. Epub 2013 Sep 26.