• 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

囊性纤维化患者症状和第一秒用力呼气容积的实时每日一次监测——一项使用新型设备的可行性研究

Real-time, once-daily monitoring of symptoms and FEV in cystic fibrosis patients--a feasibility study using a novel device.

作者信息

Sarfaraz Sunny, Sund Zoe, Jarad Nabil

机构信息

Adult CF Centre, Department of Respiratory Medicine, Bristol Royal Infirmary, Bristol, UK.

出版信息

Clin Respir J. 2010 Apr;4(2):74-82. doi: 10.1111/j.1752-699X.2009.00147.x.

DOI:10.1111/j.1752-699X.2009.00147.x
PMID:20565480
Abstract

BACKGROUND AND AIMS

We investigated feasibility and value of a real-time electronic monitoring system adapted for early detection of cystic fibrosis (CF) pulmonary exacerbations (P Exs).

METHODS

This was a 6-month prospective study. Patients recorded once daily their symptom score and spirometry using an electronic diary. The data were sent daily to the research team in real time. P Ex was considered to be present when change in symptoms and lung function values met a preset criteria. Number of P Exs during the study was compared with a parallel period of the previous and of the following years.

RESULTS

Only 19 patients (37.2%) completed recording that could be evaluated. A total of 53 P Exs were identified, 26 (49.0%) of which needed intravenous (IV) antibiotics. The number of total P Exs in the study year did not differ from the previous or the following year, but the number of courses of oral antibiotics was greater than those given during the previous year.

CONCLUSION

Remote daily monitoring of symptoms and spirometry had a poor uptake among CF patients. For those who completed the study, this method early detected P Exs that were treated with oral antibiotics that might otherwise required IV antibiotics.

摘要

背景与目的

我们研究了一种适用于早期检测囊性纤维化(CF)肺部加重(P Exs)的实时电子监测系统的可行性和价值。

方法

这是一项为期6个月的前瞻性研究。患者每天使用电子日记记录一次症状评分和肺功能测定值。数据每天实时发送给研究团队。当症状和肺功能值的变化符合预设标准时,即认为存在P Ex。将研究期间的P Exs数量与前一年和后一年的平行时间段进行比较。

结果

只有19名患者(37.2%)完成了可评估的记录。共识别出53次P Exs,其中26次(49.0%)需要静脉注射(IV)抗生素。研究年度的P Exs总数与前一年或后一年没有差异,但口服抗生素疗程的数量多于前一年。

结论

CF患者对症状和肺功能测定值的远程每日监测接受度较低。对于完成研究的患者,这种方法可早期检测出原本可能需要静脉注射抗生素治疗的P Exs,现用口服抗生素治疗。

相似文献

1
Real-time, once-daily monitoring of symptoms and FEV in cystic fibrosis patients--a feasibility study using a novel device.囊性纤维化患者症状和第一秒用力呼气容积的实时每日一次监测——一项使用新型设备的可行性研究
Clin Respir J. 2010 Apr;4(2):74-82. doi: 10.1111/j.1752-699X.2009.00147.x.
2
Remote daily real-time monitoring in patients with COPD --a feasibility study using a novel device.慢性阻塞性肺疾病患者的远程日常实时监测——使用新型设备的可行性研究。
Respir Med. 2009 Sep;103(9):1320-8. doi: 10.1016/j.rmed.2009.03.017. Epub 2009 Apr 16.
3
Risk factors for increased need for intravenous antibiotics for pulmonary exacerbations in adult patients with cystic fibrosis.成年囊性纤维化患者肺部病情加重时静脉使用抗生素需求增加的危险因素。
Chron Respir Dis. 2008;5(1):29-33. doi: 10.1177/1479972307085635.
4
Telemonitoring in chronic obstructive airway disease and adult patients with cystic fibrosis.慢性阻塞性气道疾病和成年囊性纤维化患者的远程监测。
J Telemed Telecare. 2011;17(3):127-32. doi: 10.1258/jtt.2010.100309. Epub 2010 Dec 16.
5
Recurrent exacerbations affect FEV(1) decline in adult patients with cystic fibrosis.反复加重影响成年囊性纤维化患者的第一秒用力呼气容积(FEV₁)下降。
Respir Med. 2009 Mar;103(3):407-13. doi: 10.1016/j.rmed.2008.09.024. Epub 2008 Nov 22.
6
Patient compliance with assessing and monitoring of asthma.患者对哮喘评估和监测的依从性。
J Asthma. 2009 Dec;46(10):1027-31. doi: 10.3109/02770900903229685.
7
Improved lung function and body mass index associated with long-term use of Macrolide antibiotics.长期使用大环内酯类抗生素与肺功能和体重指数改善相关。
J Cyst Fibros. 2003 Jun;2(2):69-71. doi: 10.1016/S1569-1993(03)00021-3.
8
Objective monitoring of cough in children with cystic fibrosis.对囊性纤维化患儿咳嗽情况的客观监测。
Pediatr Pulmonol. 2002 Nov;34(5):331-5. doi: 10.1002/ppul.10174.
9
[Early detection of exacerbation of lung infections in patients with cystic fibrosis by means of daily spirometry].
Schweiz Med Wochenschr. 2000 Sep 30;130(39):1361-5.
10
Effectiveness and tolerability of high-dose salmeterol in cystic fibrosis.高剂量沙美特罗治疗囊性纤维化的有效性和耐受性
Pediatr Pulmonol. 2002 Oct;34(4):287-96. doi: 10.1002/ppul.10162.

引用本文的文献

1
The Feasibility and Validity of Home Spirometry for People with Cystic Fibrosis: Is It Comparable to Spirometry in the Clinic?家庭肺量计在囊性纤维化患者中的可行性和有效性:它与临床肺量计相比如何?
Children (Basel). 2025 Feb 25;12(3):277. doi: 10.3390/children12030277.
2
Assessment of Home-based Monitoring in Adults with Chronic Lung Disease: An Official American Thoracic Society Research Statement.成人慢性肺病家庭监测评估:美国胸科学会官方研究声明
Am J Respir Crit Care Med. 2025 Feb;211(2):174-193. doi: 10.1164/rccm.202410-2080ST.
3
Experiences Among Patients With Cystic Fibrosis in the MucoExocet Study of Using Connected Devices for the Management of Pulmonary Exacerbations: Grounded Theory Qualitative Research.
在使用联网设备管理肺部加重期的黏液外排研究中囊性纤维化患者的经历:扎根理论定性研究
JMIR Form Res. 2024 Jan 23;8:e38064. doi: 10.2196/38064.
4
Telemedicine and Its Application in Cystic Fibrosis.远程医疗及其在囊性纤维化中的应用。
J Pers Med. 2023 Jun 25;13(7):1041. doi: 10.3390/jpm13071041.
5
Virtual monitoring in CF - the importance of continuous monitoring in a multi-organ chronic condition.囊性纤维化中的虚拟监测——多器官慢性疾病中持续监测的重要性。
Front Digit Health. 2023 May 4;5:1196442. doi: 10.3389/fdgth.2023.1196442. eCollection 2023.
6
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.
7
A prospective randomised controlled mixed-methods pilot study of home monitoring in adults with cystic fibrosis.前瞻性随机对照混合方法成人囊性纤维化家庭监测研究
Ther Adv Respir Dis. 2022 Jan-Dec;16:17534666211070133. doi: 10.1177/17534666211070133.
8
Telemedicine in cystic fibrosis.囊性纤维化中的远程医疗
J Clin Transl Endocrinol. 2021 Oct 26;26:100270. doi: 10.1016/j.jcte.2021.100270. eCollection 2021 Dec.
9
Use of Home-Based Connected Devices in Patients With Cystic Fibrosis for the Early Detection and Treatment of Pulmonary Exacerbations: Protocol for a Qualitative Study.居家连接设备在囊性纤维化患者肺部急性加重早期检测与治疗中的应用:一项定性研究方案
JMIR Res Protoc. 2021 Aug 18;10(8):e14552. doi: 10.2196/14552.
10
A Mobile Health Platform for Self-Management of Pediatric Cystic Fibrosis: Qualitative Study of Adaptation to Stakeholder Needs and Integration in Clinical Settings.用于小儿囊性纤维化自我管理的移动健康平台:适应利益相关者需求并融入临床环境的定性研究
JMIR Form Res. 2021 Jan 26;5(1):e19413. doi: 10.2196/19413.