• 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(CF)和非CF支气管扩张症中的吸入性抗生素

Inhaled antibiotics in Cystic Fibrosis (CF) and non-CF bronchiectasis.

作者信息

Tay George T P, Reid David W, Bell Scott C

机构信息

Department of Thoracic Medicine, The Prince Charles Hospital, Brisbane, Australia.

出版信息

Semin Respir Crit Care Med. 2015 Apr;36(2):267-86. doi: 10.1055/s-0035-1547346. Epub 2015 Mar 31.

DOI:10.1055/s-0035-1547346
PMID:25826593
Abstract

Bronchiectasis is a pathological diagnosis describing dilatation of the airways and is characterized by chronic lung sepsis. Bronchiectasis has multiple etiologies, but is usually considered in terms of whether it is due to the genetic disorder cystic fibrosis (CF) or secondary to other causes (non-CF bronchiectasis, NCFB). Inhaled antibiotics are used in bronchiectasis to suppress bacterial pathogens and reduce long-term lung function decline. The majority of the literature on inhaled antibiotics comes from studies on CF where the dominant bacterial pathogen in the airway is usually Pseudomonas aeruginosa. Thus, most aerosolized antibiotic regimens target this bacterium, but the emergence of molecular diagnostic methods has questioned this approach and more tailored strategies may need to be considered in CF based on the community composition of the lung microbiome. Similarly, the lung microbiome in NCFB has been found to be a complex polymicrobial one and the current practice of employing the same inhaled antibiotic regimes as are used in CF may no longer be appropriate in many patients. In this article, the use of inhaled antibiotics in CF and NCFB is considered in the light of improved understanding of the lung microbiome and why more tailored therapy may be needed based on molecular identification of the microbial pathogens present. The evidence for the use of currently available inhaled antibiotics and advances in inhaled drug packaging and delivery devices are discussed. Finally, the urgent need for prospective randomized clinical trials in CF and NCFB is highlighted and areas for future research identified.

摘要

支气管扩张是一种描述气道扩张的病理学诊断,其特征为慢性肺脓毒症。支气管扩张有多种病因,但通常根据其是否由遗传性疾病囊性纤维化(CF)引起或继发于其他原因(非CF支气管扩张,NCFB)来考虑。吸入性抗生素用于支气管扩张以抑制细菌病原体并减少长期肺功能下降。关于吸入性抗生素的大多数文献来自对CF的研究,其中气道中的主要细菌病原体通常是铜绿假单胞菌。因此,大多数雾化抗生素方案都针对这种细菌,但分子诊断方法的出现对这种方法提出了质疑,在CF中可能需要根据肺部微生物群的群落组成考虑更具针对性的策略。同样,已发现NCFB中的肺部微生物群是一个复杂的多微生物群落,在许多患者中,目前采用与CF相同的吸入性抗生素方案的做法可能不再合适。在本文中,鉴于对肺部微生物群的认识有所提高,以及基于对存在的微生物病原体的分子鉴定为何可能需要更具针对性的治疗,对CF和NCFB中吸入性抗生素的使用进行了探讨。讨论了使用现有吸入性抗生素的证据以及吸入药物包装和递送装置的进展。最后,强调了在CF和NCFB中进行前瞻性随机临床试验的迫切需求,并确定了未来的研究领域。

相似文献

1
Inhaled antibiotics in Cystic Fibrosis (CF) and non-CF bronchiectasis.囊性纤维化(CF)和非CF支气管扩张症中的吸入性抗生素
Semin Respir Crit Care Med. 2015 Apr;36(2):267-86. doi: 10.1055/s-0035-1547346. Epub 2015 Mar 31.
2
Aerosolized Antibiotics.雾化抗生素
Respir Care. 2015 Jun;60(6):762-1; discussion 771-3. doi: 10.4187/respcare.04208.
3
Challenges with current inhaled treatments for chronic Pseudomonas aeruginosa infection in patients with cystic fibrosis.囊性纤维化患者慢性铜绿假单胞菌感染的当前吸入治疗挑战。
Curr Med Res Opin. 2012 Jun;28(6):1059-67. doi: 10.1185/03007995.2012.674500. Epub 2012 May 10.
4
Aerosolized antibiotics for non-cystic fibrosis bronchiectasis.用于非囊性纤维化支气管扩张症的雾化抗生素
Respiration. 2014;88(3):177-84. doi: 10.1159/000366000. Epub 2014 Aug 22.
5
[Inhaled antibiotics in the treatment of noncystic fibrosis bronchiectasis].吸入性抗生素治疗非囊性纤维化支气管扩张症
Arch Bronconeumol. 2011 Jun;47 Suppl 6:19-23. doi: 10.1016/S0300-2896(11)70031-X.
6
The Rationale and Evidence for Use of Inhaled Antibiotics to Control Pseudomonas aeruginosa Infection in Non-cystic Fibrosis Bronchiectasis.吸入抗生素治疗非囊性纤维化支气管扩张症铜绿假单胞菌感染的原理和证据。
J Aerosol Med Pulm Drug Deliv. 2018 Jun;31(3):121-138. doi: 10.1089/jamp.2017.1415. Epub 2017 Oct 27.
7
Inhaled antibiotics for lower respiratory tract infections: focus on ciprofloxacin.吸入性抗生素治疗下呼吸道感染:聚焦环丙沙星
Drugs Today (Barc). 2012 May;48(5):339-51. doi: 10.1358/dot.2012.48.5.1789474.
8
Assessing effects of inhaled antibiotics in adults with non-cystic fibrosis bronchiectasis--experiences from recent clinical trials.评估吸入抗生素对非囊性纤维化支气管扩张症成人的影响——来自最近临床试验的经验。
Expert Rev Respir Med. 2018 Sep;12(9):769-782. doi: 10.1080/17476348.2018.1503540. Epub 2018 Aug 3.
9
Aerosolized antibiotics for non-cystic fibrosis bronchiectasis.用于非囊性纤维化支气管扩张症的雾化抗生素
J Aerosol Med Pulm Drug Deliv. 2008 Mar;21(1):71-6. doi: 10.1089/jamp.2007.0652.
10
Addition of inhaled tobramycin to ciprofloxacin for acute exacerbations of Pseudomonas aeruginosa infection in adult bronchiectasis.在成人支气管扩张症患者中,吸入妥布霉素联合环丙沙星用于治疗铜绿假单胞菌感染急性加重期。
Chest. 2006 Nov;130(5):1503-10. doi: 10.1378/chest.130.5.1503.

引用本文的文献

1
Insights on the Pathogenesis of Infection in Patients with Cystic Fibrosis.囊性纤维化患者感染发病机制的见解
J Clin Med. 2025 May 16;14(10):3492. doi: 10.3390/jcm14103492.
2
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis.囊性纤维化和非囊性纤维化支气管扩张症的比较微生物组分析。
Respir Res. 2024 May 18;25(1):211. doi: 10.1186/s12931-024-02835-w.
3
Chronic Lung Disease in Primary Antibody Deficiency: Diagnosis and Management.原发性抗体缺陷中的慢性肺部疾病:诊断与管理。
Immunol Allergy Clin North Am. 2020 Aug;40(3):437-459. doi: 10.1016/j.iac.2020.03.003. Epub 2020 Jun 9.
4
The Rationale and Evidence for Use of Inhaled Antibiotics to Control Pseudomonas aeruginosa Infection in Non-cystic Fibrosis Bronchiectasis.吸入抗生素治疗非囊性纤维化支气管扩张症铜绿假单胞菌感染的原理和证据。
J Aerosol Med Pulm Drug Deliv. 2018 Jun;31(3):121-138. doi: 10.1089/jamp.2017.1415. Epub 2017 Oct 27.
5
Molecular Epidemiology of Mutations in Antimicrobial Resistance Loci of Pseudomonas aeruginosa Isolates from Airways of Cystic Fibrosis Patients.囊性纤维化患者气道分离的铜绿假单胞菌抗菌药物耐药位点突变的分子流行病学
Antimicrob Agents Chemother. 2016 Oct 21;60(11):6726-6734. doi: 10.1128/AAC.00724-16. Print 2016 Nov.