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成人稳定型非 CF 支气管扩张症的抗生素治疗 - 系统评价。

Antibiotic therapy for stable non-CF bronchiectasis in adults - A systematic review.

机构信息

1 Department of Pulmonary Medicine, Hvidovre Hospital, Hvidovre, Denmark.

2 Department of Infectious Disease and Pulmonary Medicine, Nordsjællands Hospital, Hillerod, Denmark.

出版信息

Chron Respir Dis. 2017 May;14(2):174-186. doi: 10.1177/1479972316661923. Epub 2016 Aug 9.

Abstract

To provide an update on efficacy and safety of antibiotic treatments for stable non-cystic fibrosis (CF) bronchiectasis (BE). Systematic review based on the Preferred Reporting Items for Systematic reviews and Meta-Analyses guidelines was done. Twenty-six studies (1.898 patients) fulfilled the inclusion criteria. Studies of inhaled tobramycin have revealed conflicting results regarding quality of life (QoL), exacerbations and admissions, but may result in sputum cultures negative for Pseudomonas aeruginosa, whereas studies investigating the effect of inhaled gentamycin have shown positive effects on sputum bacterial density, decrease in sputum cultures positive for P. aeruginosa, QoL and exacerbation rate, but no improvement in forced expiratory volume in first second (FEV). Oral azithromycin can reduce exacerbations, together with minor improvements in QoL and FEV. Furthermore, oral erythromycin reduces exacerbations, but has no effect on lung function, symptoms or QoL. Inhaled ciprofloxacin may reduce P. aeruginosa in sputum cultures, but without changes in lung function, exacerbations or QoL. Although with limited evidence, inhaled colistin may have effects on P. aeruginosa density, exacerbations and QoL, whereas studies on aztreonam revealed no significant clinical improvements in the outcomes of interest, including exacerbation rate. Adverse events, including bronchospasm, have been reported in association with tobramycin and aztreonam. Several antibiotic treatment regimens have been shown to improve QoL and exacerbation rate, whereas findings regarding sputum production, lung function and admissions have been conflicting. Evidence-based treatment algorithms for antibiotic treatment of stable non-CF BE will have to await large-scale, long-term controlled studies.

摘要

提供稳定非囊性纤维化(CF)支气管扩张症(BE)抗生素治疗疗效和安全性的最新信息。根据系统评价和荟萃分析首选报告项目进行了系统评价。有 26 项研究(1898 例患者)符合纳入标准。吸入妥布霉素的研究结果表明,生活质量(QoL)、加重和住院率方面存在相互矛盾的结果,但可能导致铜绿假单胞菌痰培养阴性,而研究吸入庆大霉素的影响表明对痰细菌密度、痰培养铜绿假单胞菌阳性率、QoL 和加重率有积极影响,但对第一秒用力呼气量(FEV)没有改善。口服阿奇霉素可减少加重,同时 QoL 和 FEV 略有改善。此外,口服红霉素可减少加重,但对肺功能、症状或 QoL 没有影响。吸入环丙沙星可能减少痰培养中的铜绿假单胞菌,但对肺功能、加重或 QoL 没有变化。尽管证据有限,但吸入黏菌素可能对铜绿假单胞菌密度、加重和 QoL 有影响,而关于氨曲南的研究表明,在感兴趣的结果方面,包括加重率,没有显著的临床改善。已经报道了与妥布霉素和氨曲南相关的不良反应,包括支气管痉挛。几种抗生素治疗方案已被证明可改善 QoL 和加重率,而关于痰产生、肺功能和住院率的研究结果则相互矛盾。稳定非 CF BE 抗生素治疗的循证治疗算法将不得不等待大规模、长期对照研究。

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本文引用的文献

1
Developing drug therapies in bronchiectasis.
Expert Opin Investig Drugs. 2015 Feb;24(2):169-81. doi: 10.1517/13543784.2015.971153. Epub 2014 Oct 11.
3
Inhaled colistin in patients with bronchiectasis and chronic Pseudomonas aeruginosa infection.
Am J Respir Crit Care Med. 2014 Apr 15;189(8):975-82. doi: 10.1164/rccm.201312-2208OC.
8
Ciprofloxacin DPI in non-cystic fibrosis bronchiectasis: a Phase II randomized study.
Expert Opin Investig Drugs. 2013 May;22(5):671-3. doi: 10.1517/13543784.2013.783565. Epub 2013 Mar 22.
9
Ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis: a phase II randomised study.
Eur Respir J. 2013 May;41(5):1107-15. doi: 10.1183/09031936.00071312. Epub 2012 Sep 27.

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