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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。

Assessing effects of inhaled antibiotics in adults with non-cystic fibrosis bronchiectasis--experiences from recent clinical trials.

机构信息

a Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine , University of Miami , Miami , FL , USA.

b Miami Children's Research Institute , Nicklaus Children's Research Institute , Miami , FL , USA.

出版信息

Expert Rev Respir Med. 2018 Sep;12(9):769-782. doi: 10.1080/17476348.2018.1503540. Epub 2018 Aug 3.

Abstract

INTRODUCTION

Non-cystic fibrosis bronchiectasis (NCFB) results from a permanent and progressive destruction of the airways leading to poor lung function. NCFB is characterized by recurrent lung infection, sputum production, and cough, often requiring long-term antibiotic therapy and hospitalization. At present, there are no approved therapies available. Clinical trials of inhaled antibiotics have shown promise against sputum bacterial load, but mixed results on clinical outcomes. Areas covered: The objective of this review is to provide an overview of NCFB and critically evaluate the evidence supporting the outcome measures used in recent clinical trials of inhaled antibiotics. These include quantitative changes in bacterial load, sputum purulence and yield, inflammatory markers, and lung function, as well as clinical changes in exacerbations, exacerbation frequency, hospitalizations, and health-related quality of life. Expert commentary: Recently completed large trials of inhaled antibiotics in NCFB did not consistently meet pre-specified end points, suggesting that we have not yet found the best enrollment criteria or outcome measures to evaluate efficacy, although reduced exacerbation frequency may be clinically most meaningful. Future trials may focus on specific patient populations at high risk with new information obtained through analyses of large international patient registries.

ABBREVIATIONS

6-MWT: Six-Minute Walk Test; AIR-BX: Aztreonam for Inhalation Solution in Patients with Non-Cystic Fibrosis Bronchiectasis trial; BSI: Bronchiectasis Severity Index; CAT: COPD Assessment Test; CF: Cystic Fibrosis; CFTR: Cystic Fibrosis Transmembrane Conductance Regulator; CFU: Colony-Forming Units; COPD: Chronic Obstructive Pulmonary Disease; CRP: C-Reactive Protein; DPI: Dry Powder for Inhalation; EMA: European Medicines Agency; ERS: European Respiratory Society; FACED: FEV1, Age, Chronic colonization by P. aeruginosa, Extension of bronchiectasis and Dyspnea; FDA: US Food and Drug Administration; FEV: Forced Expiration in 1 s; FVC: Forced Vital Capacity; HFCC: High-Frequency Chest Compression; HRCT: High-Resolution Computed Tomography; HRQoL: Health-Related Quality of Life; LCQ: Leicester Cough Questionnaire; MID: Minimal Important Difference; NCFB: Non-Cystic Fibrosis Bronchiectasis; NTM: Nontuberculous Mycobacteria; ORBIT: Once-daily Respiratory Bronchiectasis Inhalation Treatment trial; PRO: Patient-Reported Outcomes; QoL-B: Quality of Life-Bronchiectasis; SGRQ: St. George's Respiratory Questionnaire; SWT: Shuttle Walk Test; TORCH: Towards a Revolution in COPD Health trial; UPLIFT: Understanding Potential Long-term Impacts on Function with Tiotropium trial.

摘要

简介

非囊性纤维化支气管扩张症(NCFB)是气道永久性和进行性破坏导致肺功能下降的结果。NCFB 的特征是反复肺部感染、痰产生和咳嗽,常需要长期抗生素治疗和住院治疗。目前,尚无批准的治疗方法。吸入抗生素的临床试验显示出对痰细菌负荷的有希望的效果,但对临床结果的影响结果喜忧参半。

涵盖领域

本综述的目的是概述 NCFB,并批判性地评估最近吸入抗生素临床试验中支持使用的结果测量的证据。这些包括细菌负荷、痰脓性和产量、炎症标志物和肺功能的定量变化,以及加重、加重频率、住院和健康相关生活质量的临床变化。

专家评论

最近完成的 NCFB 中吸入抗生素的大型试验并未一致达到预定的终点,这表明我们尚未找到评估疗效的最佳入组标准或结果测量,尽管减少加重频率可能在临床上更有意义。未来的试验可能会针对具有通过大型国际患者登记处分析获得的新信息的高危特定患者人群进行。

缩写词

6-MWT:六分钟步行测试;AIR-BX:吸入阿佐仑治疗非囊性纤维化支气管扩张症试验;BSI:支气管扩张严重指数;CAT:慢性阻塞性肺疾病评估测试;CF:囊性纤维化;CFTR:囊性纤维化跨膜电导调节剂;CFU:集落形成单位;COPD:慢性阻塞性肺疾病;CRP:C 反应蛋白;DPI:干粉吸入器;EMA:欧洲药品管理局;ERS:欧洲呼吸学会;FACED:FEV1、年龄、慢性铜绿假单胞菌定植、支气管扩张扩展和呼吸困难;FDA:美国食品和药物管理局;FEV:1 秒用力呼气量;FVC:用力肺活量;HFCC:高频胸部压缩;HRCT:高分辨率计算机断层扫描;HRQoL:健康相关生活质量;LCQ:莱斯特咳嗽问卷;MID:最小重要差异;NCFB:非囊性纤维化支气管扩张症;NTM:非结核分枝杆菌;ORBIT:每日一次呼吸支气管扩张吸入治疗试验;PRO:患者报告的结果;QoL-B:支气管扩张生活质量;SGRQ:圣乔治呼吸问卷;SWT:穿梭步行测试;TORCH:COPD 健康研究的革命试验;UPLIFT:噻托溴铵治疗肺功能长期影响试验。

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