Antibiotic treatment of bacterial lung infections in cystic fibrosis.

IF 3 3区 医学 Q1 PEDIATRICS
Giovanni Taccetti, Vito Terlizzi, Silvia Campana, Daniela Dolce, Novella Ravenni, Cristina Fevola, Michela Francalanci, Valeria Galici, Anna Silvia Neri
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引用次数: 0

Abstract

Bacterial infections of the lower airways are the main cause of mortality and morbidity in cystic fibrosis. The most frequently isolated pathogens are S. aureus and P. aeruginosa; bacterial co-infections are frequently observed. The aim of this review is to provide, in the current context, the indications regarding the best antibiotic strategy to adopt in subjects affected by CF infected with the most common pathogens. We selected relevant publications (guidelines, systematic reviews and clinical studies published so far on these topics) and we analysed the sampling methods used and antibiotic strategies adopted. Oropharyngeal sampling methods are considered less sensitive for pathogen detection than sputum. In non-expectorating people, induced sputum is considered equivalent to two-lobe bronchoalveolar lavage, which is considered invasive. Antibiotic treatment against the main pathogens can consist in eradication treatment in the early stages of infection, chronic suppressive therapy and treatment of the pulmonary exacerbations. This scheme is valid for P. aeruginosa but remains to be demonstrated for the other pathogens. For S. aureus, no evidence-based therapeutic strategies on how to treat the different stages of bacterial infection have been established with certainty. With regard to the treatment of the other classic pathogens (B. cepacia complex, A. xylosoxidans and S. maltophilia), no evidence-based indications exist and decision is left to the clinician. The recent introduction of highly effective modulators on the CFTR protein, in addition to the favourable effects described in regulatory trials, has led to a reduction in bacterial isolations; the real effect of which in clinical practice has still to be assessed on the basis of scientific data. CONCLUSIONS: The reliability of culture examination depends on sampling methods, and expectorated sputum continues to be the best method as it is simple and non-invasive. P. aeruginosa is the pathogen for which antibiotic strategies for the various stages of infection appear best established, and the efficacy of early eradication treatment and chronic suppressive therapy have been underlined in clinical trials and systematic reviews. The recent introduction of modulators into clinical practice, despite their widely described efficacy, has not yet led to suggestions for changes in antibiotic strategies against the pathogens most frequently isolated.

囊性纤维化患者肺部细菌感染的抗生素治疗。
下呼吸道细菌感染是导致囊性纤维化患者死亡和发病的主要原因。最常分离到的病原体是金黄色葡萄球菌和铜绿假单胞菌;细菌合并感染也很常见。本综述的目的是在当前情况下,为感染了最常见病原体的囊性纤维化患者提供最佳抗生素策略的指征。我们选取了相关出版物(迄今为止发表的有关这些主题的指南、系统综述和临床研究),并分析了所采用的采样方法和抗生素策略。在病原体检测方面,口咽取样方法被认为不如痰液灵敏。在非排痰人群中,诱导痰被认为等同于双叶支气管肺泡灌洗,而后者被认为是侵入性的。针对主要病原体的抗生素治疗包括感染早期的根除治疗、慢性抑制治疗和肺部恶化治疗。这一方案对铜绿假单胞菌有效,但对其他病原体仍有待论证。至于金黄色葡萄球菌,关于如何治疗细菌感染的不同阶段,目前还没有确定的循证治疗策略。至于对其他典型病原体(复合头孢杆菌、木糖酵母菌和嗜麦芽糖酵母菌)的治疗,目前还没有基于证据的适应症,只能由临床医生自行决定。除了监管试验中描述的良好效果外,最近还推出了高效的 CFTR 蛋白调节剂,从而减少了细菌分离;其在临床实践中的实际效果仍有待根据科学数据进行评估。结论:培养检查的可靠性取决于取样方法,而排出的痰液仍然是最好的方法,因为它既简单又无创。铜绿假单胞菌是一种病原体,针对不同感染阶段的抗生素策略似乎最为成熟,早期根除治疗和慢性抑制治疗的疗效已在临床试验和系统性综述中得到强调。最近将调节剂引入临床实践,尽管其疗效已被广泛描述,但尚未导致针对最常分离的病原体改变抗生素策略的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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