Koerner-Rettberg Cordula, Ballmann Manfred
Department of Pediatric Pneumology, University Children's Hospital of Ruhr University Bochum at St Josef-Hospital, Bochum, Germany.
Core Evid. 2014 Sep 19;9:99-112. doi: 10.2147/CE.S64980. eCollection 2014.
Chronic bacterial respiratory-tract infections are a major driving force in the pathogenesis of cystic fibrosis (CF) lung disease and promote chronic lung-function decline, destruction, and progression to respiratory failure at a premature age. Gram-negative bacteria colonizing the airways in CF are a major problem in CF therapy due to their tendency to develop a high degree of resistance to antibiotic agents over time. Pseudomonas aeruginosa is the dominating bacterial strain infecting the CF lung from early childhood on, and multiresistant strains frequently develop after years of therapy. Colistin has been used for treating pulmonary bacterial infections in CF for decades due to its very good Gram-negative activity. However, drawbacks include concerns regarding toxicity when being applied systemically, and the lack of approval for application by inhalation in the USA for many years. Other antibiotic substances for systemic use are available with good to excellent Gram-negative and anti-Pseudomonas activity, while there are only three substances approved for inhalation use in the treatment of chronic pulmonary infection with proven benefit in CF. The emergence of multiresistant strains leaving nearly no antibiotic substance as a treatment option, the limited number of antibiotics with high activity against P. aeruginosa, the concerns about increasing the risk of antibiotic resistance by continuous antibiotic therapy, the development of new drug formulations and drug-delivery devices, and, finally, the differing treatment strategies used in CF centers call for defining the place of this "old" drug, colistimethate, in today's CF therapy. This article reviews the available evidence to reflect on the place of colistimethate sodium in the therapy of chronic pulmonary infection in CF.
慢性细菌性呼吸道感染是囊性纤维化(CF)肺病发病机制的主要驱动力,会促使肺功能慢性下降、肺组织破坏,并过早发展为呼吸衰竭。由于随着时间推移,CF气道中定植的革兰氏阴性菌容易对抗生素产生高度耐药性,因此它是CF治疗中的一个主要问题。铜绿假单胞菌是从儿童早期就开始感染CF肺部的主要菌株,经过数年治疗后经常会出现多重耐药菌株。由于多粘菌素对革兰氏阴性菌具有良好的活性,因此几十年来一直用于治疗CF中的肺部细菌感染。然而,其缺点包括全身应用时的毒性问题,以及在美国多年来未获吸入给药批准。其他可供全身使用的抗生素物质对革兰氏阴性菌和抗铜绿假单胞菌具有良好至优异的活性,而在治疗CF慢性肺部感染方面,只有三种物质被批准用于吸入治疗且已证实有疗效。多重耐药菌株的出现使得几乎没有抗生素物质可作为治疗选择,对铜绿假单胞菌具有高活性的抗生素数量有限,持续使用抗生素治疗会增加抗生素耐药性风险,新型药物制剂和给药装置的开发,以及CF中心采用的不同治疗策略,都需要明确这种“老”药——多粘菌素甲磺酸钠——在当今CF治疗中的地位。本文回顾现有证据,以思考多粘菌素甲磺酸钠在CF慢性肺部感染治疗中的地位。