Treatment of Resistant Gram-negative bacilli in children

IF 2.9 4区 医学 Q2 INFECTIOUS DISEASES
Robert Cohen , Laurent Dortet , Marion Caseris , Josette Raymond , Mathie Lorrot , Julie Toubiana
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Abstract

Resistance of Gram-negative bacteria to the most widely used antibiotics, particularly β-lactams, is now considered as major public health problem. The main resistance mechanisms to β-lactams in Enterobacterales are the production of extended spectrum β-lactamases (ESBL) or carbapenemases, which hydrolyze virtually all β-lactams. However, a substantial proportion of carbapenem-resistant Gram-negative bacilli do not produce carbapenemase but combine overproduction of a cephalosporinase and/or ESBL with very low penem hydrolysis and reduced outer membrane permeability. The arrival of new antibacterial agents active on some of these multidrug-resistant strains, such as new β-lactam inhibitors, has marked a turning point in treatment and represents real progress. In-depth knowledge of resistance mechanisms is crucial to the choice of the most effective molecule, and their prescription requires close collaboration between microbiologists, infectious disease specialists and intensive care physicians. While these compounds are significantly more active against resistant strains than those previously available, their spectrum of activity does not cover all resistance mechanisms in Gram-negatives, nor in other bacterial species potentially involved in polymicrobial infections. The use of these new compounds does not alter antibiotic regimens in terms of duration and indication of combined antibiotic therapy, which remain very limited.

儿童耐药革兰氏阴性杆菌的治疗。
革兰氏阴性菌对最广泛使用的抗生素,特别是β-内酰胺类抗生素的耐药性,现在被认为是一个主要的公共卫生问题。肠杆菌对β-内酰胺类抗生素的主要耐药性机制是产生超广谱β-内酶(ESBL)或碳青霉烯酶,它们几乎能水解所有的β-内胺类药物。然而,相当大比例的碳青霉烯抗性革兰氏阴性杆菌不产生碳青霉烯酶,而是将头孢菌素酶和/或ESBL的过量产生与非常低的培南水解和降低的外膜通透性结合在一起。对其中一些耐多药菌株具有活性的新抗菌剂的出现,如新的β-内酰胺抑制剂,标志着治疗的转折点,代表着真正的进展。深入了解耐药性机制对于选择最有效的分子至关重要,它们的处方需要微生物学家、传染病专家和重症监护医生之间的密切合作。虽然这些化合物对耐药菌株的活性明显高于以前的那些,但它们的活性谱并不能涵盖革兰氏阴性菌的所有耐药机制,也不能涵盖其他可能参与多种微生物感染的细菌物种的所有耐药机理。就联合抗生素治疗的持续时间和适应症而言,这些新化合物的使用不会改变抗生素方案,这仍然非常有限。
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
Infectious diseases now
Infectious diseases now Medicine-Infectious Diseases
CiteScore
7.10
自引率
2.90%
发文量
116
审稿时长
40 days
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