Romandini Alessandra, Pani Arianna, Schenardi Paolo Andrea, Pattarino Giulia Angela Carla, De Giacomo Costantino, Scaglione Francesco
Department of Oncology and Hemato-Oncology, Postgraduate School of Clinical Pharmacology and Toxicology, Università degli Studi di Milano, 20122 Milan, Italy.
Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Antibiotics (Basel). 2021 Apr 6;10(4):393. doi: 10.3390/antibiotics10040393.
Antibiotic resistance is a public health threat of the utmost importance, especially when it comes to children: according to WHO data, infections caused by multidrug resistant bacteria produce 700,000 deaths across all ages, of which around 200,000 are newborns. This surging issue has multipronged roots that are specific to the pediatric age. For instance, the problematic overuse and misuse of antibiotics (for wrong diagnoses and indications, or at wrong dosage) is also fueled by the lack of pediatric-specific data and trials. The ever-evolving nature of this age group also poses another issue: the partly age-dependent changes of a developing system of cytochromes determine a rather diverse population in terms of biochemical characteristics and pharmacokinetics profiles, hard to easily codify in an age- or weight-dependent dosage. The pediatric population is also penalized by the contraindications of tetracyclines and fluoroquinolones, and by congenital malformations which often require repeated hospitalizations and pharmacological and surgical treatments from a very young age. Emerging threats for the pediatric age are , , ESBL-producing , carbapenem-resistant and the alarming colistin resistance. Urgent actions need to be taken in order to step back from a now likely post-antibiotic era, where simple infections might cause infant death once again.
抗生素耐药性是一个极其重要的公共卫生威胁,尤其是对儿童而言:根据世界卫生组织的数据,耐多药细菌引起的感染在所有年龄段导致70万人死亡,其中约20万是新生儿。这个日益严重的问题有多个根源,这些根源在儿科年龄段是特有的。例如,抗生素的过度使用和滥用问题(用于错误的诊断和适应症,或剂量错误)也因缺乏儿科专用数据和试验而加剧。这个年龄组不断变化的性质也带来了另一个问题:发育中的细胞色素系统部分依赖年龄的变化决定了在生化特征和药代动力学方面相当多样化的人群,很难简单地按照年龄或体重依赖的剂量进行编码。儿科人群还受到四环素和氟喹诺酮类药物禁忌的影响,以及先天性畸形的影响,先天性畸形往往需要从很小的时候就反复住院以及进行药物和手术治疗。儿科面临的新威胁包括产超广谱β-内酰胺酶(ESBL)细菌、耐碳青霉烯类细菌以及令人担忧的对黏菌素的耐药性。需要采取紧急行动,以避免进入一个可能的后抗生素时代,在这个时代,简单的感染可能再次导致婴儿死亡。