Clinical Department of Medical, Surgical and Health Sciences. Trieste University, Trieste, Italy.
Clinica Malattie Infettive, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
J Glob Antimicrob Resist. 2021 Jun;25:268-281. doi: 10.1016/j.jgar.2021.04.001. Epub 2021 Apr 23.
Ceftazidime/avibactam (CAZ-AVI), approved in 2015, is an important first-line option for Klebsiella pneumoniae carbapenemase-producing Enterobacterales (KPC-E). Although still uncommon, resistance to CAZ-AVI has emerged and may represent a serious cause of concern.
We performed a systematic literature review of clinical and microbiological features of infections and colonisations by CAZ-AVI-resistant KPC-E, focused on the in vivo emergence of CAZ-AVI resistance in different clinical scenarios.
Twenty-three papers were retrieved accounting for 42 patients and 57 isolates, mostly belonging to K. pneumoniae ST258 harbouring D179Y substitution in the KPC enzyme. The USA, Greece and Italy accounted for 80% of cases. In one-third of isolates resistance was not associated with previous CAZ-AVI exposure. Moreover, 20% of the strains were colistin-resistant and 80% were extended-spectrum β-lactamase (ESBL)-producers. The majority of infected patients had severe underlying diseases (39% cancer, 22% solid-organ transplantation) and 37% died. The abdomen, lung and blood were the most involved infection sites. Infections by CAZ-AVI-resistant strains were mainly treated with combination therapy (85% of cases), with meropenem being the most common (65%) followed by tigecycline (30%), gentamicin (25%), colistin (25%) and fosfomycin (10%). Despite the emergence of resistance, 35% of patients received CAZ-AVI.
Taken together, these data highlight the need for prompt susceptibility testing including CAZ-AVI for Enterobacterales, at least in critical areas. Resistance to CAZ-AVI is an urgent issue to monitor in order to improve both empirical and targeted CAZ-AVI use as well as the management of patients with infections caused by CAZ-AVI-resistant strains.
头孢他啶/阿维巴坦(CAZ-AVI)于 2015 年获得批准,是治疗产碳青霉烯酶肠杆菌科(KPC-E)的重要一线选择。尽管仍然不常见,但 CAZ-AVI 的耐药性已经出现,可能成为一个严重的关注问题。
我们对 CAZ-AVI 耐药的 KPC-E 引起的感染和定植的临床和微生物学特征进行了系统的文献回顾,重点关注不同临床情况下 CAZ-AVI 耐药性的体内出现。
共检索到 23 篇论文,涉及 42 名患者和 57 株分离株,主要属于携带 KPC 酶 D179Y 取代的肺炎克雷伯菌 ST258。美国、希腊和意大利占病例的 80%。三分之一的分离株的耐药性与之前的 CAZ-AVI 暴露无关。此外,20%的菌株对黏菌素耐药,80%的菌株产超广谱β-内酰胺酶(ESBL)。受感染的患者大多患有严重的基础疾病(39%为癌症,22%为实体器官移植),37%死亡。腹部、肺部和血液是最常见的感染部位。CAZ-AVI 耐药株引起的感染主要采用联合治疗(85%的病例),其中美罗培南最为常见(65%),其次是替加环素(30%)、庆大霉素(25%)、黏菌素(25%)和磷霉素(10%)。尽管出现了耐药性,但仍有 35%的患者接受了 CAZ-AVI 治疗。
综上所述,这些数据强调了需要及时进行药敏试验,包括对肠杆菌科进行 CAZ-AVI 药敏试验,至少在关键区域进行。需要密切监测 CAZ-AVI 的耐药性,以改善经验性和靶向 CAZ-AVI 的使用,并改善 CAZ-AVI 耐药株引起的感染患者的管理。