From the JMI Laboratories, North Liberty, Iowa.
Pediatr Infect Dis J. 2018 Jun;37(6):549-554. doi: 10.1097/INF.0000000000001859.
Ceftazidime-avibactam was approved by the US Food and Drug Administration in 2015 to treat complicated intra-abdominal and urinary tract infections in adults and is under clinical development for treating pediatric patients.
Among 53,381 Gram-negative organisms (1 per patient) collected in 2011-2015, 8461 (15.9%) were from pediatric (≤17 years old) patients. The isolates were collected from 82 US medical centers and susceptibility tested against ceftazidime-avibactam (avibactam at fixed 4 μg/mL) and comparators by reference broth microdilution methods. Susceptibility results were stratified by patient age: ≤1 (3671 isolates); 2-5 (1900); 6-12 (1644) and 13-17 years old (1246). Enterobacteriaceae with an extended-spectrum β-lactamase (ESBL) screening-positive phenotype were evaluated by microarray-based assay for genes encoding ESBLs, KPC, NDM and transferable AmpC enzymes.
Ceftazidime-avibactam inhibited >99.9% of all Enterobacteriaceae at the ≤8 μg/mL susceptible break point and was highly active against ESBL screening-positive phenotype Escherichia coli and Klebsiella pneumoniae. Overall, 83.6% of ESBL screening-positive phenotype K. pneumoniae were susceptible to meropenem. Only 1 of 4724 Enterobacteriaceae (0.02%) isolates was nonsusceptible to ceftazidime-avibactam, an Enterobacter aerogenes with a ceftazidime-avibactam minimum inhibitory concentration (MIC) value of 16 μg/mL and negative results for all β-lactamase tested. Ceftazidime-avibactam was very active against Pseudomonas aeruginosa (MIC50/90, 1/4 μg/mL; 99.1% susceptible), including isolates nonsusceptible to meropenem (94.0% susceptible to ceftazidime-avibactam) or piperacillin-tazobactam (91.7% susceptible) or ceftazidime (89.6% susceptible). Ceftazidime-avibactam activity against P. aeruginosa did not vary substantially among age groups (98.8%-99.3% susceptible) or year of isolation (98.5%-100.0% susceptible).
Ceftazidime-avibactam was very active against a large collection of Gram-negative bacilli isolated from pediatric patients, including P. aeruginosa and Enterobacteriaceae with an ESBL screening-positive phenotype and resistant to carbapenems.
头孢他啶-阿维巴坦于 2015 年获得美国食品和药物管理局批准,用于治疗成人复杂性腹腔内和尿路感染,目前正在临床开发用于治疗儿科患者。
在 2011 年至 2015 年间收集的 53381 株革兰氏阴性菌(每例患者 1 株)中,8461 株(15.9%)来自儿科(≤17 岁)患者。这些分离株来自 82 个美国医疗中心,采用参考肉汤微量稀释法对抗头孢他啶-阿维巴坦(阿维巴坦固定 4μg/ml)和对照药物进行药敏试验。根据患者年龄对药敏结果进行分层:≤1 岁(3671 株);2-5 岁(1900 株);6-12 岁(1644 株)和 13-17 岁(1246 株)。用基于微阵列的检测方法检测具有超广谱β-内酰胺酶(ESBL)筛选阳性表型的肠杆菌科,检测 ESBL、KPC、NDM 和可转移 AmpC 酶的编码基因。
头孢他啶-阿维巴坦在≤8μg/ml 的敏感折点抑制了所有肠杆菌科的>99.9%,对 ESBL 筛选阳性表型的大肠埃希菌和肺炎克雷伯菌具有高度活性。总体而言,83.6%的 ESBL 筛选阳性表型肺炎克雷伯菌对美罗培南敏感。在 4724 株肠杆菌科中,只有 1 株(0.02%)对头孢他啶-阿维巴坦不敏感,为产头孢他啶-阿维巴坦 MIC 值为 16μg/ml 的阴沟肠杆菌,所有β-内酰胺酶检测均为阴性。头孢他啶-阿维巴坦对铜绿假单胞菌(MIC50/90,1/4μg/ml;99.1%敏感)非常有效,包括对美罗培南(94.0%敏感)、哌拉西林-他唑巴坦(91.7%敏感)或头孢他啶(89.6%敏感)不敏感的分离株。头孢他啶-阿维巴坦对铜绿假单胞菌的活性在不同年龄组(98.8%-99.3%敏感)或分离年份(98.5%-100.0%敏感)之间差异不大。
头孢他啶-阿维巴坦对儿科患者分离的大量革兰氏阴性杆菌具有很强的活性,包括对 ESBL 筛选阳性表型和碳青霉烯类耐药的铜绿假单胞菌和肠杆菌科。