Di Pietrantonio Maria, Brescini Lucia, Candi Jennifer, Gianluca Morroni, Pallotta Francesco, Mazzanti Sara, Mantini Paolo, Candelaresi Bianca, Olivieri Silvia, Ginevri Francesco, Cesaretti Giulia, Castelletti Sefora, Cocci Emanuele, Polo Rosaria G, Cerutti Elisabetta, Simonetti Oriana, Cirioni Oscar, Tavio Marcello, Giacometti Andrea, Barchiesi Francesco
Infectious Diseases Clinic, Ospedali Riuniti Umberto I, Via Conca 71, 60126 Ancona, Torrette, Italy.
Department of Biomedical Sciences and Public Health, Polytechnic University of Marche Medical School, Via Tronto 10/a, 60020 Ancona, Torrette, Italy.
Antibiotics (Basel). 2022 Feb 28;11(3):321. doi: 10.3390/antibiotics11030321.
Background: Ceftazidime/avibactam is a new cephalosporin/beta-lactamase inhibitor combination approved in 2015 by the FDA for the treatment of complicated intra-abdominal and urinary tract infection, hospital-acquired pneumoniae and Gram-negative infections with limited treatment options. Methods: In this retrospective study, we evaluate the efficacy of ceftazidime/avibactam treatment in 81 patients with Gram-negative infection treated in our center from January 2018 to December 2019. The outcome evaluated was 30-days survival or relapse of infection after the first positive blood culture. Results: the majority of patients were 56 male (69%), with median age of 67. Charlson’s Comorbidity Index was >3 in 58 patients. In total, 46% of the patients were admitted into the medical unit, 41% in the ICU, and 14% in the surgical ward. Of the patients, 78% had nosocomial infections, and 22% had healthcare-related infections. The clinical failure rate was 35%: 13 patients died within 30 days from the onset of infection. The outcome was influenced by the clinical condition of the patients: solid organ transplantation (p = 0.003) emerged as an independent predictor of mortality; non-survival patients most frequently had pneumonia (p = 0.009) or mechanical ventilation (p = 0.049). Conclusion: Ceftazidime−avibactam showed high efficacy in infections caused by MDR Gram-negative pathogens with limited therapeutic options.
头孢他啶/阿维巴坦是一种新型头孢菌素/β-内酰胺酶抑制剂组合,于2015年获美国食品药品监督管理局(FDA)批准,用于治疗复杂性腹腔内感染、泌尿道感染、医院获得性肺炎以及治疗选择有限的革兰氏阴性菌感染。方法:在这项回顾性研究中,我们评估了2018年1月至2019年12月在本中心接受治疗的81例革兰氏阴性菌感染患者使用头孢他啶/阿维巴坦治疗的疗效。评估的结果是首次血培养阳性后30天的生存率或感染复发情况。结果:大多数患者为男性,共56例(69%),中位年龄为67岁。58例患者的查尔森合并症指数>3。总体而言,46%的患者入住内科病房,41%入住重症监护病房(ICU),14%入住外科病房。在这些患者中,78%患有医院感染,22%患有与医疗保健相关的感染。临床失败率为35%:13例患者在感染发作后30天内死亡。结果受患者临床状况的影响:实体器官移植(p = 0.003)是死亡率的独立预测因素;未存活患者最常见的是肺炎(p = 0.009)或机械通气(p = 0.049)。结论:头孢他啶-阿维巴坦在治疗选择有限的耐多药革兰氏阴性病原体引起的感染中显示出高效性。