Rashid Mamun-Ur, Rosenborg Staffan, Panagiotidis Georgios, Söderberg-Löfdal Karin, Weintraub Andrej, Nord Carl Erik
Department of Laboratory Medicine, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Department of Laboratory Medicine, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden
Antimicrob Agents Chemother. 2015 Aug;59(8):4504-9. doi: 10.1128/AAC.00530-15. Epub 2015 May 18.
Ceftaroline-avibactam is a new combination of the antibiotic ceftaroline with a novel non-β-lactam β-lactamase inhibitor, avibactam. The purpose of the present study was to investigate the effect of ceftaroline-avibactam on the human intestinal microbiota. Fourteen healthy volunteers received ceftaroline-avibactam (600 mg ceftaroline fosamil and 600 mg avibactam) intravenously over 2 h every 8 h on days 1 to 6 and as a single dose on day 7. Fecal samples were collected on day -1 (within 24 h of the first infusion on day 1) and on days 2, 5, 7, 9, 14, and 21. Escherichia coli numbers decreased during the study and normalized on day 21. An increased number of Klebsiella bacteria appeared on day 14 and normalized on day 21. The number of other enterobacteria decreased during the study, and the number of enterococci decreased from days 2 to 7 and normalized on day 9. Candida numbers increased from days 5 to 9 and normalized after day 14. The number of lactobacilli decreased during the study and recovered on day 14. The number of bifidobacteria decreased on day 2 and normalized on day 21. The number of Bacteroides bacteria was unchanged. Clostridium difficile numbers decreased on days 7 and 9 and increased on days 14 and 21. A toxigenic C. difficile strain was detected in one volunteer on day 21 with no reported adverse events. Plasma samples were collected on days -1, 2, 5, and 7. Ceftaroline and avibactam concentrations were 0 to 34.5 mg/liter and 0 to 61.6 mg/liter, respectively, in plasma and 0 to 35.4 mg/kg and 0 to 98.5 mg/kg, respectively, in feces. (This study is registered in the European Clinical Trials Database [https://eudract.ema.europa.eu/] under number EudraCT 2012 004921-25.).
头孢洛林-阿维巴坦是抗生素头孢洛林与新型非β-内酰胺类β-内酰胺酶抑制剂阿维巴坦的新组合。本研究的目的是调查头孢洛林-阿维巴坦对人体肠道微生物群的影响。14名健康志愿者在第1至6天每8小时静脉输注头孢洛林-阿维巴坦(600毫克头孢洛林磷霉素和600毫克阿维巴坦),持续2小时,第7天给予单剂量。在第-1天(第1天首次输注后24小时内)以及第2、5、7、9、14和21天采集粪便样本。研究期间大肠杆菌数量减少,在第21天恢复正常。肺炎克雷伯菌数量在第14天增加,在第21天恢复正常。其他肠杆菌数量在研究期间减少,肠球菌数量从第2天至第7天减少,在第9天恢复正常。念珠菌数量从第5天至第9天增加,在第14天后恢复正常。乳酸杆菌数量在研究期间减少,在第14天恢复。双歧杆菌数量在第2天减少,在第21天恢复正常。拟杆菌数量未变。艰难梭菌数量在第7天和第9天减少,在第14天和第21天增加。在第21天,一名志愿者检测到一株产毒艰难梭菌菌株,未报告不良事件。在第-1、2、5和7天采集血浆样本。血浆中头孢洛林和阿维巴坦浓度分别为0至34.5毫克/升和0至61.6毫克/升,粪便中分别为0至35.4毫克/千克和0至98.5毫克/千克。(本研究已在欧洲临床试验数据库[https://eudract.ema.europa.eu/]注册,编号为EudraCT 2012 004921-25。)