International Health Management Associates, Inc., 2122 Palmer Drive, Schaumburg, IL 60173, USA.
Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ 07033, USA.
J Glob Antimicrob Resist. 2020 Mar;20:209-213. doi: 10.1016/j.jgar.2019.07.017. Epub 2019 Jul 24.
Infections caused by Pseudomonas aeruginosa are often difficult to treat. Knowledge of the risk of infection with resistant P. aeruginosa would allow more discriminatory prescribing of broad-spectrum antimicrobials. Using clinical isolates collected as part of the Study for Monitoring Antimicrobial Resistance Trends (SMART), we examined the activity of commonly used β-lactams, levofloxacin, and ceftolozane-tazobactam (C/T), an antipseudomonal cephalosporin/β-lactamase inhibitor approved in the United States and over 60 countries worldwide, against P. aeruginosa isolates from patients in different risk strata.
In 2016-2017, 25 hospitals in the US each collected up to 250 consecutive gram-negative bacilli per year from respiratory tract (RTI), intraabdominal (IAI), and urinary tract (UTI) infections. MICs of 9,964 isolates (including 1,887 P. aeruginosa) were determined using CLSI broth microdilution and interpreted with CLSI breakpoints.
Susceptibility of all P. aeruginosa isolates combined was 94.7% to C/T and 76.8%, 77.0%, 70.2%, and 69.0% to ceftazidime, meropenem, piperacillin-tazobactam, and levofloxacin, respectively. Susceptibility to the β-lactam comparators was 8-11 percentage points lower among ICU than non-ICU isolates, 7-11 points lower in isolates collected ≥48h than <48h post-admission, 1-5 points lower in patients <65 years of age than older patients, and 3-12 points lower in RTI than IAI and UTI isolates. C/T maintained activity against >90% of P. aeruginosa isolates in all risk strata and against 75-88% of isolates nonsusceptible to ceftazidime, meropenem, or piperacillin-tazobactam.
C/T represents a promising new treatment option even in strata in which the risk of infection with β-lactam-nonsusceptible P. aeruginosa appeared higher.
铜绿假单胞菌引起的感染通常难以治疗。了解耐铜绿假单胞菌感染的风险,可以更有针对性地开具广谱抗菌药物。本研究使用作为监测抗菌药物耐药趋势研究(SMART)一部分收集的临床分离株,检测了常用的β-内酰胺类药物、左氧氟沙星和头孢他唑巴坦-他唑巴坦(C/T)对不同危险分层患者的铜绿假单胞菌分离株的活性。C/T 是一种在美国和全球 60 多个国家批准的抗假单胞菌头孢菌素/β-内酰胺酶抑制剂。
2016-2017 年,美国 25 家医院每年从呼吸道(RTI)、腹腔内(IAI)和尿路感染(UTI)感染中各收集 250 株连续的革兰氏阴性杆菌。使用 CLSI 肉汤微量稀释法测定 9964 株分离株(包括 1887 株铜绿假单胞菌)的 MIC,并使用 CLSI 折点进行解释。
所有铜绿假单胞菌分离株的 C/T 药敏率为 94.7%,头孢他啶、美罗培南、哌拉西林-他唑巴坦和左氧氟沙星的药敏率分别为 76.8%、77.0%、70.2%和 69.0%。与非 ICU 分离株相比,ICU 分离株对β-内酰胺类药物的敏感性低 8-11 个百分点,与入院后 48 小时内采集的分离株相比,48 小时后采集的分离株低 7-11 个百分点,与<65 岁的患者相比,≥65 岁的患者低 1-5 个百分点,与 RTI 分离株相比,IAI 和 UTI 分离株低 3-12 个百分点。C/T 对所有危险分层中>90%的铜绿假单胞菌分离株保持活性,对 75-88%的头孢他啶、美罗培南或哌拉西林-他唑巴坦不敏感的分离株也保持活性。
即使在感染β-内酰胺类药物不敏感铜绿假单胞菌风险较高的分层中,C/T 也是一种有前途的新治疗选择。