Branton Alexander C, Vu Catherine H, Venugopalan Veena, Santevecchi Barbara A, Cherabuddi Kartikeya, Ramphal Reuben, Manohar Tanvi, Desear Kathryn E
Department of Pharmacy, St. Anthony's Hospital, St. Petersburg, FL, USA.
Department of Pharmacy, University Medical Center New Orleans, New Orleans, LA, USA.
JAC Antimicrob Resist. 2023 Mar 17;5(2):dlad021. doi: 10.1093/jacamr/dlad021. eCollection 2023 Apr.
To re-examine the use of non-carbapenems (NCBPs), specifically piperacillin/tazobactam and cefepime, for ESBL-producing Enterobacterales (ESBL-E) urinary tract infections (UTIs).
Retrospective cohort study of adults hospitalized between January 2016 and June 2020 with pyuria on urinalysis, a urine culture positive for ESBL-E treated with a study antibiotic (meropenem, ertapenem, cefepime or piperacillin/tazobactam) and did not meet criteria for study exclusion.
To compare carbapenems (CBPs) with cefepime or piperacillin/tazobactam for the treatment of ESBL-E UTI. The primary outcome was clinical cure, defined as complete resolution of signs and symptoms of infection. Secondary outcomes included in-hospital mortality, recurrence within 30 days and resistance emergence within 30 days.
One-hundred and thirty-three patients were included, based on definitive therapy received; 69 (51.9%) received CBP and 64 (48.1%) received NCBP therapy. Of the total patient population, 17 (12.8%) were admitted to the ICU, 84 (63.1%) had a complicated UTI and 64 (48.1%) had pyelonephritis. There was no difference in clinical cure between the CBP and NCBP groups (95.7% versus 96.9%, = 0.999). Additionally, no differences in secondary outcomes were observed.
When compared with CBPs, cefepime and piperacillin/tazobactam resulted in similar clinical cure, in-hospital mortality, recurrence and resistance emergence in the treatment of ESBL-E UTI.
重新审视非碳青霉烯类药物(NCBPs),特别是哌拉西林/他唑巴坦和头孢吡肟,用于产超广谱β-内酰胺酶肠杆菌科细菌(ESBL-E)所致尿路感染(UTIs)的情况。
对2016年1月至2020年6月期间住院的成年人进行回顾性队列研究,这些患者尿液分析显示脓尿,尿培养ESBL-E阳性,接受了研究用抗生素(美罗培南、厄他培南、头孢吡肟或哌拉西林/他唑巴坦)治疗,且不符合研究排除标准。
比较碳青霉烯类药物(CBPs)与头孢吡肟或哌拉西林/他唑巴坦治疗ESBL-E UTI的效果。主要结局为临床治愈,定义为感染的体征和症状完全消退。次要结局包括院内死亡率、30天内复发及30天内出现耐药。
根据接受的确定性治疗,纳入133例患者;69例(51.9%)接受CBP治疗,64例(48.1%)接受NCBP治疗。在全部患者中,17例(12.8%)入住重症监护病房,84例(63.1%)患有复杂性UTI,64例(48.1%)患有肾盂肾炎。CBP组和NCBP组的临床治愈率无差异(95.7%对96.9%,P = 0.999)。此外,次要结局也未观察到差异。
与CBPs相比,头孢吡肟和哌拉西林/他唑巴坦在治疗ESBL-E UTI时,临床治愈率、院内死亡率、复发率及耐药出现情况相似。