Infectious Diseases Department, Rouen University Hospital, Rouen, France.
EA 2656 (GRAM 2.0), IRIB, Normandie Univ, Unirouen, Rouen, France.
J Antimicrob Chemother. 2021 Feb 11;76(3):784-788. doi: 10.1093/jac/dkaa486.
EUCAST recently advised against temocillin use, except for non-serious urinary tract infections (UTI) caused by Escherichia coli, Klebsiella spp. (except Klebsiella aerogenes) and Proteus mirabilis (EKP) treated with a dose of 2 g q8h. We aimed to analyse our practice in the context of a larger temocillin use in France.
All ≥3 day temocillin prescriptions from 2016 to 2019 were reviewed, with reference to French recommendations and a susceptibility breakpoint of 8 mg/L. The primary outcome was early clinical failure (antibiotic switch, relapse or death within 10 days after the completion of antibiotic treatment).
Overall, 153 cases were analysed: 123 cases of UTI (80.4%) and 133 cases of monomicrobial infection with Enterobacterales (86.9%). A total of 160 Enterobacterales were isolated, comprising 108 (67.5%) ESBL producers and 30 (20.7%) non-EKP species. The rate of early clinical failure was 9.2% and was significantly lower for UTI compared with non-UTI (4.9% versus 26.7%, P = 0.001) and for sepsis compared with severe sepsis or septic shock (6.2% versus 25%, P = 0.011). It was not different between 2 g q12h and 2 g q8h doses (10% versus 7.4%, P = 0.81) and between EKP and other Enterobacterales (8.7% versus 14.3%, P = 0.41).
EUCAST recommendations on urinary isolates seem to be too restrictive. Our data support the efficacy of temocillin at a dose of 2 g q12h to treat patients with non-severe complicated UTI caused by MDR Enterobacterales with an MIC of ≤8 mg/L, whatever the species.
EUCAST 最近建议除了治疗由大肠埃希菌、克雷伯菌属(除肺炎克雷伯菌外)和奇异变形杆菌引起的非严重尿路感染(UTI)外,不使用替莫西林,这些感染的治疗剂量为 2 g,q8h。我们旨在根据法国更大规模使用替莫西林的情况分析我们的实践。
回顾了 2016 年至 2019 年所有≥3 天的替莫西林处方,参考了法国的建议和 8mg/L 的药敏折点。主要结局是早期临床失败(抗生素转换、治疗结束后 10 天内复发或死亡)。
共分析了 153 例病例:123 例 UTI(80.4%)和 133 例单一微生物感染的肠杆菌科(86.9%)。共分离出 160 株肠杆菌科,其中 108 株(67.5%)为 ESBL 产酶菌,30 株(20.7%)为非 EKP 菌。早期临床失败率为 9.2%,UTI 明显低于非 UTI(4.9%比 26.7%,P=0.001),败血症明显低于严重败血症或感染性休克(6.2%比 25%,P=0.011)。2 g,q12h 和 2 g,q8h 剂量之间(10%比 7.4%,P=0.81)和 EKP 和其他肠杆菌科之间(8.7%比 14.3%,P=0.41)没有差异。
EUCAST 对尿分离株的建议似乎过于严格。我们的数据支持在 MIC≤8mg/L 时,2 g,q12h 的剂量治疗由 MDR 肠杆菌科引起的非严重复杂 UTI 的疗效,无论哪种物种。