Heard Katie L, Killington Kieran, Mughal Nabeela, Moore Luke S P, Hughes Stephen
Chelsea and Westminster NHS Foundation Trust, 369 Fulham Road, London SW10 9NH, UK.
North West London Pathology, Imperial College Healthcare NHS Trust, Fulham Palace Road. London W6 8RF, UK.
JAC Antimicrob Resist. 2021 Feb 14;3(1):dlab005. doi: 10.1093/jacamr/dlab005. eCollection 2021 Mar.
With increasing frequency of resistant Gram-negative bacteria, temocillin has potential utility in reducing carbapenem use. The 2020 EUCAST guideline changes temocillin breakpoints and reclassifies isolates with an MIC of 0.001-16 mg/L as 'susceptible, increased exposure' necessitating 6 g/day rather than the previous 4 g/day, associated with significant cost implications.
We explore the clinical utility and treatment failure rate of temocillin at 4 g/day dosing.
All adult inpatient electronic prescriptions of temocillin (3 days or greater) from March 2016 to October 2019 were retrieved using a clinical decision support system (ICNET). Treatment success was defined as survival, no switch to broad-spectrum agent for the same indication and no subsequent recrudescence of infection, occurring within 30 days.
Temocillin was used in 205 eligible patient-episodes, median age 79 years (IQR : 71-87 years), 42.4% female. Median temocillin course length was 5.9 days (IQR : 4.6-7.8 days). Indications for use: urinary tract infection (UTI) (=141), pneumonia (=53), other (=11). In total, 144 (70.2%) patients had targeted treatment; 74 (36.1%) against , 70 (34.4%) other Enterobacterales. A total of 130 (63%) patients received 4 g/day; the remaining patients had reduced renal function with dosing in accordance with guidance. Overall temocillin treatment success was 79.5%; highest when used to treat UTI 85.8% (versus 67.9% in respiratory infections, =0.008). Empirical treatment demonstrated 82.0% (50/61) success [versus 78.5% (113/144) among targeted treatment, =0. 71].
Temocillin at 4 g/day is an effective and safe alternative in treating patients with Gram-negative infections, but should be considered in the context of patient age and comorbidities. Increased dosing or alternate strategies may be indicated when the infection is not of a urinary source.
随着革兰氏阴性耐药菌的出现频率不断增加,替莫西林在减少碳青霉烯类药物使用方面具有潜在效用。2020年欧洲临床微生物学和传染病学会(EUCAST)指南更改了替莫西林的断点,并将最低抑菌浓度(MIC)为0.001 - 16mg/L的分离株重新分类为“敏感,暴露增加”,这需要每日剂量6g而非之前的4g,这带来了显著的成本影响。
我们探讨每日4g剂量替莫西林的临床效用和治疗失败率。
使用临床决策支持系统(ICNET)检索2016年3月至2019年10月所有成人住院患者开具的替莫西林电子处方(疗程为3天或更长时间)。治疗成功定义为患者存活,未因相同适应症改用广谱药物,且在30天内未出现后续感染复发。
替莫西林用于205例符合条件的患者疗程,中位年龄79岁(四分位间距:71 - 87岁),女性占42.4%。替莫西林的中位疗程为5.9天(四分位间距:4.6 - 7.8天)。使用指征:尿路感染(UTI)(=141例)、肺炎(=53例)、其他(=11例)。总共有144例(70.2%)患者接受了针对性治疗;74例(36.1%)针对 ,70例(34.4%)针对其他肠杆菌科细菌。共有130例(63%)患者接受每日4g的剂量;其余患者肾功能减退,根据指导调整剂量。替莫西林总体治疗成功率为79.5%;用于治疗UTI时成功率最高,为85.8%(而呼吸道感染为67.9%,P = 0.008)。经验性治疗的成功率为82.0%(50/61)[针对性治疗为78.5%(113/144),P = 0.71]。
每日4g剂量的替莫西林是治疗革兰氏阴性感染患者的一种有效且安全的替代药物,但应结合患者年龄和合并症情况考虑。当感染并非源于泌尿系统时,可能需要增加剂量或采用其他策略。