Oosterbos Julie, Schalkwijk Maaike, Thiessen Steven, Oris Els, Coppens Guy, Lagrou Katrien, Steensels Deborah
Ziekenhuis Oost-Limburg hospital, Genk, Belgium.
Katholieke Universiteit Leuven, Leuven, Belgium.
JAC Antimicrob Resist. 2022 Aug 23;4(4):dlac086. doi: 10.1093/jacamr/dlac086. eCollection 2022 Aug.
Expanding the use of temocillin could be an important weapon in the fight against antimicrobial resistance. However, EUCAST defined clinical breakpoints for a limited number of species and only for urinary tract infections (UTI), including urosepsis but excluding severe sepsis and septic shock. Moreover, a dosage of 2 g q8h is advised in most cases.
Evaluation of temocillin use for the treatment of bacteraemia, correlating clinical and microbiological outcomes with infection site, infection severity, temocillin dosage, Enterobacterales species and MIC.
All adult patients with blood cultures positive for temocillin-susceptible Enterobacterales and treated with temocillin for ≥72 h from June 2018 until June 2021 were considered for inclusion. The primary outcome was clinical success, defined as resolution of infection signs, no relapse of the same infection and no antibiotic switch due to insufficient clinical improvement. The secondary outcome was microbiological success.
In total, 182 episodes were included [140 UTI versus 42 non-UTI, 171 species (except ) and (EKPs) versus 11 non-EKPs]. Clinical and microbiological failure were low (8% and 3%, respectively). No difference in outcome was observed for dosages of 2 g q12h versus 2 g q8h, either for EKP versus non-EKP isolates or MIC values ≤8 versus 16 mg/L. Considering only bacteraemia episodes of UTI origin, using the 16 mg/L breakpoint, there was no difference in success rate between regimens of 2 g q12h and 2 g q8h.
Temocillin 2 g q12h can be successfully used for the treatment of systemic UTI. Prospective studies are needed to assess outcomes and evaluate non-inferiority compared with other broad-spectrum antibiotics in non-UTI infections, including bacteraemia.
扩大替莫西林的使用可能是对抗抗菌药物耐药性的一项重要武器。然而,欧洲抗菌药物敏感性试验委员会(EUCAST)仅为有限数量的菌种定义了临床断点,且仅针对尿路感染(UTI),包括尿脓毒症,但不包括严重脓毒症和感染性休克。此外,在大多数情况下建议剂量为2g每8小时一次。
评估替莫西林用于治疗菌血症的情况,将临床和微生物学结果与感染部位、感染严重程度﹑替莫西林剂量、肠杆菌科菌种及最低抑菌浓度(MIC)相关联。
纳入2018年6月至2021年6月期间所有血培养对替莫西林敏感的肠杆菌科菌种呈阳性且接受替莫西林治疗≥72小时的成年患者。主要结局为临床成功,定义为感染体征消退、同一感染无复发且未因临床改善不足而更换抗生素。次要结局为微生物学成功。
共纳入182例病例[140例UTI与42例非UTI,171例肠杆菌科菌种(除外 )和 (产超广谱β-内酰胺酶菌)与11例非产超广谱β-内酰胺酶菌]。临床和微生物学失败率较低(分别为8%和3%)。对于每12小时2g与每8小时2g的剂量,无论是产超广谱β-内酰胺酶菌与非产超广谱β-内酰胺酶菌分离株,还是MIC值≤8mg/L与16mg/L,结局均无差异。仅考虑UTI来源的菌血症病例,使用16mg/L的断点时,每12小时2g与每8小时2g方案的成功率无差异。
每12小时2g的替莫西林可成功用于治疗全身性UTI。需要进行前瞻性研究以评估结局,并与其他广谱抗生素在包括菌血症在内的非UTI感染中进行非劣效性评估。