Patjas Anu, Jokiranta T Sakari, Kantele Anu
Department of Infectious Diseases, Meilahti Vaccine Research Centre, MeVac, University of Helsinki and Helsinki University Hospital, P.O. Box 700, FI-00029 HUS Helsinki, Finland.
Human Microbiome Research Unit, University of Helsinki, Haartmaninkatu 3, FI-00290 Helsinki, Finland.
JAC Antimicrob Resist. 2024 Nov 26;6(6):dlae188. doi: 10.1093/jacamr/dlae188. eCollection 2024 Dec.
With the global spread of antimicrobial resistance, treating urinary tract infections (UTIs) is becoming more challenging. Clinical data on UTI outcomes are scarce in cases with antimicrobial treatment mismatching the uropathogens' susceptibility profiles. We explored the association of (mis)matching antimicrobial treatment and clinical outcomes among patients with either ESBL-producing Enterobacterales (ESBL-PE) or non-ESBL-PE identified in urine samples.
In 2015-2019, we recruited 18-65-year-old patients with laboratory-confirmed, community-acquired ESBL-PE ( = 130) or non-ESBL-PE ( = 187) UTI. Our study involved collecting data on susceptibility profiles, antimicrobial therapy (microbiological match/mismatch) and clinical outcomes, and a follow-up of relapses/reinfections.
Non-beta-lactam co-resistance was found more frequent among ESBL-PE than non-ESBL-PE isolates. The initial antimicrobial matched the susceptibility for 91.6% (164/179) of those with non-ESBL-PE and 46.9% (38/81) with ESBL-PE UTI ( < 0.001). The clinical cure rates in the non-ESBL-PE and ESBL-PE UTI groups were 82.6% (142/172) and 62.2% (74/119) ( < 0.001) for all, 87.3% (131/150) and 83.3% (30/36) for those treated with matching antimicrobials, and 33.3% (5/15) and 41.9% (18/43) for those given mismatching antimicrobials, respectively. Mismatching antimicrobial therapy was not associated with relapse/reinfection over the 3-month follow-up ( = 0.943).
In our data, (mis)matching microbiological susceptibility is only partially associated with the clinical outcome of UTI: microbiological matching appears to predict clinical cure better than mismatching predicts clinical failure.
随着抗菌药物耐药性在全球范围内的传播,治疗尿路感染(UTIs)正变得更具挑战性。在抗菌治疗与尿路病原体药敏谱不匹配的情况下,关于UTI治疗结果的临床数据稀缺。我们探讨了在尿样中检测到产超广谱β-内酰胺酶肠杆菌(ESBL-PE)或非ESBL-PE的患者中,抗菌治疗(不)匹配与临床结局之间的关联。
在2015年至2019年期间,我们招募了18至65岁、实验室确诊为社区获得性ESBL-PE(n = 130)或非ESBL-PE(n = 187)UTI的患者。我们的研究包括收集药敏谱、抗菌治疗(微生物学匹配/不匹配)和临床结局的数据,并对复发/再感染进行随访。
与非ESBL-PE分离株相比,ESBL-PE中发现非β-内酰胺类共耐药更为常见。初始抗菌药物与91.6%(164/179)的非ESBL-PE患者和46.9%(38/81)的ESBL-PE UTI患者的药敏匹配(P < 0.001)。非ESBL-PE和ESBL-PE UTI组的总体临床治愈率分别为82.6%(142/172)和62.2%(74/119)(P < 0.001),接受匹配抗菌药物治疗的患者分别为87.3%(131/150)和83.3%(30/36),接受不匹配抗菌药物治疗的患者分别为33.3%(5/15)和41.9%(18/43)。在3个月的随访中,不匹配的抗菌治疗与复发/再感染无关(P = 0.943)。
在我们的数据中,微生物学药敏(不)匹配仅部分与UTI的临床结局相关:微生物学匹配似乎比不匹配更能预测临床治愈,而不匹配比匹配更能预测临床失败。