Merchante Nicolás, Herrero Rocío, Valverde-Fredet María Dolores, Rodríguez-Fernández Miguel, Pinagorte Héctor, Martínez-Marcos Francisco J, Gil-Anguita Concepción, García-López María, Tasias Pitarch María, Abril López De Medrano Vicente, Navarrete Lorite Miguel Nicolás, Gómez-Ayerbe Cristina, León Eva, González-De La Aleja Pilar, Ruiz Castillo Ana, Aller Ana I, Rodríguez Juan Carlos, Ternero Fonseca Julia, Corzo Juan E, Naranjo Pérez Alberto, Trigo-Rodríguez Marta, Merino Esperanza
Unidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario de Valme, Instituto de Biomedicina de Sevilla (IBiS), Universidad de Sevilla, Avenida de Bellavista s/n, 41014, Sevilla, Spain.
Unidad de Enfermedades Infecciosas, Hospital General Universitario Dr. Balmis, Instituto de Investigación Biomédica de Alicante (ISABIAL), Alicante, Spain.
JAC Antimicrob Resist. 2023 Mar 23;5(2):dlad033. doi: 10.1093/jacamr/dlad033. eCollection 2023 Apr.
To investigate the role of previous antibiotic therapy in the risk of recurrence after a infection (CDI) treated with vancomycin.
Multicentre observational study. Patients with a CDI episode achieving clinical cure with oral vancomycin and followed up 8 weeks were included. Previous antibiotic exposure up to 90 days was collected. Multivariate analysis of predictors of recurrence adjusted by the propensity score (PS) of being previously treated with each non-CDI antibiotic was performed.
Two hundred and forty-one patients were included; 216 (90%) had received systemic antibiotics. Fifty-three patients (22%) had a CDI recurrence. Rates of recurrence were lower in those treated with piperacillin/tazobactam in the last month when compared with those not receiving piperacillin/tazobactam [3 (7%) versus 50 (25%); = 0.01], whereas higher rates were seen in those treated with cephalosporins in the last month [26/87 (30%) versus 27/154 (17%); = 0.03]. In multivariate analysis controlled by the inverse probability of treatment weighting by PS, receiving 5 days of piperacillin/tazobactam in the last month as the last antibiotic regimen prior to CDI was independently associated with a lower risk of recurrence [adjusted OR (AOR) 0.13; 95% CI: 0.06-0.29; < 0.0001] whereas exposure for 5 days to cephalosporins (versus piperacillin/tazobactam) was associated with an increased risk (AOR 10.9; 95% CI: 4.4-27.1; < 0.0001).
Recent use of piperacillin/tazobactam might be associated with a lower risk of CDI recurrence, while recent use of cephalosporins might promote an increased risk. These findings should be considered when treating hospitalized patients.
探讨既往抗生素治疗在万古霉素治疗艰难梭菌感染(CDI)后复发风险中的作用。
多中心观察性研究。纳入口服万古霉素实现临床治愈并随访8周的CDI发作患者。收集既往90天内的抗生素暴露情况。对根据每种非CDI抗生素既往治疗倾向评分(PS)调整的复发预测因素进行多变量分析。
纳入241例患者;216例(90%)接受过全身用抗生素治疗。53例患者(22%)出现CDI复发。与未接受哌拉西林/他唑巴坦治疗的患者相比,最后1个月接受哌拉西林/他唑巴坦治疗的患者复发率较低[3例(7%)对50例(25%);P = 0.01],而最后1个月接受头孢菌素治疗的患者复发率较高[26/87例(30%)对27/154例(17%);P = 0.03]。在通过PS进行治疗权重逆概率控制的多变量分析中,最后1个月作为CDI前最后一种抗生素方案接受5天哌拉西林/他唑巴坦治疗与较低的复发风险独立相关[调整后比值比(AOR)0.13;95%置信区间:0.06 - 0.29;P < 0.0001],而暴露于头孢菌素5天(与哌拉西林/他唑巴坦相比)与复发风险增加相关(AOR 10.9;95%置信区间:4.4 - 27.1;P < 0.0001)。
近期使用哌拉西林/他唑巴坦可能与较低的CDI复发风险相关,而近期使用头孢菌素可能会增加复发风险。在治疗住院患者时应考虑这些发现。