Hirai Jun, Mori Nobuaki, Hanai Yuki, Asai Nobuhiro, Hagihara Mao, Mikamo Hiroshige
Department of Clinical Infectious Diseases, Aichi Medical University Hospital, Aichi 480-1195, Japan.
Department of Infection Control and Prevention, Aichi Medical University Hospital, Aichi 480-1195, Japan.
Antibiotics (Basel). 2025 Feb 24;14(3):228. doi: 10.3390/antibiotics14030228.
infection (CDI) poses a significant healthcare challenge, with recurrence rates reaching 30%, leading to substantial morbidity and costs. Fidaxomicin (FDX) and bezlotoxumab (BEZ) have shown potential in reducing recurrence; however, real-world data on the efficacy of their combination in high-risk CDI patients remain limited. This study aimed to evaluate the efficacy and safety of FDX + BEZ compared with FDX alone in CDI patients with recurrence risk factors. CDI patients with ≥two recurrence risk factors treated with FDX alone or FDX + BEZ were analyzed. Sixteen factors were evaluated as risk factors for recurrent CDI based on findings from previous studies. Patients with FDX treatment duration <10 days or other CDI treatment prior to FDX were excluded. Outcomes included recurrence within 2 months, global and clinical cure rates, and adverse events. Univariate and multivariate analyses were performed to evaluate efficacy. Among 82 patients, the FDX + BEZ group ( = 30) demonstrated significantly higher global (86.7% vs. 65.4%; < 0.05) and clinical cure rates (90.0% vs. 69.2%; < 0.05) compared with the FDX-alone group ( = 52), despite more severe cases in the combination group. Recurrence rates were non-significantly lower in the FDX + BEZ group (3.3% vs. 11.5%). Combination therapy also accelerated diarrhea resolution without additional adverse events. Multivariate analysis identified FDX + BEZ as significantly associated with improved clinical cure (adjusted odds ratio 4.167; 95% CI: 1.029-16.885). FDX + BEZ therapy offers superior efficacy and safety in CDI patients with recurrence risk factors, presenting a promising strategy for optimizing CDI management.
艰难梭菌感染(CDI)对医疗保健构成重大挑战,复发率高达30%,会导致严重的发病率和成本。非达霉素(FDX)和贝佐托昔单抗(BEZ)在降低复发率方面已显示出潜力;然而,关于它们联合使用对高危CDI患者疗效的真实世界数据仍然有限。本研究旨在评估FDX + BEZ与单独使用FDX相比,在具有复发风险因素的CDI患者中的疗效和安全性。分析了单独使用FDX或FDX + BEZ治疗的具有≥两个复发风险因素的CDI患者。根据先前研究的结果,评估了16个因素作为复发性CDI的风险因素。排除FDX治疗持续时间<10天或在FDX之前接受过其他CDI治疗的患者。结局包括2个月内的复发、总体治愈率和临床治愈率以及不良事件。进行单因素和多因素分析以评估疗效。在82例患者中,与单独使用FDX组(n = 52)相比,FDX + BEZ组(n = 30)的总体治愈率(86.7%对65.4%;P < 0.05)和临床治愈率(90.0%对69.2%;P < 0.05)显著更高,尽管联合治疗组的病例更严重。FDX + BEZ组的复发率略低于单独使用FDX组(3.3%对11.5%),差异无统计学意义。联合治疗还加速了腹泻的缓解,且无额外不良事件。多因素分析确定FDX + BEZ与改善临床治愈显著相关(调整后的优势比4.167;95%置信区间:1.029 - 16.885)。FDX + BEZ疗法在具有复发风险因素的CDI患者中具有卓越的疗效和安全性,为优化CDI管理提供了一种有前景的策略。